Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 88455 |
| ensemblid | ENSG00000076513.17 |
| hgncid | 21268 |
| symbol | ANKRD13A |
| name | ankyrin repeat domain 13A |
| refseq_nuc | NM_033121.2 |
| refseq_prot | NP_149112.1 |
| ensembl_nuc | ENST00000261739.9 |
| ensembl_prot | ENSP00000261739.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109999430 |
| end | 110039763 |
| strand | + |
| ver | v1.2 |
| region | chr12:109999430-110039763 |
| region5000 | chr12:109994430-110044763 |
| regionname0 | ANKRD13A_chr12_109999430_110039763 |
| regionname5000 | ANKRD13A_chr12_109994430_110044763 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 590 | 237 | 71 | 57 | 65 | 10 | 32 | 48 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | MSSAC others(585): Show |
chr12 | 109994430 | 110044763 |
| a0002 | 0/0 | 590 | 35 | 12 | 1 | 20 | 0 | 2 | 16 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | MSSAC others(585): Show |
chr12 | 109994430 | 110044763 |
| a0003 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | MSSAC others(585): Show |
chr12 | 109994430 | 110044763 |
| a0004 | 0/0 | 590 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | MSSAC others(585): Show |
chr12 | 109994430 | 110044763 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1770 | 163 | 25 | 41 | 58 | 9 | 28 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 | ||
| a0001c0002 | 0/0 | 1770 | 71 | 43 | 16 | 7 | 1 | 4 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 | ||
| a0001c0004 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 | ||
| a0001c0006 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 | ||
| a0002c0003 | 0/0 | 1770 | 35 | 12 | 1 | 20 | 0 | 2 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 | ||
| a0003c0005 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 | ||
| a0004c0007 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | ATGTC others(1765): Show |
chr12 | 109994430 | 110044763 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4241 | 151 | 23 | 37 | 56 | 9 | 24 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0006 | 0/0 | 4242 | 4 | 2 | 0 | 2 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0009 | 0/0 | 4241 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0012 | 0/0 | 4241 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0013 | 0/0 | 4241 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0014 | 0/0 | 4241 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0015 | 0/0 | 4241 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0018 | 0/0 | 4241 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0019 | 0/0 | 4241 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0001t0021 | 0/0 | 4241 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0001 | 0/0 | 4241 | 13 | 5 | 7 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0002 | 0/0 | 4241 | 29 | 21 | 1 | 6 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0003 | 0/0 | 4242 | 18 | 11 | 5 | 1 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0005 | 0/0 | 4242 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0007 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0008 | 0/0 | 4241 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0010 | 0/0 | 4241 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0016 | 0/0 | 4241 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0002t0017 | 0/0 | 4241 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0004t0001 | 0/0 | 4241 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0001c0006t0004 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0002c0003t0003 | 0/0 | 4242 | 8 | 7 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0002c0003t0004 | 0/0 | 4242 | 25 | 4 | 0 | 19 | 0 | 2 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0002c0003t0011 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0002c0003t0020 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| a0003c0005t0001 | 0/0 | 4241 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4236): Show |
chr12 | 109994430 | 110044763 |
| a0004c0007t0005 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | AGAAG others(4237): Show |
chr12 | 109994430 | 110044763 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 7 | 1 | 3 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 1 | 5 | 0 | 3 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0011 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0012g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0013g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0014g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0015g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0018g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0019g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0001t0021g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0006 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0008g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0016g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0002t0017g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0001c0006t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0002c0003t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0003c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| a0004c0007t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0137 | EUR | FIN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00423 | hp1 | a0002 | c0003 | t0004 | g0192 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00558 | hp2 | a0002 | c0003 | t0004 | g0181 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0016 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00738 | hp1 | a0001 | c0002 | t0008 | g0030 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01069 | hp2 | a0001 | c0002 | t0008 | g0030 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01099 | hp1 | a0001 | c0002 | t0005 | g0167 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0171 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01109 | hp2 | a0002 | c0003 | t0003 | g0187 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0132 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0145 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01192 | hp2 | a0001 | c0001 | t0015 | g0011 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0146 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01258 | hp1 | a0001 | c0001 | t0014 | g0069 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01884 | hp1 | a0002 | c0003 | t0004 | g0185 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01884 | hp2 | a0002 | c0003 | t0003 | g0190 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0138 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02040 | hp2 | a0002 | c0003 | t0004 | g0033 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0160 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02071 | hp1 | a0003 | c0005 | t0001 | g0087 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02071 | hp2 | a0002 | c0003 | t0004 | g0193 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0168 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02257 | hp1 | a0002 | c0003 | t0003 | g0035 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02257 | hp2 | a0004 | c0007 | t0005 | g0141 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02258 | hp2 | a0002 | c0003 | t0004 | g0178 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02293 | hp2 | a0001 | c0001 | t0018 | g0007 | AMR | PEL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0175 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02572 | hp2 | a0001 | c0006 | t0004 | g0041 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02698 | hp2 | a0002 | c0003 | t0004 | g0195 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02717 | hp2 | a0001 | c0002 | t0005 | g0166 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0031 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0003 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0179 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02970 | hp2 | a0002 | c0003 | t0004 | g0034 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0156 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03041 | hp1 | a0002 | c0003 | t0003 | g0035 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03098 | hp1 | a0002 | c0003 | t0011 | g0186 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03139 | hp2 | a0002 | c0003 | t0003 | g0191 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0139 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0164 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0143 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03490 | hp2 | a0001 | c0002 | t0016 | g0150 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0140 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0072 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03942 | hp1 | a0001 | c0001 | t0019 | g0005 | SAS | BEB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03942 | hp2 | a0001 | c0002 | t0017 | g0172 | SAS | BEB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG04115 | hp1 | a0002 | c0003 | t0004 | g0198 | SAS | STU | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0155 | SAS | BEB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0103 | SAS | STU | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18522 | hp1 | a0002 | c0003 | t0004 | g0034 | AFR | YRI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | YRI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18947 | hp2 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18948 | hp1 | a0002 | c0003 | t0004 | g0182 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18949 | hp1 | a0002 | c0003 | t0004 | g0184 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18954 | hp2 | a0002 | c0003 | t0004 | g0176 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18959 | hp1 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18973 | hp2 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18989 | hp2 | a0002 | c0003 | t0004 | g0177 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19001 | hp2 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19010 | hp1 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0154 | AFR | LWK | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | LWK | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19056 | hp2 | a0002 | c0003 | t0004 | g0183 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19063 | hp2 | a0002 | c0003 | t0004 | g0196 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19075 | hp1 | a0002 | c0003 | t0020 | g0194 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19077 | hp1 | a0002 | c0003 | t0004 | g0197 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19081 | hp1 | a0002 | c0003 | t0004 | g0014 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19088 | hp1 | a0002 | c0003 | t0004 | g0033 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19090 | hp2 | a0002 | c0003 | t0004 | g0180 | EAS | JPT | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | YRI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0162 | AFR | YRI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA20905 | hp1 | a0001 | c0001 | t0021 | g0076 | SAS | GIH | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02109 | hp1 | a0002 | c0003 | t0003 | g0188 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0144 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02486 | hp1 | a0001 | c0002 | t0007 | g0159 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0163 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | ACB | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03471 | hp1 | a0001 | c0002 | t0010 | g0161 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0149 | AFR | MSL | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA20300 | hp2 | a0002 | c0003 | t0003 | g0189 | AFR | USA | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | LWK | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0057 | REF | REF | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | ANKRD13A_chr12_109994430_110044763 | ANKRD13A | chr12 | 109994430 | 110044763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110028576 | A | G | 1 | a0004 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1010A>G | p.Asn337Ser | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/15 | 1269/4241 | 1010/1773 | 337/590 | chr12 | 110028576 | |||
| chr12:110033884 | A | G | 1 | a0003 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1436A>G | p.His479Arg | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/15 | 1695/4241 | 1436/1773 | 479/590 | chr12 | 110033884 | |||
| chr12:110036265 | T | C | 1 | a0002 | 35 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(32): Show |
missense_variant | MODERATE | c.1514T>C | p.Leu505Pro | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/15 | 1773/4241 | 1514/1773 | 505/590 | chr12 | 110036265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110018370 | A | G | 4 | a0001c0002 a0001c0006 a0002c0003 others(1): Show |
108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
synonymous_variant | LOW | c.426A>G | p.Pro142Pro | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 5/15 | 685/4241 | 426/1773 | 142/590 | chr12 | 110018370 | |||
| chr12:110033828 | A | G | 2 | a0001c0004 a0001c0006 |
3 | HG02559.hp1 HG02572.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.1380A>G | p.Gln460Gln | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/15 | 1639/4241 | 1380/1773 | 460/590 | chr12 | 110033828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109999499 | G | A | 1 | a0001c0001t0009 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-190G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/15 | 190 | chr12 | 109999499 | ||||||
| chr12:109999557 | A | C | 1 | a0001c0001t0021 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/15 | 132 | chr12 | 109999557 | ||||||
| chr12:110037732 | C | T | 3 | a0001c0006t0004 a0002c0003t0004 a0002c0003t0020 |
27 | HG00423.hp1 HG00558.hp2 HG01884.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*178C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 178 | chr12 | 110037732 | ||||||
| chr12:110037875 | T | C | 2 | a0001c0002t0007 a0001c0002t0010 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*321T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 321 | chr12 | 110037875 | ||||||
| chr12:110038042 | A | T | 1 | a0002c0003t0020 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 488 | chr12 | 110038042 | ||||||
| chr12:110038043 | T | A | 1 | a0002c0003t0020 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 489 | chr12 | 110038043 | ||||||
| chr12:110038080 | T | A | 1 | a0002c0003t0011 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*526T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 526 | chr12 | 110038080 | ||||||
| chr12:110038306 | G | A | 1 | a0001c0001t0012 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*752G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 752 | chr12 | 110038306 | ||||||
| chr12:110038327 | C | T | 1 | a0002c0003t0020 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 773 | chr12 | 110038327 | ||||||
| chr12:110038328 | A | C | 1 | a0002c0003t0020 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 774 | chr12 | 110038328 | ||||||
| chr12:110038489 | C | T | 1 | a0001c0002t0008 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*935C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 935 | chr12 | 110038489 | ||||||
| chr12:110038573 | T | C | 1 | a0001c0001t0013 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1019 | chr12 | 110038573 | ||||||
| chr12:110038594 | T | G | 1 | a0001c0001t0014 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1040T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1040 | chr12 | 110038594 | ||||||
| chr12:110038741 | T | C | 1 | a0001c0001t0015 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1187 | chr12 | 110038741 | ||||||
| chr12:110038790 | T | A | 12 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0007 others(9): Show |
90 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1236T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1236 | chr12 | 110038790 | ||||||
| chr12:110039068 | G | GT | 8 | a0001c0001t0006 a0001c0002t0003 a0001c0002t0007 others(5): Show |
60 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1526dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1527 | INFO_REALIGN_3_PRIME | chr12 | 110039068 | |||||
| chr12:110039068 | G | T | 1 | a0001c0002t0017 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1514G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1514 | chr12 | 110039068 | ||||||
| chr12:110039069 | T | G | 1 | a0001c0001t0018 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1515T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1515 | chr12 | 110039069 | ||||||
| chr12:110039535 | G | A | 1 | a0001c0001t0019 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 1981 | chr12 | 110039535 | ||||||
| chr12:110039630 | C | G | 1 | a0001c0002t0016 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2076C>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 2076 | chr12 | 110039630 | ||||||
| chr12:110039727 | C | CA | 2 | a0001c0002t0005 a0004c0007t0005 |
5 | HG01099.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2174dupA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 15/15 | 2175 | INFO_REALIGN_3_PRIME | chr12 | 110039727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109999792 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | NA19054.hp2 NA19074.hp2 NA19088.hp2 |
splice_region_variant&intron_variant | LOW | c.96+8G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 109999792 | |||||||
| chr12:109999816 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.96+32T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 109999816 | |||||||
| chr12:109999957 | G | A | 1 | a0001c0006t0004g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.96+173G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 109999957 | |||||||
| chr12:110000349 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.96+565T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110000349 | |||||||
| chr12:110000351 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.96+567A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110000351 | |||||||
| chr12:110000433 | G | T | 83 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(80): Show |
108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.96+649G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110000433 | |||||||
| chr12:110000504 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG00609.hp2 HG00621.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.96+720A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110000504 | |||||||
| chr12:110000714 | C | T | 29 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(26): Show |
36 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+930C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110000714 | |||||||
| chr12:110000755 | C | CT | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0026 others(46): Show |
65 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.96+990dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110000755 | ||||||
| chr12:110000755 | CT | C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
11 | HG00323.hp1 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+990delT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110000755 | ||||||
| chr12:110001105 | G | C | 40 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(37): Show |
53 | HG00735.hp2 HG01106.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.96+1321G>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001105 | |||||||
| chr12:110001391 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.96+1607G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001391 | |||||||
| chr12:110001402 | G | GA | 29 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(26): Show |
36 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+1620dupA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110001402 | ||||||
| chr12:110001404 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.96+1620A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001404 | |||||||
| chr12:110001436 | CT | C | 6 | a0001c0001t0001g0050 a0001c0002t0003g0031 a0001c0002t0003g0132 others(3): Show |
7 | HG00735.hp2 HG01106.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+1667delT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110001436 | ||||||
| chr12:110001446 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.96+1662T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001446 | |||||||
| chr12:110001468 | C | A | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.96+1684C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001468 | |||||||
| chr12:110001479 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+1695A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001479 | |||||||
| chr12:110001526 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.96+1742G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001526 | |||||||
| chr12:110001542 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+1758C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001542 | |||||||
| chr12:110001575 | G | A | 1 | a0002c0003t0004g0181 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.96+1791G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001575 | |||||||
| chr12:110001637 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(21): Show |
30 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.96+1853T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001637 | |||||||
| chr12:110001709 | T | C | 4 | a0002c0003t0004g0013 a0002c0003t0004g0181 a0002c0003t0004g0182 others(1): Show |
6 | HG00558.hp2 NA18947.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1925T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001709 | |||||||
| chr12:110001830 | T | G | 16 | a0001c0002t0003g0012 a0001c0002t0003g0031 a0001c0002t0003g0132 others(13): Show |
19 | HG00735.hp2 HG01106.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+2046T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110001830 | |||||||
| chr12:110002254 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+2470A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110002254 | |||||||
| chr12:110002313 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.96+2529A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110002313 | |||||||
| chr12:110002354 | T | C | 70 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(67): Show |
91 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+2570T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110002354 | |||||||
| chr12:110002784 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.96+3000G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110002784 | |||||||
| chr12:110003248 | G | A | 1 | a0001c0002t0005g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+3464G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110003248 | |||||||
| chr12:110003321 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.96+3537C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110003321 | |||||||
| chr12:110003498 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.96+3714G>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110003498 | |||||||
| chr12:110003797 | G | A | 3 | a0002c0003t0004g0033 a0002c0003t0004g0176 a0002c0003t0004g0184 |
4 | HG02040.hp2 NA18949.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4013G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110003797 | |||||||
| chr12:110003896 | C | T | 1 | a0001c0002t0002g0162 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.96+4112C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110003896 | |||||||
| chr12:110003925 | A | G | 30 | a0001c0002t0008g0030 a0001c0006t0004g0041 a0002c0003t0003g0035 others(27): Show |
38 | HG00423.hp1 HG00558.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+4141A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110003925 | |||||||
| chr12:110004036 | T | C | 30 | a0001c0002t0008g0030 a0001c0006t0004g0041 a0002c0003t0003g0035 others(27): Show |
38 | HG00423.hp1 HG00558.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+4252T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004036 | |||||||
| chr12:110004063 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.96+4279T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004063 | |||||||
| chr12:110004168 | T | A | 1 | a0002c0003t0004g0177 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.96+4384T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004168 | |||||||
| chr12:110004229 | G | A | 2 | a0001c0002t0003g0138 a0001c0002t0003g0139 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.96+4445G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004229 | |||||||
| chr12:110004236 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.96+4452C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004236 | |||||||
| chr12:110004254 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.96+4470G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004254 | |||||||
| chr12:110004315 | A | G | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4531A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004315 | |||||||
| chr12:110004420 | A | T | 1 | a0002c0003t0004g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.96+4636A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004420 | |||||||
| chr12:110004445 | G | A | 1 | a0001c0002t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.96+4661G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004445 | |||||||
| chr12:110004612 | C | T | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96+4828C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004612 | |||||||
| chr12:110004686 | T | C | 1 | a0002c0003t0004g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+4902T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004686 | |||||||
| chr12:110004842 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.96+5058C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004842 | |||||||
| chr12:110004927 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.96+5143C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110004927 | |||||||
| chr12:110005001 | G | C | 70 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(67): Show |
91 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+5217G>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110005001 | |||||||
| chr12:110005006 | A | AT | 83 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(80): Show |
108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.96+5228dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110005006 | ||||||
| chr12:110005308 | A | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0100 others(7): Show |
13 | HG01928.hp1 HG02698.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+5524A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110005308 | |||||||
| chr12:110005509 | C | T | 1 | a0001c0001t0006g0047 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.96+5725C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110005509 | |||||||
| chr12:110005654 | G | A | 70 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(67): Show |
91 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.96+5870G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110005654 | |||||||
| chr12:110005800 | G | T | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.96+6016G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110005800 | |||||||
| chr12:110006041 | T | C | 1 | a0002c0003t0004g0184 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.97-5964T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110006041 | |||||||
| chr12:110006388 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.97-5617G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110006388 | |||||||
| chr12:110006602 | C | CT | 7 | a0001c0001t0001g0025 a0001c0002t0003g0012 a0001c0002t0003g0132 others(4): Show |
10 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-5392dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110006602 | ||||||
| chr12:110006745 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0104 a0001c0001t0013g0103 |
3 | HG02698.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.97-5260C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110006745 | |||||||
| chr12:110006870 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0100 others(7): Show |
13 | HG01928.hp1 HG02698.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-5135A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110006870 | |||||||
| chr12:110006895 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.97-5110C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110006895 | |||||||
| chr12:110006965 | C | T | 8 | a0002c0003t0004g0014 a0002c0003t0004g0177 a0002c0003t0004g0180 others(5): Show |
10 | HG02698.hp2 HG04115.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-5040C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110006965 | |||||||
| chr12:110007124 | T | C | 2 | a0001c0002t0007g0159 a0001c0002t0007g0160 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-4881T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007124 | |||||||
| chr12:110007287 | G | A | 4 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0147 others(1): Show |
9 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-4718G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007287 | |||||||
| chr12:110007437 | A | G | 2 | a0001c0002t0007g0159 a0001c0002t0007g0160 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-4568A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007437 | |||||||
| chr12:110007537 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0099 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.97-4468C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007537 | |||||||
| chr12:110007611 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-4394C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007611 | |||||||
| chr12:110007612 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-4393T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007612 | |||||||
| chr12:110007692 | A | G | 29 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(26): Show |
36 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.97-4313A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110007692 | |||||||
| chr12:110008169 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | NA19054.hp2 NA19074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.97-3836C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008169 | |||||||
| chr12:110008340 | A | G | 2 | a0001c0002t0003g0138 a0001c0002t0003g0139 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.97-3665A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008340 | |||||||
| chr12:110008449 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97-3556G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008449 | |||||||
| chr12:110008496 | G | C | 69 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(66): Show |
89 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.97-3509G>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008496 | |||||||
| chr12:110008559 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.97-3446A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008559 | |||||||
| chr12:110008621 | G | A | 73 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0062 others(70): Show |
97 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.97-3384G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008621 | |||||||
| chr12:110008715 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.97-3290A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008715 | |||||||
| chr12:110008783 | G | A | 20 | a0001c0006t0004g0041 a0002c0003t0004g0013 a0002c0003t0004g0014 others(17): Show |
26 | HG00558.hp2 HG01884.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.97-3222G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008783 | |||||||
| chr12:110008860 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97-3145G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008860 | |||||||
| chr12:110008873 | A | G | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-3132A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008873 | |||||||
| chr12:110008885 | G | GA | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0116 others(2): Show |
5 | HG01081.hp1 HG02293.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-3112dupA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110008885 | ||||||
| chr12:110008917 | T | G | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97-3088T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008917 | |||||||
| chr12:110008981 | CTTTTT | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
6 | HG01192.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-3023_97-3019del others(5): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110008981 | |||||||
| chr12:110009146 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97-2859A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009146 | |||||||
| chr12:110009150 | C | T | 2 | a0001c0002t0005g0167 a0001c0002t0005g0168 |
2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.97-2855C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009150 | |||||||
| chr12:110009175 | G | A | 1 | a0001c0002t0010g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-2830G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009175 | |||||||
| chr12:110009450 | T | C | 29 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(26): Show |
36 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.97-2555T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009450 | |||||||
| chr12:110009474 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.97-2531T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009474 | |||||||
| chr12:110009609 | A | G | 3 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0158 |
5 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-2396A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009609 | |||||||
| chr12:110009708 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.97-2297A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009708 | |||||||
| chr12:110009896 | G | A | 1 | a0001c0002t0002g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97-2109G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009896 | |||||||
| chr12:110009920 | A | G | 1 | a0001c0002t0010g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-2085A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110009920 | |||||||
| chr12:110010118 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.97-1887C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010118 | |||||||
| chr12:110010138 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97-1867A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010138 | |||||||
| chr12:110010273 | C | T | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-1732C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010273 | |||||||
| chr12:110010357 | C | A | 1 | a0001c0002t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.97-1648C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010357 | |||||||
| chr12:110010378 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(162): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.97-1627T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010378 | |||||||
| chr12:110010397 | G | T | 27 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(24): Show |
34 | HG00558.hp2 HG01109.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.97-1608G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010397 | |||||||
| chr12:110010451 | A | G | 81 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(78): Show |
106 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-1554A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010451 | |||||||
| chr12:110010600 | T | C | 18 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(15): Show |
28 | HG01167.hp1 HG02055.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.97-1405T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010600 | |||||||
| chr12:110010747 | A | G | 2 | a0001c0002t0007g0159 a0001c0002t0007g0160 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-1258A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010747 | |||||||
| chr12:110010868 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.97-1137G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110010868 | |||||||
| chr12:110011108 | GA | G | 68 | a0001c0002t0001g0137 a0001c0002t0002g0003 a0001c0002t0002g0009 others(65): Show |
89 | HG00323.hp1 HG00558.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.97-883delA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110011108 | ||||||
| chr12:110011144 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0086 a0001c0002t0001g0170 |
4 | HG03041.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-861A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011144 | |||||||
| chr12:110011274 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.97-731G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011274 | |||||||
| chr12:110011368 | G | A | 8 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(5): Show |
12 | HG00323.hp1 HG00642.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-637G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011368 | |||||||
| chr12:110011406 | C | T | 1 | a0001c0004t0001g0021 | 2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.97-599C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011406 | |||||||
| chr12:110011472 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.97-533G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011472 | |||||||
| chr12:110011487 | G | A | 1 | a0001c0002t0003g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97-518G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011487 | |||||||
| chr12:110011495 | C | A | 11 | a0001c0002t0002g0009 a0001c0002t0002g0028 a0001c0002t0002g0029 others(8): Show |
16 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-510C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011495 | |||||||
| chr12:110011567 | T | C | 2 | a0001c0002t0003g0140 a0001c0002t0003g0163 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.97-438T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011567 | |||||||
| chr12:110011934 | A | G | 11 | a0001c0002t0002g0009 a0001c0002t0002g0028 a0001c0002t0002g0029 others(8): Show |
16 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-71A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 1/14 | chr12 | 110011934 | |||||||
| chr12:110012227 | C | T | 5 | a0002c0003t0003g0035 a0002c0003t0003g0179 a0002c0003t0003g0189 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.229+90C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012227 | |||||||
| chr12:110012476 | G | A | 2 | a0002c0003t0003g0187 a0002c0003t0003g0188 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.229+339G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012476 | |||||||
| chr12:110012534 | C | T | 1 | a0002c0003t0004g0197 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.229+397C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012534 | |||||||
| chr12:110012742 | T | C | 3 | a0001c0002t0002g0157 a0001c0002t0002g0174 a0001c0002t0002g0175 |
3 | HG02572.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.230-383T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012742 | |||||||
| chr12:110012779 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.230-346C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012779 | |||||||
| chr12:110012787 | C | G | 21 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(18): Show |
31 | HG01167.hp1 HG02055.hp2 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.230-338C>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012787 | |||||||
| chr12:110012818 | A | G | 1 | a0001c0001t0006g0020 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.230-307A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012818 | |||||||
| chr12:110012881 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0105 |
2 | NA18959.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.230-244G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012881 | |||||||
| chr12:110012882 | C | G | 83 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(80): Show |
108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.230-243C>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012882 | |||||||
| chr12:110012917 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.230-208A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012917 | |||||||
| chr12:110012962 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.230-163A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110012962 | |||||||
| chr12:110013100 | T | C | 3 | a0001c0002t0002g0157 a0001c0002t0002g0174 a0001c0002t0002g0175 |
3 | HG02572.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.230-25T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 2/14 | chr12 | 110013100 | |||||||
| chr12:110013320 | A | T | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.354+71A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110013320 | |||||||
| chr12:110013375 | A | C | 4 | a0001c0002t0005g0164 a0001c0002t0005g0166 a0001c0002t0005g0167 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+126A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110013375 | |||||||
| chr12:110013800 | T | C | 40 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(37): Show |
53 | HG00735.hp2 HG01106.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.354+551T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110013800 | |||||||
| chr12:110013876 | T | TAGGTGCC others(327): Show |
1 | a0002c0003t0003g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.354+643_354+644ins others(334): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110013876 | ||||||
| chr12:110014085 | T | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0099 a0001c0001t0014g0069 |
3 | HG01167.hp2 HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.354+836T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110014085 | |||||||
| chr12:110014209 | G | A | 3 | a0002c0003t0004g0033 a0002c0003t0004g0176 a0002c0003t0004g0184 |
4 | HG02040.hp2 NA18949.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+960G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110014209 | |||||||
| chr12:110014269 | G | A | 2 | a0001c0001t0001g0051 a0003c0005t0001g0087 |
2 | HG02071.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.354+1020G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110014269 | |||||||
| chr12:110014320 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.354+1071G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110014320 | |||||||
| chr12:110014789 | C | CTTTTTTT others(5): Show |
14 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(11): Show |
24 | HG01167.hp1 HG02055.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.354+1541_354+1552d others(14): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110014789 | ||||||
| chr12:110014789 | C | CTTTTTTT others(6): Show |
23 | a0001c0002t0002g0148 a0001c0002t0002g0153 a0001c0002t0002g0154 others(20): Show |
27 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.354+1552_354+1553i others(15): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110014789 | ||||||
| chr12:110014789 | C | CTTTTTTT others(7): Show |
22 | a0001c0002t0002g0175 a0001c0002t0003g0146 a0001c0002t0007g0159 others(19): Show |
29 | HG00423.hp1 HG00558.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.354+1552_354+1553i others(16): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110014789 | ||||||
| chr12:110014789 | C | CTTTTTTT others(8): Show |
9 | a0001c0002t0003g0173 a0001c0002t0007g0160 a0002c0003t0004g0180 others(6): Show |
9 | HG02055.hp1 HG02071.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.354+1552_354+1553i others(17): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110014789 | ||||||
| chr12:110014789 | C | CTTTTTTT others(9): Show |
2 | a0002c0003t0003g0187 a0002c0003t0003g0188 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.354+1552_354+1553i others(18): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110014789 | ||||||
| chr12:110014909 | G | A | 21 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(18): Show |
31 | HG01167.hp1 HG02055.hp2 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.355-1479G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110014909 | |||||||
| chr12:110014950 | A | AT | 3 | a0001c0002t0003g0142 a0002c0003t0004g0014 a0004c0007t0005g0141 |
5 | HG02257.hp2 HG02559.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-1427dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110014950 | ||||||
| chr12:110015068 | G | A | 3 | a0001c0002t0002g0157 a0001c0002t0002g0174 a0001c0002t0002g0175 |
3 | HG02572.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.355-1320G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015068 | |||||||
| chr12:110015104 | A | G | 3 | a0001c0002t0002g0157 a0001c0002t0002g0174 a0001c0002t0002g0175 |
3 | HG02572.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.355-1284A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015104 | |||||||
| chr12:110015140 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.355-1248G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015140 | |||||||
| chr12:110015398 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.355-990C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015398 | |||||||
| chr12:110015523 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.355-865A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015523 | |||||||
| chr12:110015767 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.355-621G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015767 | |||||||
| chr12:110015953 | C | CT | 32 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0002t0002g0147 others(29): Show |
38 | HG00423.hp1 HG00558.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.355-420dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110015953 | ||||||
| chr12:110015953 | C | CTT | 7 | a0001c0002t0002g0156 a0001c0002t0005g0168 a0002c0003t0003g0035 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-421_355-420dup others(2): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110015953 | ||||||
| chr12:110015957 | T | C | 1 | a0001c0002t0010g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.355-431T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015957 | |||||||
| chr12:110015983 | G | A | 2 | a0001c0001t0001g0129 a0001c0002t0002g0162 |
2 | HG00609.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.355-405G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110015983 | |||||||
| chr12:110016181 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.355-207G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110016181 | |||||||
| chr12:110016282 | T | C | 5 | a0001c0002t0005g0164 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01099.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-106T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 3/14 | chr12 | 110016282 | |||||||
| chr12:110016585 | C | T | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.400+152C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110016585 | |||||||
| chr12:110016626 | G | A | 2 | a0001c0002t0003g0138 a0001c0002t0003g0139 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.400+193G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110016626 | |||||||
| chr12:110016682 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG01934.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.400+249T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110016682 | |||||||
| chr12:110016713 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.400+280A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110016713 | |||||||
| chr12:110016883 | A | T | 9 | a0001c0002t0003g0012 a0001c0002t0003g0132 a0001c0002t0003g0138 others(6): Show |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.400+450A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110016883 | |||||||
| chr12:110016919 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0099 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.400+486C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110016919 | |||||||
| chr12:110017052 | G | A | 1 | a0001c0002t0002g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400+619G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017052 | |||||||
| chr12:110017130 | G | A | 1 | a0001c0002t0003g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.400+697G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017130 | |||||||
| chr12:110017384 | C | T | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.400+951C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017384 | |||||||
| chr12:110017553 | G | A | 11 | a0001c0002t0002g0009 a0001c0002t0002g0028 a0001c0002t0002g0029 others(8): Show |
16 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.401-792G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017553 | |||||||
| chr12:110017761 | C | T | 5 | a0002c0003t0003g0035 a0002c0003t0003g0179 a0002c0003t0003g0189 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-584C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017761 | |||||||
| chr12:110017788 | C | T | 2 | a0001c0002t0003g0132 a0001c0002t0003g0145 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.401-557C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017788 | |||||||
| chr12:110017946 | G | A | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-399G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110017946 | |||||||
| chr12:110018222 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.401-123C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 4/14 | chr12 | 110018222 | |||||||
| chr12:110018678 | T | C | 1 | a0001c0002t0003g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544+190T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 5/14 | chr12 | 110018678 | |||||||
| chr12:110018833 | C | G | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.545-306C>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 5/14 | chr12 | 110018833 | |||||||
| chr12:110018899 | G | A | 69 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(66): Show |
90 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.545-240G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 5/14 | chr12 | 110018899 | |||||||
| chr12:110019769 | A | ATGTT | 2 | a0001c0001t0001g0064 a0001c0002t0008g0030 |
3 | HG00438.hp2 HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.734+467_734+470dup others(4): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 110019769 | ||||||
| chr12:110019769 | ATGTT | A | 4 | a0001c0002t0005g0164 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.734+467_734+470del others(4): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 110019769 | ||||||
| chr12:110019861 | G | T | 1 | a0001c0002t0003g0144 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.734+533G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110019861 | |||||||
| chr12:110020058 | G | T | 1 | a0001c0006t0004g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.734+730G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020058 | |||||||
| chr12:110020212 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0058 |
3 | HG00642.hp2 HG02258.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.734+884T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020212 | |||||||
| chr12:110020296 | C | T | 29 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(26): Show |
36 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.734+968C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020296 | |||||||
| chr12:110020417 | T | C | 1 | a0002c0003t0004g0181 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.734+1089T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020417 | |||||||
| chr12:110020422 | T | C | 6 | a0001c0002t0003g0012 a0001c0002t0003g0132 a0001c0002t0003g0143 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.734+1094T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020422 | |||||||
| chr12:110020727 | A | G | 83 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(80): Show |
108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.734+1399A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020727 | |||||||
| chr12:110020728 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.734+1400G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020728 | |||||||
| chr12:110020753 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.734+1425C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110020753 | |||||||
| chr12:110021032 | G | A | 1 | a0001c0002t0007g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.734+1704G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110021032 | |||||||
| chr12:110021417 | T | C | 2 | a0002c0003t0003g0187 a0002c0003t0003g0188 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.734+2089T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110021417 | |||||||
| chr12:110021425 | C | CT | 7 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0093 others(4): Show |
8 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.734+2115dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 110021425 | ||||||
| chr12:110021425 | CT | C | 57 | a0001c0001t0001g0054 a0001c0001t0001g0083 a0001c0001t0009g0072 others(54): Show |
73 | HG00423.hp1 HG00558.hp2 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.734+2115delT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 110021425 | ||||||
| chr12:110021499 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0054 others(6): Show |
11 | HG00280.hp2 HG01070.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+2171C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110021499 | |||||||
| chr12:110021627 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.734+2299G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110021627 | |||||||
| chr12:110021680 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0092 |
6 | HG00423.hp2 HG02040.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.734+2352C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110021680 | |||||||
| chr12:110022059 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0099 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.735-1987T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022059 | |||||||
| chr12:110022145 | T | C | 1 | a0001c0002t0002g0162 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.735-1901T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022145 | |||||||
| chr12:110022199 | C | T | 4 | a0001c0002t0002g0009 a0001c0002t0002g0151 a0001c0002t0002g0152 others(1): Show |
7 | HG04184.hp1 NA18948.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.735-1847C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022199 | |||||||
| chr12:110022221 | G | A | 11 | a0001c0002t0002g0009 a0001c0002t0002g0028 a0001c0002t0002g0029 others(8): Show |
16 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.735-1825G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022221 | |||||||
| chr12:110022238 | G | A | 4 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0147 others(1): Show |
9 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.735-1808G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022238 | |||||||
| chr12:110022387 | T | C | 3 | a0001c0002t0002g0157 a0001c0002t0002g0174 a0001c0002t0002g0175 |
3 | HG02572.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.735-1659T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022387 | |||||||
| chr12:110022485 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0081 |
5 | HG02647.hp1 HG03516.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-1561A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110022485 | |||||||
| chr12:110023496 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.735-550T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110023496 | |||||||
| chr12:110023673 | G | A | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.735-373G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110023673 | |||||||
| chr12:110023755 | C | T | 5 | a0001c0002t0005g0164 a0001c0002t0005g0166 a0001c0002t0005g0167 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.735-291C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 6/14 | chr12 | 110023755 | |||||||
| chr12:110024143 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.801+31T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110024143 | |||||||
| chr12:110024411 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.801+299A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110024411 | |||||||
| chr12:110024576 | G | A | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.801+464G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110024576 | |||||||
| chr12:110024661 | G | T | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.801+549G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110024661 | |||||||
| chr12:110024663 | T | C | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.801+551T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110024663 | |||||||
| chr12:110024664 | TTTGGTG | T | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.801+557_801+562del others(6): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 110024664 | ||||||
| chr12:110024720 | A | G | 1 | a0001c0002t0002g0029 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.801+608A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110024720 | |||||||
| chr12:110025070 | C | T | 68 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(65): Show |
88 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.802-672C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110025070 | |||||||
| chr12:110025184 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802-558C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110025184 | |||||||
| chr12:110025263 | C | T | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.802-479C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110025263 | |||||||
| chr12:110025271 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0079 |
4 | HG02717.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-471G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110025271 | |||||||
| chr12:110025355 | C | CA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0062 others(8): Show |
11 | HG00609.hp2 HG02071.hp2 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.802-367dupA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 110025355 | ||||||
| chr12:110025355 | CA | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0056 others(12): Show |
16 | HG01069.hp1 HG01257.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.802-367delA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 110025355 | ||||||
| chr12:110025574 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.802-168A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 7/14 | chr12 | 110025574 | |||||||
| chr12:110025986 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.883+163A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110025986 | |||||||
| chr12:110026065 | G | A | 1 | a0001c0002t0003g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883+242G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026065 | |||||||
| chr12:110026089 | GTAGCTGG others(3): Show |
G | 1 | a0002c0003t0004g0183 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.883+269_883+278del others(10): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 110026089 | ||||||
| chr12:110026134 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.883+311T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026134 | |||||||
| chr12:110026151 | C | T | 1 | a0002c0003t0004g0177 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.883+328C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026151 | |||||||
| chr12:110026255 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0120 others(1): Show |
4 | HG00280.hp2 HG01070.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+432G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026255 | |||||||
| chr12:110026321 | C | G | 4 | a0001c0002t0003g0031 a0001c0002t0003g0171 a0001c0002t0003g0173 others(1): Show |
5 | HG00735.hp2 HG01106.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+498C>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026321 | |||||||
| chr12:110026363 | C | T | 2 | a0001c0002t0007g0159 a0001c0002t0007g0160 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.883+540C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026363 | |||||||
| chr12:110026421 | T | A | 1 | a0001c0002t0017g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.883+598T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026421 | |||||||
| chr12:110026532 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.883+709G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026532 | |||||||
| chr12:110026577 | C | CA | 5 | a0001c0001t0001g0118 a0001c0002t0002g0003 a0001c0002t0002g0032 others(2): Show |
10 | HG01167.hp1 HG01934.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.883+770dupA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 110026577 | ||||||
| chr12:110026577 | CA | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0128 a0001c0002t0001g0006 others(9): Show |
16 | HG00323.hp1 HG00642.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.883+770delA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 110026577 | ||||||
| chr12:110026610 | G | A | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883+787G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026610 | |||||||
| chr12:110026650 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.883+827G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026650 | |||||||
| chr12:110026756 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.883+933C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026756 | |||||||
| chr12:110026776 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.884-929G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026776 | |||||||
| chr12:110026812 | G | T | 1 | a0002c0003t0004g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.884-893G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110026812 | |||||||
| chr12:110027145 | ACATCCCA others(4): Show |
A | 1 | a0001c0002t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.884-546_884-536del others(11): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 110027145 | ||||||
| chr12:110027642 | T | A | 3 | a0001c0002t0002g0149 a0001c0002t0002g0153 a0001c0002t0002g0154 |
3 | HG03471.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.884-63T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 8/14 | chr12 | 110027642 | |||||||
| chr12:110027796 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.945+30G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 9/14 | chr12 | 110027796 | |||||||
| chr12:110027875 | A | G | 3 | a0001c0002t0007g0159 a0001c0002t0007g0160 a0001c0002t0010g0161 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945+109A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 9/14 | chr12 | 110027875 | |||||||
| chr12:110027885 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.945+119C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 9/14 | chr12 | 110027885 | |||||||
| chr12:110028018 | G | T | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.945+252G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 9/14 | chr12 | 110028018 | |||||||
| chr12:110028063 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.945+297A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 9/14 | chr12 | 110028063 | |||||||
| chr12:110028407 | G | A | 2 | a0001c0002t0007g0159 a0001c0002t0007g0160 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.946-105G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 9/14 | chr12 | 110028407 | |||||||
| chr12:110028807 | G | A | 9 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0107 others(6): Show |
14 | HG00738.hp2 HG01167.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1076+165G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110028807 | |||||||
| chr12:110028824 | G | A | 1 | a0001c0002t0010g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+182G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110028824 | |||||||
| chr12:110028927 | A | G | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1076+285A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110028927 | |||||||
| chr12:110028979 | G | A | 1 | a0002c0003t0004g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1076+337G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110028979 | |||||||
| chr12:110029133 | C | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0100 others(7): Show |
13 | HG01928.hp1 HG02698.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077-345C>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110029133 | |||||||
| chr12:110029339 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0082 |
2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.1077-139C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110029339 | |||||||
| chr12:110029463 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1077-15G>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 10/14 | chr12 | 110029463 | |||||||
| chr12:110030240 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1235-405C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 11/14 | chr12 | 110030240 | |||||||
| chr12:110030455 | C | A | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1235-190C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 11/14 | chr12 | 110030455 | |||||||
| chr12:110030860 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1348+102C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110030860 | |||||||
| chr12:110030927 | T | C | 4 | a0001c0002t0003g0031 a0001c0002t0003g0171 a0001c0002t0003g0173 others(1): Show |
5 | HG00735.hp2 HG01106.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+169T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110030927 | |||||||
| chr12:110030963 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1348+205C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110030963 | |||||||
| chr12:110031123 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1348+365A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031123 | |||||||
| chr12:110031262 | T | C | 3 | a0001c0002t0005g0164 a0001c0002t0005g0167 a0001c0002t0005g0168 |
3 | HG01099.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1348+504T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031262 | |||||||
| chr12:110031299 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1348+541T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031299 | |||||||
| chr12:110031357 | AT | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0099 a0001c0001t0014g0069 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348+613delT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 110031357 | ||||||
| chr12:110031455 | G | A | 1 | a0001c0002t0003g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1348+697G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031455 | |||||||
| chr12:110031489 | T | C | 22 | a0001c0006t0004g0041 a0002c0003t0004g0013 a0002c0003t0004g0014 others(19): Show |
28 | HG00423.hp1 HG00558.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1348+731T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031489 | |||||||
| chr12:110031581 | C | T | 29 | a0001c0006t0004g0041 a0002c0003t0003g0035 a0002c0003t0003g0179 others(26): Show |
36 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1348+823C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031581 | |||||||
| chr12:110031808 | G | A | 9 | a0001c0002t0001g0006 a0001c0002t0001g0133 a0001c0002t0001g0134 others(6): Show |
13 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1348+1050G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110031808 | |||||||
| chr12:110031870 | CT | C | 12 | a0001c0001t0001g0043 a0001c0002t0002g0009 a0001c0002t0002g0028 others(9): Show |
17 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(14): Show |
intron_variant | MODIFIER | c.1348+1122delT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 110031870 | ||||||
| chr12:110032093 | T | C | 2 | a0001c0002t0005g0166 a0004c0007t0005g0141 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1348+1335T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032093 | |||||||
| chr12:110032152 | A | G | 2 | a0001c0002t0007g0159 a0001c0002t0007g0160 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1348+1394A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032152 | |||||||
| chr12:110032276 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0064 |
5 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348+1518T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032276 | |||||||
| chr12:110032351 | G | T | 1 | a0002c0003t0011g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1349-1446G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032351 | |||||||
| chr12:110032361 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0126 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1349-1436G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032361 | |||||||
| chr12:110032554 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0042 |
3 | HG02155.hp1 HG02523.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1349-1243C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032554 | |||||||
| chr12:110032824 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1349-973T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032824 | |||||||
| chr12:110032890 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0100 others(7): Show |
13 | HG01928.hp1 HG02698.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.1349-907T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110032890 | |||||||
| chr12:110033055 | C | CT | 9 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0093 others(6): Show |
9 | HG01175.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1349-724dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 110033055 | ||||||
| chr12:110033211 | G | A | 2 | a0001c0002t0003g0138 a0001c0002t0003g0139 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1349-586G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110033211 | |||||||
| chr12:110033220 | A | AT | 22 | a0001c0001t0001g0040 a0001c0001t0001g0105 a0001c0002t0002g0028 others(19): Show |
27 | HG00735.hp2 HG01106.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1349-562dupT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 110033220 | ||||||
| chr12:110033220 | A | ATT | 5 | a0001c0001t0001g0037 a0001c0002t0002g0009 a0001c0002t0002g0151 others(2): Show |
8 | HG03579.hp2 NA18948.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1349-563_1349-562d others(4): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 110033220 | ||||||
| chr12:110033221 | T | A | 1 | a0002c0003t0011g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1349-576T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110033221 | |||||||
| chr12:110033545 | G | A | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1349-252G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110033545 | |||||||
| chr12:110033587 | T | G | 1 | a0002c0003t0011g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1349-210T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110033587 | |||||||
| chr12:110033671 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1349-126A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 12/14 | chr12 | 110033671 | |||||||
| chr12:110034119 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1509+162A>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110034119 | |||||||
| chr12:110034190 | T | G | 6 | a0001c0002t0003g0012 a0001c0002t0003g0132 a0001c0002t0003g0143 others(3): Show |
8 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1509+233T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110034190 | |||||||
| chr12:110034728 | G | T | 1 | a0002c0003t0011g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1509+771G>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110034728 | |||||||
| chr12:110034904 | C | T | 28 | a0002c0003t0003g0035 a0002c0003t0003g0179 a0002c0003t0003g0187 others(25): Show |
35 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1509+947C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110034904 | |||||||
| chr12:110035445 | A | T | 1 | a0001c0002t0003g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1510-816A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110035445 | |||||||
| chr12:110035445 | AT | A | 43 | a0001c0001t0001g0102 a0001c0002t0001g0170 a0001c0002t0003g0012 others(40): Show |
53 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1510-801delT | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 110035445 | ||||||
| chr12:110035446 | T | A | 1 | a0002c0003t0011g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1510-815T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110035446 | |||||||
| chr12:110035447 | T | A | 27 | a0002c0003t0003g0035 a0002c0003t0003g0179 a0002c0003t0003g0187 others(24): Show |
34 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1510-814T>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110035447 | |||||||
| chr12:110035586 | A | T | 1 | a0002c0003t0004g0196 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1510-675A>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110035586 | |||||||
| chr12:110035597 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0055 others(2): Show |
6 | HG02698.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1510-664G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110035597 | |||||||
| chr12:110036037 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1510-224G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110036037 | |||||||
| chr12:110036094 | GTGT | G | 37 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(34): Show |
50 | HG00735.hp2 HG01106.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.1510-162_1510-160d others(5): Show |
ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 110036094 | ||||||
| chr12:110036136 | A | G | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1510-125A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 13/14 | chr12 | 110036136 | |||||||
| chr12:110036342 | G | A | 11 | a0001c0002t0002g0009 a0001c0002t0002g0028 a0001c0002t0002g0029 others(8): Show |
16 | HG02055.hp2 HG02809.hp2 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.1577+14G>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036342 | |||||||
| chr12:110036431 | C | T | 1 | a0001c0002t0008g0030 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1577+103C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036431 | |||||||
| chr12:110036477 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1577+149C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036477 | |||||||
| chr12:110036515 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1577+187C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036515 | |||||||
| chr12:110036540 | A | G | 68 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(65): Show |
89 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.1577+212A>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036540 | |||||||
| chr12:110036698 | C | T | 1 | a0001c0001t0021g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1577+370C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036698 | |||||||
| chr12:110036749 | C | CA | 14 | a0001c0002t0003g0012 a0001c0002t0003g0031 a0001c0002t0003g0132 others(11): Show |
17 | HG00735.hp2 HG01106.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1577+433dupA | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 110036749 | ||||||
| chr12:110036791 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1577+463T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036791 | |||||||
| chr12:110036948 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0042 |
3 | HG02155.hp1 HG02523.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1578-411C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110036948 | |||||||
| chr12:110037037 | C | T | 1 | a0001c0002t0010g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1578-322C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110037037 | |||||||
| chr12:110037055 | C | T | 28 | a0002c0003t0003g0035 a0002c0003t0003g0179 a0002c0003t0003g0187 others(25): Show |
35 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1578-304C>T | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110037055 | |||||||
| chr12:110037178 | T | G | 69 | a0001c0002t0002g0003 a0001c0002t0002g0009 a0001c0002t0002g0028 others(66): Show |
90 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1578-181T>G | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110037178 | |||||||
| chr12:110037297 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1578-62T>C | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110037297 | |||||||
| chr12:110037329 | C | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0065 others(3): Show |
7 | HG02630.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578-30C>A | ANKRD13A | ENSG00000076513.17 | transcript | ENST00000261739.9 | protein_coding | 14/14 | chr12 | 110037329 |