Item | Value |
---|---|
geneid | 286 |
ensemblid | ENSG00000029534.22 |
hgncid | 492 |
symbol | ANK1 |
name | ankyrin 1 |
refseq_nuc | NM_000037.4 |
refseq_prot | NP_000028.3 |
ensembl_nuc | ENST00000289734.13 |
ensembl_prot | ENSP00000289734.8 |
mane_status | MANE Select |
chr | chr8 |
start | 41653225 |
end | 41797622 |
strand | - |
ver | v1.2 |
region | chr8:41653225-41797622 |
region5000 | chr8:41648225-41802622 |
regionname0 | ANK1_chr8_41653225_41797622 |
regionname5000 | ANK1_chr8_41648225_41802622 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1880 | 233 | 58 | 46 | 84 | 12 | 31 | 61 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0002 | 0/0 | 1880 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0003 | 0/0 | 1880 | 10 | 3 | 1 | 3 | 0 | 3 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0004 | 0/0 | 1880 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0005 | 0/0 | 1880 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0006 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0007 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0008 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0009 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0010 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0011 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0012 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0013 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0014 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0015 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(1875): Show |
chr8 | 41648225 | 41802622 |
a0016 | 0/0 | 492 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | MPYSV others(487): Show |
chr8 | 41648225 | 41802622 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5640 | 45 | 7 | 6 | 26 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0002 | 0/0 | 5640 | 38 | 4 | 11 | 12 | 4 | 7 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0003 | 0/1 | 5640 | 27 | 1 | 8 | 7 | 2 | 8 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0004 | 0/0 | 5640 | 24 | 1 | 3 | 13 | 0 | 7 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0005 | 1/0 | 5640 | 24 | 12 | 5 | 6 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0006 | 0/0 | 5640 | 12 | 12 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0008 | 0/0 | 5640 | 7 | 0 | 0 | 5 | 2 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0009 | 0/0 | 5640 | 7 | 0 | 5 | 0 | 1 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0010 | 0/0 | 5640 | 6 | 0 | 0 | 6 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0012 | 0/0 | 5640 | 5 | 3 | 1 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0013 | 0/0 | 5640 | 4 | 4 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0016 | 0/0 | 5640 | 3 | 2 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0017 | 0/0 | 5640 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0018 | 0/0 | 5640 | 3 | 1 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0019 | 0/0 | 5640 | 3 | 0 | 1 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0022 | 0/0 | 5640 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0023 | 0/0 | 5640 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0025 | 0/0 | 5640 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0026 | 0/0 | 5640 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0028 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0029 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0030 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0032 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0034 | 0/0 | 5640 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0037 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0038 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0040 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0046 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0051 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0052 | 0/0 | 5640 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0054 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0056 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0001c0058 | 0/0 | 5640 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0002c0007 | 0/0 | 5640 | 8 | 7 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0002c0039 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0002c0042 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0002c0043 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0002c0057 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0003c0014 | 0/0 | 5640 | 4 | 0 | 1 | 0 | 0 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0003c0015 | 0/0 | 5640 | 3 | 0 | 0 | 3 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0003c0024 | 0/0 | 5640 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0003c0049 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0004c0011 | 0/0 | 5640 | 5 | 5 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0004c0020 | 0/0 | 5640 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0004c0044 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0005c0021 | 0/0 | 5640 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0005c0035 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0006c0036 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0007c0055 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0008c0041 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0009c0027 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0010c0050 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0011c0048 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0012c0033 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0013c0047 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0014c0031 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0015c0045 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5635): Show |
chr8 | 41648225 | 41802622 | ||
a0016c0053 | 0/0 | 5660 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | ATGCC others(5655): Show |
chr8 | 41648225 | 41802622 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8283 | 12 | 0 | 0 | 12 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0001t0002 | 0/0 | 8290 | 31 | 7 | 5 | 13 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0001t0013 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0001t0023 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0002t0001 | 0/0 | 8283 | 27 | 3 | 9 | 9 | 2 | 4 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0002t0002 | 0/0 | 8290 | 4 | 0 | 0 | 3 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0002t0003 | 0/0 | 8275 | 3 | 0 | 0 | 0 | 1 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0002t0009 | 0/0 | 8279 | 2 | 1 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8274): Show |
chr8 | 41648225 | 41802622 |
a0001c0002t0012 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8280): Show |
chr8 | 41648225 | 41802622 |
a0001c0002t0014 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8277): Show |
chr8 | 41648225 | 41802622 |
a0001c0003t0001 | 0/1 | 8283 | 21 | 0 | 8 | 5 | 2 | 5 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0003t0002 | 0/0 | 8290 | 3 | 1 | 0 | 1 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0003t0009 | 0/0 | 8279 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8274): Show |
chr8 | 41648225 | 41802622 |
a0001c0003t0014 | 0/0 | 8282 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8277): Show |
chr8 | 41648225 | 41802622 |
a0001c0003t0019 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0004t0001 | 0/0 | 8283 | 2 | 1 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0004t0002 | 0/0 | 8290 | 21 | 0 | 3 | 12 | 0 | 6 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0004t0024 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0001 | 0/0 | 8283 | 8 | 1 | 3 | 4 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0002 | 0/0 | 8290 | 3 | 1 | 1 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0004 | 1/0 | 8292 | 7 | 6 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8287): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0010 | 0/0 | 8296 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8291): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0013 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0020 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0028 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0005t0029 | 0/0 | 8282 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8277): Show |
chr8 | 41648225 | 41802622 |
a0001c0006t0001 | 0/0 | 8283 | 7 | 7 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0006t0003 | 0/0 | 8275 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0006t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8274): Show |
chr8 | 41648225 | 41802622 |
a0001c0006t0018 | 0/0 | 8281 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8276): Show |
chr8 | 41648225 | 41802622 |
a0001c0008t0002 | 0/0 | 8290 | 6 | 0 | 0 | 5 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0008t0015 | 0/0 | 8289 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8284): Show |
chr8 | 41648225 | 41802622 |
a0001c0009t0002 | 0/0 | 8290 | 7 | 0 | 5 | 0 | 1 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0010t0002 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0010t0003 | 0/0 | 8275 | 5 | 0 | 0 | 5 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0012t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0012t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8274): Show |
chr8 | 41648225 | 41802622 |
a0001c0012t0006 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0012t0015 | 0/0 | 8289 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8284): Show |
chr8 | 41648225 | 41802622 |
a0001c0013t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0013t0006 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0016t0002 | 0/0 | 8290 | 3 | 2 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0017t0005 | 0/0 | 8279 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8274): Show |
chr8 | 41648225 | 41802622 |
a0001c0018t0001 | 0/0 | 8283 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0018t0026 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8271): Show |
chr8 | 41648225 | 41802622 |
a0001c0019t0002 | 0/0 | 8290 | 3 | 0 | 1 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0022t0002 | 0/0 | 8290 | 2 | 0 | 2 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0023t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0025t0011 | 0/0 | 8294 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8289): Show |
chr8 | 41648225 | 41802622 |
a0001c0026t0001 | 0/0 | 8283 | 2 | 0 | 0 | 2 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0028t0003 | 0/0 | 8275 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0029t0001 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0030t0017 | 0/0 | 8293 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8288): Show |
chr8 | 41648225 | 41802622 |
a0001c0032t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0034t0002 | 0/0 | 8290 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0037t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0038t0002 | 0/0 | 8290 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0001c0040t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0046t0030 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0051t0008 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8273): Show |
chr8 | 41648225 | 41802622 |
a0001c0052t0001 | 0/0 | 8283 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0054t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0001c0056t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0001c0058t0022 | 0/0 | 8292 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8287): Show |
chr8 | 41648225 | 41802622 |
a0002c0007t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0002c0007t0007 | 0/0 | 8294 | 4 | 3 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8289): Show |
chr8 | 41648225 | 41802622 |
a0002c0007t0021 | 0/0 | 8291 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8286): Show |
chr8 | 41648225 | 41802622 |
a0002c0007t0027 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0002c0039t0010 | 0/0 | 8296 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8291): Show |
chr8 | 41648225 | 41802622 |
a0002c0042t0016 | 0/0 | 8294 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8289): Show |
chr8 | 41648225 | 41802622 |
a0002c0043t0002 | 0/0 | 8290 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0002c0057t0005 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8274): Show |
chr8 | 41648225 | 41802622 |
a0003c0014t0002 | 0/0 | 8290 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0003c0014t0008 | 0/0 | 8278 | 3 | 0 | 0 | 0 | 0 | 3 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8273): Show |
chr8 | 41648225 | 41802622 |
a0003c0015t0003 | 0/0 | 8275 | 3 | 0 | 0 | 3 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0003c0024t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0003c0024t0003 | 0/0 | 8275 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8270): Show |
chr8 | 41648225 | 41802622 |
a0003c0049t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0004c0011t0001 | 0/0 | 8283 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0004c0011t0002 | 0/0 | 8290 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0004c0020t0001 | 0/0 | 8283 | 3 | 3 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0004c0044t0004 | 0/0 | 8292 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8287): Show |
chr8 | 41648225 | 41802622 |
a0005c0021t0002 | 0/0 | 8290 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0005c0035t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0006c0036t0002 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0007c0055t0006 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0008c0041t0012 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8280): Show |
chr8 | 41648225 | 41802622 |
a0009c0027t0002 | 0/0 | 8290 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0010c0050t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0011c0048t0001 | 0/0 | 8283 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0012c0033t0001 | 0/0 | 8283 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8278): Show |
chr8 | 41648225 | 41802622 |
a0013c0047t0002 | 0/0 | 8290 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0014c0031t0002 | 0/0 | 8290 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8285): Show |
chr8 | 41648225 | 41802622 |
a0015c0045t0025 | 0/0 | 8276 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8271): Show |
chr8 | 41648225 | 41802622 |
a0016c0053t0002 | 0/0 | 8310 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | AGAGG others(8305): Show |
chr8 | 41648225 | 41802622 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0013g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0001t0023g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0009g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0012g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0002t0014g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0009g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0014g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0003t0019g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0004t0024g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0004g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0013g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0020g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0028g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0005t0029g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0006t0018g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0008t0015g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0009t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0010t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0010t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0010t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0010t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0010t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0010t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0012t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0012t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0012t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0012t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0012t0015g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0013t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0013t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0013t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0013t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0016t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0016t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0016t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0017t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0017t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0017t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0018t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0018t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0018t0026g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0019t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0019t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0019t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0022t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0022t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0023t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0023t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0025t0011g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0026t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0026t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0028t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0029t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0030t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0032t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0034t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0037t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0038t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0040t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0046t0030g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0051t0008g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0052t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0054t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0056t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0001c0058t0022g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0021g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0007t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0039t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0042t0016g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0043t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0002c0057t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0014t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0014t0008g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0014t0008g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0014t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0015t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0015t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0015t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0024t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0024t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0003c0049t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0011t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0011t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0011t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0020t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0020t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0020t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0004c0044t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0005c0021t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0005c0021t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0005c0035t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0006c0036t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0007c0055t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0008c0041t0012g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0009c0027t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0010c0050t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0011c0048t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0012c0033t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0013c0047t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0014c0031t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0015c0045t0025g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
a0016c0053t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0056 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0069 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0124 | EUR | GBR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | FIN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00323 | hp2 | a0001 | c0052 | t0001 | g0235 | EUR | FIN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00408 | hp2 | a0001 | c0005 | t0002 | g0189 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00423 | hp1 | a0006 | c0036 | t0002 | g0075 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00423 | hp2 | a0001 | c0004 | t0002 | g0202 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00438 | hp1 | a0001 | c0026 | t0001 | g0158 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00438 | hp2 | a0001 | c0008 | t0002 | g0217 | EAS | CHS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00639 | hp1 | a0003 | c0014 | t0002 | g0198 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00639 | hp2 | a0001 | c0009 | t0002 | g0055 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00733 | hp2 | a0001 | c0022 | t0002 | g0232 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00738 | hp1 | a0001 | c0051 | t0008 | g0273 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00738 | hp2 | a0001 | c0009 | t0002 | g0047 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00741 | hp1 | a0001 | c0054 | t0001 | g0126 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01069 | hp1 | a0001 | c0004 | t0002 | g0120 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01070 | hp1 | a0001 | c0009 | t0002 | g0083 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01070 | hp2 | a0001 | c0005 | t0013 | g0005 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01071 | hp1 | a0001 | c0001 | t0013 | g0090 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01071 | hp2 | a0001 | c0005 | t0002 | g0004 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01081 | hp1 | a0001 | c0009 | t0002 | g0048 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0137 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01106 | hp1 | a0001 | c0009 | t0002 | g0062 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01106 | hp2 | a0007 | c0055 | t0006 | g0012 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01167 | hp1 | a0002 | c0042 | t0016 | g0046 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01168 | hp1 | a0001 | c0004 | t0002 | g0220 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01175 | hp1 | a0009 | c0027 | t0002 | g0071 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01192 | hp2 | a0001 | c0016 | t0002 | g0008 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01243 | hp1 | a0001 | c0019 | t0002 | g0155 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01243 | hp2 | a0002 | c0007 | t0007 | g0022 | AMR | PUR | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0054 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01258 | hp1 | a0001 | c0038 | t0002 | g0223 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0135 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01261 | hp1 | a0001 | c0002 | t0012 | g0031 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01261 | hp2 | a0001 | c0005 | t0001 | g0086 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0092 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01515 | hp1 | a0001 | c0008 | t0002 | g0204 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01515 | hp2 | a0001 | c0002 | t0014 | g0123 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0122 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01517 | hp2 | a0001 | c0008 | t0015 | g0206 | EUR | IBS | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01891 | hp1 | a0002 | c0057 | t0005 | g0265 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01891 | hp2 | a0001 | c0023 | t0001 | g0275 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01928 | hp1 | a0010 | c0050 | t0001 | g0171 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01928 | hp2 | a0001 | c0012 | t0001 | g0138 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0140 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01952 | hp2 | a0011 | c0048 | t0001 | g0181 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01975 | hp1 | a0001 | c0005 | t0001 | g0258 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01975 | hp2 | a0001 | c0002 | t0009 | g0125 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01978 | hp1 | a0001 | c0004 | t0002 | g0063 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0139 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02004 | hp2 | a0001 | c0022 | t0002 | g0231 | AMR | PEL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02015 | hp2 | a0001 | c0008 | t0002 | g0212 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02071 | hp1 | a0001 | c0005 | t0001 | g0225 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02071 | hp2 | a0001 | c0010 | t0002 | g0081 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02074 | hp1 | a0001 | c0028 | t0003 | g0066 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02074 | hp2 | a0001 | c0010 | t0003 | g0188 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02080 | hp1 | a0001 | c0010 | t0003 | g0003 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02080 | hp2 | a0001 | c0004 | t0002 | g0200 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02083 | hp1 | a0001 | c0004 | t0002 | g0244 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02145 | hp1 | a0001 | c0006 | t0001 | g0263 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02258 | hp1 | a0002 | c0007 | t0007 | g0025 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02280 | hp1 | a0005 | c0021 | t0002 | g0131 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02280 | hp2 | a0001 | c0005 | t0003 | g0033 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02451 | hp1 | a0001 | c0018 | t0026 | g0113 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02451 | hp2 | a0002 | c0007 | t0021 | g0115 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02572 | hp1 | a0001 | c0017 | t0005 | g0116 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02572 | hp2 | a0004 | c0020 | t0001 | g0034 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02602 | hp1 | a0001 | c0004 | t0002 | g0270 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0221 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02622 | hp1 | a0001 | c0012 | t0006 | g0097 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0267 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02630 | hp1 | a0001 | c0006 | t0001 | g0100 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02630 | hp2 | a0004 | c0020 | t0001 | g0037 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02647 | hp1 | a0001 | c0056 | t0003 | g0026 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02647 | hp2 | a0001 | c0016 | t0002 | g0007 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02683 | hp2 | a0001 | c0004 | t0002 | g0176 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02698 | hp1 | a0001 | c0004 | t0002 | g0205 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02717 | hp1 | a0001 | c0037 | t0003 | g0234 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02717 | hp2 | a0001 | c0005 | t0002 | g0019 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02723 | hp1 | a0002 | c0043 | t0002 | g0045 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02723 | hp2 | a0001 | c0046 | t0030 | g0276 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0070 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02809 | hp1 | a0001 | c0012 | t0005 | g0101 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02809 | hp2 | a0004 | c0011 | t0001 | g0185 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02818 | hp1 | a0001 | c0005 | t0004 | g0099 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02818 | hp2 | a0003 | c0024 | t0003 | g0102 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02886 | hp1 | a0001 | c0005 | t0004 | g0011 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02886 | hp2 | a0002 | c0007 | t0001 | g0041 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02895 | hp1 | a0012 | c0033 | t0001 | g0107 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02895 | hp2 | a0001 | c0005 | t0029 | g0111 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02897 | hp1 | a0001 | c0005 | t0004 | g0030 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02897 | hp2 | a0001 | c0005 | t0028 | g0112 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02922 | hp1 | a0001 | c0005 | t0004 | g0044 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02922 | hp2 | a0001 | c0016 | t0002 | g0009 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02965 | hp1 | a0001 | c0002 | t0009 | g0098 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02965 | hp2 | a0001 | c0005 | t0004 | g0029 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02970 | hp1 | a0001 | c0005 | t0004 | g0043 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02970 | hp2 | a0001 | c0013 | t0001 | g0038 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02976 | hp1 | a0001 | c0013 | t0001 | g0027 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02976 | hp2 | a0003 | c0024 | t0001 | g0272 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03017 | hp1 | a0001 | c0003 | t0014 | g0061 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03041 | hp1 | a0001 | c0006 | t0003 | g0006 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03041 | hp2 | a0004 | c0020 | t0001 | g0035 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03098 | hp1 | a0001 | c0013 | t0006 | g0130 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03098 | hp2 | a0001 | c0012 | t0006 | g0096 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0266 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03130 | hp2 | a0001 | c0017 | t0005 | g0119 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03139 | hp1 | a0002 | c0007 | t0001 | g0039 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03139 | hp2 | a0001 | c0005 | t0010 | g0020 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03195 | hp1 | a0003 | c0049 | t0001 | g0103 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03195 | hp2 | a0004 | c0011 | t0002 | g0001 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0268 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03225 | hp1 | a0002 | c0039 | t0010 | g0018 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0108 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03239 | hp1 | a0003 | c0014 | t0008 | g0191 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03239 | hp2 | a0001 | c0009 | t0002 | g0052 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03453 | hp1 | a0001 | c0006 | t0003 | g0015 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03453 | hp2 | a0001 | c0006 | t0001 | g0040 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03486 | hp1 | a0002 | c0007 | t0027 | g0036 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03486 | hp2 | a0013 | c0047 | t0002 | g0016 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03490 | hp2 | a0003 | c0014 | t0008 | g0094 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03491 | hp2 | a0001 | c0025 | t0011 | g0002 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03492 | hp1 | a0001 | c0025 | t0011 | g0002 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03492 | hp2 | a0003 | c0014 | t0008 | g0093 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03516 | hp1 | a0001 | c0040 | t0001 | g0085 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03540 | hp2 | a0002 | c0007 | t0007 | g0024 | AFR | GWD | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03579 | hp1 | a0001 | c0017 | t0005 | g0117 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03688 | hp1 | a0001 | c0004 | t0002 | g0073 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0050 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03704 | hp2 | a0001 | c0003 | t0009 | g0163 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0148 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03710 | hp2 | a0001 | c0058 | t0022 | g0088 | SAS | PJL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03834 | hp1 | a0001 | c0004 | t0002 | g0252 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0143 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0162 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | STU | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18522 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18522 | hp2 | a0004 | c0044 | t0004 | g0042 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18612 | hp1 | a0001 | c0019 | t0002 | g0238 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18747 | hp2 | a0001 | c0004 | t0024 | g0199 | EAS | CHB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18950 | hp1 | a0001 | c0004 | t0002 | g0213 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18950 | hp2 | a0003 | c0015 | t0003 | g0250 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18960 | hp1 | a0001 | c0019 | t0002 | g0174 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18967 | hp2 | a0001 | c0004 | t0002 | g0201 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18969 | hp2 | a0001 | c0012 | t0015 | g0239 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18973 | hp1 | a0001 | c0008 | t0002 | g0253 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18979 | hp1 | a0001 | c0010 | t0003 | g0110 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18980 | hp1 | a0001 | c0010 | t0003 | g0236 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18981 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18986 | hp1 | a0014 | c0031 | t0002 | g0256 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18988 | hp1 | a0001 | c0003 | t0019 | g0065 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18992 | hp1 | a0001 | c0005 | t0001 | g0078 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18992 | hp2 | a0001 | c0008 | t0002 | g0246 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18998 | hp2 | a0001 | c0018 | t0001 | g0145 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18999 | hp1 | a0001 | c0004 | t0002 | g0208 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19004 | hp1 | a0001 | c0005 | t0001 | g0228 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19004 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19007 | hp2 | a0001 | c0004 | t0002 | g0152 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19010 | hp1 | a0003 | c0015 | t0003 | g0136 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19010 | hp2 | a0001 | c0004 | t0002 | g0249 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19012 | hp2 | a0001 | c0010 | t0003 | g0269 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19043 | hp1 | a0015 | c0045 | t0025 | g0187 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19043 | hp2 | a0001 | c0030 | t0017 | g0058 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19056 | hp2 | a0001 | c0004 | t0002 | g0259 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19057 | hp1 | a0001 | c0026 | t0001 | g0156 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19057 | hp2 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19063 | hp1 | a0001 | c0004 | t0002 | g0247 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19066 | hp2 | a0001 | c0029 | t0001 | g0254 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19067 | hp1 | a0001 | c0018 | t0001 | g0144 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19068 | hp1 | a0003 | c0015 | t0003 | g0214 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19068 | hp2 | a0001 | c0005 | t0020 | g0178 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19076 | hp1 | a0016 | c0053 | t0002 | g0251 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19079 | hp2 | a0001 | c0005 | t0001 | g0229 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19084 | hp1 | a0001 | c0001 | t0023 | g0072 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19084 | hp2 | a0001 | c0004 | t0002 | g0260 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19087 | hp2 | a0001 | c0008 | t0002 | g0203 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19240 | hp1 | a0004 | c0011 | t0002 | g0001 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA19240 | hp2 | a0005 | c0035 | t0001 | g0129 | AFR | YRI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20129 | hp1 | a0001 | c0005 | t0001 | g0084 | AFR | ASW | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ASW | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20752 | hp1 | a0001 | c0009 | t0002 | g0067 | EUR | TSI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0079 | EUR | TSI | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20905 | hp1 | a0001 | c0034 | t0002 | g0146 | SAS | GIH | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20905 | hp2 | a0001 | c0004 | t0002 | g0068 | SAS | GIH | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01123 | hp1 | a0001 | c0005 | t0001 | g0257 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG01123 | hp2 | a0008 | c0041 | t0012 | g0167 | AMR | CLM | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02109 | hp2 | a0001 | c0006 | t0005 | g0014 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02486 | hp2 | a0001 | c0003 | t0002 | g0064 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02559 | hp1 | a0004 | c0011 | t0002 | g0095 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG02559 | hp2 | a0005 | c0021 | t0002 | g0114 | AFR | ACB | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03471 | hp1 | a0001 | c0013 | t0006 | g0128 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG03471 | hp2 | a0004 | c0011 | t0001 | g0186 | AFR | MSL | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG06807 | hp1 | a0001 | c0006 | t0018 | g0118 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20300 | hp1 | a0001 | c0023 | t0001 | g0274 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA20300 | hp2 | a0001 | c0006 | t0003 | g0013 | AFR | USA | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA21309 | hp1 | a0002 | c0007 | t0007 | g0028 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
NA21309 | hp2 | a0001 | c0032 | t0003 | g0104 | AFR | LWK | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0082 | REF | REF | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
homoSapiens | grch38p0 | a0001 | c0005 | t0004 | g0196 | REF | REF | ANK1_chr8_41648225_41802622 | ANK1 | chr8 | 41648225 | 41802622 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41684589 | G | A | 1 | a0015 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4492C>T | p.Arg1498Trp | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/43 | 4576/8292 | 4492/5643 | 1498/1880 | chr8 | 41684589 | |||
chr8:41686157 | G | A | 1 | a0008 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.4385C>T | p.Ala1462Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/43 | 4469/8292 | 4385/5643 | 1462/1880 | chr8 | 41686157 | |||
chr8:41690485 | T | C | 2 | a0002 a0007 |
13 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(10): Show |
missense_variant | MODERATE | c.3973A>G | p.Met1325Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 32/43 | 4057/8292 | 3973/5643 | 1325/1880 | chr8 | 41690485 | |||
chr8:41692838 | A | G | 1 | a0006 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.3668T>C | p.Val1223Ala | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/43 | 3752/8292 | 3668/5643 | 1223/1880 | chr8 | 41692838 | |||
chr8:41693954 | G | A | 1 | a0010 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.3476C>T | p.Pro1159Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/43 | 3560/8292 | 3476/5643 | 1159/1880 | chr8 | 41693954 | |||
chr8:41694695 | G | A | 2 | a0004 a0012 |
10 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.3224C>T | p.Thr1075Ile | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/43 | 3308/8292 | 3224/5643 | 1075/1880 | chr8 | 41694695 | |||
chr8:41696493 | C | T | 1 | a0007 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.2830G>A | p.Ala944Thr | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/43 | 2914/8292 | 2830/5643 | 944/1880 | chr8 | 41696493 | |||
chr8:41699467 | G | A | 1 | a0011 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.2543C>T | p.Pro848Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/43 | 2627/8292 | 2543/5643 | 848/1880 | chr8 | 41699467 | |||
chr8:41699515 | C | T | 2 | a0005 a0012 |
4 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.2495G>A | p.Arg832Gln | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/43 | 2579/8292 | 2495/5643 | 832/1880 | chr8 | 41699515 | |||
chr8:41704438 | T | C | 1 | a0013 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2132A>G | p.Tyr711Cys | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 19/43 | 2216/8292 | 2132/5643 | 711/1880 | chr8 | 41704438 | |||
chr8:41708920 | C | T | 2 | a0003 a0010 |
11 | HG00639.hp1 HG01928.hp1 HG02818.hp2 others(8): Show |
missense_variant | MODERATE | c.1856G>A | p.Arg619His | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/43 | 1940/8292 | 1856/5643 | 619/1880 | chr8 | 41708920 | |||
chr8:41715771 | T | G | 1 | a0012 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1483A>C | p.Asn495His | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 14/43 | 1567/8292 | 1483/5643 | 495/1880 | chr8 | 41715771 | |||
chr8:41717010 | G | GTGCCCGG others(13): Show |
1 | a0016 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1327_1346dupATGGCA others(14): Show |
p.His449fs | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/43 | 1430/8292 | 1346/5643 | 449/1880 | chr8 | 41717010 | |||
chr8:41719771 | C | T | 1 | a0009 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.997G>A | p.Asp333Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/43 | 1081/8292 | 997/5643 | 333/1880 | chr8 | 41719771 | |||
chr8:41724473 | C | T | 1 | a0014 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.694G>A | p.Val232Ile | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/43 | 778/8292 | 694/5643 | 232/1880 | chr8 | 41724473 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41668396 | C | T | 14 | a0001c0004 a0001c0009 a0001c0016 others(11): Show |
55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
synonymous_variant | LOW | c.5265G>A | p.Val1755Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/43 | 5349/8292 | 5265/5643 | 1755/1880 | chr8 | 41668396 | |||
chr8:41684575 | G | A | 1 | a0008c0041 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.4506C>T | p.Arg1502Arg | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/43 | 4590/8292 | 4506/5643 | 1502/1880 | chr8 | 41684575 | |||
chr8:41690230 | G | A | 21 | a0001c0006 a0001c0010 a0001c0013 others(18): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
synonymous_variant | LOW | c.4101C>T | p.Ala1367Ala | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/43 | 4185/8292 | 4101/5643 | 1367/1880 | chr8 | 41690230 | |||
chr8:41690323 | C | T | 1 | a0001c0022 | 2 | HG00733.hp2 HG02004.hp2 |
synonymous_variant | LOW | c.4008G>A | p.Pro1336Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/43 | 4092/8292 | 4008/5643 | 1336/1880 | chr8 | 41690323 | |||
chr8:41692693 | C | T | 2 | a0001c0037 a0003c0024 |
3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.3813G>A | p.Glu1271Glu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/43 | 3897/8292 | 3813/5643 | 1271/1880 | chr8 | 41692693 | |||
chr8:41693944 | G | A | 6 | a0001c0013 a0003c0049 a0004c0011 others(3): Show |
15 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(12): Show |
synonymous_variant | LOW | c.3486C>T | p.Ser1162Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/43 | 3570/8292 | 3486/5643 | 1162/1880 | chr8 | 41693944 | |||
chr8:41695253 | G | A | 1 | a0015c0045 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.3039C>T | p.Asn1013Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/43 | 3123/8292 | 3039/5643 | 1013/1880 | chr8 | 41695253 | |||
chr8:41695259 | G | A | 1 | a0001c0023 | 2 | HG01891.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.3033C>T | p.Ser1011Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/43 | 3117/8292 | 3033/5643 | 1011/1880 | chr8 | 41695259 | |||
chr8:41695322 | G | A | 1 | a0001c0017 | 3 | HG02572.hp1 HG03130.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.2970C>T | p.Ile990Ile | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/43 | 3054/8292 | 2970/5643 | 990/1880 | chr8 | 41695322 | |||
chr8:41696410 | C | G | 15 | a0001c0001 a0001c0003 a0001c0009 others(12): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
synonymous_variant | LOW | c.2913G>C | p.Leu971Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/43 | 2997/8292 | 2913/5643 | 971/1880 | chr8 | 41696410 | |||
chr8:41696563 | G | A | 1 | a0001c0029 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2760C>T | p.Asp920Asp | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/43 | 2844/8292 | 2760/5643 | 920/1880 | chr8 | 41696563 | |||
chr8:41698091 | G | A | 1 | a0001c0046 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2589C>T | p.Pro863Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/43 | 2673/8292 | 2589/5643 | 863/1880 | chr8 | 41698091 | |||
chr8:41701608 | C | T | 1 | a0001c0051 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.2403G>A | p.Lys801Lys | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/43 | 2487/8292 | 2403/5643 | 801/1880 | chr8 | 41701608 | |||
chr8:41702091 | G | A | 6 | a0001c0003 a0001c0009 a0001c0018 others(3): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
synonymous_variant | LOW | c.2349C>T | p.Thr783Thr | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/43 | 2433/8292 | 2349/5643 | 783/1880 | chr8 | 41702091 | |||
chr8:41704125 | G | C | 2 | a0001c0010 a0004c0011 |
11 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(8): Show |
synonymous_variant | LOW | c.2211C>G | p.Pro737Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/43 | 2295/8292 | 2211/5643 | 737/1880 | chr8 | 41704125 | |||
chr8:41706167 | G | A | 6 | a0001c0003 a0001c0009 a0001c0018 others(3): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
synonymous_variant | LOW | c.2073C>T | p.Gly691Gly | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/43 | 2157/8292 | 2073/5643 | 691/1880 | chr8 | 41706167 | |||
chr8:41708808 | C | T | 1 | a0001c0054 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1968G>A | p.Ser656Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/43 | 2052/8292 | 1968/5643 | 656/1880 | chr8 | 41708808 | |||
chr8:41714174 | G | T | 1 | a0001c0034 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1782C>A | p.Ser594Ser | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/43 | 1866/8292 | 1782/5643 | 594/1880 | chr8 | 41714174 | |||
chr8:41715787 | C | T | 1 | a0012c0033 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1467G>A | p.Leu489Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 14/43 | 1551/8292 | 1467/5643 | 489/1880 | chr8 | 41715787 | |||
chr8:41717037 | C | T | 2 | a0001c0013 a0001c0032 |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.1320G>A | p.Pro440Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/43 | 1404/8292 | 1320/5643 | 440/1880 | chr8 | 41717037 | |||
chr8:41724492 | G | A | 1 | a0001c0026 | 2 | HG00438.hp1 NA19057.hp1 |
synonymous_variant | LOW | c.675C>T | p.Leu225Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/43 | 759/8292 | 675/5643 | 225/1880 | chr8 | 41724492 | |||
chr8:41725776 | C | T | 6 | a0001c0004 a0001c0008 a0001c0028 others(3): Show |
35 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.597G>A | p.Pro199Pro | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/43 | 681/8292 | 597/5643 | 199/1880 | chr8 | 41725776 | |||
chr8:41725884 | G | A | 1 | a0003c0024 | 2 | HG02818.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.489C>T | p.Leu163Leu | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/43 | 573/8292 | 489/5643 | 163/1880 | chr8 | 41725884 | |||
chr8:41725923 | T | C | 5 | a0001c0051 a0001c0052 a0003c0014 others(2): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
synonymous_variant | LOW | c.450A>G | p.Val150Val | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/43 | 534/8292 | 450/5643 | 150/1880 | chr8 | 41725923 | |||
chr8:41727920 | G | A | 13 | a0001c0002 a0001c0012 a0001c0019 others(10): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/43 | 399/8292 | 315/5643 | 105/1880 | chr8 | 41727920 | |||
chr8:41727998 | G | A | 1 | a0001c0058 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.237C>T | p.Asn79Asn | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/43 | 321/8292 | 237/5643 | 79/1880 | chr8 | 41727998 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41653618 | G | T | 1 | a0001c0005t0020 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2172C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7848 | chr8 | 41653618 | ||||||
chr8:41653638 | A | C | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 others(91): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*2152T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7828 | chr8 | 41653638 | ||||||
chr8:41653667 | C | A | 2 | a0001c0001t0013 a0001c0005t0013 |
2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2123G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7799 | chr8 | 41653667 | ||||||
chr8:41653768 | C | T | 2 | a0002c0007t0007 a0002c0042t0016 |
5 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2022G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7698 | chr8 | 41653768 | ||||||
chr8:41653891 | C | T | 6 | a0001c0005t0010 a0001c0025t0011 a0001c0030t0017 others(3): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1899G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7575 | chr8 | 41653891 | ||||||
chr8:41654122 | C | T | 1 | a0001c0004t0024 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1668G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7344 | chr8 | 41654122 | ||||||
chr8:41654123 | A | T | 1 | a0001c0001t0023 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7343 | chr8 | 41654123 | ||||||
chr8:41654181 | G | C | 6 | a0001c0005t0010 a0001c0025t0011 a0001c0030t0017 others(3): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1609C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7285 | chr8 | 41654181 | ||||||
chr8:41654388 | C | A | 1 | a0001c0018t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 7078 | chr8 | 41654388 | ||||||
chr8:41654933 | G | T | 1 | a0001c0003t0019 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*857C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6533 | chr8 | 41654933 | ||||||
chr8:41654969 | G | A | 1 | a0002c0007t0021 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6497 | chr8 | 41654969 | ||||||
chr8:41655016 | T | C | 3 | a0001c0012t0006 a0001c0013t0006 a0007c0055t0006 |
5 | HG01106.hp2 HG02622.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*774A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6450 | chr8 | 41655016 | ||||||
chr8:41655026 | CAGAG | C | 5 | a0001c0006t0005 a0001c0006t0018 a0001c0012t0005 others(2): Show |
7 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*760_*763delCTCT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6436 | chr8 | 41655026 | ||||||
chr8:41655062 | CACAGCAG others(7): Show |
C | 60 | a0001c0001t0001 a0001c0001t0013 a0001c0002t0001 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*714_*727delATAGAC others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6390 | chr8 | 41655062 | ||||||
chr8:41655129 | G | GGT | 4 | a0001c0025t0011 a0001c0030t0017 a0002c0007t0007 others(1): Show |
8 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*660dupAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6336 | chr8 | 41655129 | ||||||
chr8:41655129 | G | GGTGT | 42 | a0001c0001t0001 a0001c0001t0013 a0001c0002t0001 others(39): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*660dupACAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6336 | chr8 | 41655129 | ||||||
chr8:41655129 | G | GGTGTGT | 3 | a0001c0002t0012 a0001c0006t0018 a0008c0041t0012 |
3 | HG01123.hp2 HG01261.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655_*660dupACACAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6336 | chr8 | 41655129 | ||||||
chr8:41655129 | GGT | G | 40 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(37): Show |
126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*660delAC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6335 | chr8 | 41655129 | ||||||
chr8:41655171 | G | A | 1 | a0002c0042t0016 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6295 | chr8 | 41655171 | ||||||
chr8:41655305 | C | CT | 48 | a0001c0001t0001 a0001c0001t0013 a0001c0002t0001 others(45): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*484dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6160 | chr8 | 41655305 | ||||||
chr8:41655305 | CT | C | 13 | a0001c0002t0003 a0001c0005t0003 a0001c0006t0003 others(10): Show |
23 | HG01517.hp2 HG02074.hp1 HG02074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*484delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6160 | chr8 | 41655305 | ||||||
chr8:41655358 | T | C | 1 | a0002c0007t0027 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6108 | chr8 | 41655358 | ||||||
chr8:41655404 | AC | A | 6 | a0001c0005t0010 a0001c0025t0011 a0001c0030t0017 others(3): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*385delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 6061 | chr8 | 41655404 | ||||||
chr8:41655552 | A | G | 6 | a0001c0005t0010 a0001c0025t0011 a0001c0030t0017 others(3): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*238T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 5914 | chr8 | 41655552 | ||||||
chr8:41655674 | G | A | 2 | a0001c0005t0028 a0001c0005t0029 |
2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 43/43 | 5792 | chr8 | 41655674 | ||||||
chr8:41797603 | G | A | 1 | a0001c0046t0030 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/43 | 65 | chr8 | 41797603 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:41655932 | G | A | 1 | a0001c0018t0026g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*37-179C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41655932 | |||||||
chr8:41655934 | C | T | 17 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0002t0003g0143 others(14): Show |
17 | HG02074.hp1 HG02280.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.*37-181G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41655934 | |||||||
chr8:41656012 | T | C | 164 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.*37-259A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656012 | |||||||
chr8:41656020 | T | C | 9 | a0001c0005t0010g0020 a0001c0025t0011g0002 a0001c0030t0017g0058 others(6): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.*37-267A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656020 | |||||||
chr8:41656100 | C | T | 2 | a0001c0037t0003g0234 a0003c0024t0003g0102 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.*37-347G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656100 | |||||||
chr8:41656277 | G | C | 10 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0025t0011g0002 others(7): Show |
11 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.*37-524C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656277 | |||||||
chr8:41656290 | T | C | 164 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.*37-537A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656290 | |||||||
chr8:41656532 | C | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.*37-779G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656532 | |||||||
chr8:41656596 | C | T | 1 | a0001c0016t0002g0008 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.*37-843G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656596 | |||||||
chr8:41656646 | G | A | 1 | a0001c0006t0001g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*37-893C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656646 | |||||||
chr8:41656721 | G | A | 1 | a0013c0047t0002g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*37-968C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656721 | |||||||
chr8:41656743 | A | G | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*37-990T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656743 | |||||||
chr8:41656778 | G | C | 45 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(42): Show |
45 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.*37-1025C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41656778 | |||||||
chr8:41657239 | G | A | 9 | a0001c0005t0010g0020 a0001c0025t0011g0002 a0001c0030t0017g0058 others(6): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.*37-1486C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657239 | |||||||
chr8:41657369 | G | A | 165 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.*37-1616C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657369 | |||||||
chr8:41657380 | A | G | 1 | a0001c0018t0026g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*37-1627T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657380 | |||||||
chr8:41657496 | T | G | 18 | a0001c0001t0013g0090 a0001c0002t0009g0098 a0001c0005t0010g0020 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.*37-1743A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657496 | |||||||
chr8:41657571 | C | A | 1 | a0001c0010t0003g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.*37-1818G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657571 | |||||||
chr8:41657611 | A | G | 164 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.*37-1858T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657611 | |||||||
chr8:41657769 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.*37-2016C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41657769 | |||||||
chr8:41658012 | A | G | 164 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.*37-2259T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658012 | |||||||
chr8:41658106 | A | G | 1 | a0001c0003t0001g0069 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*37-2353T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658106 | |||||||
chr8:41658263 | C | T | 1 | a0001c0006t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*37-2510G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658263 | |||||||
chr8:41658298 | G | A | 21 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0002t0003g0143 others(18): Show |
21 | HG02074.hp1 HG02074.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.*37-2545C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658298 | |||||||
chr8:41658427 | C | T | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37-2674G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658427 | |||||||
chr8:41658474 | G | A | 163 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(160): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.*37-2721C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658474 | |||||||
chr8:41658662 | G | A | 1 | a0001c0002t0001g0240 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.*36+2768C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658662 | |||||||
chr8:41658750 | A | C | 3 | a0002c0007t0027g0036 a0004c0011t0001g0185 a0004c0011t0001g0186 |
3 | HG02809.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.*36+2680T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658750 | |||||||
chr8:41658845 | A | G | 2 | a0001c0037t0003g0234 a0003c0024t0003g0102 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.*36+2585T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658845 | |||||||
chr8:41658897 | T | TATAA | 76 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0190 others(73): Show |
76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.*36+2529_*36+2532d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | |||||||
chr8:41658897 | T | TATAAATA others(1): Show |
4 | a0001c0001t0002g0010 a0001c0002t0001g0059 a0001c0004t0002g0176 others(1): Show |
4 | HG02083.hp1 HG02683.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.*36+2525_*36+2532d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | |||||||
chr8:41658897 | TATAA | T | 20 | a0001c0001t0002g0169 a0001c0002t0001g0182 a0001c0002t0001g0264 others(17): Show |
20 | HG00735.hp2 HG02074.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.*36+2529_*36+2532d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | |||||||
chr8:41658897 | TATAAATA others(5): Show |
T | 7 | a0001c0001t0002g0021 a0001c0001t0002g0076 a0001c0001t0002g0233 others(4): Show |
8 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.*36+2521_*36+2532d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | |||||||
chr8:41658897 | TATAAATA others(9): Show |
T | 85 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.*36+2517_*36+2532d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658897 | |||||||
chr8:41658911 | TAAATAAA others(4): Show |
T | 1 | a0001c0003t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*36+2508_*36+2518d others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658911 | |||||||
chr8:41658966 | T | C | 87 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.*36+2464A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658966 | |||||||
chr8:41658970 | C | T | 2 | a0001c0019t0002g0174 a0016c0053t0002g0251 |
2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.*36+2460G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41658970 | |||||||
chr8:41659062 | A | G | 182 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.*36+2368T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659062 | |||||||
chr8:41659065 | C | T | 1 | a0001c0002t0012g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.*36+2365G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659065 | |||||||
chr8:41659081 | C | T | 3 | a0001c0008t0002g0204 a0001c0008t0015g0206 a0005c0021t0002g0114 |
3 | HG01515.hp1 HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.*36+2349G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659081 | |||||||
chr8:41659134 | G | A | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*36+2296C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659134 | |||||||
chr8:41659154 | G | C | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.*36+2276C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659154 | |||||||
chr8:41659184 | T | G | 1 | a0001c0003t0001g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.*36+2246A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659184 | |||||||
chr8:41659221 | C | T | 6 | a0001c0006t0005g0014 a0001c0006t0018g0118 a0001c0012t0005g0101 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*36+2209G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659221 | |||||||
chr8:41659271 | A | G | 60 | a0001c0001t0002g0010 a0001c0001t0002g0023 a0001c0001t0002g0057 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.*36+2159T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659271 | |||||||
chr8:41659396 | C | T | 105 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0190 others(102): Show |
106 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.*36+2034G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659396 | |||||||
chr8:41659422 | G | A | 1 | a0002c0007t0027g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*36+2008C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659422 | |||||||
chr8:41659468 | T | C | 23 | a0001c0003t0001g0147 a0001c0004t0001g0148 a0001c0005t0001g0084 others(20): Show |
23 | HG01167.hp1 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.*36+1962A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659468 | |||||||
chr8:41659472 | G | A | 64 | a0001c0001t0001g0142 a0001c0001t0001g0219 a0001c0001t0002g0010 others(61): Show |
64 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.*36+1958C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659472 | |||||||
chr8:41659539 | T | C | 1 | a0001c0037t0003g0234 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.*36+1891A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659539 | |||||||
chr8:41659545 | T | C | 13 | a0001c0001t0002g0021 a0001c0002t0009g0098 a0001c0005t0002g0019 others(10): Show |
14 | HG00738.hp1 HG01106.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.*36+1885A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659545 | |||||||
chr8:41659576 | C | T | 1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*36+1854G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659576 | |||||||
chr8:41659667 | G | A | 2 | a0003c0014t0008g0093 a0003c0014t0008g0094 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.*36+1763C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659667 | |||||||
chr8:41659813 | G | A | 1 | a0003c0014t0008g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.*36+1617C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41659813 | |||||||
chr8:41660155 | C | G | 1 | a0001c0004t0002g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*36+1275G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660155 | |||||||
chr8:41660341 | G | A | 71 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0023 others(68): Show |
72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.*36+1089C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660341 | |||||||
chr8:41660342 | G | T | 3 | a0001c0002t0001g0157 a0001c0002t0001g0166 a0001c0002t0001g0177 |
3 | NA18972.hp2 NA18986.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.*36+1088C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660342 | |||||||
chr8:41660437 | C | T | 2 | a0001c0001t0013g0090 a0001c0005t0013g0005 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.*36+993G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660437 | |||||||
chr8:41660463 | G | A | 1 | a0001c0005t0003g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*36+967C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660463 | |||||||
chr8:41660586 | G | A | 1 | a0001c0003t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*36+844C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660586 | |||||||
chr8:41660690 | C | T | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.*36+740G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41660690 | |||||||
chr8:41661062 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.*36+368C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661062 | |||||||
chr8:41661137 | A | T | 1 | a0001c0003t0001g0215 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.*36+293T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661137 | |||||||
chr8:41661197 | C | T | 19 | a0001c0004t0001g0108 a0001c0005t0001g0084 a0001c0006t0001g0100 others(16): Show |
19 | HG01891.hp2 HG02109.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.*36+233G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661197 | |||||||
chr8:41661307 | C | T | 1 | a0001c0008t0002g0217 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*36+123G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661307 | |||||||
chr8:41661354 | G | C | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.*36+76C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 42/42 | chr8 | 41661354 | |||||||
chr8:41661725 | T | G | 1 | a0001c0003t0001g0056 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5544+151A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661725 | |||||||
chr8:41661730 | T | C | 217 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.5544+146A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661730 | |||||||
chr8:41661731 | G | A | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5544+145C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661731 | |||||||
chr8:41661797 | G | A | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5544+79C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661797 | |||||||
chr8:41661830 | C | T | 2 | a0001c0037t0003g0234 a0003c0024t0003g0102 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5544+46G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 41/42 | chr8 | 41661830 | |||||||
chr8:41661944 | A | G | 211 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
splice_region_variant&intron_variant | LOW | c.5479-3T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41661944 | |||||||
chr8:41661986 | C | T | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5479-45G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41661986 | |||||||
chr8:41662033 | G | A | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5479-92C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662033 | |||||||
chr8:41662118 | G | A | 2 | a0001c0002t0001g0122 a0001c0002t0014g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5479-177C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662118 | |||||||
chr8:41662242 | G | C | 1 | a0001c0002t0009g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5479-301C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662242 | |||||||
chr8:41662256 | C | CA | 69 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(66): Show |
69 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.5479-316dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662256 | |||||||
chr8:41662426 | T | C | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5479-485A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662426 | |||||||
chr8:41662490 | C | G | 1 | a0001c0001t0002g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5479-549G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662490 | |||||||
chr8:41662494 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5479-553G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662494 | |||||||
chr8:41662553 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5479-612G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662553 | |||||||
chr8:41662746 | G | A | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5479-805C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662746 | |||||||
chr8:41662775 | G | A | 1 | a0003c0014t0002g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5479-834C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41662775 | |||||||
chr8:41663098 | G | C | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5478+561C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | |||||||
chr8:41663098 | G | GTCTC | 7 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5478+557_5478+560d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | |||||||
chr8:41663098 | G | GTCTCTC | 72 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0023 others(69): Show |
73 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.5478+555_5478+560d others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | |||||||
chr8:41663098 | G | GTCTCTCT others(1): Show |
3 | a0001c0003t0001g0050 a0001c0037t0003g0234 a0003c0024t0001g0272 |
3 | HG02717.hp1 HG02976.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.5478+553_5478+560d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663098 | |||||||
chr8:41663100 | C | G | 13 | a0001c0005t0001g0084 a0001c0006t0001g0100 a0001c0013t0006g0128 others(10): Show |
13 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.5478+559G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663100 | |||||||
chr8:41663110 | C | CTGTGTGT others(1): Show |
3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5478+548_5478+549i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663110 | |||||||
chr8:41663112 | C | CTGTGTGT others(1): Show |
8 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.5478+546_5478+547i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663112 | |||||||
chr8:41663112 | C | CTGTGTGT others(3): Show |
1 | a0001c0006t0018g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5478+546_5478+547i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663112 | |||||||
chr8:41663112 | C | G | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5478+547G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663112 | |||||||
chr8:41663114 | C | CTCTCTCT others(3): Show |
1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5478+544_5478+545i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTCTCTG | 46 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.5478+544_5478+545i others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTCTCTGT others(1): Show |
3 | a0001c0001t0001g0245 a0001c0003t0001g0262 a0001c0003t0014g0061 |
3 | HG03017.hp1 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.5478+544_5478+545i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTCTCTGT others(3): Show |
1 | a0001c0005t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5478+544_5478+545i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTCTGTG | 7 | a0001c0001t0001g0242 a0004c0011t0001g0185 a0004c0011t0001g0186 others(4): Show |
7 | HG02015.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5478+544_5478+545i others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTCTGTGT others(3): Show |
3 | a0001c0013t0006g0128 a0001c0013t0006g0130 a0015c0045t0025g0187 |
3 | HG03098.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5478+544_5478+545i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTCTGTGT others(5): Show |
1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5478+544_5478+545i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTG | 10 | a0002c0007t0001g0039 a0002c0007t0001g0041 a0002c0007t0007g0022 others(7): Show |
10 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.5478+543_5478+544d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTGTG | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5478+541_5478+544d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | CTGTGTGT others(3): Show |
4 | a0001c0018t0026g0113 a0001c0023t0001g0274 a0001c0023t0001g0275 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.5478+535_5478+544d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | C | G | 19 | a0001c0002t0001g0183 a0001c0002t0009g0098 a0001c0004t0002g0068 others(16): Show |
19 | HG01192.hp2 HG01258.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.5478+545G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663114 | CTG | C | 2 | a0001c0025t0011g0002 a0001c0030t0017g0058 |
3 | HG03491.hp2 HG03492.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5478+543_5478+544d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663114 | |||||||
chr8:41663116 | G | C | 7 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5478+543C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663116 | |||||||
chr8:41663142 | A | G | 3 | a0002c0007t0001g0039 a0002c0007t0001g0041 a0002c0007t0027g0036 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5478+517T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663142 | |||||||
chr8:41663156 | T | A | 2 | a0001c0003t0001g0162 a0001c0003t0001g0237 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5478+503A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663156 | |||||||
chr8:41663435 | C | T | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5478+224G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 40/42 | chr8 | 41663435 | |||||||
chr8:41663842 | A | G | 1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5395-100T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663842 | |||||||
chr8:41663951 | C | G | 135 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.5395-209G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663951 | |||||||
chr8:41663955 | C | T | 6 | a0001c0005t0001g0084 a0001c0006t0001g0100 a0001c0013t0006g0128 others(3): Show |
6 | HG02630.hp1 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.5395-213G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663955 | |||||||
chr8:41663956 | G | A | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5395-214C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41663956 | |||||||
chr8:41664145 | T | C | 138 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.5395-403A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664145 | |||||||
chr8:41664165 | G | A | 2 | a0001c0001t0013g0090 a0001c0005t0013g0005 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5395-423C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664165 | |||||||
chr8:41664195 | C | T | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5395-453G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664195 | |||||||
chr8:41664244 | G | C | 3 | a0001c0003t0001g0054 a0001c0003t0001g0056 a0001c0003t0001g0070 |
3 | HG00099.hp2 HG01255.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.5395-502C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664244 | |||||||
chr8:41664424 | A | G | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5395-682T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664424 | |||||||
chr8:41664462 | T | G | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5395-720A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664462 | |||||||
chr8:41664498 | AAAGAG | A | 40 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(37): Show |
40 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.5395-761_5395-757d others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664498 | |||||||
chr8:41664672 | C | T | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5395-930G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664672 | |||||||
chr8:41664687 | T | G | 2 | a0001c0013t0006g0128 a0001c0013t0006g0130 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5395-945A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664687 | |||||||
chr8:41664694 | C | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0190 |
2 | NA18948.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.5395-952G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664694 | |||||||
chr8:41664698 | C | T | 1 | a0001c0003t0001g0147 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5395-956G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664698 | |||||||
chr8:41664708 | C | G | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5395-966G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664708 | |||||||
chr8:41664889 | G | C | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5395-1147C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41664889 | |||||||
chr8:41665028 | G | A | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5395-1286C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665028 | |||||||
chr8:41665231 | G | A | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5395-1489C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665231 | |||||||
chr8:41665322 | T | C | 1 | a0001c0026t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5395-1580A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665322 | |||||||
chr8:41665325 | C | T | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5395-1583G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665325 | |||||||
chr8:41665342 | G | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0180 |
2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.5395-1600C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665342 | |||||||
chr8:41665473 | A | G | 212 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.5395-1731T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665473 | |||||||
chr8:41665562 | A | G | 1 | a0001c0003t0001g0137 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5395-1820T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665562 | |||||||
chr8:41665610 | G | A | 3 | a0001c0004t0001g0148 a0001c0004t0002g0068 a0001c0004t0002g0176 |
3 | HG02683.hp2 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.5395-1868C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665610 | |||||||
chr8:41665645 | C | A | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5395-1903G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665645 | |||||||
chr8:41665816 | C | T | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5395-2074G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665816 | |||||||
chr8:41665840 | A | G | 53 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(50): Show |
54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.5395-2098T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665840 | |||||||
chr8:41665918 | C | T | 2 | a0001c0018t0026g0113 a0002c0057t0005g0265 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5395-2176G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41665918 | |||||||
chr8:41666149 | C | T | 2 | a0001c0001t0002g0210 a0014c0031t0002g0256 |
2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5394+2118G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666149 | |||||||
chr8:41666150 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5394+2117C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666150 | |||||||
chr8:41666170 | C | T | 2 | a0001c0001t0002g0210 a0014c0031t0002g0256 |
2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5394+2097G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666170 | |||||||
chr8:41666227 | G | A | 57 | a0001c0002t0009g0098 a0001c0004t0001g0108 a0001c0004t0001g0148 others(54): Show |
58 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.5394+2040C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666227 | |||||||
chr8:41666241 | CT | C | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+2025delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666241 | |||||||
chr8:41666257 | G | A | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+2010C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666257 | |||||||
chr8:41666323 | G | A | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5394+1944C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666323 | |||||||
chr8:41666769 | A | G | 192 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.5394+1498T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666769 | |||||||
chr8:41666872 | G | A | 1 | a0001c0004t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5394+1395C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666872 | |||||||
chr8:41666907 | A | G | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+1360T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666907 | |||||||
chr8:41666965 | T | G | 2 | a0001c0018t0026g0113 a0002c0057t0005g0265 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5394+1302A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666965 | |||||||
chr8:41666987 | A | G | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+1280T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41666987 | |||||||
chr8:41667018 | C | T | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+1249G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667018 | |||||||
chr8:41667170 | C | T | 53 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(50): Show |
54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.5394+1097G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667170 | |||||||
chr8:41667171 | G | A | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+1096C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667171 | |||||||
chr8:41667290 | G | C | 192 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.5394+977C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667290 | |||||||
chr8:41667332 | A | T | 1 | a0001c0003t0002g0154 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5394+935T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667332 | |||||||
chr8:41667381 | A | G | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5394+886T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667381 | |||||||
chr8:41667659 | C | T | 5 | a0001c0001t0002g0023 a0001c0001t0002g0132 a0001c0012t0005g0101 others(2): Show |
5 | HG02109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.5394+608G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667659 | |||||||
chr8:41667825 | G | A | 3 | a0002c0007t0001g0039 a0002c0007t0001g0041 a0002c0007t0027g0036 |
3 | HG02886.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5394+442C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667825 | |||||||
chr8:41667838 | G | A | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5394+429C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667838 | |||||||
chr8:41667866 | G | A | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5394+401C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667866 | |||||||
chr8:41667869 | A | T | 135 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.5394+398T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667869 | |||||||
chr8:41667982 | G | C | 190 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.5394+285C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41667982 | |||||||
chr8:41668070 | C | T | 76 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0023 others(73): Show |
77 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.5394+197G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668070 | |||||||
chr8:41668121 | T | C | 1 | a0001c0004t0002g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5394+146A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668121 | |||||||
chr8:41668245 | G | A | 10 | a0001c0003t0001g0147 a0001c0006t0003g0006 a0001c0006t0003g0013 others(7): Show |
10 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.5394+22C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668245 | |||||||
chr8:41668246 | C | T | 1 | a0001c0012t0005g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5394+21G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668246 | |||||||
chr8:41668256 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.5394+11G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 39/42 | chr8 | 41668256 | |||||||
chr8:41668711 | G | T | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5097-147C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41668711 | |||||||
chr8:41668880 | G | C | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5097-316C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41668880 | |||||||
chr8:41669009 | G | A | 133 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.5097-445C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669009 | |||||||
chr8:41669057 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5097-493G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669057 | |||||||
chr8:41669058 | G | A | 1 | a0001c0004t0002g0120 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.5097-494C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669058 | |||||||
chr8:41669123 | CG | C | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5097-560delC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669123 | |||||||
chr8:41669188 | T | C | 2 | a0001c0005t0001g0084 a0001c0006t0001g0100 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5097-624A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669188 | |||||||
chr8:41669267 | T | G | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.5097-703A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669267 | |||||||
chr8:41669445 | C | A | 2 | a0001c0003t0001g0162 a0001c0003t0001g0237 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5097-881G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669445 | |||||||
chr8:41669453 | C | G | 8 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0004c0011t0001g0185 others(5): Show |
8 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.5097-889G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669453 | |||||||
chr8:41669737 | C | T | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5097-1173G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669737 | |||||||
chr8:41669786 | C | T | 1 | a0001c0037t0003g0234 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5097-1222G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669786 | |||||||
chr8:41669902 | C | T | 1 | a0001c0004t0002g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5097-1338G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41669902 | |||||||
chr8:41670059 | C | T | 1 | a0001c0003t0001g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5097-1495G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670059 | |||||||
chr8:41670067 | C | T | 2 | a0001c0004t0002g0200 a0001c0004t0024g0199 |
2 | HG02080.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.5097-1503G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670067 | |||||||
chr8:41670113 | C | T | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5097-1549G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670113 | |||||||
chr8:41670178 | G | T | 2 | a0004c0020t0001g0037 a0012c0033t0001g0107 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.5097-1614C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670178 | |||||||
chr8:41670483 | G | A | 1 | a0001c0004t0002g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5096+1871C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670483 | |||||||
chr8:41670486 | C | G | 3 | a0001c0002t0001g0134 a0001c0003t0001g0140 a0001c0003t0009g0163 |
3 | HG01934.hp2 HG02004.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.5096+1868G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670486 | |||||||
chr8:41670660 | G | T | 57 | a0001c0002t0009g0098 a0001c0004t0001g0108 a0001c0004t0001g0148 others(54): Show |
58 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.5096+1694C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670660 | |||||||
chr8:41670710 | G | C | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
55 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.5096+1644C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41670710 | |||||||
chr8:41671035 | T | C | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.5096+1319A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671035 | |||||||
chr8:41671090 | C | T | 3 | a0001c0004t0001g0108 a0001c0018t0026g0113 a0002c0057t0005g0265 |
3 | HG01891.hp1 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5096+1264G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671090 | |||||||
chr8:41671161 | G | A | 1 | a0001c0003t0009g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5096+1193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671161 | |||||||
chr8:41671617 | C | CCTCCCGG others(86): Show |
50 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(47): Show |
51 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.5096+736_5096+737i others(95): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671617 | |||||||
chr8:41671654 | A | G | 4 | a0002c0007t0007g0024 a0002c0007t0007g0025 a0002c0007t0007g0028 others(1): Show |
4 | HG01167.hp1 HG02258.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.5096+700T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671654 | |||||||
chr8:41671657 | ACCCCGAT others(24): Show |
A | 1 | a0001c0018t0026g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5096+666_5096+696d others(33): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671657 | |||||||
chr8:41671715 | C | T | 1 | a0013c0047t0002g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5096+639G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671715 | |||||||
chr8:41671827 | GTGAGTCC others(50): Show |
G | 2 | a0001c0018t0026g0113 a0002c0057t0005g0265 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5096+470_5096+526d others(59): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671827 | |||||||
chr8:41671877 | G | A | 1 | a0001c0002t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.5096+477C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41671877 | |||||||
chr8:41672242 | A | C | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5096+112T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672242 | |||||||
chr8:41672243 | G | T | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5096+111C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672243 | |||||||
chr8:41672244 | A | AATTGCAC others(8): Show |
9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5096+109_5096+110i others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672244 | |||||||
chr8:41672271 | C | T | 4 | a0001c0051t0008g0273 a0003c0014t0008g0093 a0003c0014t0008g0094 others(1): Show |
4 | HG00738.hp1 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.5096+83G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672271 | |||||||
chr8:41672338 | A | G | 265 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.5096+16T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 38/42 | chr8 | 41672338 | |||||||
chr8:41672964 | C | G | 252 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4538-52G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41672964 | |||||||
chr8:41672971 | C | T | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4538-59G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41672971 | |||||||
chr8:41672980 | CCACGCAC others(3): Show |
C | 1 | a0001c0004t0002g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4538-78_4538-69del others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41672980 | |||||||
chr8:41673014 | G | A | 4 | a0001c0016t0002g0007 a0001c0016t0002g0008 a0001c0016t0002g0009 others(1): Show |
4 | HG01192.hp2 HG01258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4538-102C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673014 | |||||||
chr8:41673048 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4538-136C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673048 | |||||||
chr8:41673099 | G | T | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4538-187C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673099 | |||||||
chr8:41673485 | T | C | 134 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.4538-573A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673485 | |||||||
chr8:41673556 | T | C | 249 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4538-644A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673556 | |||||||
chr8:41673618 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4538-706T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673618 | |||||||
chr8:41673721 | T | C | 138 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.4538-809A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673721 | |||||||
chr8:41673733 | G | C | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4538-821C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673733 | |||||||
chr8:41673960 | C | T | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.4538-1048G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673960 | |||||||
chr8:41673968 | C | T | 4 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.4538-1056G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673968 | |||||||
chr8:41673997 | A | G | 2 | a0001c0018t0026g0113 a0002c0057t0005g0265 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4538-1085T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41673997 | |||||||
chr8:41674098 | C | T | 42 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.4538-1186G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674098 | |||||||
chr8:41674115 | C | CCCTCAGC others(12): Show |
2 | a0001c0002t0001g0183 a0001c0004t0002g0220 |
2 | HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4538-1222_4538-120 others(23): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674115 | |||||||
chr8:41674195 | A | G | 1 | a0001c0004t0002g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4538-1283T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674195 | |||||||
chr8:41674324 | C | A | 1 | a0001c0005t0001g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4538-1412G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674324 | |||||||
chr8:41674597 | T | C | 1 | a0001c0004t0002g0120 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4538-1685A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674597 | |||||||
chr8:41674615 | A | T | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-1703T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674615 | |||||||
chr8:41674674 | C | T | 3 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0013c0047t0002g0016 |
3 | HG02965.hp1 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4538-1762G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674674 | |||||||
chr8:41674738 | C | G | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-1826G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674738 | |||||||
chr8:41674824 | T | G | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4538-1912A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41674824 | |||||||
chr8:41675073 | T | C | 1 | a0005c0021t0002g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4538-2161A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675073 | |||||||
chr8:41675129 | T | C | 192 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.4538-2217A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675129 | |||||||
chr8:41675151 | T | C | 2 | a0001c0019t0002g0174 a0016c0053t0002g0251 |
2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.4538-2239A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675151 | |||||||
chr8:41675245 | C | T | 7 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4538-2333G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675245 | |||||||
chr8:41675253 | C | T | 9 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(6): Show |
9 | HG02074.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-2341G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675253 | |||||||
chr8:41675260 | C | G | 1 | a0001c0016t0002g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4538-2348G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675260 | |||||||
chr8:41675682 | C | A | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4538-2770G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675682 | |||||||
chr8:41675683 | T | C | 192 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.4538-2771A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675683 | |||||||
chr8:41675727 | C | A | 1 | a0001c0001t0002g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4538-2815G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675727 | |||||||
chr8:41675879 | C | T | 193 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.4538-2967G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675879 | |||||||
chr8:41675995 | C | T | 1 | a0001c0004t0002g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4538-3083G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675995 | |||||||
chr8:41675996 | A | G | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4538-3084T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41675996 | |||||||
chr8:41676248 | T | C | 11 | a0001c0040t0001g0085 a0002c0007t0001g0039 a0002c0007t0001g0041 others(8): Show |
11 | HG01167.hp1 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4538-3336A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676248 | |||||||
chr8:41676329 | A | T | 192 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.4538-3417T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676329 | |||||||
chr8:41676550 | T | C | 54 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4538-3638A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676550 | |||||||
chr8:41676668 | G | A | 1 | a0001c0013t0006g0128 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4538-3756C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676668 | |||||||
chr8:41676900 | C | T | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4538-3988G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676900 | |||||||
chr8:41676939 | A | G | 138 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.4538-4027T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676939 | |||||||
chr8:41676966 | C | T | 9 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(6): Show |
9 | HG02074.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.4538-4054G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676966 | |||||||
chr8:41676967 | A | G | 211 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.4538-4055T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41676967 | |||||||
chr8:41677092 | G | A | 2 | a0001c0013t0006g0128 a0001c0013t0006g0130 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4538-4180C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677092 | |||||||
chr8:41677584 | C | T | 254 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.4538-4672G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677584 | |||||||
chr8:41677594 | G | GT | 100 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(97): Show |
101 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.4538-4683dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677594 | |||||||
chr8:41677594 | G | GTT | 6 | a0001c0002t0001g0160 a0001c0030t0017g0058 a0002c0007t0001g0039 others(3): Show |
6 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4538-4684_4538-468 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677594 | |||||||
chr8:41677665 | C | T | 1 | a0001c0002t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4538-4753G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677665 | |||||||
chr8:41677693 | G | A | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.4538-4781C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677693 | |||||||
chr8:41677885 | T | C | 192 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.4538-4973A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677885 | |||||||
chr8:41677922 | T | G | 138 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.4538-5010A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41677922 | |||||||
chr8:41678130 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4538-5218A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678130 | |||||||
chr8:41678152 | T | A | 1 | a0001c0028t0003g0066 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4538-5240A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678152 | |||||||
chr8:41678229 | C | T | 2 | a0001c0012t0006g0096 a0001c0012t0006g0097 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4538-5317G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678229 | |||||||
chr8:41678242 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4538-5330C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678242 | |||||||
chr8:41678368 | C | T | 43 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(40): Show |
44 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.4538-5456G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678368 | |||||||
chr8:41678774 | T | C | 3 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0245 |
3 | NA19002.hp2 NA19005.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.4537+5770A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41678774 | |||||||
chr8:41679304 | T | C | 265 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.4537+5240A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679304 | |||||||
chr8:41679558 | C | CT | 13 | a0001c0001t0001g0211 a0001c0001t0002g0077 a0001c0001t0002g0197 others(10): Show |
13 | HG00323.hp1 HG00408.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.4537+4985dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | |||||||
chr8:41679558 | C | CTT | 113 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.4537+4984_4537+498 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | |||||||
chr8:41679558 | C | CTTT | 13 | a0001c0002t0001g0134 a0001c0003t0001g0050 a0001c0003t0001g0140 others(10): Show |
13 | HG00438.hp1 HG01891.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.4537+4983_4537+498 others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | |||||||
chr8:41679558 | CT | C | 54 | a0001c0001t0002g0241 a0001c0002t0001g0159 a0001c0004t0001g0108 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.4537+4985delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679558 | |||||||
chr8:41679586 | A | G | 193 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.4537+4958T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679586 | |||||||
chr8:41679610 | G | T | 1 | a0001c0010t0003g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4537+4934C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679610 | |||||||
chr8:41679636 | C | T | 1 | a0001c0004t0001g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4537+4908G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679636 | |||||||
chr8:41679656 | G | A | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4537+4888C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679656 | |||||||
chr8:41679665 | C | T | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.4537+4879G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679665 | |||||||
chr8:41679708 | G | A | 4 | a0001c0037t0003g0234 a0003c0024t0001g0272 a0003c0024t0003g0102 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4537+4836C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679708 | |||||||
chr8:41679723 | A | C | 254 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.4537+4821T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679723 | |||||||
chr8:41679800 | G | A | 54 | a0001c0001t0002g0241 a0001c0004t0001g0108 a0001c0004t0001g0148 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.4537+4744C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679800 | |||||||
chr8:41679956 | T | C | 1 | a0004c0011t0001g0185 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4537+4588A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679956 | |||||||
chr8:41679958 | T | G | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4537+4586A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41679958 | |||||||
chr8:41680097 | G | C | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4537+4447C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680097 | |||||||
chr8:41680285 | G | A | 8 | a0001c0003t0001g0060 a0001c0003t0001g0135 a0001c0003t0001g0137 others(5): Show |
8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4537+4259C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680285 | |||||||
chr8:41680392 | C | T | 51 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(48): Show |
51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.4537+4152G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680392 | |||||||
chr8:41680421 | G | A | 2 | a0001c0026t0001g0156 a0001c0029t0001g0254 |
2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4537+4123C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680421 | |||||||
chr8:41680431 | C | T | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4537+4113G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680431 | |||||||
chr8:41680520 | G | T | 5 | a0001c0010t0003g0269 a0001c0028t0003g0066 a0003c0015t0003g0136 others(2): Show |
5 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.4537+4024C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680520 | |||||||
chr8:41680565 | CA | C | 86 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(83): Show |
88 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.4537+3978delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680565 | |||||||
chr8:41680565 | CAA | C | 55 | a0001c0001t0001g0151 a0001c0001t0001g0211 a0001c0001t0002g0057 others(52): Show |
55 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.4537+3977_4537+397 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680565 | |||||||
chr8:41680749 | G | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0008t0002g0253 |
3 | HG01952.hp1 HG02683.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.4537+3795C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680749 | |||||||
chr8:41680768 | A | G | 189 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0207 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.4537+3776T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41680768 | |||||||
chr8:41681096 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4537+3448C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681096 | |||||||
chr8:41681180 | C | T | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4537+3364G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681180 | |||||||
chr8:41681330 | C | A | 1 | a0001c0030t0017g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4537+3214G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681330 | |||||||
chr8:41681330 | C | T | 1 | a0001c0016t0002g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4537+3214G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681330 | |||||||
chr8:41681353 | T | C | 45 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(42): Show |
46 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.4537+3191A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681353 | |||||||
chr8:41681404 | A | G | 10 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0016t0002g0007 others(7): Show |
10 | HG00738.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4537+3140T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681404 | |||||||
chr8:41681678 | C | T | 5 | a0001c0006t0005g0014 a0001c0006t0018g0118 a0001c0017t0005g0116 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+2866G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681678 | |||||||
chr8:41681679 | A | G | 5 | a0001c0006t0005g0014 a0001c0006t0018g0118 a0001c0017t0005g0116 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+2865T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681679 | |||||||
chr8:41681681 | G | GCTGGTTG others(4): Show |
5 | a0001c0006t0005g0014 a0001c0006t0018g0118 a0001c0017t0005g0116 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+2862_4537+286 others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681681 | |||||||
chr8:41681689 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4537+2855C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41681689 | |||||||
chr8:41682079 | C | T | 1 | a0001c0012t0001g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4537+2465G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682079 | |||||||
chr8:41682266 | G | A | 7 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4537+2278C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682266 | |||||||
chr8:41682380 | C | G | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4537+2164G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682380 | |||||||
chr8:41682410 | C | T | 2 | a0001c0008t0002g0212 a0001c0008t0002g0217 |
2 | HG00438.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.4537+2134G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682410 | |||||||
chr8:41682452 | G | A | 14 | a0001c0006t0001g0100 a0001c0028t0003g0066 a0003c0015t0003g0136 others(11): Show |
15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4537+2092C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682452 | |||||||
chr8:41682553 | C | A | 3 | a0001c0037t0003g0234 a0003c0024t0001g0272 a0003c0024t0003g0102 |
3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4537+1991G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682553 | |||||||
chr8:41682557 | C | A | 1 | a0001c0006t0001g0268 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4537+1987G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682557 | |||||||
chr8:41682578 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(2): Show |
5 | NA18948.hp2 NA18979.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.4537+1966G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682578 | |||||||
chr8:41682674 | G | A | 14 | a0001c0006t0001g0100 a0001c0028t0003g0066 a0003c0015t0003g0136 others(11): Show |
15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4537+1870C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682674 | |||||||
chr8:41682869 | C | T | 64 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(61): Show |
65 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.4537+1675G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682869 | |||||||
chr8:41682917 | T | C | 2 | a0001c0005t0001g0084 a0005c0035t0001g0129 |
2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4537+1627A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41682917 | |||||||
chr8:41683031 | C | CACGGACA others(13): Show |
14 | a0001c0006t0001g0100 a0001c0028t0003g0066 a0003c0015t0003g0136 others(11): Show |
15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4537+1493_4537+151 others(24): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683031 | |||||||
chr8:41683097 | C | A | 1 | a0001c0008t0002g0203 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4537+1447G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683097 | |||||||
chr8:41683098 | G | A | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4537+1446C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683098 | |||||||
chr8:41683103 | C | T | 2 | a0001c0001t0002g0021 a0002c0043t0002g0045 |
2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4537+1441G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683103 | |||||||
chr8:41683104 | A | G | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4537+1440T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683104 | |||||||
chr8:41683115 | TACGC | T | 8 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4537+1425_4537+142 others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683115 | |||||||
chr8:41683211 | C | T | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4537+1333G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683211 | |||||||
chr8:41683226 | GGACAGTG others(2): Show |
G | 4 | a0001c0028t0003g0066 a0003c0015t0003g0136 a0003c0015t0003g0214 others(1): Show |
4 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537+1309_4537+131 others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683226 | |||||||
chr8:41683253 | GCACGATA others(1276): Show |
G | 1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.4537+8_4537+1290de others(1): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683253 | |||||||
chr8:41683282 | G | A | 4 | a0001c0028t0003g0066 a0003c0015t0003g0136 a0003c0015t0003g0214 others(1): Show |
4 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537+1262C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683282 | |||||||
chr8:41683292 | G | C | 5 | a0001c0051t0008g0273 a0003c0014t0002g0198 a0003c0014t0008g0093 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.4537+1252C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683292 | |||||||
chr8:41683310 | T | C | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4537+1234A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683310 | |||||||
chr8:41683366 | G | A | 52 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.4537+1178C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683366 | |||||||
chr8:41683437 | C | T | 1 | a0001c0010t0002g0081 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4537+1107G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683437 | |||||||
chr8:41683455 | G | A | 3 | a0001c0037t0003g0234 a0003c0024t0001g0272 a0003c0024t0003g0102 |
3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4537+1089C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683455 | |||||||
chr8:41683531 | C | T | 133 | a0001c0001t0001g0149 a0001c0001t0001g0207 a0001c0001t0001g0209 others(130): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.4537+1013G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683531 | |||||||
chr8:41683768 | C | T | 1 | a0001c0002t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4537+776G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683768 | |||||||
chr8:41683802 | G | A | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4537+742C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41683802 | |||||||
chr8:41684121 | A | G | 1 | a0001c0005t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4537+423T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684121 | |||||||
chr8:41684150 | C | T | 1 | a0003c0014t0002g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4537+394G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684150 | |||||||
chr8:41684223 | A | G | 260 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.4537+321T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684223 | |||||||
chr8:41684229 | C | T | 1 | a0002c0007t0007g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4537+315G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684229 | |||||||
chr8:41684328 | G | A | 3 | a0001c0037t0003g0234 a0003c0024t0001g0272 a0003c0024t0003g0102 |
3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4537+216C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684328 | |||||||
chr8:41684345 | G | A | 4 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(1): Show |
4 | HG02647.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537+199C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684345 | |||||||
chr8:41684443 | C | T | 1 | a0001c0004t0002g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4537+101G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684443 | |||||||
chr8:41684460 | C | T | 2 | a0001c0002t0001g0183 a0001c0002t0001g0184 |
2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4537+84G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 37/42 | chr8 | 41684460 | |||||||
chr8:41684735 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4391-45G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684735 | |||||||
chr8:41684739 | G | A | 15 | a0001c0006t0001g0100 a0001c0028t0003g0066 a0003c0015t0003g0136 others(12): Show |
16 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.4391-49C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684739 | |||||||
chr8:41684810 | G | A | 3 | a0001c0002t0009g0098 a0001c0046t0030g0276 a0013c0047t0002g0016 |
3 | HG02723.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4391-120C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684810 | |||||||
chr8:41684937 | A | T | 4 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(1): Show |
4 | HG02647.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4391-247T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684937 | |||||||
chr8:41684942 | A | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4391-252T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41684942 | |||||||
chr8:41685025 | C | T | 138 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0087 others(135): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.4391-335G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685025 | |||||||
chr8:41685054 | G | A | 1 | a0001c0003t0019g0065 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4391-364C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685054 | |||||||
chr8:41685086 | G | A | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4391-396C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685086 | |||||||
chr8:41685149 | G | A | 1 | a0001c0040t0001g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4391-459C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685149 | |||||||
chr8:41685398 | A | G | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4391-708T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685398 | |||||||
chr8:41685456 | C | T | 5 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4390+696G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685456 | |||||||
chr8:41685632 | C | G | 2 | a0001c0002t0001g0183 a0001c0002t0001g0184 |
2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4390+520G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685632 | |||||||
chr8:41685645 | AT | A | 138 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0087 others(135): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.4390+506delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685645 | |||||||
chr8:41685670 | T | G | 1 | a0003c0015t0003g0250 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4390+482A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685670 | |||||||
chr8:41685823 | C | A | 6 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4390+329G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685823 | |||||||
chr8:41685944 | G | C | 1 | a0001c0002t0002g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4390+208C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 36/42 | chr8 | 41685944 | |||||||
chr8:41686355 | C | T | 1 | a0001c0004t0002g0208 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4259-72G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686355 | |||||||
chr8:41686424 | G | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0005t0001g0257 |
3 | HG01123.hp1 HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4259-141C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686424 | |||||||
chr8:41686812 | A | G | 29 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(26): Show |
29 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.4259-529T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686812 | |||||||
chr8:41686967 | C | T | 2 | a0001c0002t0009g0098 a0013c0047t0002g0016 |
2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4259-684G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686967 | |||||||
chr8:41686974 | ACACT | A | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.4259-695_4259-692d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41686974 | |||||||
chr8:41687236 | C | T | 5 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4258+920G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687236 | |||||||
chr8:41687340 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4258+816C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687340 | |||||||
chr8:41687456 | C | A | 1 | a0003c0049t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4258+700G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687456 | |||||||
chr8:41687474 | C | T | 4 | a0001c0028t0003g0066 a0003c0015t0003g0136 a0003c0015t0003g0214 others(1): Show |
4 | HG02074.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4258+682G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687474 | |||||||
chr8:41687558 | C | G | 92 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0087 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.4258+598G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687558 | |||||||
chr8:41687585 | C | T | 27 | a0001c0006t0001g0040 a0001c0006t0001g0263 a0001c0006t0001g0266 others(24): Show |
27 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.4258+571G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687585 | |||||||
chr8:41687677 | T | C | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4258+479A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687677 | |||||||
chr8:41687740 | T | C | 2 | a0001c0002t0001g0032 a0001c0002t0012g0031 |
2 | HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4258+416A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687740 | |||||||
chr8:41687765 | G | A | 1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4258+391C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687765 | |||||||
chr8:41687987 | G | A | 1 | a0001c0019t0002g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4258+169C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687987 | |||||||
chr8:41687995 | A | G | 1 | a0001c0005t0001g0257 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4258+161T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687995 | |||||||
chr8:41687998 | G | T | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4258+158C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41687998 | |||||||
chr8:41688123 | A | G | 31 | a0001c0006t0001g0100 a0001c0006t0003g0006 a0001c0006t0003g0013 others(28): Show |
32 | HG02074.hp1 HG02109.hp2 HG02559.hp1 others(29): Show |
intron_variant | MODIFIER | c.4258+33T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 35/42 | chr8 | 41688123 | |||||||
chr8:41688297 | G | A | 1 | a0001c0012t0005g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4184-67C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 34/42 | chr8 | 41688297 | |||||||
chr8:41688614 | G | T | 1 | a0001c0002t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4105-25C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688614 | |||||||
chr8:41688675 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4105-86C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688675 | |||||||
chr8:41688735 | A | G | 4 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0046t0030g0276 others(1): Show |
4 | HG02723.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4105-146T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688735 | |||||||
chr8:41688782 | G | A | 1 | a0001c0004t0002g0201 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4105-193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688782 | |||||||
chr8:41688814 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4105-225C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688814 | |||||||
chr8:41688876 | G | A | 9 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.4105-287C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688876 | |||||||
chr8:41688908 | C | A | 19 | a0001c0006t0001g0100 a0001c0013t0001g0027 a0001c0013t0001g0038 others(16): Show |
20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-319G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688908 | |||||||
chr8:41688966 | A | G | 260 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.4105-377T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688966 | |||||||
chr8:41688983 | A | G | 1 | a0001c0010t0003g0269 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4105-394T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688983 | |||||||
chr8:41688994 | T | C | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4105-405A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41688994 | |||||||
chr8:41689138 | G | A | 19 | a0001c0006t0001g0100 a0001c0013t0001g0027 a0001c0013t0001g0038 others(16): Show |
20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-549C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689138 | |||||||
chr8:41689195 | TC | T | 19 | a0001c0006t0001g0100 a0001c0013t0001g0027 a0001c0013t0001g0038 others(16): Show |
20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-607delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689195 | |||||||
chr8:41689216 | C | T | 3 | a0001c0002t0001g0134 a0001c0003t0009g0163 a0001c0012t0001g0138 |
3 | HG01928.hp2 HG02004.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.4105-627G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689216 | |||||||
chr8:41689217 | G | A | 1 | a0001c0058t0022g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4105-628C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689217 | |||||||
chr8:41689221 | T | C | 5 | a0001c0001t0002g0023 a0001c0001t0002g0132 a0001c0012t0005g0101 others(2): Show |
5 | HG02109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4105-632A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689221 | |||||||
chr8:41689251 | G | A | 2 | a0001c0004t0002g0200 a0001c0004t0024g0199 |
2 | HG02080.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.4105-662C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689251 | |||||||
chr8:41689296 | A | AT | 124 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0087 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.4105-708dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689296 | |||||||
chr8:41689302 | T | A | 19 | a0001c0006t0001g0100 a0001c0013t0001g0027 a0001c0013t0001g0038 others(16): Show |
20 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.4105-713A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689302 | |||||||
chr8:41689403 | C | T | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4105-814G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689403 | |||||||
chr8:41689420 | G | A | 2 | a0001c0005t0001g0084 a0005c0035t0001g0129 |
2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4104+807C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689420 | |||||||
chr8:41689541 | A | G | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4104+686T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689541 | |||||||
chr8:41689601 | G | C | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.4104+626C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689601 | |||||||
chr8:41689615 | G | C | 3 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0005t0001g0257 |
3 | HG01123.hp1 HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4104+612C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689615 | |||||||
chr8:41689666 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4104+561T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689666 | |||||||
chr8:41689868 | A | G | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.4104+359T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689868 | |||||||
chr8:41689937 | C | A | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4104+290G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41689937 | |||||||
chr8:41690035 | C | A | 3 | a0001c0037t0003g0234 a0003c0024t0001g0272 a0003c0024t0003g0102 |
3 | HG02717.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4104+192G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690035 | |||||||
chr8:41690056 | A | G | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.4104+171T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690056 | |||||||
chr8:41690142 | G | A | 39 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(36): Show |
40 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.4104+85C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690142 | |||||||
chr8:41690160 | G | T | 3 | a0001c0040t0001g0085 a0005c0021t0002g0114 a0005c0021t0002g0131 |
3 | HG02280.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4104+67C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690160 | |||||||
chr8:41690165 | T | C | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.4104+62A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 33/42 | chr8 | 41690165 | |||||||
chr8:41690689 | C | T | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-90G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690689 | |||||||
chr8:41690691 | C | T | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-92G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690691 | |||||||
chr8:41690780 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3859-181A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690780 | |||||||
chr8:41690794 | C | T | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-195G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690794 | |||||||
chr8:41690908 | A | AAAC | 5 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-312_3859-310d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690908 | |||||||
chr8:41690917 | C | T | 52 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(49): Show |
53 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.3859-318G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41690917 | |||||||
chr8:41691011 | T | G | 1 | a0001c0038t0002g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3859-412A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691011 | |||||||
chr8:41691070 | A | T | 60 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(57): Show |
61 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.3859-471T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691070 | |||||||
chr8:41691077 | C | T | 57 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0100 others(54): Show |
58 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.3859-478G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691077 | |||||||
chr8:41691282 | C | G | 28 | a0001c0006t0001g0100 a0001c0006t0003g0006 a0001c0006t0003g0013 others(25): Show |
29 | HG02074.hp1 HG02109.hp2 HG02559.hp1 others(26): Show |
intron_variant | MODIFIER | c.3859-683G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691282 | |||||||
chr8:41691339 | T | C | 1 | a0001c0005t0001g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3859-740A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691339 | |||||||
chr8:41691368 | G | C | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3859-769C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691368 | |||||||
chr8:41691393 | A | T | 29 | a0001c0006t0001g0100 a0001c0006t0003g0006 a0001c0006t0003g0013 others(26): Show |
30 | HG01123.hp2 HG02074.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3859-794T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691393 | |||||||
chr8:41691440 | C | G | 5 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3859-841G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691440 | |||||||
chr8:41691498 | G | A | 2 | a0001c0001t0002g0210 a0014c0031t0002g0256 |
2 | NA18986.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3859-899C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691498 | |||||||
chr8:41691595 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3859-996C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691595 | |||||||
chr8:41691676 | T | C | 29 | a0001c0006t0001g0100 a0001c0006t0003g0006 a0001c0006t0003g0013 others(26): Show |
30 | HG01123.hp2 HG02074.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3858+972A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691676 | |||||||
chr8:41691893 | C | T | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3858+755G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691893 | |||||||
chr8:41691931 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3858+717C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691931 | |||||||
chr8:41691973 | G | A | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3858+675C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41691973 | |||||||
chr8:41692059 | CT | C | 34 | a0001c0001t0001g0209 a0001c0002t0001g0159 a0001c0002t0003g0080 others(31): Show |
34 | HG01070.hp2 HG01106.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.3858+588delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692059 | |||||||
chr8:41692081 | G | C | 1 | a0001c0001t0002g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3858+567C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692081 | |||||||
chr8:41692097 | C | T | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3858+551G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692097 | |||||||
chr8:41692119 | C | T | 19 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(16): Show |
19 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.3858+529G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692119 | |||||||
chr8:41692167 | C | T | 5 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3858+481G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692167 | |||||||
chr8:41692300 | G | A | 28 | a0001c0006t0001g0100 a0001c0006t0003g0006 a0001c0006t0003g0013 others(25): Show |
29 | HG02074.hp1 HG02109.hp2 HG02559.hp1 others(26): Show |
intron_variant | MODIFIER | c.3858+348C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692300 | |||||||
chr8:41692344 | A | G | 1 | a0001c0009t0002g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3858+304T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692344 | |||||||
chr8:41692353 | G | A | 21 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(18): Show |
21 | HG02074.hp1 HG02109.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.3858+295C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692353 | |||||||
chr8:41692377 | C | T | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3858+271G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692377 | |||||||
chr8:41692500 | T | C | 4 | a0001c0006t0005g0014 a0001c0006t0018g0118 a0001c0017t0005g0116 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3858+148A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692500 | |||||||
chr8:41692562 | C | T | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3858+86G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692562 | |||||||
chr8:41692580 | T | C | 10 | a0001c0006t0001g0100 a0004c0011t0001g0185 a0004c0011t0001g0186 others(7): Show |
11 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3858+68A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 31/42 | chr8 | 41692580 | |||||||
chr8:41692948 | GC | G | 28 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(25): Show |
28 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.3630-73delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 30/42 | chr8 | 41692948 | |||||||
chr8:41692992 | C | T | 7 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(4): Show |
7 | HG01243.hp2 HG02071.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3629+113G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 30/42 | chr8 | 41692992 | |||||||
chr8:41693265 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3533-64T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693265 | |||||||
chr8:41693269 | C | T | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3533-68G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693269 | |||||||
chr8:41693417 | CTTTTTTT others(2): Show |
C | 7 | a0001c0002t0001g0157 a0001c0002t0001g0216 a0001c0025t0011g0002 others(4): Show |
8 | HG01123.hp2 HG02818.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.3533-225_3533-217d others(11): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | |||||||
chr8:41693417 | CTTTTTTT others(3): Show |
C | 37 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.3533-226_3533-217d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | |||||||
chr8:41693417 | CTTTTTTT others(4): Show |
C | 73 | a0001c0001t0002g0021 a0001c0001t0002g0150 a0001c0001t0002g0172 others(70): Show |
74 | HG00140.hp1 HG00423.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.3533-227_3533-217d others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | |||||||
chr8:41693417 | CTTTTTTT others(5): Show |
C | 139 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.3533-228_3533-217d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | |||||||
chr8:41693417 | CTTTTTTT others(6): Show |
C | 4 | a0001c0003t0001g0147 a0001c0004t0002g0260 a0001c0005t0013g0005 others(1): Show |
4 | HG01070.hp2 NA18969.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.3533-229_3533-217d others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693417 | |||||||
chr8:41693491 | G | A | 1 | a0005c0035t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3533-290C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693491 | |||||||
chr8:41693645 | G | A | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+253C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693645 | |||||||
chr8:41693766 | A | T | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+132T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693766 | |||||||
chr8:41693767 | G | C | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+131C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693767 | |||||||
chr8:41693769 | ACCTC | A | 9 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3532+125_3532+128d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693769 | |||||||
chr8:41693780 | G | A | 6 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0018t0026g0113 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3532+118C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693780 | |||||||
chr8:41693853 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3532+45G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693853 | |||||||
chr8:41693885 | G | T | 1 | a0001c0005t0003g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3532+13C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 29/42 | chr8 | 41693885 | |||||||
chr8:41694163 | A | G | 7 | a0001c0003t0001g0060 a0001c0003t0001g0135 a0001c0003t0001g0137 others(4): Show |
7 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3328-61T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694163 | |||||||
chr8:41694202 | G | A | 7 | a0001c0002t0001g0184 a0001c0002t0009g0098 a0001c0005t0010g0020 others(4): Show |
7 | HG02451.hp1 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3328-100C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694202 | |||||||
chr8:41694210 | G | A | 19 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(16): Show |
19 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.3328-108C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694210 | |||||||
chr8:41694305 | A | G | 1 | a0001c0003t0001g0175 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3328-203T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694305 | |||||||
chr8:41694372 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3327+220C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694372 | |||||||
chr8:41694528 | T | C | 5 | a0001c0051t0008g0273 a0003c0014t0002g0198 a0003c0014t0008g0093 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3327+64A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694528 | |||||||
chr8:41694571 | G | C | 14 | a0001c0006t0001g0100 a0001c0028t0003g0066 a0003c0015t0003g0136 others(11): Show |
15 | HG02074.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.3327+21C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 28/42 | chr8 | 41694571 | |||||||
chr8:41694925 | G | A | 15 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(12): Show |
16 | HG02145.hp1 HG02559.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.3116-122C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41694925 | |||||||
chr8:41695004 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3115+173G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695004 | |||||||
chr8:41695026 | C | T | 1 | a0001c0004t0002g0208 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3115+151G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695026 | |||||||
chr8:41695070 | T | C | 1 | a0001c0004t0002g0208 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3115+107A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695070 | |||||||
chr8:41695168 | C | T | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3115+9G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 27/42 | chr8 | 41695168 | |||||||
chr8:41695595 | G | A | 2 | a0001c0004t0002g0205 a0001c0004t0002g0270 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2961-264C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695595 | |||||||
chr8:41695715 | A | G | 5 | a0003c0014t0002g0198 a0003c0014t0008g0093 a0003c0014t0008g0094 others(2): Show |
5 | HG00639.hp1 HG01123.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2961-384T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695715 | |||||||
chr8:41695720 | C | T | 2 | a0001c0018t0026g0113 a0015c0045t0025g0187 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2961-389G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695720 | |||||||
chr8:41695726 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2961-395G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695726 | |||||||
chr8:41695762 | C | T | 7 | a0001c0005t0002g0004 a0001c0005t0003g0033 a0001c0005t0013g0005 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2961-431G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695762 | |||||||
chr8:41695764 | C | T | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2961-433G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695764 | |||||||
chr8:41695828 | A | T | 179 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.2961-497T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695828 | |||||||
chr8:41695906 | T | C | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2960+457A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695906 | |||||||
chr8:41695940 | C | T | 5 | a0001c0002t0001g0157 a0003c0015t0003g0136 a0003c0015t0003g0214 others(2): Show |
5 | HG03195.hp1 NA18950.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.2960+423G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695940 | |||||||
chr8:41695951 | G | GC | 36 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(33): Show |
36 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2960+411dupG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41695951 | |||||||
chr8:41696170 | G | A | 6 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2960+193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696170 | |||||||
chr8:41696179 | C | T | 1 | a0001c0002t0009g0125 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2960+184G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696179 | |||||||
chr8:41696307 | C | T | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2960+56G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696307 | |||||||
chr8:41696317 | G | A | 93 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(90): Show |
94 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2960+46C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 26/42 | chr8 | 41696317 | |||||||
chr8:41696666 | C | T | 1 | a0005c0035t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2735+10G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 25/42 | chr8 | 41696666 | |||||||
chr8:41696862 | C | A | 1 | a0001c0006t0001g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2638-89G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41696862 | |||||||
chr8:41696930 | C | G | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2638-157G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41696930 | |||||||
chr8:41697084 | GC | G | 232 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2638-312delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697084 | |||||||
chr8:41697230 | T | C | 233 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2638-457A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697230 | |||||||
chr8:41697290 | G | A | 1 | a0001c0010t0002g0081 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2638-517C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697290 | |||||||
chr8:41697293 | A | G | 266 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2638-520T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697293 | |||||||
chr8:41697318 | C | T | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2638-545G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697318 | |||||||
chr8:41697333 | G | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2638-560C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697333 | |||||||
chr8:41697392 | A | G | 239 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.2638-619T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697392 | |||||||
chr8:41697463 | A | G | 140 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2637+580T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697463 | |||||||
chr8:41697559 | C | T | 91 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(88): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2637+484G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697559 | |||||||
chr8:41697562 | C | A | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2637+481G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697562 | |||||||
chr8:41697632 | C | T | 1 | a0001c0013t0001g0038 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2637+411G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697632 | |||||||
chr8:41697648 | G | A | 1 | a0002c0057t0005g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2637+395C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697648 | |||||||
chr8:41697847 | T | C | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2637+196A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697847 | |||||||
chr8:41697848 | T | C | 103 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(100): Show |
103 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2637+195A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697848 | |||||||
chr8:41697855 | G | A | 102 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(99): Show |
102 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2637+188C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697855 | |||||||
chr8:41697896 | G | A | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2637+147C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697896 | |||||||
chr8:41697955 | T | C | 113 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(110): Show |
114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2637+88A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697955 | |||||||
chr8:41697971 | C | T | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2637+72G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 24/42 | chr8 | 41697971 | |||||||
chr8:41698218 | C | T | 10 | a0003c0014t0002g0198 a0003c0014t0008g0093 a0003c0014t0008g0094 others(7): Show |
10 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2559-97G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698218 | |||||||
chr8:41698222 | A | G | 199 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(196): Show |
200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2559-101T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698222 | |||||||
chr8:41698286 | A | G | 34 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0005t0028g0112 others(31): Show |
34 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.2559-165T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698286 | |||||||
chr8:41698292 | C | T | 16 | a0001c0002t0009g0098 a0001c0006t0001g0267 a0001c0012t0005g0101 others(13): Show |
16 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2559-171G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698292 | |||||||
chr8:41698388 | C | G | 1 | a0001c0004t0002g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2559-267G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698388 | |||||||
chr8:41698407 | T | G | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2559-286A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698407 | |||||||
chr8:41698417 | T | C | 1 | a0001c0004t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2559-296A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698417 | |||||||
chr8:41698436 | C | T | 192 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(189): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2559-315G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698436 | |||||||
chr8:41698587 | T | C | 1 | a0002c0007t0007g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2559-466A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698587 | |||||||
chr8:41698600 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2559-479G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698600 | |||||||
chr8:41698680 | T | C | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2559-559A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698680 | |||||||
chr8:41698697 | G | A | 1 | a0001c0013t0001g0038 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2559-576C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698697 | |||||||
chr8:41698757 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0219 |
2 | NA18988.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2559-636C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698757 | |||||||
chr8:41698801 | A | AT | 63 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2558+650dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698801 | |||||||
chr8:41698801 | A | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+651T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698801 | |||||||
chr8:41698887 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+565G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698887 | |||||||
chr8:41698962 | A | ATTTTT | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+485_2558+489d others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41698962 | |||||||
chr8:41699091 | A | G | 75 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.2558+361T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699091 | |||||||
chr8:41699185 | G | A | 3 | a0005c0021t0002g0114 a0005c0021t0002g0131 a0005c0035t0001g0129 |
3 | HG02280.hp1 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2558+267C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699185 | |||||||
chr8:41699218 | G | A | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2558+234C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699218 | |||||||
chr8:41699233 | G | A | 4 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2558+219C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699233 | |||||||
chr8:41699255 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+197G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699255 | |||||||
chr8:41699274 | G | A | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2558+178C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699274 | |||||||
chr8:41699324 | C | T | 12 | a0001c0005t0010g0020 a0003c0014t0002g0198 a0003c0014t0008g0093 others(9): Show |
12 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.2558+128G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699324 | |||||||
chr8:41699336 | C | T | 1 | a0001c0005t0003g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2558+116G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699336 | |||||||
chr8:41699368 | T | C | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2558+84A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 23/42 | chr8 | 41699368 | |||||||
chr8:41699578 | G | A | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2462-30C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699578 | |||||||
chr8:41699583 | A | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2462-35T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699583 | |||||||
chr8:41699631 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2462-83C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699631 | |||||||
chr8:41699946 | G | A | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2462-398C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41699946 | |||||||
chr8:41700000 | T | C | 78 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.2462-452A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700000 | |||||||
chr8:41700096 | C | T | 1 | a0001c0001t0023g0072 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2462-548G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700096 | |||||||
chr8:41700364 | C | G | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2462-816G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700364 | |||||||
chr8:41700519 | A | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2462-971T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700519 | |||||||
chr8:41700577 | C | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2461+973G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700577 | |||||||
chr8:41700648 | T | C | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2461+902A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700648 | |||||||
chr8:41700741 | T | C | 3 | a0002c0007t0007g0024 a0002c0007t0007g0025 a0002c0007t0007g0028 |
3 | HG02258.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2461+809A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700741 | |||||||
chr8:41700751 | T | G | 112 | a0001c0002t0009g0098 a0001c0003t0001g0049 a0001c0003t0001g0050 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.2461+799A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700751 | |||||||
chr8:41700814 | G | T | 3 | a0003c0015t0003g0136 a0003c0015t0003g0214 a0003c0015t0003g0250 |
3 | NA18950.hp2 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2461+736C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700814 | |||||||
chr8:41700942 | A | C | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+608T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700942 | |||||||
chr8:41700943 | T | A | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+607A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700943 | |||||||
chr8:41700958 | G | A | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+592C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41700958 | |||||||
chr8:41701168 | T | A | 10 | a0003c0014t0002g0198 a0003c0014t0008g0093 a0003c0014t0008g0094 others(7): Show |
10 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2461+382A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701168 | |||||||
chr8:41701264 | C | T | 4 | a0001c0005t0001g0225 a0001c0005t0001g0228 a0001c0005t0002g0189 others(1): Show |
4 | HG00408.hp2 HG02071.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461+286G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701264 | |||||||
chr8:41701284 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+266G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701284 | |||||||
chr8:41701380 | T | G | 113 | a0001c0002t0001g0160 a0001c0002t0009g0098 a0001c0003t0001g0049 others(110): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2461+170A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701380 | |||||||
chr8:41701436 | T | C | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2461+114A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 22/42 | chr8 | 41701436 | |||||||
chr8:41701664 | C | T | 4 | a0004c0011t0001g0185 a0004c0011t0001g0186 a0004c0011t0002g0001 others(1): Show |
5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2389-42G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701664 | |||||||
chr8:41701666 | CA | C | 12 | a0001c0005t0010g0020 a0003c0014t0002g0198 a0003c0014t0008g0093 others(9): Show |
12 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.2389-45delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701666 | |||||||
chr8:41701766 | C | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2389-144G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701766 | |||||||
chr8:41701841 | C | G | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2388+211G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701841 | |||||||
chr8:41701874 | C | T | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2388+178G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701874 | |||||||
chr8:41701914 | C | T | 1 | a0001c0038t0002g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2388+138G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701914 | |||||||
chr8:41701952 | C | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2388+100G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701952 | |||||||
chr8:41701962 | G | C | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2388+90C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 21/42 | chr8 | 41701962 | |||||||
chr8:41702164 | G | A | 4 | a0004c0011t0001g0185 a0004c0011t0001g0186 a0004c0011t0002g0001 others(1): Show |
5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2296-20C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702164 | |||||||
chr8:41702179 | G | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-35C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702179 | |||||||
chr8:41702251 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2296-107G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702251 | |||||||
chr8:41702409 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-265G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702409 | |||||||
chr8:41702825 | T | TTG | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-683_2296-682d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702825 | |||||||
chr8:41702881 | G | A | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-737C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702881 | |||||||
chr8:41702986 | A | AT | 15 | a0001c0003t0001g0140 a0001c0005t0002g0019 a0001c0005t0010g0020 others(12): Show |
15 | HG00639.hp1 HG01934.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2296-843dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702986 | |||||||
chr8:41702986 | A | ATT | 5 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2296-844_2296-843d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41702986 | |||||||
chr8:41703022 | T | C | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-878A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703022 | |||||||
chr8:41703204 | A | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2295+837T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703204 | |||||||
chr8:41703251 | T | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2295+790A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703251 | |||||||
chr8:41703383 | CAT | C | 8 | a0001c0005t0028g0112 a0001c0005t0029g0111 a0001c0013t0001g0027 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+656_2295+657d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703383 | |||||||
chr8:41703400 | A | ATGTGTGT others(1): Show |
4 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2295+633_2295+640d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703400 | |||||||
chr8:41703400 | A | G | 1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2295+641T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703400 | |||||||
chr8:41703420 | G | A | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2295+621C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | |||||||
chr8:41703420 | G | GTA | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2295+620_2295+621i others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | |||||||
chr8:41703420 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2295+620_2295+621i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | |||||||
chr8:41703420 | G | GTATATAT others(5): Show |
1 | a0001c0012t0001g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2295+620_2295+621i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703420 | |||||||
chr8:41703422 | G | A | 16 | a0001c0001t0001g0149 a0001c0001t0002g0197 a0001c0005t0002g0019 others(13): Show |
16 | HG01928.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2295+619C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTATATAT others(3): Show |
5 | a0001c0001t0002g0241 a0001c0004t0002g0247 a0001c0005t0003g0033 others(2): Show |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2295+609_2295+618d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTATATAT others(5): Show |
1 | a0001c0022t0002g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2295+607_2295+618d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTATATAT others(7): Show |
8 | a0001c0001t0001g0211 a0001c0001t0002g0057 a0001c0001t0002g0164 others(5): Show |
8 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2295+605_2295+618d others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTATATAT others(9): Show |
3 | a0001c0001t0002g0021 a0001c0001t0002g0210 a0001c0034t0002g0146 |
3 | HG03516.hp2 NA19087.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2295+603_2295+618d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTATATAT others(11): Show |
1 | a0001c0001t0002g0218 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2295+601_2295+618d others(20): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2295+599_2295+618d others(22): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTATAT others(3): Show |
3 | a0001c0004t0002g0270 a0001c0029t0001g0254 a0008c0041t0012g0167 |
3 | HG01123.hp2 HG02602.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2295+618_2295+619i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTATAT others(5): Show |
1 | a0001c0028t0003g0066 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2295+618_2295+619i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTATAT others(19): Show |
1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2295+618_2295+619i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTGTAT others(1): Show |
6 | a0001c0002t0001g0160 a0001c0002t0003g0079 a0001c0002t0003g0080 others(3): Show |
6 | HG01192.hp2 HG02723.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2295+618_2295+619i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTGTAT others(3): Show |
26 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(23): Show |
27 | HG00140.hp2 HG00408.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2295+618_2295+619i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTGTAT others(5): Show |
10 | a0001c0002t0001g0121 a0001c0002t0001g0133 a0001c0002t0009g0125 others(7): Show |
10 | HG00733.hp1 HG00741.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2295+618_2295+619i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTGTAT others(9): Show |
3 | a0001c0002t0001g0134 a0001c0019t0002g0238 a0001c0026t0001g0158 |
3 | HG00438.hp1 HG02004.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2295+618_2295+619i others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTGTGT others(3): Show |
1 | a0001c0002t0002g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2295+618_2295+619i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | G | GTGTGTGT others(5): Show |
2 | a0001c0002t0002g0179 a0001c0002t0002g0192 |
2 | HG04115.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2295+618_2295+619i others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | GTA | G | 8 | a0001c0005t0004g0030 a0001c0005t0004g0043 a0001c0005t0004g0044 others(5): Show |
8 | HG01167.hp1 HG01891.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2295+617_2295+618d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | GTATA | G | 11 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0207 others(8): Show |
11 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(8): Show |
intron_variant | MODIFIER | c.2295+615_2295+618d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | GTATATA | G | 9 | a0001c0001t0001g0190 a0001c0001t0001g0224 a0001c0005t0001g0078 others(6): Show |
9 | HG01123.hp1 HG02071.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.2295+613_2295+618d others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703422 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2295+603_2295+618d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703422 | |||||||
chr8:41703424 | A | G | 48 | a0001c0001t0001g0242 a0001c0002t0001g0173 a0001c0002t0001g0184 others(45): Show |
49 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2295+617T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703424 | |||||||
chr8:41703426 | A | G | 11 | a0001c0002t0001g0184 a0001c0010t0002g0081 a0001c0010t0003g0003 others(8): Show |
12 | HG00738.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2295+615T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703426 | |||||||
chr8:41703428 | A | G | 2 | a0001c0001t0002g0076 a0001c0005t0002g0189 |
2 | HG00408.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2295+613T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703428 | |||||||
chr8:41703446 | A | T | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2295+595T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703446 | |||||||
chr8:41703447 | TATA | T | 8 | a0001c0003t0001g0060 a0001c0003t0001g0135 a0001c0003t0001g0137 others(5): Show |
8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+591_2295+593d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703447 | |||||||
chr8:41703448 | A | ATTT | 5 | a0001c0005t0010g0020 a0003c0015t0003g0136 a0003c0015t0003g0214 others(2): Show |
5 | HG03139.hp2 HG03195.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.2295+592_2295+593i others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703448 | |||||||
chr8:41703448 | A | T | 4 | a0001c0005t0002g0019 a0001c0013t0001g0027 a0001c0013t0001g0038 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2295+593T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703448 | |||||||
chr8:41703448 | ATAT | A | 8 | a0001c0001t0002g0150 a0001c0003t0001g0050 a0001c0003t0001g0162 others(5): Show |
8 | HG00738.hp1 HG02965.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+590_2295+592d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703448 | |||||||
chr8:41703450 | A | AT | 7 | a0001c0002t0001g0157 a0001c0002t0001g0166 a0001c0002t0001g0182 others(4): Show |
8 | HG00438.hp1 HG00735.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.2295+590dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(4): Show |
12 | a0001c0004t0002g0120 a0001c0004t0002g0152 a0001c0004t0002g0200 others(9): Show |
12 | HG00438.hp2 HG01069.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2295+590_2295+591i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(6): Show |
5 | a0001c0001t0002g0255 a0001c0004t0002g0249 a0001c0004t0002g0252 others(2): Show |
5 | HG02717.hp1 HG03834.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.2295+590_2295+591i others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(8): Show |
2 | a0001c0001t0002g0010 a0001c0008t0002g0203 |
2 | HG03209.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(19): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(35): Show |
1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(44): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(27): Show |
1 | a0002c0007t0007g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(36): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(23): Show |
1 | a0002c0057t0005g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(32): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(26): Show |
1 | a0002c0007t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(35): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(19): Show |
1 | a0002c0007t0021g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(22): Show |
1 | a0002c0007t0001g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(31): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(9): Show |
5 | a0001c0001t0002g0089 a0001c0001t0002g0172 a0001c0001t0013g0090 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.2295+590_2295+591i others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(19): Show |
1 | a0001c0012t0005g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(20): Show |
2 | a0001c0002t0009g0098 a0004c0020t0001g0035 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(29): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(21): Show |
1 | a0004c0020t0001g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(30): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(22): Show |
1 | a0002c0007t0027g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(31): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(17): Show |
2 | a0001c0012t0006g0096 a0001c0012t0006g0097 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(26): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(18): Show |
1 | a0004c0020t0001g0037 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(27): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(16): Show |
1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(25): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(19): Show |
1 | a0002c0007t0007g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(28): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(4): Show |
3 | a0001c0004t0002g0244 a0001c0008t0002g0204 a0001c0008t0015g0206 |
3 | HG01515.hp1 HG01517.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.2295+590_2295+591i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(16): Show |
1 | a0001c0056t0003g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(25): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(4): Show |
1 | a0001c0004t0002g0201 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2295+590_2295+591i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | ATATATAT others(15): Show |
1 | a0002c0007t0007g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2295+590_2295+591i others(24): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | A | T | 24 | a0001c0001t0001g0151 a0001c0002t0001g0177 a0001c0005t0001g0078 others(21): Show |
24 | HG01123.hp1 HG01123.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2295+591T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | AT | A | 10 | a0001c0001t0002g0226 a0001c0002t0001g0161 a0001c0005t0004g0011 others(7): Show |
10 | HG01175.hp2 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2295+590delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703450 | ATTT | A | 25 | a0001c0001t0002g0271 a0001c0003t0001g0049 a0001c0003t0001g0054 others(22): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2295+588_2295+590d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703450 | |||||||
chr8:41703451 | T | TA | 32 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | |||||||
chr8:41703451 | T | TATA | 3 | a0003c0014t0008g0093 a0004c0011t0002g0001 a0004c0011t0002g0095 |
4 | HG02559.hp1 HG03195.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | |||||||
chr8:41703451 | T | TATATATA others(4): Show |
5 | a0001c0002t0001g0173 a0001c0004t0001g0108 a0001c0004t0001g0148 others(2): Show |
5 | HG00741.hp2 HG01243.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | |||||||
chr8:41703451 | T | TATATATA others(6): Show |
4 | a0001c0001t0002g0169 a0001c0001t0002g0194 a0001c0001t0002g0261 others(1): Show |
4 | HG02683.hp1 NA18612.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.2295+589_2295+590i others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | |||||||
chr8:41703451 | T | TATATATA others(10): Show |
2 | a0001c0001t0001g0242 a0001c0004t0002g0220 |
2 | HG01168.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.2295+589_2295+590i others(19): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703451 | |||||||
chr8:41703452 | T | A | 9 | a0001c0001t0001g0149 a0001c0001t0002g0197 a0001c0002t0001g0160 others(6): Show |
9 | HG01928.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2295+589A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703452 | |||||||
chr8:41703453 | T | A | 13 | a0001c0002t0001g0124 a0001c0003t0001g0051 a0001c0004t0002g0176 others(10): Show |
14 | HG00140.hp2 HG02040.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2295+588A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703453 | |||||||
chr8:41703454 | T | A | 3 | a0001c0005t0003g0033 a0004c0011t0001g0185 a0004c0011t0001g0186 |
3 | HG02280.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2295+587A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703454 | |||||||
chr8:41703455 | T | A | 3 | a0001c0001t0002g0271 a0001c0003t0001g0056 a0001c0003t0001g0147 |
3 | HG00099.hp2 NA18969.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2295+586A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703455 | |||||||
chr8:41703471 | C | G | 63 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(60): Show |
63 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2295+570G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703471 | |||||||
chr8:41703545 | G | A | 1 | a0001c0005t0001g0258 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2295+496C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703545 | |||||||
chr8:41703663 | T | A | 108 | a0001c0002t0009g0098 a0001c0003t0001g0049 a0001c0003t0001g0050 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2295+378A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703663 | |||||||
chr8:41703865 | G | A | 50 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(47): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2295+176C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703865 | |||||||
chr8:41703869 | A | C | 1 | a0001c0010t0003g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2295+172T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703869 | |||||||
chr8:41703928 | C | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2295+113G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703928 | |||||||
chr8:41703967 | C | T | 1 | a0001c0034t0002g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2295+74G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 20/42 | chr8 | 41703967 | |||||||
chr8:41704268 | A | C | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2196+106T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 19/42 | chr8 | 41704268 | |||||||
chr8:41704511 | G | C | 4 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2098-39C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704511 | |||||||
chr8:41704563 | C | T | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2098-91G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704563 | |||||||
chr8:41704723 | G | A | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-251C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704723 | |||||||
chr8:41704744 | G | A | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2098-272C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704744 | |||||||
chr8:41704849 | A | T | 10 | a0001c0005t0004g0043 a0001c0013t0001g0027 a0001c0013t0001g0038 others(7): Show |
10 | HG02280.hp1 HG02559.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.2098-377T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41704849 | |||||||
chr8:41705034 | G | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2098-562C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705034 | |||||||
chr8:41705049 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2098-577A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705049 | |||||||
chr8:41705170 | G | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2098-698C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705170 | |||||||
chr8:41705198 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0219 |
2 | NA18988.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2098-726C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705198 | |||||||
chr8:41705210 | C | T | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2098-738G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705210 | |||||||
chr8:41705211 | C | T | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2098-739G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705211 | |||||||
chr8:41705381 | C | T | 3 | a0003c0015t0003g0136 a0003c0015t0003g0214 a0003c0015t0003g0250 |
3 | NA18950.hp2 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2097+762G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705381 | |||||||
chr8:41705731 | G | A | 13 | a0001c0005t0001g0084 a0001c0005t0003g0033 a0001c0006t0001g0017 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2097+412C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705731 | |||||||
chr8:41705841 | T | G | 12 | a0001c0005t0010g0020 a0003c0014t0002g0198 a0003c0014t0008g0093 others(9): Show |
12 | HG00639.hp1 HG02818.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.2097+302A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 18/42 | chr8 | 41705841 | |||||||
chr8:41706258 | G | A | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1999-17C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706258 | |||||||
chr8:41706273 | T | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1999-32A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706273 | |||||||
chr8:41706665 | C | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0037t0003g0234 |
3 | HG02258.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1999-424G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706665 | |||||||
chr8:41706665 | C | T | 1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1999-424G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706665 | |||||||
chr8:41706909 | G | A | 39 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1999-668C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41706909 | |||||||
chr8:41707013 | T | C | 78 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1999-772A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707013 | |||||||
chr8:41707145 | C | T | 39 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1999-904G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707145 | |||||||
chr8:41707179 | G | A | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1999-938C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707179 | |||||||
chr8:41707270 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0002g0197 a0001c0012t0001g0138 |
3 | HG01928.hp2 NA18747.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1999-1029G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707270 | |||||||
chr8:41707336 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1999-1095C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707336 | |||||||
chr8:41707425 | C | T | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1999-1184G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707425 | |||||||
chr8:41707464 | C | G | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1999-1223G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707464 | |||||||
chr8:41707488 | C | A | 13 | a0001c0005t0001g0084 a0001c0005t0003g0033 a0001c0006t0001g0017 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1999-1247G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707488 | |||||||
chr8:41707629 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1998+1149C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707629 | |||||||
chr8:41707824 | T | C | 61 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1998+954A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707824 | |||||||
chr8:41707945 | C | T | 7 | a0001c0005t0001g0084 a0001c0005t0003g0033 a0001c0006t0003g0006 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1998+833G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41707945 | |||||||
chr8:41708051 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1998+727C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708051 | |||||||
chr8:41708063 | C | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1998+715G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708063 | |||||||
chr8:41708064 | G | A | 46 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(43): Show |
47 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1998+714C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708064 | |||||||
chr8:41708214 | CT | C | 20 | a0001c0001t0002g0106 a0001c0002t0009g0098 a0001c0003t0002g0221 others(17): Show |
20 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1998+563delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708214 | |||||||
chr8:41708223 | T | G | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1998+555A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708223 | |||||||
chr8:41708260 | T | C | 1 | a0002c0007t0021g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1998+518A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708260 | |||||||
chr8:41708281 | T | C | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1998+497A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708281 | |||||||
chr8:41708313 | G | A | 1 | a0001c0010t0002g0081 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1998+465C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708313 | |||||||
chr8:41708376 | A | G | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1998+402T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708376 | |||||||
chr8:41708439 | G | A | 1 | a0002c0007t0021g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1998+339C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708439 | |||||||
chr8:41708464 | G | A | 1 | a0003c0049t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1998+314C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708464 | |||||||
chr8:41708511 | T | C | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1998+267A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708511 | |||||||
chr8:41708524 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1998+254C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708524 | |||||||
chr8:41708645 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1998+133A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708645 | |||||||
chr8:41708737 | T | A | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1998+41A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708737 | |||||||
chr8:41708761 | G | A | 1 | a0001c0012t0005g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1998+17C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 17/42 | chr8 | 41708761 | |||||||
chr8:41709025 | A | T | 3 | a0001c0016t0002g0007 a0001c0016t0002g0008 a0001c0016t0002g0009 |
3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1801-50T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709025 | |||||||
chr8:41709093 | G | A | 9 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1801-118C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709093 | |||||||
chr8:41709117 | T | TAAAC | 245 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1801-146_1801-143d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709117 | |||||||
chr8:41709117 | T | TAAACAAA others(1): Show |
18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1801-150_1801-143d others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709117 | |||||||
chr8:41709401 | C | T | 39 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1801-426G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709401 | |||||||
chr8:41709564 | A | T | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1801-589T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41709564 | |||||||
chr8:41710113 | C | T | 1 | a0001c0002t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1801-1138G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710113 | |||||||
chr8:41710131 | G | T | 1 | a0001c0002t0009g0098 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1801-1156C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710131 | |||||||
chr8:41710132 | C | CA | 75 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(72): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1801-1158dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710132 | |||||||
chr8:41710134 | T | G | 75 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(72): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1801-1159A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710134 | |||||||
chr8:41710152 | C | T | 2 | a0001c0019t0002g0174 a0016c0053t0002g0251 |
2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1801-1177G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710152 | |||||||
chr8:41710353 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-1378G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710353 | |||||||
chr8:41710577 | T | G | 1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1801-1602A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710577 | |||||||
chr8:41710632 | G | A | 11 | a0003c0014t0002g0198 a0003c0014t0008g0093 a0003c0014t0008g0094 others(8): Show |
11 | HG00639.hp1 HG01928.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1801-1657C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710632 | |||||||
chr8:41710640 | C | T | 57 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(54): Show |
59 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1801-1665G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710640 | |||||||
chr8:41710657 | C | G | 1 | a0001c0017t0005g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1801-1682G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41710657 | |||||||
chr8:41711185 | C | T | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1801-2210G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711185 | |||||||
chr8:41711721 | A | G | 2 | a0001c0013t0001g0027 a0001c0013t0001g0038 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1800+2435T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711721 | |||||||
chr8:41711795 | A | G | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2361T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711795 | |||||||
chr8:41711844 | C | A | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1800+2312G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711844 | |||||||
chr8:41711844 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2312G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711844 | |||||||
chr8:41711845 | G | A | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2311C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711845 | |||||||
chr8:41711856 | G | A | 34 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0006t0018g0118 others(31): Show |
35 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1800+2300C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711856 | |||||||
chr8:41711870 | G | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2286C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711870 | |||||||
chr8:41711931 | C | CT | 8 | a0001c0001t0001g0142 a0001c0001t0001g0219 a0001c0013t0001g0027 others(5): Show |
8 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1800+2224dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711931 | |||||||
chr8:41711931 | CT | C | 48 | a0001c0001t0002g0193 a0001c0003t0001g0049 a0001c0003t0001g0050 others(45): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1800+2224delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41711931 | |||||||
chr8:41712083 | C | G | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1800+2073G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712083 | |||||||
chr8:41712221 | G | C | 40 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1800+1935C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712221 | |||||||
chr8:41712294 | C | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1800+1862G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712294 | |||||||
chr8:41712326 | G | A | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1800+1830C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712326 | |||||||
chr8:41712455 | G | A | 6 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+1701C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712455 | |||||||
chr8:41712457 | A | G | 6 | a0001c0009t0002g0047 a0001c0009t0002g0048 a0001c0009t0002g0052 others(3): Show |
6 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+1699T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712457 | |||||||
chr8:41712486 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1800+1670T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712486 | |||||||
chr8:41712533 | A | T | 2 | a0004c0020t0001g0034 a0004c0020t0001g0035 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1800+1623T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712533 | |||||||
chr8:41712547 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0219 |
2 | NA18988.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1800+1609A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712547 | |||||||
chr8:41712629 | C | T | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1800+1527G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712629 | |||||||
chr8:41712904 | A | C | 1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1800+1252T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41712904 | |||||||
chr8:41713062 | G | A | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1800+1094C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713062 | |||||||
chr8:41713064 | C | T | 1 | a0001c0004t0002g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1800+1092G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713064 | |||||||
chr8:41713171 | C | T | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1800+985G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713171 | |||||||
chr8:41713223 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1800+933G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713223 | |||||||
chr8:41713285 | G | A | 4 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1800+871C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713285 | |||||||
chr8:41713303 | T | C | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1800+853A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713303 | |||||||
chr8:41713310 | C | G | 29 | a0001c0002t0009g0098 a0001c0005t0002g0019 a0001c0005t0010g0020 others(26): Show |
30 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1800+846G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713310 | |||||||
chr8:41713310 | C | T | 6 | a0001c0006t0001g0017 a0001c0006t0001g0040 a0001c0006t0001g0263 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+846G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713310 | |||||||
chr8:41713327 | G | C | 29 | a0001c0002t0009g0098 a0001c0005t0002g0019 a0001c0005t0010g0020 others(26): Show |
30 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1800+829C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713327 | |||||||
chr8:41713364 | C | T | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+792G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713364 | |||||||
chr8:41713365 | A | G | 35 | a0001c0002t0009g0098 a0001c0005t0002g0019 a0001c0005t0010g0020 others(32): Show |
36 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1800+791T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713365 | |||||||
chr8:41713421 | C | T | 28 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0006t0018g0118 others(25): Show |
29 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1800+735G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713421 | |||||||
chr8:41713508 | C | T | 2 | a0001c0046t0030g0276 a0004c0020t0001g0037 |
2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1800+648G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713508 | |||||||
chr8:41713715 | T | C | 104 | a0001c0001t0001g0153 a0001c0001t0001g0190 a0001c0001t0001g0245 others(101): Show |
106 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1800+441A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713715 | |||||||
chr8:41713873 | G | A | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1800+283C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713873 | |||||||
chr8:41713915 | C | T | 102 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(99): Show |
102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1800+241G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 16/42 | chr8 | 41713915 | |||||||
chr8:41714284 | C | G | 12 | a0001c0051t0008g0273 a0003c0014t0002g0198 a0003c0014t0008g0093 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1702-30G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714284 | |||||||
chr8:41714308 | C | G | 39 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1702-54G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714308 | |||||||
chr8:41714387 | T | G | 35 | a0001c0002t0009g0098 a0001c0005t0002g0019 a0001c0005t0010g0020 others(32): Show |
36 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1702-133A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714387 | |||||||
chr8:41714445 | A | T | 39 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1702-191T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714445 | |||||||
chr8:41714447 | G | A | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1702-193C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714447 | |||||||
chr8:41714583 | G | A | 1 | a0001c0005t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1702-329C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714583 | |||||||
chr8:41714595 | T | C | 6 | a0001c0013t0001g0027 a0001c0013t0001g0038 a0001c0013t0006g0128 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1702-341A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714595 | |||||||
chr8:41714678 | A | G | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1701+298T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714678 | |||||||
chr8:41714839 | A | G | 2 | a0001c0005t0002g0019 a0001c0005t0004g0029 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1701+137T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714839 | |||||||
chr8:41714867 | A | G | 37 | a0001c0002t0009g0098 a0001c0005t0002g0019 a0001c0005t0004g0029 others(34): Show |
38 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.1701+109T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 15/42 | chr8 | 41714867 | |||||||
chr8:41715222 | C | T | 2 | a0001c0009t0002g0047 a0001c0009t0002g0048 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1603-148G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 14/42 | chr8 | 41715222 | |||||||
chr8:41715970 | G | A | 63 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(60): Show |
63 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1405-121C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41715970 | |||||||
chr8:41716021 | C | T | 1 | a0001c0005t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1405-172G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716021 | |||||||
chr8:41716039 | C | T | 20 | a0001c0002t0009g0098 a0001c0005t0010g0020 a0001c0012t0005g0101 others(17): Show |
20 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1405-190G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716039 | |||||||
chr8:41716164 | T | G | 152 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(149): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1405-315A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716164 | |||||||
chr8:41716195 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1405-346T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716195 | |||||||
chr8:41716355 | C | T | 1 | a0001c0004t0002g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1405-506G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716355 | |||||||
chr8:41716504 | G | A | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1404+449C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716504 | |||||||
chr8:41716570 | G | A | 4 | a0003c0015t0003g0136 a0003c0015t0003g0214 a0003c0015t0003g0250 others(1): Show |
4 | HG03195.hp1 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1404+383C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716570 | |||||||
chr8:41716772 | C | T | 265 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1404+181G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716772 | |||||||
chr8:41716914 | C | T | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1404+39G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 13/42 | chr8 | 41716914 | |||||||
chr8:41717092 | G | C | 1 | a0001c0006t0018g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306-41C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717092 | |||||||
chr8:41717218 | A | C | 273 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(270): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1306-167T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717218 | |||||||
chr8:41717378 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1305+226G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717378 | |||||||
chr8:41717580 | G | A | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1305+24C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 12/42 | chr8 | 41717580 | |||||||
chr8:41717761 | A | G | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1207-59T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717761 | |||||||
chr8:41717865 | T | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1207-163A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717865 | |||||||
chr8:41717902 | A | C | 64 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(61): Show |
66 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1207-200T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717902 | |||||||
chr8:41717902 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1207-200T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717902 | |||||||
chr8:41717921 | G | A | 97 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(94): Show |
99 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1206+185C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 11/42 | chr8 | 41717921 | |||||||
chr8:41718231 | CA | C | 10 | a0001c0051t0008g0273 a0003c0014t0002g0198 a0003c0014t0008g0093 others(7): Show |
10 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1108-28delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718231 | |||||||
chr8:41718262 | C | T | 1 | a0001c0010t0003g0110 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1108-58G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718262 | |||||||
chr8:41718263 | G | A | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1108-59C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718263 | |||||||
chr8:41718326 | T | C | 4 | a0004c0011t0001g0185 a0004c0011t0001g0186 a0004c0011t0002g0001 others(1): Show |
5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-122A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718326 | |||||||
chr8:41718583 | T | C | 1 | a0002c0007t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1108-379A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718583 | |||||||
chr8:41718616 | T | G | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1108-412A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718616 | |||||||
chr8:41718684 | T | C | 1 | a0001c0003t0001g0175 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1108-480A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718684 | |||||||
chr8:41718718 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0261 |
2 | NA18948.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1108-514G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718718 | |||||||
chr8:41718731 | T | G | 6 | a0001c0005t0001g0084 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG02109.hp2 HG03041.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-527A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718731 | |||||||
chr8:41718736 | G | A | 2 | a0001c0022t0002g0231 a0001c0022t0002g0232 |
2 | HG00733.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1108-532C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718736 | |||||||
chr8:41718766 | T | C | 2 | a0001c0005t0002g0019 a0001c0005t0004g0029 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1108-562A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718766 | |||||||
chr8:41718846 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1108-642C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718846 | |||||||
chr8:41718907 | G | A | 38 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1108-703C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718907 | |||||||
chr8:41718942 | G | A | 2 | a0001c0005t0002g0019 a0001c0005t0004g0029 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1107+719C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41718942 | |||||||
chr8:41719010 | A | G | 72 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(69): Show |
74 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1107+651T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719010 | |||||||
chr8:41719078 | A | G | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1107+583T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719078 | |||||||
chr8:41719101 | G | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1107+560C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719101 | |||||||
chr8:41719228 | A | G | 65 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(62): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1107+433T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719228 | |||||||
chr8:41719338 | T | A | 63 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(60): Show |
65 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1107+323A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719338 | |||||||
chr8:41719397 | G | A | 2 | a0001c0008t0002g0212 a0001c0008t0002g0217 |
2 | HG00438.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1107+264C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719397 | |||||||
chr8:41719425 | C | T | 4 | a0001c0005t0001g0078 a0001c0005t0001g0229 a0001c0005t0001g0257 others(1): Show |
4 | HG01123.hp1 HG01975.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1107+236G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719425 | |||||||
chr8:41719496 | A | G | 152 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(149): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1107+165T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719496 | |||||||
chr8:41719503 | C | T | 3 | a0001c0016t0002g0007 a0001c0016t0002g0008 a0001c0016t0002g0009 |
3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1107+158G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719503 | |||||||
chr8:41719603 | C | G | 37 | a0001c0002t0009g0098 a0001c0006t0001g0017 a0001c0006t0001g0263 others(34): Show |
37 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1107+58G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 10/42 | chr8 | 41719603 | |||||||
chr8:41719977 | T | C | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-119A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41719977 | |||||||
chr8:41720005 | C | T | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-147G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720005 | |||||||
chr8:41720016 | C | T | 1 | a0003c0015t0003g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.910-158G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720016 | |||||||
chr8:41720165 | C | T | 7 | a0001c0005t0001g0084 a0001c0005t0003g0033 a0001c0006t0003g0006 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-307G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720165 | |||||||
chr8:41720214 | C | T | 153 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(150): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.910-356G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720214 | |||||||
chr8:41720224 | T | C | 265 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.910-366A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720224 | |||||||
chr8:41720232 | C | T | 49 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.910-374G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720232 | |||||||
chr8:41720351 | G | A | 1 | a0001c0005t0001g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.910-493C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720351 | |||||||
chr8:41720510 | T | C | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-652A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720510 | |||||||
chr8:41720719 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.910-861C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720719 | |||||||
chr8:41720846 | G | A | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-988C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41720846 | |||||||
chr8:41721203 | A | C | 2 | a0001c0005t0002g0019 a0001c0005t0004g0029 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.910-1345T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721203 | |||||||
chr8:41721230 | C | G | 35 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(32): Show |
35 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.910-1372G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721230 | |||||||
chr8:41721322 | C | T | 2 | a0001c0001t0002g0089 a0001c0001t0013g0090 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.910-1464G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721322 | |||||||
chr8:41721395 | C | T | 1 | a0005c0035t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.910-1537G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721395 | |||||||
chr8:41721407 | C | A | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-1549G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721407 | |||||||
chr8:41721410 | A | G | 38 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(35): Show |
38 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.910-1552T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721410 | |||||||
chr8:41721569 | A | G | 1 | a0001c0004t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.909+1556T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721569 | |||||||
chr8:41721608 | G | A | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.909+1517C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721608 | |||||||
chr8:41721656 | C | CA | 16 | a0001c0001t0001g0153 a0001c0001t0002g0074 a0001c0001t0002g0132 others(13): Show |
16 | HG01175.hp1 HG01891.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.909+1468dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721656 | C | CAAAAAAA others(3): Show |
1 | a0003c0014t0008g0093 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.909+1459_909+1468d others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721656 | CA | C | 24 | a0001c0001t0001g0219 a0001c0004t0002g0120 a0001c0004t0024g0199 others(21): Show |
24 | HG00438.hp2 HG01069.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+1468delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721656 | CAAAAAAA others(5): Show |
C | 65 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(62): Show |
66 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.909+1457_909+1468d others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721656 | CAAAAAAA others(6): Show |
C | 2 | a0008c0041t0012g0167 a0016c0053t0002g0251 |
2 | HG01123.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.909+1456_909+1468d others(15): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721656 | CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0209 a0001c0003t0001g0147 a0001c0006t0001g0040 others(6): Show |
9 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+1455_909+1468d others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721656 | CAAAAAAA others(8): Show |
C | 49 | a0001c0001t0001g0207 a0001c0003t0001g0049 a0001c0003t0001g0050 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.909+1454_909+1468d others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721656 | |||||||
chr8:41721726 | T | C | 8 | a0001c0006t0001g0017 a0001c0006t0001g0263 a0001c0006t0001g0266 others(5): Show |
8 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1399A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721726 | |||||||
chr8:41721735 | G | A | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1390C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721735 | |||||||
chr8:41721880 | A | G | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1245T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721880 | |||||||
chr8:41721973 | A | G | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.909+1152T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41721973 | |||||||
chr8:41722089 | T | A | 4 | a0004c0011t0001g0185 a0004c0011t0001g0186 a0004c0011t0002g0001 others(1): Show |
5 | HG02559.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+1036A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722089 | |||||||
chr8:41722182 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.909+943G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722182 | |||||||
chr8:41722288 | T | C | 1 | a0001c0005t0004g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+837A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722288 | |||||||
chr8:41722308 | C | T | 4 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+817G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722308 | |||||||
chr8:41722485 | C | G | 2 | a0001c0005t0002g0019 a0001c0005t0004g0029 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.909+640G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722485 | |||||||
chr8:41722628 | G | A | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+497C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722628 | |||||||
chr8:41722637 | T | C | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+488A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722637 | |||||||
chr8:41722667 | C | T | 1 | a0001c0004t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.909+458G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722667 | |||||||
chr8:41722877 | C | A | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.909+248G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722877 | |||||||
chr8:41722942 | C | G | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.909+183G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41722942 | |||||||
chr8:41723078 | C | A | 1 | a0001c0001t0002g0218 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.909+47G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41723078 | |||||||
chr8:41723089 | T | C | 101 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(98): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909+36A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41723089 | |||||||
chr8:41723118 | T | C | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.909+7A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 9/42 | chr8 | 41723118 | |||||||
chr8:41723388 | G | A | 40 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.810+147C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 8/42 | chr8 | 41723388 | |||||||
chr8:41723662 | C | A | 1 | a0001c0009t0002g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.712-29G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723662 | |||||||
chr8:41723665 | G | A | 5 | a0001c0010t0003g0003 a0001c0010t0003g0110 a0001c0010t0003g0188 others(2): Show |
5 | HG02074.hp2 HG02080.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-32C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723665 | |||||||
chr8:41723769 | T | C | 163 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.712-136A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723769 | |||||||
chr8:41723778 | T | TA | 7 | a0001c0052t0001g0235 a0003c0014t0002g0198 a0003c0014t0008g0093 others(4): Show |
7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-146_712-145ins others(1): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723778 | |||||||
chr8:41723781 | T | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.712-148A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723781 | |||||||
chr8:41723785 | A | T | 7 | a0001c0052t0001g0235 a0003c0014t0002g0198 a0003c0014t0008g0093 others(4): Show |
7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-152T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723785 | |||||||
chr8:41723789 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.712-156A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723789 | |||||||
chr8:41723792 | A | AT | 10 | a0001c0001t0002g0170 a0001c0005t0010g0020 a0001c0052t0001g0235 others(7): Show |
10 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-160dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723792 | |||||||
chr8:41723792 | A | T | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.712-159T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723792 | |||||||
chr8:41723796 | T | A | 5 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-163A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723796 | |||||||
chr8:41723799 | T | A | 11 | a0001c0003t0001g0054 a0001c0003t0001g0056 a0001c0003t0001g0070 others(8): Show |
11 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.712-166A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723799 | |||||||
chr8:41723812 | C | T | 6 | a0001c0005t0001g0084 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG02109.hp2 HG03041.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-179G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723812 | |||||||
chr8:41723829 | G | T | 2 | a0001c0005t0010g0020 a0013c0047t0002g0016 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.712-196C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723829 | |||||||
chr8:41723883 | G | A | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.712-250C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723883 | |||||||
chr8:41723887 | T | C | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.712-254A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723887 | |||||||
chr8:41723938 | C | A | 18 | a0001c0005t0002g0019 a0001c0005t0004g0029 a0001c0006t0018g0118 others(15): Show |
19 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.712-305G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723938 | |||||||
chr8:41723951 | G | A | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-318C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41723951 | |||||||
chr8:41724021 | C | G | 1 | a0001c0001t0002g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.712-388G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724021 | |||||||
chr8:41724031 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.712-398C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724031 | |||||||
chr8:41724039 | C | T | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-406G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724039 | |||||||
chr8:41724040 | G | A | 2 | a0001c0005t0002g0019 a0001c0005t0004g0029 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.712-407C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724040 | |||||||
chr8:41724080 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.711+376C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724080 | |||||||
chr8:41724081 | C | A | 3 | a0001c0003t0001g0056 a0001c0003t0001g0070 a0001c0009t0002g0055 |
3 | HG00099.hp2 HG00639.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.711+375G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724081 | |||||||
chr8:41724092 | A | G | 1 | a0001c0012t0001g0138 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.711+364T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724092 | |||||||
chr8:41724187 | G | C | 2 | a0001c0026t0001g0156 a0001c0026t0001g0158 |
2 | HG00438.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.711+269C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724187 | |||||||
chr8:41724200 | A | T | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+256T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724200 | |||||||
chr8:41724289 | T | C | 10 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(7): Show |
11 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.711+167A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724289 | |||||||
chr8:41724423 | C | T | 3 | a0001c0002t0003g0143 a0001c0005t0001g0084 a0001c0040t0001g0085 |
3 | HG03516.hp1 HG03834.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.711+33G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 7/42 | chr8 | 41724423 | |||||||
chr8:41724576 | G | A | 2 | a0001c0013t0001g0027 a0001c0013t0001g0038 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.613-22C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724576 | |||||||
chr8:41724644 | C | A | 2 | a0004c0011t0002g0001 a0004c0011t0002g0095 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.613-90G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724644 | |||||||
chr8:41724722 | A | C | 1 | a0001c0004t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.613-168T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724722 | |||||||
chr8:41724796 | C | T | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.613-242G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724796 | |||||||
chr8:41724844 | T | G | 1 | a0001c0056t0003g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.613-290A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724844 | |||||||
chr8:41724892 | G | T | 2 | a0001c0004t0002g0208 a0001c0028t0003g0066 |
2 | HG02074.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.613-338C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724892 | |||||||
chr8:41724983 | C | T | 4 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-429G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41724983 | |||||||
chr8:41725023 | C | A | 1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.613-469G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725023 | |||||||
chr8:41725031 | A | T | 2 | a0001c0003t0001g0060 a0002c0057t0005g0265 |
2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.613-477T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725031 | |||||||
chr8:41725352 | G | A | 1 | a0003c0015t0003g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.612+409C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725352 | |||||||
chr8:41725409 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.612+352G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725409 | |||||||
chr8:41725451 | G | C | 1 | a0001c0002t0001g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.612+310C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725451 | |||||||
chr8:41725513 | T | G | 1 | a0001c0004t0002g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.612+248A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725513 | |||||||
chr8:41725684 | G | A | 7 | a0001c0052t0001g0235 a0003c0014t0002g0198 a0003c0014t0008g0093 others(4): Show |
7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+77C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725684 | |||||||
chr8:41725697 | C | T | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+64G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725697 | |||||||
chr8:41725743 | C | G | 19 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(16): Show |
19 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.612+18G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 6/42 | chr8 | 41725743 | |||||||
chr8:41726029 | C | T | 2 | a0001c0009t0002g0047 a0001c0009t0002g0048 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.427-83G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726029 | |||||||
chr8:41726037 | C | G | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.427-91G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726037 | |||||||
chr8:41726108 | C | A | 1 | a0001c0009t0002g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.427-162G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726108 | |||||||
chr8:41726180 | T | C | 1 | a0001c0005t0001g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.427-234A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726180 | |||||||
chr8:41726196 | T | C | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-250A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726196 | |||||||
chr8:41726372 | A | C | 1 | a0001c0006t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.427-426T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726372 | |||||||
chr8:41726399 | T | A | 8 | a0001c0003t0001g0147 a0001c0006t0001g0040 a0001c0013t0001g0027 others(5): Show |
8 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.427-453A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726399 | |||||||
chr8:41726548 | C | A | 1 | a0001c0005t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.427-602G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726548 | |||||||
chr8:41726678 | C | T | 3 | a0001c0016t0002g0007 a0001c0016t0002g0008 a0001c0016t0002g0009 |
3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.426+572G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726678 | |||||||
chr8:41726686 | C | T | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.426+564G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726686 | |||||||
chr8:41726723 | T | C | 18 | a0001c0002t0009g0098 a0001c0012t0005g0101 a0001c0012t0006g0096 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.426+527A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726723 | |||||||
chr8:41726923 | C | T | 10 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(7): Show |
11 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.426+327G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41726923 | |||||||
chr8:41727046 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.426+204C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41727046 | |||||||
chr8:41727055 | C | T | 1 | a0001c0058t0022g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.426+195G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41727055 | |||||||
chr8:41727124 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.426+126G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 5/42 | chr8 | 41727124 | |||||||
chr8:41727618 | C | A | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.328-270G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727618 | |||||||
chr8:41727677 | C | T | 3 | a0001c0002t0001g0157 a0001c0002t0001g0166 a0001c0002t0001g0177 |
3 | NA18972.hp2 NA18986.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.327+231G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727677 | |||||||
chr8:41727820 | C | T | 2 | a0001c0002t0001g0248 a0001c0019t0002g0238 |
2 | NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.327+88G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727820 | |||||||
chr8:41727839 | G | A | 2 | a0001c0005t0002g0004 a0001c0005t0013g0005 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.327+69C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727839 | |||||||
chr8:41727866 | T | G | 46 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.327+42A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727866 | |||||||
chr8:41727905 | T | C | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.327+3A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 4/42 | chr8 | 41727905 | |||||||
chr8:41728053 | C | T | 148 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.229-47G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728053 | |||||||
chr8:41728059 | G | A | 40 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.229-53C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728059 | |||||||
chr8:41728061 | G | A | 8 | a0001c0051t0008g0273 a0001c0052t0001g0235 a0003c0014t0002g0198 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-55C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728061 | |||||||
chr8:41728115 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.229-109T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728115 | |||||||
chr8:41728319 | G | A | 1 | a0003c0015t0003g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.229-313C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728319 | |||||||
chr8:41728349 | C | T | 2 | a0001c0003t0001g0054 a0001c0003t0002g0064 |
2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.229-343G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728349 | |||||||
chr8:41728377 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0261 |
2 | NA18948.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.229-371G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728377 | |||||||
chr8:41728442 | A | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.229-436T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728442 | |||||||
chr8:41728462 | C | T | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.229-456G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728462 | |||||||
chr8:41728471 | C | A | 2 | a0001c0005t0028g0112 a0001c0005t0029g0111 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229-465G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728471 | |||||||
chr8:41728680 | C | A | 1 | a0005c0021t0002g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229-674G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728680 | |||||||
chr8:41728838 | G | A | 123 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.229-832C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728838 | |||||||
chr8:41728874 | C | G | 7 | a0001c0002t0009g0098 a0002c0007t0001g0039 a0002c0007t0001g0041 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-868G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728874 | |||||||
chr8:41728963 | G | C | 2 | a0001c0004t0002g0202 a0001c0004t0002g0213 |
2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.229-957C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41728963 | |||||||
chr8:41729000 | G | A | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229-994C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729000 | |||||||
chr8:41729002 | C | A | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229-996G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729002 | |||||||
chr8:41729132 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.229-1126C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729132 | |||||||
chr8:41729159 | G | A | 1 | a0002c0057t0005g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.229-1153C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729159 | |||||||
chr8:41729177 | A | G | 3 | a0001c0002t0001g0195 a0001c0002t0001g0216 a0001c0002t0001g0222 |
3 | HG00408.hp1 HG02129.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.229-1171T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729177 | |||||||
chr8:41729232 | T | C | 55 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.229-1226A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729232 | |||||||
chr8:41729255 | A | G | 55 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.229-1249T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729255 | |||||||
chr8:41729304 | G | T | 40 | a0001c0003t0001g0147 a0001c0005t0002g0019 a0001c0005t0004g0029 others(37): Show |
41 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.229-1298C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729304 | |||||||
chr8:41729311 | T | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.229-1305A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729311 | |||||||
chr8:41729334 | A | C | 1 | a0001c0004t0002g0208 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.229-1328T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729334 | |||||||
chr8:41729910 | T | C | 3 | a0001c0005t0028g0112 a0001c0005t0029g0111 a0008c0041t0012g0167 |
3 | HG01123.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229-1904A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41729910 | |||||||
chr8:41730208 | G | A | 132 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(129): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.229-2202C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730208 | |||||||
chr8:41730288 | T | A | 1 | a0001c0001t0002g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.229-2282A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730288 | |||||||
chr8:41730326 | T | C | 6 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-2320A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730326 | |||||||
chr8:41730450 | T | C | 40 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.229-2444A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730450 | |||||||
chr8:41730451 | C | CT | 86 | a0001c0001t0002g0023 a0001c0001t0002g0074 a0001c0002t0001g0032 others(83): Show |
87 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.229-2446dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730451 | |||||||
chr8:41730598 | T | TCCATTGG others(3): Show |
3 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0037t0003g0234 |
3 | HG02258.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.229-2593_229-2592i others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730598 | |||||||
chr8:41730668 | A | G | 134 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0023 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.229-2662T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730668 | |||||||
chr8:41730749 | C | T | 41 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.229-2743G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730749 | |||||||
chr8:41730880 | C | T | 3 | a0001c0005t0028g0112 a0001c0005t0029g0111 a0008c0041t0012g0167 |
3 | HG01123.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229-2874G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41730880 | |||||||
chr8:41731157 | C | T | 7 | a0001c0052t0001g0235 a0003c0014t0002g0198 a0003c0014t0008g0093 others(4): Show |
7 | HG00323.hp2 HG00639.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+2814G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731157 | |||||||
chr8:41731201 | T | G | 1 | a0001c0002t0012g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.228+2770A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731201 | |||||||
chr8:41731346 | T | C | 2 | a0001c0003t0001g0056 a0001c0009t0002g0055 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.228+2625A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731346 | |||||||
chr8:41731526 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0132 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.228+2445A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731526 | |||||||
chr8:41731580 | CT | C | 13 | a0001c0005t0004g0030 a0001c0005t0004g0099 a0001c0006t0018g0118 others(10): Show |
14 | HG01517.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.228+2390delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731580 | |||||||
chr8:41731753 | G | C | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.228+2218C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731753 | |||||||
chr8:41731779 | G | A | 1 | a0001c0003t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.228+2192C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731779 | |||||||
chr8:41731805 | C | T | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.228+2166G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731805 | |||||||
chr8:41731817 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.228+2154C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731817 | |||||||
chr8:41731908 | C | T | 1 | a0001c0058t0022g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.228+2063G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731908 | |||||||
chr8:41731950 | C | T | 2 | a0001c0003t0001g0162 a0001c0003t0009g0163 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.228+2021G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731950 | |||||||
chr8:41731963 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.228+2008C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41731963 | |||||||
chr8:41732210 | C | T | 11 | a0001c0001t0002g0233 a0001c0003t0001g0147 a0001c0005t0002g0019 others(8): Show |
11 | HG02258.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.228+1761G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732210 | |||||||
chr8:41732227 | C | A | 5 | a0001c0006t0001g0017 a0001c0006t0001g0263 a0001c0006t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.228+1744G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732227 | |||||||
chr8:41732453 | C | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0261 |
2 | NA18948.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.228+1518G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732453 | |||||||
chr8:41732522 | C | T | 1 | a0001c0017t0005g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.228+1449G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732522 | |||||||
chr8:41732527 | C | T | 2 | a0002c0039t0010g0018 a0003c0049t0001g0103 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.228+1444G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732527 | |||||||
chr8:41732554 | A | G | 1 | a0001c0017t0005g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.228+1417T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732554 | |||||||
chr8:41732569 | C | T | 3 | a0001c0002t0001g0173 a0001c0002t0001g0180 a0001c0025t0011g0002 |
4 | HG00741.hp2 HG01192.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+1402G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732569 | |||||||
chr8:41732610 | G | A | 7 | a0001c0002t0009g0098 a0001c0056t0003g0026 a0002c0007t0007g0022 others(4): Show |
7 | HG01106.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+1361C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732610 | |||||||
chr8:41732631 | T | G | 1 | a0001c0003t0009g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.228+1340A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732631 | |||||||
chr8:41732632 | C | T | 2 | a0001c0003t0001g0054 a0001c0003t0002g0064 |
2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.228+1339G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732632 | |||||||
chr8:41732820 | C | T | 2 | a0001c0051t0008g0273 a0002c0043t0002g0045 |
2 | HG00738.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.228+1151G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41732820 | |||||||
chr8:41733028 | G | A | 1 | a0002c0057t0005g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.228+943C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733028 | |||||||
chr8:41733029 | C | T | 38 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.228+942G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733029 | |||||||
chr8:41733162 | G | C | 6 | a0001c0005t0003g0033 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.228+809C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733162 | |||||||
chr8:41733228 | C | T | 1 | a0002c0007t0007g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.228+743G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733228 | |||||||
chr8:41733282 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.228+689C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733282 | |||||||
chr8:41733473 | G | A | 2 | a0001c0022t0002g0231 a0001c0022t0002g0232 |
2 | HG00733.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.228+498C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733473 | |||||||
chr8:41733540 | T | C | 14 | a0001c0001t0002g0023 a0001c0005t0001g0084 a0001c0005t0010g0020 others(11): Show |
14 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.228+431A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733540 | |||||||
chr8:41733712 | G | C | 2 | a0001c0002t0001g0182 a0001c0002t0001g0264 |
2 | HG00735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.228+259C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733712 | |||||||
chr8:41733756 | G | A | 38 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.228+215C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733756 | |||||||
chr8:41733838 | C | G | 1 | a0001c0003t0001g0147 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.228+133G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 3/42 | chr8 | 41733838 | |||||||
chr8:41734125 | C | T | 37 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0063 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.130-56G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734125 | |||||||
chr8:41734247 | C | T | 4 | a0001c0003t0001g0147 a0001c0013t0006g0128 a0001c0013t0006g0130 others(1): Show |
4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-178G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734247 | |||||||
chr8:41734389 | C | CTTAATTA others(4): Show |
1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.130-331_130-321dup others(11): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734389 | |||||||
chr8:41734733 | G | GA | 6 | a0001c0005t0003g0033 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-665dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734733 | |||||||
chr8:41734761 | G | C | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-692C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734761 | |||||||
chr8:41734996 | AAAAC | A | 5 | a0001c0006t0001g0017 a0001c0006t0001g0263 a0001c0006t0001g0266 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-931_130-928del others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41734996 | |||||||
chr8:41735102 | T | C | 55 | a0001c0001t0002g0109 a0001c0002t0001g0032 a0001c0002t0001g0053 others(52): Show |
56 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.130-1033A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735102 | |||||||
chr8:41735153 | T | A | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-1084A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735153 | |||||||
chr8:41735265 | T | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-1196A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735265 | |||||||
chr8:41735303 | C | A | 1 | a0001c0016t0002g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.130-1234G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735303 | |||||||
chr8:41735410 | T | G | 1 | a0001c0017t0005g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.130-1341A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735410 | |||||||
chr8:41735420 | C | T | 6 | a0002c0007t0001g0039 a0002c0007t0001g0041 a0002c0007t0027g0036 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-1351G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735420 | |||||||
chr8:41735455 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-1386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735455 | |||||||
chr8:41735611 | C | G | 2 | a0001c0046t0030g0276 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.130-1542G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735611 | |||||||
chr8:41735705 | C | T | 165 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.130-1636G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735705 | |||||||
chr8:41735791 | G | A | 9 | a0001c0003t0001g0092 a0001c0052t0001g0235 a0002c0039t0010g0018 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.130-1722C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735791 | |||||||
chr8:41735861 | G | A | 4 | a0001c0003t0001g0147 a0001c0013t0006g0128 a0001c0013t0006g0130 others(1): Show |
4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1792C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735861 | |||||||
chr8:41735863 | G | A | 3 | a0001c0002t0001g0157 a0001c0002t0001g0166 a0001c0002t0001g0177 |
3 | NA18972.hp2 NA18986.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.130-1794C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735863 | |||||||
chr8:41735915 | AC | A | 4 | a0001c0003t0001g0147 a0001c0013t0006g0128 a0001c0013t0006g0130 others(1): Show |
4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1847delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735915 | |||||||
chr8:41735973 | G | T | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130-1904C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735973 | |||||||
chr8:41735999 | C | T | 2 | a0001c0002t0001g0122 a0001c0002t0014g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-1930G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41735999 | |||||||
chr8:41736108 | T | C | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130-2039A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736108 | |||||||
chr8:41736265 | A | G | 6 | a0001c0005t0003g0033 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-2196T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736265 | |||||||
chr8:41736284 | C | T | 38 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.130-2215G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736284 | |||||||
chr8:41736410 | G | T | 1 | a0001c0003t0001g0215 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.130-2341C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736410 | |||||||
chr8:41736436 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-2367C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736436 | |||||||
chr8:41736519 | T | C | 10 | a0001c0006t0001g0017 a0001c0006t0001g0263 a0001c0006t0001g0266 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.130-2450A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736519 | |||||||
chr8:41736526 | A | T | 53 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(50): Show |
54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.130-2457T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736526 | |||||||
chr8:41736634 | C | T | 23 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0012t0005g0101 others(20): Show |
24 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.130-2565G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736634 | |||||||
chr8:41736665 | T | C | 2 | a0001c0004t0002g0252 a0001c0008t0002g0253 |
2 | HG03834.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.130-2596A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736665 | |||||||
chr8:41736741 | G | A | 1 | a0001c0003t0001g0162 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.130-2672C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736741 | |||||||
chr8:41736780 | A | G | 6 | a0001c0006t0001g0100 a0001c0006t0018g0118 a0001c0017t0005g0116 others(3): Show |
6 | HG02572.hp1 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-2711T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41736780 | |||||||
chr8:41737110 | A | G | 97 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0032 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.130-3041T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737110 | |||||||
chr8:41737253 | C | G | 42 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.130-3184G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737253 | |||||||
chr8:41737507 | G | A | 1 | a0003c0049t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.130-3438C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737507 | |||||||
chr8:41737567 | C | T | 1 | a0003c0015t0003g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.130-3498G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737567 | |||||||
chr8:41737644 | C | T | 1 | a0001c0003t0001g0147 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.130-3575G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737644 | |||||||
chr8:41737687 | C | T | 7 | a0001c0006t0001g0017 a0001c0006t0001g0100 a0001c0006t0018g0118 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-3618G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737687 | |||||||
chr8:41737773 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.130-3704C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737773 | |||||||
chr8:41737817 | T | C | 29 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0005t0003g0033 others(26): Show |
30 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130-3748A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737817 | |||||||
chr8:41737879 | G | A | 1 | a0001c0004t0002g0249 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.130-3810C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41737879 | |||||||
chr8:41738010 | C | T | 1 | a0001c0003t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130-3941G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738010 | |||||||
chr8:41738077 | CAGAAG | C | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-4013_130-4009d others(7): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738077 | |||||||
chr8:41738095 | T | C | 147 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(144): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.130-4026A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738095 | |||||||
chr8:41738202 | T | TGTATCTG others(1): Show |
134 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(131): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.130-4134_130-4133i others(10): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738202 | |||||||
chr8:41738205 | T | C | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.130-4136A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738205 | |||||||
chr8:41738236 | T | C | 1 | a0001c0040t0001g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-4167A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738236 | |||||||
chr8:41738258 | C | T | 1 | a0001c0003t0019g0065 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.130-4189G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738258 | |||||||
chr8:41738415 | G | A | 2 | a0001c0002t0001g0122 a0001c0002t0014g0123 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-4346C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738415 | |||||||
chr8:41738645 | T | A | 7 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-4576A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738645 | |||||||
chr8:41738902 | A | G | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-4833T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738902 | |||||||
chr8:41738962 | A | G | 3 | a0005c0021t0002g0114 a0005c0021t0002g0131 a0005c0035t0001g0129 |
3 | HG02280.hp1 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.130-4893T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41738962 | |||||||
chr8:41739199 | G | T | 35 | a0001c0004t0001g0108 a0001c0004t0001g0148 a0001c0004t0002g0068 others(32): Show |
35 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.130-5130C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739199 | |||||||
chr8:41739215 | C | T | 5 | a0001c0056t0003g0026 a0002c0007t0007g0024 a0002c0007t0007g0025 others(2): Show |
5 | HG01106.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-5146G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739215 | |||||||
chr8:41739260 | T | A | 1 | a0003c0024t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-5191A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739260 | |||||||
chr8:41739325 | T | C | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-5256A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739325 | |||||||
chr8:41739509 | G | GTTTTTTT others(9): Show |
1 | a0001c0003t0019g0065 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.130-5456_130-5441d others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739509 | |||||||
chr8:41739521 | CT | C | 210 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(207): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.130-5453delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739521 | |||||||
chr8:41739521 | CTT | C | 5 | a0001c0001t0001g0153 a0001c0001t0001g0242 a0001c0005t0001g0084 others(2): Show |
5 | HG02015.hp1 HG02630.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-5454_130-5453d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739521 | |||||||
chr8:41739522 | T | TTTTTTTT others(7): Show |
4 | a0001c0009t0002g0047 a0001c0009t0002g0048 a0001c0009t0002g0052 others(1): Show |
4 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-5454_130-5453i others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739522 | |||||||
chr8:41739522 | T | TTTTTTTT others(8): Show |
33 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.130-5454_130-5453i others(17): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739522 | |||||||
chr8:41739523 | T | TTTTTTTT others(7): Show |
1 | a0001c0003t0002g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.130-5455_130-5454i others(16): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739523 | |||||||
chr8:41739614 | T | C | 134 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(131): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.130-5545A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739614 | |||||||
chr8:41739616 | C | T | 1 | a0001c0005t0010g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130-5547G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739616 | |||||||
chr8:41739764 | G | A | 6 | a0001c0001t0001g0242 a0001c0001t0002g0172 a0001c0001t0002g0193 others(3): Show |
6 | HG02015.hp1 HG04115.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-5695C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739764 | |||||||
chr8:41739770 | C | T | 1 | a0001c0009t0002g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.130-5701G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41739770 | |||||||
chr8:41740050 | C | T | 4 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-5981G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740050 | |||||||
chr8:41740162 | A | AT | 91 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0023 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.130-6094dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740162 | |||||||
chr8:41740162 | AT | A | 130 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(127): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.130-6094delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740162 | |||||||
chr8:41740306 | G | A | 39 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.130-6237C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740306 | |||||||
chr8:41740334 | G | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-6265C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740334 | |||||||
chr8:41740335 | C | T | 232 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.130-6266G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740335 | |||||||
chr8:41740368 | C | T | 3 | a0001c0005t0004g0029 a0001c0013t0001g0027 a0001c0013t0001g0038 |
3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-6299G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740368 | |||||||
chr8:41740385 | C | G | 2 | a0001c0002t0003g0079 a0001c0002t0003g0080 |
2 | HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.130-6316G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740385 | |||||||
chr8:41740402 | T | C | 47 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.130-6333A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740402 | |||||||
chr8:41740455 | CA | C | 74 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(71): Show |
74 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.130-6387delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740455 | |||||||
chr8:41740749 | T | C | 1 | a0001c0026t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.130-6680A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41740749 | |||||||
chr8:41741202 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-7133C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741202 | |||||||
chr8:41741494 | C | A | 132 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(129): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.130-7425G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741494 | |||||||
chr8:41741579 | G | GA | 133 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.130-7511dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741579 | |||||||
chr8:41741617 | C | T | 6 | a0001c0010t0002g0081 a0001c0010t0003g0003 a0001c0010t0003g0110 others(3): Show |
6 | HG02071.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-7548G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741617 | |||||||
chr8:41741637 | C | T | 3 | a0001c0046t0030g0276 a0002c0007t0021g0115 a0014c0031t0002g0256 |
3 | HG02451.hp2 HG02723.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.130-7568G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741637 | |||||||
chr8:41741663 | C | T | 1 | a0001c0004t0002g0176 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.130-7594G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741663 | |||||||
chr8:41741721 | C | T | 1 | a0001c0056t0003g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.130-7652G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741721 | |||||||
chr8:41741825 | A | C | 6 | a0001c0005t0003g0033 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-7756T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741825 | |||||||
chr8:41741899 | T | C | 232 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.130-7830A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741899 | |||||||
chr8:41741963 | C | G | 37 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.130-7894G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41741963 | |||||||
chr8:41742042 | G | A | 84 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0023 others(81): Show |
85 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.130-7973C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742042 | |||||||
chr8:41742167 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130-8098A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742167 | |||||||
chr8:41742282 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.130-8213C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742282 | |||||||
chr8:41742507 | C | T | 2 | a0001c0003t0001g0092 a0010c0050t0001g0171 |
2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.130-8438G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742507 | |||||||
chr8:41742591 | C | T | 3 | a0001c0005t0004g0029 a0001c0013t0001g0027 a0001c0013t0001g0038 |
3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-8522G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742591 | |||||||
chr8:41742607 | T | G | 49 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.130-8538A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742607 | |||||||
chr8:41742609 | G | A | 3 | a0001c0005t0004g0029 a0001c0013t0001g0027 a0001c0013t0001g0038 |
3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-8540C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742609 | |||||||
chr8:41742749 | G | A | 1 | a0001c0004t0002g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.130-8680C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742749 | |||||||
chr8:41742839 | C | G | 4 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(1): Show |
4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-8770G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41742839 | |||||||
chr8:41743037 | G | C | 232 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.130-8968C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743037 | |||||||
chr8:41743130 | G | A | 148 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.130-9061C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743130 | |||||||
chr8:41743178 | C | G | 54 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.130-9109G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743178 | |||||||
chr8:41743303 | G | A | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130-9234C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743303 | |||||||
chr8:41743588 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.130-9519C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743588 | |||||||
chr8:41743809 | CAT | C | 54 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0003t0001g0049 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.130-9742_130-9741d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743809 | |||||||
chr8:41743914 | G | A | 2 | a0001c0046t0030g0276 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.130-9845C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41743914 | |||||||
chr8:41744006 | T | C | 133 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.130-9937A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744006 | |||||||
chr8:41744167 | C | T | 133 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.130-10098G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744167 | |||||||
chr8:41744363 | A | G | 3 | a0001c0005t0004g0029 a0001c0013t0001g0027 a0001c0013t0001g0038 |
3 | HG02965.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.130-10294T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744363 | |||||||
chr8:41744536 | C | CT | 72 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0009g0098 others(69): Show |
73 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.130-10468dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744536 | |||||||
chr8:41744536 | C | CTT | 8 | a0001c0001t0002g0023 a0001c0003t0001g0139 a0001c0003t0002g0064 others(5): Show |
8 | HG01978.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-10469_130-1046 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744536 | |||||||
chr8:41744536 | CTT | C | 129 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(126): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.130-10469_130-1046 others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744536 | |||||||
chr8:41744543 | T | C | 2 | a0003c0049t0001g0103 a0012c0033t0001g0107 |
2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.130-10474A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744543 | |||||||
chr8:41744597 | T | C | 232 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.130-10528A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744597 | |||||||
chr8:41744663 | A | G | 1 | a0001c0002t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.130-10594T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744663 | |||||||
chr8:41744684 | G | A | 3 | a0001c0004t0002g0252 a0001c0008t0002g0253 a0003c0015t0003g0214 |
3 | HG03834.hp1 NA18973.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.130-10615C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744684 | |||||||
chr8:41744691 | C | T | 4 | a0001c0003t0001g0147 a0001c0013t0006g0128 a0001c0013t0006g0130 others(1): Show |
4 | HG03098.hp1 HG03471.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-10622G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744691 | |||||||
chr8:41744825 | G | A | 4 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-10756C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744825 | |||||||
chr8:41744827 | G | A | 1 | a0001c0013t0006g0128 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130-10758C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744827 | |||||||
chr8:41744839 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-10770G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744839 | |||||||
chr8:41744874 | T | C | 138 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(135): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.130-10805A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744874 | |||||||
chr8:41744982 | G | A | 7 | a0001c0005t0004g0030 a0001c0006t0001g0017 a0001c0006t0001g0100 others(4): Show |
7 | HG02572.hp1 HG02630.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-10913C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41744982 | |||||||
chr8:41745047 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.130-10978T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745047 | |||||||
chr8:41745091 | AACAG | A | 135 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(132): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.130-11026_130-1102 others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745091 | |||||||
chr8:41745150 | G | A | 60 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(57): Show |
61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.130-11081C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745150 | |||||||
chr8:41745257 | A | T | 60 | a0001c0002t0001g0032 a0001c0002t0001g0053 a0001c0002t0001g0059 others(57): Show |
61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.130-11188T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745257 | |||||||
chr8:41745455 | C | T | 1 | a0001c0003t0001g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.130-11386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745455 | |||||||
chr8:41745489 | A | T | 2 | a0001c0002t0001g0059 a0001c0002t0001g0159 |
2 | HG01167.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.130-11420T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745489 | |||||||
chr8:41745895 | G | T | 231 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.130-11826C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41745895 | |||||||
chr8:41746028 | G | A | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130-11959C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746028 | |||||||
chr8:41746155 | C | G | 76 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(73): Show |
76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.129+11881G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746155 | |||||||
chr8:41746705 | C | G | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.129+11331G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746705 | |||||||
chr8:41746851 | G | A | 4 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(1): Show |
4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+11185C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746851 | |||||||
chr8:41746868 | T | TA | 75 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(72): Show |
75 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.129+11167dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746868 | |||||||
chr8:41746868 | TA | T | 19 | a0001c0001t0002g0023 a0001c0002t0003g0143 a0001c0003t0001g0147 others(16): Show |
19 | HG00639.hp2 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+11167delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41746868 | |||||||
chr8:41747022 | G | A | 1 | a0004c0044t0004g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+11014C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747022 | |||||||
chr8:41747220 | T | A | 6 | a0001c0005t0003g0033 a0001c0006t0003g0006 a0001c0006t0003g0013 others(3): Show |
6 | HG00738.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+10816A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747220 | |||||||
chr8:41747542 | T | C | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+10494A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747542 | |||||||
chr8:41747630 | C | T | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0001c0046t0030g0276 others(2): Show |
5 | HG02717.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+10406G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747630 | |||||||
chr8:41747748 | C | T | 1 | a0001c0005t0004g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.129+10288G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747748 | |||||||
chr8:41747769 | G | A | 1 | a0001c0002t0009g0125 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.129+10267C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41747769 | |||||||
chr8:41748053 | C | A | 1 | a0001c0010t0003g0110 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.129+9983G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748053 | |||||||
chr8:41748090 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+9946G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748090 | |||||||
chr8:41748114 | T | A | 4 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+9922A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748114 | |||||||
chr8:41748119 | G | C | 110 | a0001c0001t0001g0153 a0001c0001t0001g0207 a0001c0001t0001g0209 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.129+9917C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748119 | |||||||
chr8:41748201 | A | G | 5 | a0001c0010t0002g0081 a0001c0010t0003g0110 a0001c0010t0003g0188 others(2): Show |
5 | HG02071.hp2 HG02074.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+9835T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748201 | |||||||
chr8:41748312 | C | T | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.129+9724G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748312 | |||||||
chr8:41748435 | T | A | 1 | a0002c0007t0007g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.129+9601A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748435 | |||||||
chr8:41748461 | C | T | 73 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(70): Show |
73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.129+9575G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748461 | |||||||
chr8:41748709 | G | A | 7 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+9327C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748709 | |||||||
chr8:41748771 | T | C | 4 | a0001c0005t0001g0078 a0001c0005t0001g0229 a0001c0005t0001g0257 others(1): Show |
4 | HG01123.hp1 HG01975.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+9265A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748771 | |||||||
chr8:41748791 | T | C | 5 | a0001c0005t0004g0030 a0001c0005t0010g0020 a0001c0006t0001g0017 others(2): Show |
5 | HG02451.hp2 HG02897.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+9245A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748791 | |||||||
chr8:41748801 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129+9235A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748801 | |||||||
chr8:41748802 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129+9234T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748802 | |||||||
chr8:41748818 | G | A | 1 | a0001c0003t0014g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9218C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748818 | |||||||
chr8:41748831 | C | G | 1 | a0001c0003t0014g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9205G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748831 | |||||||
chr8:41748832 | A | G | 45 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0003t0014g0061 others(42): Show |
46 | HG01106.hp2 HG01192.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.129+9204T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748832 | |||||||
chr8:41748842 | C | T | 1 | a0001c0003t0014g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9194G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748842 | |||||||
chr8:41748843 | A | G | 1 | a0001c0003t0014g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+9193T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748843 | |||||||
chr8:41748852 | A | G | 3 | a0001c0002t0001g0195 a0001c0002t0001g0216 a0001c0002t0001g0222 |
3 | HG00408.hp1 HG02129.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.129+9184T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748852 | |||||||
chr8:41748859 | T | C | 2 | a0003c0024t0001g0272 a0003c0049t0001g0103 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.129+9177A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748859 | |||||||
chr8:41748903 | C | T | 4 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(1): Show |
4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+9133G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748903 | |||||||
chr8:41748952 | A | G | 15 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0124 others(12): Show |
15 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.129+9084T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748952 | |||||||
chr8:41748959 | T | C | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+9077A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41748959 | |||||||
chr8:41749000 | C | A | 5 | a0001c0006t0003g0006 a0001c0006t0003g0013 a0001c0006t0003g0015 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+9036G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749000 | |||||||
chr8:41749022 | A | G | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+9014T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749022 | |||||||
chr8:41749034 | C | CA | 63 | a0001c0001t0001g0153 a0001c0001t0002g0023 a0001c0002t0001g0032 others(60): Show |
64 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.129+9001dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749034 | |||||||
chr8:41749034 | C | CAA | 6 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0018t0001g0144 others(3): Show |
6 | HG02895.hp1 HG03195.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+9000_129+9001d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749034 | |||||||
chr8:41749226 | A | G | 7 | a0001c0005t0002g0019 a0001c0005t0004g0030 a0001c0005t0010g0020 others(4): Show |
7 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+8810T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749226 | |||||||
chr8:41749295 | C | CT | 32 | a0001c0001t0002g0172 a0001c0001t0002g0218 a0001c0002t0001g0121 others(29): Show |
32 | HG00140.hp2 HG00438.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.129+8740dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749295 | |||||||
chr8:41749295 | C | CTTT | 26 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.129+8738_129+8740d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749295 | |||||||
chr8:41749295 | CT | C | 44 | a0001c0001t0001g0142 a0001c0001t0001g0190 a0001c0001t0001g0207 others(41): Show |
44 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.129+8740delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749295 | |||||||
chr8:41749390 | C | T | 20 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0013t0001g0027 others(17): Show |
20 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+8646G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749390 | |||||||
chr8:41749437 | G | A | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+8599C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749437 | |||||||
chr8:41749449 | C | G | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+8587G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749449 | |||||||
chr8:41749631 | A | G | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.129+8405T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749631 | |||||||
chr8:41749670 | T | C | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+8366A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749670 | |||||||
chr8:41749761 | C | T | 61 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0002t0001g0032 others(58): Show |
62 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.129+8275G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749761 | |||||||
chr8:41749855 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.129+8181C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749855 | |||||||
chr8:41749960 | C | T | 11 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(8): Show |
11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+8076G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41749960 | |||||||
chr8:41750072 | G | A | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+7964C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750072 | |||||||
chr8:41750174 | C | T | 266 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.129+7862G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750174 | |||||||
chr8:41750197 | G | A | 106 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0219 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+7839C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750197 | |||||||
chr8:41750339 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.129+7697C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750339 | |||||||
chr8:41750350 | C | A | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+7686G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750350 | |||||||
chr8:41750393 | C | T | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+7643G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750393 | |||||||
chr8:41750495 | G | C | 11 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(8): Show |
11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+7541C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750495 | |||||||
chr8:41750515 | T | G | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+7521A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750515 | |||||||
chr8:41750558 | A | G | 11 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(8): Show |
11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+7478T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750558 | |||||||
chr8:41750565 | CT | C | 76 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0002g0210 others(73): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.129+7470delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750565 | |||||||
chr8:41750646 | C | G | 238 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.129+7390G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750646 | |||||||
chr8:41750841 | C | T | 267 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.129+7195G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750841 | |||||||
chr8:41750847 | A | G | 267 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.129+7189T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750847 | |||||||
chr8:41750848 | G | C | 11 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(8): Show |
11 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+7188C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750848 | |||||||
chr8:41750909 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.129+7127T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41750909 | |||||||
chr8:41751306 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.129+6730C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751306 | |||||||
chr8:41751333 | T | C | 1 | a0001c0003t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+6703A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751333 | |||||||
chr8:41751348 | T | C | 273 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(270): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.129+6688A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751348 | |||||||
chr8:41751385 | C | T | 1 | a0002c0057t0005g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.129+6651G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751385 | |||||||
chr8:41751582 | G | T | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+6454C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751582 | |||||||
chr8:41751792 | C | T | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+6244G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41751792 | |||||||
chr8:41752050 | G | A | 20 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0013t0001g0027 others(17): Show |
20 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+5986C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752050 | |||||||
chr8:41752105 | C | T | 105 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0002t0001g0032 others(102): Show |
107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+5931G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752105 | |||||||
chr8:41752325 | G | A | 105 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0002t0001g0032 others(102): Show |
107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+5711C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752325 | |||||||
chr8:41752398 | C | T | 1 | a0001c0009t0002g0062 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.129+5638G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752398 | |||||||
chr8:41752399 | G | A | 1 | a0001c0038t0002g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.129+5637C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752399 | |||||||
chr8:41752444 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.129+5592T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752444 | |||||||
chr8:41752596 | C | T | 105 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0211 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.129+5440G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752596 | |||||||
chr8:41752655 | C | T | 13 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(10): Show |
14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+5381G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752655 | |||||||
chr8:41752716 | G | A | 106 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0211 others(103): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+5320C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752716 | |||||||
chr8:41752748 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129+5288G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752748 | |||||||
chr8:41752798 | G | GC | 68 | a0001c0001t0001g0142 a0001c0001t0002g0091 a0001c0001t0002g0169 others(65): Show |
70 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.129+5237dupG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752798 | |||||||
chr8:41752798 | G | GCC | 88 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0211 others(85): Show |
88 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.129+5236_129+5237d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752798 | |||||||
chr8:41752798 | G | GCCC | 21 | a0001c0001t0002g0010 a0001c0001t0002g0077 a0001c0001t0002g0172 others(18): Show |
21 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+5235_129+5237d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752798 | |||||||
chr8:41752816 | G | A | 2 | a0001c0003t0001g0060 a0001c0003t0014g0061 |
2 | HG01934.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.129+5220C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752816 | |||||||
chr8:41752827 | C | T | 14 | a0001c0001t0001g0142 a0001c0002t0001g0121 a0001c0002t0001g0122 others(11): Show |
14 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+5209G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752827 | |||||||
chr8:41752828 | G | A | 106 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0211 others(103): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.129+5208C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752828 | |||||||
chr8:41752925 | C | T | 42 | a0001c0001t0001g0153 a0001c0002t0001g0032 a0001c0002t0001g0053 others(39): Show |
43 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.129+5111G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752925 | |||||||
chr8:41752972 | A | G | 1 | a0003c0024t0003g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.129+5064T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752972 | |||||||
chr8:41752976 | A | C | 59 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0002t0001g0032 others(56): Show |
60 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.129+5060T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752976 | |||||||
chr8:41752991 | G | A | 212 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.129+5045C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41752991 | |||||||
chr8:41753060 | C | CT | 27 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(24): Show |
27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+4975dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753060 | |||||||
chr8:41753060 | CT | C | 80 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0002g0023 others(77): Show |
81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.129+4975delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753060 | |||||||
chr8:41753125 | C | T | 105 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0002t0001g0032 others(102): Show |
107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.129+4911G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753125 | |||||||
chr8:41753173 | T | C | 20 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0013t0001g0027 others(17): Show |
20 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+4863A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753173 | |||||||
chr8:41753317 | C | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.129+4719G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753317 | |||||||
chr8:41753318 | G | A | 13 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(10): Show |
14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+4718C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753318 | |||||||
chr8:41753345 | T | C | 212 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.129+4691A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753345 | |||||||
chr8:41753362 | G | A | 7 | a0001c0013t0001g0038 a0002c0007t0001g0039 a0002c0007t0001g0041 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+4674C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753362 | |||||||
chr8:41753424 | G | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.129+4612C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753424 | |||||||
chr8:41753451 | G | A | 105 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0219 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.129+4585C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753451 | |||||||
chr8:41753520 | C | G | 1 | a0001c0058t0022g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.129+4516G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753520 | |||||||
chr8:41753774 | G | GCC | 105 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0219 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.129+4260_129+4261d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753774 | |||||||
chr8:41753857 | T | C | 105 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0219 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.129+4179A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753857 | |||||||
chr8:41753966 | C | T | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+4070G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41753966 | |||||||
chr8:41754030 | T | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.129+4006A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754030 | |||||||
chr8:41754227 | A | G | 212 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.129+3809T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754227 | |||||||
chr8:41754276 | C | T | 212 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.129+3760G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754276 | |||||||
chr8:41754288 | C | T | 2 | a0001c0009t0002g0067 a0001c0009t0002g0083 |
2 | HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.129+3748G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754288 | |||||||
chr8:41754542 | A | G | 1 | a0001c0005t0004g0030 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.129+3494T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754542 | |||||||
chr8:41754737 | C | T | 106 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(103): Show |
108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.129+3299G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754737 | |||||||
chr8:41754969 | C | T | 105 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0219 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.129+3067G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41754969 | |||||||
chr8:41755033 | T | C | 212 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.129+3003A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755033 | |||||||
chr8:41755069 | C | A | 17 | a0001c0001t0001g0142 a0001c0002t0001g0121 a0001c0002t0001g0122 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.129+2967G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755069 | |||||||
chr8:41755146 | G | A | 1 | a0001c0003t0001g0060 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.129+2890C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755146 | |||||||
chr8:41755219 | C | T | 1 | a0001c0002t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.129+2817G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755219 | |||||||
chr8:41755272 | C | T | 3 | a0001c0032t0003g0104 a0003c0049t0001g0103 a0012c0033t0001g0107 |
3 | HG02895.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129+2764G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755272 | |||||||
chr8:41755294 | C | T | 1 | a0001c0005t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.129+2742G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755294 | |||||||
chr8:41755297 | A | C | 1 | a0001c0005t0003g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129+2739T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755297 | |||||||
chr8:41755305 | A | G | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2731T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755305 | |||||||
chr8:41755542 | T | G | 66 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(63): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.129+2494A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755542 | |||||||
chr8:41755551 | G | A | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2485C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755551 | |||||||
chr8:41755627 | G | A | 13 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(10): Show |
14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+2409C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755627 | |||||||
chr8:41755664 | G | C | 1 | a0001c0005t0003g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129+2372C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755664 | |||||||
chr8:41755684 | C | T | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+2352G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755684 | |||||||
chr8:41755822 | A | G | 21 | a0001c0001t0002g0023 a0001c0002t0009g0098 a0001c0013t0001g0027 others(18): Show |
21 | HG01106.hp2 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+2214T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755822 | |||||||
chr8:41755885 | C | T | 13 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(10): Show |
14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+2151G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755885 | |||||||
chr8:41755903 | A | T | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.129+2133T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755903 | |||||||
chr8:41755978 | T | C | 108 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(105): Show |
110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.129+2058A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755978 | |||||||
chr8:41755980 | A | G | 1 | a0001c0009t0002g0083 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129+2056T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41755980 | |||||||
chr8:41756070 | A | G | 1 | a0001c0003t0001g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.129+1966T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756070 | |||||||
chr8:41756128 | ATTTATTT others(10): Show |
A | 2 | a0001c0005t0002g0004 a0001c0005t0013g0005 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.129+1891_129+1907d others(19): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756128 | |||||||
chr8:41756231 | C | T | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00423.hp2 HG01168.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.129+1805G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756231 | |||||||
chr8:41756365 | C | T | 3 | a0001c0032t0003g0104 a0003c0049t0001g0103 a0012c0033t0001g0107 |
3 | HG02895.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129+1671G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756365 | |||||||
chr8:41756379 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0209 |
2 | NA19002.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.129+1657G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756379 | |||||||
chr8:41756435 | C | T | 4 | a0001c0013t0001g0027 a0002c0007t0007g0024 a0002c0007t0007g0025 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1601G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756435 | |||||||
chr8:41756670 | T | G | 1 | a0001c0002t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.129+1366A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756670 | |||||||
chr8:41756683 | T | C | 34 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(31): Show |
34 | HG00140.hp1 HG00423.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.129+1353A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756683 | |||||||
chr8:41756738 | G | A | 67 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.129+1298C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756738 | |||||||
chr8:41756740 | A | C | 28 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.129+1296T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756740 | |||||||
chr8:41756769 | G | C | 67 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.129+1267C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756769 | |||||||
chr8:41756811 | T | C | 1 | a0001c0002t0002g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.129+1225A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756811 | |||||||
chr8:41756859 | G | A | 15 | a0001c0006t0001g0017 a0001c0006t0001g0100 a0001c0006t0001g0263 others(12): Show |
16 | HG00738.hp1 HG02145.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.129+1177C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756859 | |||||||
chr8:41756985 | G | A | 83 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(80): Show |
85 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.129+1051C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41756985 | |||||||
chr8:41757049 | G | A | 110 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(107): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.129+987C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757049 | |||||||
chr8:41757197 | C | T | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.129+839G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757197 | |||||||
chr8:41757321 | G | A | 1 | a0001c0004t0002g0176 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.129+715C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757321 | |||||||
chr8:41757402 | G | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.129+634C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757402 | |||||||
chr8:41757541 | A | G | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129+495T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757541 | |||||||
chr8:41757562 | C | T | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.129+474G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757562 | |||||||
chr8:41757620 | G | A | 77 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.129+416C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757620 | |||||||
chr8:41757648 | G | A | 1 | a0003c0024t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.129+388C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757648 | |||||||
chr8:41757911 | G | A | 268 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.129+125C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 2/42 | chr8 | 41757911 | |||||||
chr8:41758220 | C | T | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-83G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758220 | |||||||
chr8:41758221 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.28-84T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758221 | |||||||
chr8:41758288 | G | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-151C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758288 | |||||||
chr8:41758333 | G | T | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-196C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758333 | |||||||
chr8:41758685 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.28-548T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758685 | |||||||
chr8:41758839 | G | A | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-702C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758839 | |||||||
chr8:41758960 | G | A | 76 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.28-823C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758960 | |||||||
chr8:41758983 | G | A | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-846C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41758983 | |||||||
chr8:41759010 | C | G | 76 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.28-873G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759010 | |||||||
chr8:41759058 | C | G | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-921G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759058 | |||||||
chr8:41759157 | G | A | 2 | a0001c0013t0006g0128 a0001c0013t0006g0130 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.28-1020C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759157 | |||||||
chr8:41759195 | A | G | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-1058T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759195 | |||||||
chr8:41759291 | A | G | 2 | a0001c0003t0001g0060 a0001c0003t0014g0061 |
2 | HG01934.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.28-1154T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759291 | |||||||
chr8:41759361 | C | A | 76 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.28-1224G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759361 | |||||||
chr8:41759431 | G | A | 60 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(57): Show |
61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.28-1294C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759431 | |||||||
chr8:41759431 | G | C | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-1294C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759431 | |||||||
chr8:41759443 | T | C | 1 | a0001c0016t0002g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.28-1306A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759443 | |||||||
chr8:41759506 | A | AAAACAAA others(1): Show |
27 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(24): Show |
27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1377_28-1370dup others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759506 | |||||||
chr8:41759506 | A | AAAACAAA others(5): Show |
49 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(46): Show |
50 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-1381_28-1370dup others(12): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759506 | |||||||
chr8:41759547 | G | A | 1 | a0001c0013t0006g0128 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-1410C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759547 | |||||||
chr8:41759674 | T | A | 266 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.28-1537A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759674 | |||||||
chr8:41759986 | G | A | 1 | a0001c0006t0003g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-1849C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41759986 | |||||||
chr8:41760017 | C | T | 27 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(24): Show |
27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1880G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760017 | |||||||
chr8:41760039 | A | G | 4 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(1): Show |
4 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-1902T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760039 | |||||||
chr8:41760202 | C | T | 13 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(10): Show |
14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-2065G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760202 | |||||||
chr8:41760309 | C | T | 77 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-2172G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760309 | |||||||
chr8:41760433 | T | C | 4 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-2296A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760433 | |||||||
chr8:41760505 | G | A | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-2368C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760505 | |||||||
chr8:41760573 | C | T | 1 | a0001c0001t0002g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.28-2436G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760573 | |||||||
chr8:41760659 | G | A | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.28-2522C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760659 | |||||||
chr8:41760695 | G | A | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-2558C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760695 | |||||||
chr8:41760977 | TGAA | T | 60 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(57): Show |
61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.28-2843_28-2841del others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760977 | |||||||
chr8:41760998 | A | G | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-2861T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41760998 | |||||||
chr8:41761123 | G | GCA | 14 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0005t0001g0078 others(11): Show |
14 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-2988_28-2987dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761123 | |||||||
chr8:41761123 | GCA | G | 63 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.28-2988_28-2987del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761123 | |||||||
chr8:41761142 | CAT | C | 15 | a0001c0005t0004g0030 a0001c0006t0001g0100 a0001c0006t0001g0263 others(12): Show |
16 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-3007_28-3006del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761142 | |||||||
chr8:41761172 | TGCACACA others(11): Show |
T | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-3053_28-3036del others(18): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761172 | |||||||
chr8:41761205 | TCA | T | 144 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(141): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.28-3070_28-3069del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761205 | |||||||
chr8:41761300 | C | T | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-3163G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761300 | |||||||
chr8:41761303 | A | C | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-3166T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761303 | |||||||
chr8:41761308 | C | T | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28-3171G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761308 | |||||||
chr8:41761335 | C | A | 77 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-3198G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761335 | |||||||
chr8:41761371 | G | GCA | 146 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(143): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.28-3236_28-3235dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761371 | |||||||
chr8:41761371 | GCA | G | 34 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(31): Show |
34 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.28-3236_28-3235del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761371 | |||||||
chr8:41761371 | GCACA | G | 42 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(39): Show |
43 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.28-3238_28-3235del others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761371 | |||||||
chr8:41761373 | A | G | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-3236T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761373 | |||||||
chr8:41761390 | T | C | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-3253A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761390 | |||||||
chr8:41761402 | C | T | 77 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-3265G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761402 | |||||||
chr8:41761439 | A | C | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-3302T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761439 | |||||||
chr8:41761488 | C | T | 1 | a0001c0002t0002g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.28-3351G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761488 | |||||||
chr8:41761518 | C | T | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-3381G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761518 | |||||||
chr8:41761637 | C | T | 6 | a0001c0009t0002g0047 a0001c0009t0002g0048 a0001c0009t0002g0052 others(3): Show |
6 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-3500G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761637 | |||||||
chr8:41761653 | CTCATGCA others(7): Show |
C | 1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-3530_28-3517del others(14): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761653 | |||||||
chr8:41761855 | G | A | 1 | a0001c0005t0020g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.28-3718C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41761855 | |||||||
chr8:41762020 | G | A | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-3883C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762020 | |||||||
chr8:41762038 | T | C | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-3901A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762038 | |||||||
chr8:41762044 | A | C | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-3907T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762044 | |||||||
chr8:41762195 | A | G | 136 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(133): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.28-4058T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762195 | |||||||
chr8:41762250 | A | G | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4113T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762250 | |||||||
chr8:41762510 | T | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-4373A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762510 | |||||||
chr8:41762541 | G | A | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4404C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762541 | |||||||
chr8:41762594 | A | G | 27 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(24): Show |
27 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-4457T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762594 | |||||||
chr8:41762654 | A | G | 13 | a0001c0006t0001g0100 a0001c0006t0001g0263 a0001c0006t0001g0266 others(10): Show |
14 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-4517T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762654 | |||||||
chr8:41762667 | G | A | 1 | a0001c0009t0002g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-4530C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762667 | |||||||
chr8:41762672 | G | C | 1 | a0001c0002t0001g0127 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28-4535C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41762672 | |||||||
chr8:41763093 | G | A | 1 | a0001c0004t0002g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-4956C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763093 | |||||||
chr8:41763120 | G | A | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-4983C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763120 | |||||||
chr8:41763193 | G | A | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-5056C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763193 | |||||||
chr8:41763213 | C | CA | 6 | a0001c0001t0002g0164 a0001c0003t0001g0237 a0001c0003t0002g0221 others(3): Show |
6 | HG00099.hp1 HG01123.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5077dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763213 | |||||||
chr8:41763213 | C | CAA | 131 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0219 others(128): Show |
131 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.28-5078_28-5077dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763213 | |||||||
chr8:41763213 | C | CAAA | 53 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0211 others(50): Show |
54 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.28-5079_28-5077dup others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763213 | |||||||
chr8:41763564 | C | A | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-5427G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763564 | |||||||
chr8:41763627 | A | G | 25 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(22): Show |
25 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.28-5490T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763627 | |||||||
chr8:41763657 | T | C | 7 | a0001c0005t0002g0019 a0001c0005t0004g0030 a0001c0005t0010g0020 others(4): Show |
7 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-5520A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763657 | |||||||
chr8:41763678 | A | G | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-5541T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763678 | |||||||
chr8:41763805 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.28-5668G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763805 | |||||||
chr8:41763806 | G | A | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-5669C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763806 | |||||||
chr8:41763858 | C | A | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-5721G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763858 | |||||||
chr8:41763869 | C | T | 76 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0002g0057 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.28-5732G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763869 | |||||||
chr8:41763881 | C | CT | 9 | a0001c0003t0001g0056 a0001c0003t0001g0060 a0001c0003t0002g0064 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-5745dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763881 | |||||||
chr8:41763881 | CTTTTTTT others(6): Show |
C | 1 | a0001c0010t0003g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.28-5757_28-5745del others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763881 | |||||||
chr8:41763884 | TTTTTC | T | 32 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0002g0057 others(29): Show |
32 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-5752_28-5748del others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763884 | |||||||
chr8:41763886 | TTTC | T | 11 | a0001c0002t0009g0098 a0001c0006t0001g0100 a0001c0006t0001g0263 others(8): Show |
12 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-5752_28-5750del others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763886 | |||||||
chr8:41763889 | C | CT | 110 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(107): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.28-5753dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | |||||||
chr8:41763889 | C | CTT | 16 | a0001c0001t0002g0076 a0001c0001t0002g0172 a0001c0001t0002g0241 others(13): Show |
16 | HG00423.hp1 HG01123.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-5754_28-5753dup others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | |||||||
chr8:41763889 | C | CTTT | 6 | a0001c0001t0002g0010 a0001c0001t0002g0074 a0001c0001t0002g0218 others(3): Show |
6 | HG02071.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5755_28-5753dup others(3): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | |||||||
chr8:41763889 | C | T | 25 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0056 others(22): Show |
25 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.28-5752G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | |||||||
chr8:41763889 | CT | C | 37 | a0001c0001t0001g0153 a0001c0001t0001g0211 a0001c0002t0001g0053 others(34): Show |
38 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.28-5753delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | |||||||
chr8:41763889 | CTTTTTTT others(6): Show |
C | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28-5765_28-5753del others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763889 | |||||||
chr8:41763983 | G | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-5846C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41763983 | |||||||
chr8:41764040 | A | G | 3 | a0001c0016t0002g0007 a0001c0016t0002g0008 a0001c0016t0002g0009 |
3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.28-5903T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764040 | |||||||
chr8:41764110 | G | A | 76 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.28-5973C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764110 | |||||||
chr8:41764167 | AT | A | 145 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0190 others(142): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.28-6031delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764167 | |||||||
chr8:41764286 | C | T | 35 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-6149G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764286 | |||||||
chr8:41764385 | C | T | 76 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.28-6248G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764385 | |||||||
chr8:41764512 | G | A | 1 | a0001c0005t0003g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-6375C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764512 | |||||||
chr8:41764589 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-6452G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764589 | |||||||
chr8:41764606 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.28-6469C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764606 | |||||||
chr8:41764684 | T | C | 1 | a0001c0006t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-6547A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764684 | |||||||
chr8:41764719 | G | A | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.28-6582C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764719 | |||||||
chr8:41764722 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-6585G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764722 | |||||||
chr8:41764869 | A | G | 2 | a0001c0005t0001g0084 a0001c0040t0001g0085 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-6732T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41764869 | |||||||
chr8:41765103 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-6966G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765103 | |||||||
chr8:41765159 | C | T | 14 | a0001c0002t0009g0098 a0001c0006t0001g0100 a0001c0006t0001g0263 others(11): Show |
15 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-7022G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765159 | |||||||
chr8:41765173 | C | CCTTT | 52 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(49): Show |
53 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.28-7040_28-7037dup others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765173 | |||||||
chr8:41765173 | CCTTT | C | 28 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.28-7040_28-7037del others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765173 | |||||||
chr8:41765243 | A | G | 1 | a0001c0003t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-7106T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765243 | |||||||
chr8:41765266 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-7129G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765266 | |||||||
chr8:41765411 | T | TA | 144 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(141): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.28-7275dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765411 | |||||||
chr8:41765431 | G | A | 26 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(23): Show |
26 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.28-7294C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765431 | |||||||
chr8:41765483 | G | A | 99 | a0001c0001t0001g0149 a0001c0001t0001g0219 a0001c0001t0001g0224 others(96): Show |
99 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.28-7346C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765483 | |||||||
chr8:41765528 | T | C | 268 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.28-7391A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765528 | |||||||
chr8:41765531 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0076 |
2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.28-7394C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765531 | |||||||
chr8:41765533 | C | T | 5 | a0001c0005t0002g0019 a0001c0005t0010g0020 a0002c0039t0010g0018 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-7396G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765533 | |||||||
chr8:41765639 | G | A | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-7502C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765639 | |||||||
chr8:41765845 | C | T | 1 | a0001c0038t0002g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.28-7708G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41765845 | |||||||
chr8:41766020 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-7883G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766020 | |||||||
chr8:41766084 | G | A | 45 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(42): Show |
46 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.28-7947C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766084 | |||||||
chr8:41766331 | G | A | 3 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0013g0090 |
3 | HG01069.hp2 HG01071.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-8194C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766331 | |||||||
chr8:41766429 | C | T | 1 | a0001c0016t0002g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.28-8292G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766429 | |||||||
chr8:41766566 | A | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-8429T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766566 | |||||||
chr8:41766587 | C | T | 63 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(60): Show |
64 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-8450G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766587 | |||||||
chr8:41766672 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-8535G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766672 | |||||||
chr8:41766807 | A | T | 1 | a0001c0003t0001g0147 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28-8670T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41766807 | |||||||
chr8:41767015 | G | A | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-8878C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767015 | |||||||
chr8:41767184 | C | G | 1 | a0001c0003t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.28-9047G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767184 | |||||||
chr8:41767271 | C | G | 1 | a0001c0001t0002g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.28-9134G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767271 | |||||||
chr8:41767290 | G | A | 4 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-9153C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767290 | |||||||
chr8:41767310 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-9173C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767310 | |||||||
chr8:41767312 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-9175G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767312 | |||||||
chr8:41767381 | C | G | 2 | a0001c0005t0001g0084 a0001c0040t0001g0085 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-9244G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767381 | |||||||
chr8:41767415 | C | G | 1 | a0001c0038t0002g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.28-9278G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767415 | |||||||
chr8:41767423 | C | T | 2 | a0001c0003t0001g0060 a0001c0003t0014g0061 |
2 | HG01934.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.28-9286G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767423 | |||||||
chr8:41767473 | G | A | 43 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(40): Show |
44 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-9336C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767473 | |||||||
chr8:41767665 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-9528C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767665 | |||||||
chr8:41767666 | C | A | 2 | a0001c0002t0001g0059 a0001c0002t0001g0159 |
2 | HG01167.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.28-9529G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767666 | |||||||
chr8:41767883 | A | G | 44 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(41): Show |
45 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.28-9746T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41767883 | |||||||
chr8:41768186 | A | T | 44 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(41): Show |
45 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.28-10049T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768186 | |||||||
chr8:41768269 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.28-10132C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768269 | |||||||
chr8:41768375 | G | T | 1 | a0012c0033t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-10238C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768375 | |||||||
chr8:41768430 | C | G | 268 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.28-10293G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768430 | |||||||
chr8:41768549 | G | T | 10 | a0001c0002t0009g0098 a0001c0006t0001g0100 a0001c0006t0018g0118 others(7): Show |
11 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-10412C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768549 | |||||||
chr8:41768629 | C | A | 42 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0002g0057 others(39): Show |
43 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.28-10492G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768629 | |||||||
chr8:41768629 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-10492G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768629 | |||||||
chr8:41768800 | CA | C | 211 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.28-10664delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768800 | |||||||
chr8:41768800 | CAA | C | 14 | a0001c0002t0009g0098 a0001c0003t0001g0051 a0001c0003t0001g0237 others(11): Show |
15 | HG02040.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-10665_28-10664d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768800 | |||||||
chr8:41768800 | CAAAA | C | 31 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(28): Show |
31 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.28-10667_28-10664d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768800 | |||||||
chr8:41768844 | G | A | 4 | a0001c0010t0002g0081 a0001c0010t0003g0110 a0001c0010t0003g0188 others(1): Show |
4 | HG02071.hp2 HG02074.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-10707C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768844 | |||||||
chr8:41768936 | G | A | 2 | a0001c0004t0002g0068 a0001c0004t0002g0176 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.28-10799C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41768936 | |||||||
chr8:41769054 | CAG | C | 34 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(31): Show |
34 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.28-10919_28-10918d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769054 | |||||||
chr8:41769169 | A | T | 10 | a0001c0002t0009g0098 a0001c0006t0001g0100 a0001c0006t0018g0118 others(7): Show |
11 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-11032T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769169 | |||||||
chr8:41769349 | G | A | 3 | a0001c0001t0002g0164 a0001c0003t0001g0162 a0001c0003t0009g0163 |
3 | HG00099.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.28-11212C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769349 | |||||||
chr8:41769436 | T | C | 6 | a0001c0001t0002g0168 a0001c0001t0002g0230 a0001c0003t0001g0237 others(3): Show |
6 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-11299A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769436 | |||||||
chr8:41769523 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.28-11386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769523 | |||||||
chr8:41769540 | T | A | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-11403A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769540 | |||||||
chr8:41769567 | G | A | 2 | a0001c0005t0001g0084 a0001c0040t0001g0085 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-11430C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769567 | |||||||
chr8:41769797 | G | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-11660C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769797 | |||||||
chr8:41769867 | A | T | 6 | a0001c0001t0002g0074 a0001c0005t0002g0019 a0001c0005t0010g0020 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-11730T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769867 | |||||||
chr8:41769967 | TTTC | T | 41 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0002g0057 others(38): Show |
42 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.28-11833_28-11831d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769967 | |||||||
chr8:41769977 | C | CT | 110 | a0001c0001t0001g0149 a0001c0001t0001g0219 a0001c0001t0001g0224 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.28-11841dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | |||||||
chr8:41769977 | C | CTT | 10 | a0001c0001t0023g0072 a0001c0002t0001g0216 a0001c0003t0001g0175 others(7): Show |
10 | HG01106.hp2 HG02109.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-11842_28-11841d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | |||||||
chr8:41769977 | CT | C | 6 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0184 others(3): Show |
6 | HG01081.hp1 HG01168.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-11841delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | |||||||
chr8:41769977 | CTT | C | 24 | a0001c0001t0001g0207 a0001c0001t0002g0261 a0001c0004t0002g0068 others(21): Show |
24 | HG00423.hp2 HG01168.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-11842_28-11841d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | |||||||
chr8:41769977 | CTTT | C | 8 | a0001c0001t0001g0190 a0001c0001t0002g0057 a0001c0002t0001g0264 others(5): Show |
8 | HG00140.hp1 HG00735.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-11843_28-11841d others(5): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769977 | |||||||
chr8:41769997 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.28-11860A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41769997 | |||||||
chr8:41770027 | G | C | 31 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(28): Show |
31 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.28-11890C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770027 | |||||||
chr8:41770131 | A | G | 240 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(237): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.28-11994T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770131 | |||||||
chr8:41770258 | C | T | 1 | a0001c0017t0005g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-12121G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770258 | |||||||
chr8:41770620 | T | C | 10 | a0001c0002t0009g0098 a0001c0006t0001g0100 a0001c0006t0018g0118 others(7): Show |
11 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-12483A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770620 | |||||||
chr8:41770743 | G | T | 1 | a0005c0035t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.28-12606C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770743 | |||||||
chr8:41770892 | C | A | 4 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-12755G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41770892 | |||||||
chr8:41771132 | A | G | 101 | a0001c0001t0001g0149 a0001c0001t0001g0219 a0001c0001t0001g0224 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.28-12995T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771132 | |||||||
chr8:41771277 | A | G | 1 | a0001c0008t0002g0246 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.28-13140T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771277 | |||||||
chr8:41771345 | A | T | 8 | a0001c0001t0002g0197 a0001c0003t0001g0135 a0001c0003t0001g0137 others(5): Show |
8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-13208T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771345 | |||||||
chr8:41771409 | C | T | 1 | a0001c0019t0002g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.28-13272G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771409 | |||||||
chr8:41771481 | C | T | 43 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(40): Show |
44 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-13344G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771481 | |||||||
chr8:41771682 | A | T | 1 | a0001c0017t0005g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-13545T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771682 | |||||||
chr8:41771721 | G | A | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.28-13584C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771721 | |||||||
chr8:41771767 | G | A | 1 | a0001c0008t0002g0203 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.28-13630C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771767 | |||||||
chr8:41771815 | G | A | 39 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(36): Show |
39 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.28-13678C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771815 | |||||||
chr8:41771828 | T | G | 1 | a0001c0005t0001g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.28-13691A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771828 | |||||||
chr8:41771951 | C | T | 1 | a0001c0008t0002g0246 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.28-13814G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771951 | |||||||
chr8:41771975 | G | C | 3 | a0001c0052t0001g0235 a0003c0014t0008g0093 a0003c0014t0008g0094 |
3 | HG00323.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.28-13838C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41771975 | |||||||
chr8:41772010 | C | A | 2 | a0001c0005t0004g0030 a0002c0007t0021g0115 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.28-13873G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772010 | |||||||
chr8:41772143 | G | A | 4 | a0001c0002t0001g0032 a0001c0002t0012g0031 a0001c0005t0004g0030 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-14006C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772143 | |||||||
chr8:41772144 | C | T | 1 | a0001c0003t0001g0147 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28-14007G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772144 | |||||||
chr8:41772156 | C | T | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.28-14019G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772156 | |||||||
chr8:41772317 | G | A | 33 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(30): Show |
33 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.28-14180C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772317 | |||||||
chr8:41772367 | G | A | 1 | a0008c0041t0012g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.28-14230C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772367 | |||||||
chr8:41772453 | G | A | 6 | a0001c0009t0002g0047 a0001c0009t0002g0048 a0001c0009t0002g0052 others(3): Show |
6 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-14316C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772453 | |||||||
chr8:41772498 | G | A | 9 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0124 others(6): Show |
9 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-14361C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772498 | |||||||
chr8:41772565 | T | C | 240 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(237): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.28-14428A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772565 | |||||||
chr8:41772655 | A | G | 4 | a0001c0006t0001g0263 a0001c0006t0001g0266 a0001c0006t0001g0267 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-14518T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772655 | |||||||
chr8:41772706 | T | A | 1 | a0001c0040t0001g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-14569A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772706 | |||||||
chr8:41772715 | G | A | 1 | a0001c0002t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-14578C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772715 | |||||||
chr8:41772813 | A | G | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-14676T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772813 | |||||||
chr8:41772838 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-14701G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772838 | |||||||
chr8:41772887 | G | A | 111 | a0001c0001t0001g0224 a0001c0001t0001g0242 a0001c0001t0001g0245 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.28-14750C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772887 | |||||||
chr8:41772929 | G | A | 112 | a0001c0001t0001g0224 a0001c0001t0001g0242 a0001c0001t0001g0245 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.28-14792C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41772929 | |||||||
chr8:41773055 | AC | A | 9 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0124 others(6): Show |
9 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-14919delG | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773055 | |||||||
chr8:41773056 | C | G | 24 | a0001c0001t0002g0023 a0001c0005t0001g0084 a0001c0006t0001g0263 others(21): Show |
24 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-14919G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773056 | |||||||
chr8:41773059 | C | A | 1 | a0009c0027t0002g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.28-14922G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773059 | |||||||
chr8:41773103 | G | A | 1 | a0001c0005t0001g0258 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.28-14966C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773103 | |||||||
chr8:41773184 | G | A | 15 | a0001c0001t0002g0023 a0001c0013t0001g0027 a0001c0013t0001g0038 others(12): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-15047C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773184 | |||||||
chr8:41773226 | C | T | 4 | a0001c0009t0002g0047 a0001c0009t0002g0048 a0001c0009t0002g0052 others(1): Show |
4 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-15089G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773226 | |||||||
chr8:41773326 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.28-15189C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773326 | |||||||
chr8:41773414 | G | T | 118 | a0001c0001t0001g0142 a0001c0001t0001g0190 a0001c0001t0001g0207 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.28-15277C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773414 | |||||||
chr8:41773494 | T | A | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28-15357A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773494 | |||||||
chr8:41773555 | G | A | 8 | a0001c0001t0002g0197 a0001c0003t0001g0135 a0001c0003t0001g0137 others(5): Show |
8 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-15418C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773555 | |||||||
chr8:41773603 | C | A | 267 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.28-15466G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773603 | |||||||
chr8:41773627 | A | T | 1 | a0002c0007t0001g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-15490T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773627 | |||||||
chr8:41773724 | C | T | 6 | a0001c0002t0009g0098 a0001c0005t0004g0029 a0001c0012t0006g0096 others(3): Show |
7 | HG02559.hp1 HG02622.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-15587G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773724 | |||||||
chr8:41773786 | A | G | 4 | a0001c0003t0001g0060 a0001c0003t0014g0061 a0003c0014t0008g0093 others(1): Show |
4 | HG01934.hp1 HG03017.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-15649T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773786 | |||||||
chr8:41773862 | G | A | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-15725C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773862 | |||||||
chr8:41773963 | A | C | 25 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0002g0193 others(22): Show |
25 | HG01070.hp2 HG01071.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.28-15826T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773963 | |||||||
chr8:41773965 | C | T | 4 | a0001c0004t0002g0205 a0001c0004t0002g0270 a0001c0008t0002g0204 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-15828G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41773965 | |||||||
chr8:41774040 | CAGAATTC others(4): Show |
C | 126 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.28-15914_28-15904d others(13): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774040 | |||||||
chr8:41774107 | C | T | 16 | a0001c0001t0002g0023 a0001c0006t0001g0040 a0001c0013t0001g0027 others(13): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-15970G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774107 | |||||||
chr8:41774115 | C | T | 116 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.28-15978G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774115 | |||||||
chr8:41774227 | T | C | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-16090A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774227 | |||||||
chr8:41774244 | T | C | 49 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(46): Show |
50 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-16107A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774244 | |||||||
chr8:41774270 | G | C | 118 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.28-16133C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774270 | |||||||
chr8:41774315 | G | A | 98 | a0001c0001t0002g0010 a0001c0001t0002g0023 a0001c0001t0002g0057 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.28-16178C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774315 | |||||||
chr8:41774348 | T | C | 1 | a0001c0010t0003g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.28-16211A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774348 | |||||||
chr8:41774379 | A | G | 5 | a0001c0001t0002g0021 a0001c0005t0002g0019 a0001c0005t0010g0020 others(2): Show |
5 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-16242T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774379 | |||||||
chr8:41774412 | A | C | 53 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.28-16275T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774412 | |||||||
chr8:41774712 | C | T | 91 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(88): Show |
91 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.28-16575G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774712 | |||||||
chr8:41774737 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.28-16600C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774737 | |||||||
chr8:41774760 | C | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-16623G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774760 | |||||||
chr8:41774894 | C | T | 1 | a0007c0055t0006g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.28-16757G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774894 | |||||||
chr8:41774913 | C | T | 1 | a0001c0002t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-16776G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774913 | |||||||
chr8:41774967 | G | A | 256 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.28-16830C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41774967 | |||||||
chr8:41775061 | CT | C | 50 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.28-16925delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775061 | |||||||
chr8:41775164 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.28-17027G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775164 | |||||||
chr8:41775228 | A | G | 263 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.28-17091T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775228 | |||||||
chr8:41775255 | G | A | 5 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0010t0002g0081 others(2): Show |
5 | HG02071.hp2 HG02074.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-17118C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775255 | |||||||
chr8:41775334 | C | T | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0003c0024t0001g0272 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.28-17197G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775334 | |||||||
chr8:41775802 | G | A | 49 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.28-17665C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775802 | |||||||
chr8:41775937 | A | T | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17800T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775937 | |||||||
chr8:41775980 | C | A | 49 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.28-17843G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41775980 | |||||||
chr8:41776004 | C | A | 3 | a0001c0003t0001g0175 a0001c0005t0020g0178 a0003c0015t0003g0136 |
3 | NA18981.hp2 NA19010.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.28-17867G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776004 | |||||||
chr8:41776089 | G | T | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17952C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776089 | |||||||
chr8:41776090 | T | G | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17953A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776090 | |||||||
chr8:41776092 | G | T | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.28-17955C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776092 | |||||||
chr8:41776339 | G | A | 91 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(88): Show |
91 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.28-18202C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776339 | |||||||
chr8:41776501 | A | G | 4 | a0001c0012t0005g0101 a0001c0046t0030g0276 a0003c0024t0003g0102 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-18364T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776501 | |||||||
chr8:41776836 | G | A | 4 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0010t0002g0081 others(1): Show |
4 | HG02071.hp2 HG02074.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-18699C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776836 | |||||||
chr8:41776873 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28-18736C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776873 | |||||||
chr8:41776962 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0012g0031 |
2 | HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.28-18825G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41776962 | |||||||
chr8:41777238 | G | C | 4 | a0001c0013t0001g0027 a0002c0007t0007g0024 a0002c0007t0007g0025 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-19101C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777238 | |||||||
chr8:41777275 | G | A | 8 | a0001c0004t0001g0108 a0001c0005t0004g0029 a0001c0005t0004g0030 others(5): Show |
8 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-19138C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777275 | |||||||
chr8:41777303 | A | G | 1 | a0001c0004t0001g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.28-19166T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777303 | |||||||
chr8:41777377 | C | T | 10 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0005t0002g0019 others(7): Show |
10 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-19240G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777377 | |||||||
chr8:41777406 | C | T | 3 | a0001c0010t0002g0081 a0001c0010t0003g0110 a0001c0010t0003g0188 |
3 | HG02071.hp2 HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.28-19269G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777406 | |||||||
chr8:41777497 | C | T | 10 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0124 others(7): Show |
10 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-19360G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777497 | |||||||
chr8:41777515 | T | C | 164 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.28-19378A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777515 | |||||||
chr8:41777609 | T | A | 55 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(52): Show |
56 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.28-19472A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777609 | |||||||
chr8:41777611 | A | C | 55 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(52): Show |
56 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.28-19474T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777611 | |||||||
chr8:41777611 | AAAAC | A | 4 | a0001c0001t0002g0226 a0001c0005t0001g0225 a0001c0010t0003g0003 others(1): Show |
4 | HG00738.hp1 HG02071.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-19478_28-19475d others(6): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777611 | |||||||
chr8:41777778 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-19641C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777778 | |||||||
chr8:41777818 | A | C | 2 | a0001c0001t0001g0142 a0001c0003t0001g0147 |
2 | NA18969.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.28-19681T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41777818 | |||||||
chr8:41778063 | G | C | 1 | a0001c0004t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+19449C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778063 | |||||||
chr8:41778269 | G | T | 1 | a0001c0001t0002g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.27+19243C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778269 | |||||||
chr8:41778484 | T | A | 29 | a0001c0001t0002g0057 a0001c0001t0002g0109 a0001c0001t0023g0072 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.27+19028A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778484 | |||||||
chr8:41778493 | A | G | 64 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.27+19019T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778493 | |||||||
chr8:41778546 | C | T | 3 | a0001c0012t0005g0101 a0001c0046t0030g0276 a0003c0024t0003g0102 |
3 | HG02723.hp2 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.27+18966G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778546 | |||||||
chr8:41778553 | C | T | 45 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.27+18959G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778553 | |||||||
chr8:41778636 | G | A | 16 | a0001c0001t0002g0023 a0001c0006t0001g0040 a0001c0013t0001g0027 others(13): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+18876C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778636 | |||||||
chr8:41778733 | T | C | 101 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.27+18779A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778733 | |||||||
chr8:41778886 | G | T | 45 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.27+18626C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778886 | |||||||
chr8:41778921 | G | C | 1 | a0001c0002t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.27+18591C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41778921 | |||||||
chr8:41779081 | G | A | 1 | a0001c0019t0002g0174 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.27+18431C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779081 | |||||||
chr8:41779358 | C | G | 1 | a0001c0003t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+18154G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779358 | |||||||
chr8:41779398 | C | T | 16 | a0001c0001t0002g0023 a0001c0006t0001g0040 a0001c0013t0001g0027 others(13): Show |
16 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+18114G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779398 | |||||||
chr8:41779628 | A | C | 1 | a0001c0046t0030g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.27+17884T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779628 | |||||||
chr8:41779637 | AT | A | 46 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.27+17874delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779637 | |||||||
chr8:41779684 | C | A | 2 | a0001c0005t0001g0084 a0001c0040t0001g0085 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.27+17828G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779684 | |||||||
chr8:41779720 | G | A | 3 | a0001c0005t0028g0112 a0001c0005t0029g0111 a0001c0006t0003g0006 |
3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.27+17792C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779720 | |||||||
chr8:41779806 | G | A | 29 | a0001c0001t0002g0057 a0001c0001t0002g0109 a0001c0001t0023g0072 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.27+17706C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779806 | |||||||
chr8:41779842 | C | T | 45 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.27+17670G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779842 | |||||||
chr8:41779854 | G | C | 29 | a0001c0001t0002g0057 a0001c0001t0002g0109 a0001c0001t0023g0072 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.27+17658C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779854 | |||||||
chr8:41779968 | G | A | 29 | a0001c0001t0002g0057 a0001c0001t0002g0109 a0001c0001t0023g0072 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.27+17544C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41779968 | |||||||
chr8:41780068 | A | G | 1 | a0002c0039t0010g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27+17444T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780068 | |||||||
chr8:41780154 | G | A | 5 | a0001c0001t0002g0021 a0001c0005t0002g0019 a0001c0005t0010g0020 others(2): Show |
5 | HG02717.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+17358C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780154 | |||||||
chr8:41780287 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+17225G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780287 | |||||||
chr8:41780376 | T | C | 4 | a0001c0006t0003g0013 a0001c0006t0003g0015 a0001c0006t0005g0014 others(1): Show |
4 | HG01106.hp2 HG02109.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+17136A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780376 | |||||||
chr8:41780476 | C | T | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0003c0024t0001g0272 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+17036G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780476 | |||||||
chr8:41780573 | T | C | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0003c0024t0001g0272 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+16939A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780573 | |||||||
chr8:41780620 | T | C | 261 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(258): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.27+16892A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780620 | |||||||
chr8:41780648 | T | C | 1 | a0001c0002t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27+16864A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780648 | |||||||
chr8:41780713 | C | T | 47 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0109 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.27+16799G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780713 | |||||||
chr8:41780727 | C | T | 4 | a0001c0012t0005g0101 a0001c0046t0030g0276 a0003c0024t0003g0102 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+16785G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41780727 | |||||||
chr8:41781240 | C | G | 2 | a0001c0005t0001g0084 a0001c0040t0001g0085 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.27+16272G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781240 | |||||||
chr8:41781455 | C | T | 64 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0087 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.27+16057G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781455 | |||||||
chr8:41781722 | G | A | 61 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0087 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.27+15790C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781722 | |||||||
chr8:41781730 | G | A | 3 | a0001c0002t0001g0240 a0001c0012t0015g0239 a0001c0019t0002g0238 |
3 | NA18612.hp1 NA18969.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.27+15782C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781730 | |||||||
chr8:41781748 | C | A | 88 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(85): Show |
88 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.27+15764G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781748 | |||||||
chr8:41781857 | G | T | 1 | a0002c0007t0007g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.27+15655C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41781857 | |||||||
chr8:41782242 | A | G | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+15270T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782242 | |||||||
chr8:41782248 | G | A | 6 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0002g0241 others(3): Show |
6 | HG02015.hp1 HG02083.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+15264C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782248 | |||||||
chr8:41782257 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.27+15255G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782257 | |||||||
chr8:41782324 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.27+15188C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782324 | |||||||
chr8:41782572 | C | T | 4 | a0001c0001t0002g0057 a0001c0002t0001g0059 a0001c0030t0017g0058 others(1): Show |
4 | HG00735.hp1 HG02698.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+14940G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782572 | |||||||
chr8:41782607 | C | T | 44 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(41): Show |
44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.27+14905G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782607 | |||||||
chr8:41782628 | G | C | 7 | a0001c0002t0001g0248 a0001c0004t0002g0247 a0001c0004t0002g0249 others(4): Show |
7 | NA18950.hp2 NA18979.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+14884C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782628 | |||||||
chr8:41782651 | G | A | 6 | a0001c0002t0001g0248 a0001c0004t0002g0247 a0001c0004t0002g0249 others(3): Show |
6 | NA18950.hp2 NA18992.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+14861C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782651 | |||||||
chr8:41782755 | C | G | 5 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0010t0002g0081 others(2): Show |
5 | HG02071.hp2 HG02074.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+14757G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782755 | |||||||
chr8:41782794 | C | T | 4 | a0001c0005t0028g0112 a0001c0005t0029g0111 a0001c0006t0003g0006 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+14718G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782794 | |||||||
chr8:41782803 | A | G | 11 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0005t0002g0019 others(8): Show |
11 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+14709T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41782803 | |||||||
chr8:41783057 | C | T | 1 | a0001c0002t0002g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+14455G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783057 | |||||||
chr8:41783128 | G | C | 78 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0074 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.27+14384C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783128 | |||||||
chr8:41783139 | G | A | 45 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.27+14373C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783139 | |||||||
chr8:41783388 | C | T | 201 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(198): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.27+14124G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783388 | |||||||
chr8:41783401 | G | A | 1 | a0001c0003t0001g0054 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.27+14111C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783401 | |||||||
chr8:41783557 | C | T | 54 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.27+13955G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783557 | |||||||
chr8:41783617 | GGAGACT | G | 122 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0209 others(119): Show |
122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.27+13889_27+13894d others(8): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783617 | |||||||
chr8:41783633 | T | C | 33 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.27+13879A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783633 | |||||||
chr8:41783821 | G | A | 1 | a0003c0049t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.27+13691C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783821 | |||||||
chr8:41783875 | C | T | 49 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.27+13637G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783875 | |||||||
chr8:41783891 | C | T | 7 | a0001c0003t0001g0135 a0001c0003t0001g0137 a0001c0003t0001g0139 others(4): Show |
7 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+13621G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41783891 | |||||||
chr8:41784039 | C | T | 31 | a0001c0001t0002g0106 a0001c0001t0002g0132 a0001c0002t0001g0121 others(28): Show |
31 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.27+13473G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784039 | |||||||
chr8:41784057 | C | CA | 36 | a0001c0001t0001g0190 a0001c0001t0002g0106 a0001c0001t0002g0132 others(33): Show |
36 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.27+13454dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784057 | |||||||
chr8:41784057 | CAA | C | 131 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.27+13453_27+13454d others(4): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784057 | |||||||
chr8:41784106 | G | A | 75 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0074 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.27+13406C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784106 | |||||||
chr8:41784232 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0005t0002g0019 others(3): Show |
6 | HG02717.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+13280G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784232 | |||||||
chr8:41784239 | A | G | 21 | a0001c0001t0002g0132 a0001c0002t0001g0121 a0001c0002t0001g0122 others(18): Show |
21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+13273T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784239 | |||||||
chr8:41784252 | C | G | 1 | a0001c0032t0003g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+13260G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784252 | |||||||
chr8:41784416 | T | C | 50 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.27+13096A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784416 | |||||||
chr8:41784444 | T | C | 1 | a0014c0031t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.27+13068A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784444 | |||||||
chr8:41784598 | T | A | 133 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0023 others(130): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.27+12914A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784598 | |||||||
chr8:41784646 | C | G | 21 | a0001c0001t0002g0132 a0001c0002t0001g0121 a0001c0002t0001g0122 others(18): Show |
21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+12866G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784646 | |||||||
chr8:41784978 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.27+12534G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41784978 | |||||||
chr8:41785020 | C | G | 5 | a0001c0006t0018g0118 a0001c0017t0005g0116 a0001c0017t0005g0117 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+12492G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785020 | |||||||
chr8:41785124 | G | C | 1 | a0002c0007t0001g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.27+12388C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785124 | |||||||
chr8:41785202 | T | C | 10 | a0001c0002t0009g0098 a0001c0005t0004g0043 a0001c0005t0004g0044 others(7): Show |
11 | HG01167.hp1 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+12310A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785202 | |||||||
chr8:41785220 | G | A | 2 | a0001c0005t0001g0257 a0001c0005t0001g0258 |
2 | HG01123.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.27+12292C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785220 | |||||||
chr8:41785253 | G | A | 1 | a0001c0002t0001g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.27+12259C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785253 | |||||||
chr8:41785368 | A | G | 56 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(53): Show |
57 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.27+12144T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785368 | |||||||
chr8:41785610 | C | T | 1 | a0001c0002t0012g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.27+11902G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785610 | |||||||
chr8:41785727 | C | T | 1 | a0001c0002t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.27+11785G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785727 | |||||||
chr8:41785843 | G | A | 1 | a0001c0005t0020g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.27+11669C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785843 | |||||||
chr8:41785939 | G | C | 191 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.27+11573C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785939 | |||||||
chr8:41785993 | C | T | 132 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0023 others(129): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.27+11519G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41785993 | |||||||
chr8:41786018 | C | T | 20 | a0001c0001t0002g0023 a0001c0002t0001g0032 a0001c0002t0012g0031 others(17): Show |
20 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.27+11494G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786018 | |||||||
chr8:41786080 | A | G | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+11432T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786080 | |||||||
chr8:41786154 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+11358G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786154 | |||||||
chr8:41786304 | T | C | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+11208A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786304 | |||||||
chr8:41786310 | CT | C | 6 | a0001c0001t0002g0132 a0001c0006t0018g0118 a0001c0017t0005g0116 others(3): Show |
6 | HG02451.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+11201delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786310 | |||||||
chr8:41786591 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.27+10921T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786591 | |||||||
chr8:41786609 | C | T | 2 | a0001c0003t0001g0056 a0001c0009t0002g0055 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.27+10903G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786609 | |||||||
chr8:41786748 | A | T | 190 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+10764T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786748 | |||||||
chr8:41786980 | C | T | 5 | a0001c0005t0004g0011 a0001c0006t0003g0013 a0001c0006t0003g0015 others(2): Show |
5 | HG01106.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+10532G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41786980 | |||||||
chr8:41787059 | T | A | 1 | a0001c0002t0002g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+10453A>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787059 | |||||||
chr8:41787074 | G | A | 9 | a0001c0001t0002g0106 a0001c0002t0002g0105 a0001c0004t0001g0108 others(6): Show |
9 | HG01192.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+10438C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787074 | |||||||
chr8:41787149 | CTGGCCTG others(17): Show |
C | 1 | a0001c0002t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27+10339_27+10362d others(26): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787149 | |||||||
chr8:41787343 | T | C | 190 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+10169A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787343 | |||||||
chr8:41787344 | G | C | 3 | a0001c0010t0002g0081 a0001c0010t0003g0110 a0001c0010t0003g0188 |
3 | HG02071.hp2 HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+10168C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787344 | |||||||
chr8:41787360 | A | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | NA18612.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.27+10152T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787360 | |||||||
chr8:41787556 | A | G | 192 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+9956T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787556 | |||||||
chr8:41787600 | C | T | 1 | a0001c0002t0003g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.27+9912G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41787600 | |||||||
chr8:41788047 | C | T | 190 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+9465G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788047 | |||||||
chr8:41788176 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.27+9336C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788176 | |||||||
chr8:41788192 | C | T | 192 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+9320G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788192 | |||||||
chr8:41788227 | C | T | 1 | a0015c0045t0025g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+9285G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788227 | |||||||
chr8:41788487 | C | T | 2 | a0001c0001t0002g0023 a0002c0007t0007g0022 |
2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.27+9025G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788487 | |||||||
chr8:41788503 | A | G | 98 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0074 others(95): Show |
99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.27+9009T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788503 | |||||||
chr8:41788845 | A | G | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+8667T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41788845 | |||||||
chr8:41789132 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.27+8380G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789132 | |||||||
chr8:41789165 | A | C | 110 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.27+8347T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789165 | |||||||
chr8:41789222 | G | A | 35 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.27+8290C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789222 | |||||||
chr8:41789243 | T | C | 2 | a0001c0001t0002g0021 a0001c0005t0010g0020 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.27+8269A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789243 | |||||||
chr8:41789281 | T | C | 2 | a0001c0004t0001g0108 a0012c0033t0001g0107 |
2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.27+8231A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789281 | |||||||
chr8:41789394 | G | C | 2 | a0001c0010t0003g0110 a0001c0010t0003g0188 |
2 | HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+8118C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789394 | |||||||
chr8:41789413 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+8099C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789413 | |||||||
chr8:41789426 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0012g0031 |
2 | HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.27+8086C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789426 | |||||||
chr8:41789437 | A | G | 2 | a0001c0010t0003g0110 a0001c0010t0003g0188 |
2 | HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+8075T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789437 | |||||||
chr8:41789479 | T | G | 191 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.27+8033A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789479 | |||||||
chr8:41789503 | C | T | 1 | a0003c0049t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.27+8009G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789503 | |||||||
chr8:41789596 | C | T | 22 | a0001c0001t0002g0023 a0001c0002t0001g0032 a0001c0002t0012g0031 others(19): Show |
22 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.27+7916G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789596 | |||||||
chr8:41789663 | G | A | 4 | a0001c0006t0001g0266 a0001c0006t0001g0267 a0001c0006t0001g0268 others(1): Show |
4 | HG01891.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+7849C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789663 | |||||||
chr8:41789826 | G | A | 1 | a0001c0006t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.27+7686C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789826 | |||||||
chr8:41789845 | A | G | 13 | a0001c0001t0002g0106 a0001c0002t0002g0105 a0001c0004t0001g0108 others(10): Show |
13 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.27+7667T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789845 | |||||||
chr8:41789930 | C | G | 1 | a0001c0009t0002g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.27+7582G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789930 | |||||||
chr8:41789975 | A | C | 192 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+7537T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41789975 | |||||||
chr8:41790042 | G | A | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+7470C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790042 | |||||||
chr8:41790215 | C | T | 3 | a0001c0012t0005g0101 a0001c0046t0030g0276 a0003c0024t0003g0102 |
3 | HG02723.hp2 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.27+7297G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790215 | |||||||
chr8:41790259 | G | A | 193 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.27+7253C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790259 | |||||||
chr8:41790468 | GTCACTAT others(15): Show |
G | 1 | a0001c0001t0001g0142 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.27+7022_27+7043del others(22): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790468 | |||||||
chr8:41790495 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.27+7017C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790495 | |||||||
chr8:41790605 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0005t0002g0019 others(8): Show |
11 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+6907C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790605 | |||||||
chr8:41790662 | C | T | 1 | a0001c0005t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27+6850G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790662 | |||||||
chr8:41790663 | G | A | 41 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0132 others(38): Show |
41 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.27+6849C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790663 | |||||||
chr8:41790756 | C | T | 1 | a0003c0014t0008g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.27+6756G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790756 | |||||||
chr8:41790840 | G | A | 93 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.27+6672C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41790840 | |||||||
chr8:41791050 | G | T | 2 | a0001c0003t0001g0049 a0001c0003t0001g0050 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.27+6462C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791050 | |||||||
chr8:41791126 | C | T | 5 | a0001c0005t0004g0011 a0001c0006t0003g0013 a0001c0006t0003g0015 others(2): Show |
5 | HG01106.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+6386G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791126 | |||||||
chr8:41791194 | G | GT | 18 | a0001c0001t0002g0226 a0001c0001t0002g0271 a0001c0002t0001g0059 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.27+6317dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | |||||||
chr8:41791194 | GT | G | 70 | a0001c0001t0001g0151 a0001c0001t0001g0209 a0001c0001t0002g0057 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.27+6317delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | |||||||
chr8:41791194 | GTT | G | 87 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0153 others(84): Show |
88 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.27+6316_27+6317del others(2): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | |||||||
chr8:41791194 | GTTTTTTT others(4): Show |
G | 1 | a0016c0053t0002g0251 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.27+6307_27+6317del others(11): Show |
ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791194 | |||||||
chr8:41791209 | T | G | 2 | a0001c0002t0001g0133 a0001c0002t0001g0134 |
2 | HG00733.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.27+6303A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791209 | |||||||
chr8:41791254 | C | A | 30 | a0001c0001t0002g0132 a0001c0002t0001g0121 a0001c0002t0001g0122 others(27): Show |
30 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.27+6258G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791254 | |||||||
chr8:41791447 | C | CT | 7 | a0001c0001t0001g0190 a0001c0001t0002g0010 a0001c0006t0018g0118 others(4): Show |
7 | HG02451.hp2 HG02572.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+6064dupA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791447 | |||||||
chr8:41791447 | CT | C | 5 | a0001c0009t0002g0083 a0001c0010t0003g0003 a0001c0023t0001g0274 others(2): Show |
5 | HG00738.hp1 HG01070.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+6064delA | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791447 | |||||||
chr8:41791573 | A | G | 2 | a0001c0009t0002g0047 a0001c0009t0002g0048 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.27+5939T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791573 | |||||||
chr8:41791634 | C | T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0005t0002g0019 others(9): Show |
12 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+5878G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791634 | |||||||
chr8:41791768 | C | T | 38 | a0001c0001t0002g0057 a0001c0001t0002g0074 a0001c0001t0002g0076 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+5744G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791768 | |||||||
chr8:41791916 | T | TG | 192 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+5595dupC | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791916 | |||||||
chr8:41791921 | T | G | 194 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.27+5591A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791921 | |||||||
chr8:41791986 | A | G | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+5526T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41791986 | |||||||
chr8:41792052 | C | T | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+5460G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792052 | |||||||
chr8:41792254 | G | A | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+5258C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792254 | |||||||
chr8:41792324 | T | G | 4 | a0001c0010t0003g0003 a0001c0023t0001g0274 a0001c0023t0001g0275 others(1): Show |
4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+5188A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792324 | |||||||
chr8:41792445 | C | A | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+5067G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792445 | |||||||
chr8:41792455 | G | C | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+5057C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792455 | |||||||
chr8:41792534 | C | T | 1 | a0005c0021t0002g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+4978G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792534 | |||||||
chr8:41792854 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+4658G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792854 | |||||||
chr8:41792957 | A | G | 1 | a0001c0006t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+4555T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41792957 | |||||||
chr8:41793104 | C | T | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+4408G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793104 | |||||||
chr8:41793169 | G | C | 1 | a0003c0024t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.27+4343C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793169 | |||||||
chr8:41793187 | G | C | 1 | a0001c0002t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.27+4325C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793187 | |||||||
chr8:41793238 | C | T | 20 | a0001c0001t0002g0023 a0001c0002t0001g0032 a0001c0002t0012g0031 others(17): Show |
20 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.27+4274G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793238 | |||||||
chr8:41793394 | T | TA | 10 | a0001c0006t0001g0040 a0001c0010t0003g0003 a0001c0013t0001g0038 others(7): Show |
10 | HG02080.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+4117dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793394 | |||||||
chr8:41793436 | C | G | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+4076G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793436 | |||||||
chr8:41793782 | A | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+3730T>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793782 | |||||||
chr8:41793897 | GA | G | 4 | a0001c0005t0004g0043 a0001c0005t0004g0044 a0002c0042t0016g0046 others(1): Show |
4 | HG01167.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3614delT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793897 | |||||||
chr8:41793950 | T | C | 94 | a0001c0001t0002g0023 a0001c0001t0002g0057 a0001c0001t0002g0074 others(91): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.27+3562A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793950 | |||||||
chr8:41793950 | T | G | 4 | a0001c0006t0001g0266 a0001c0006t0001g0267 a0001c0006t0001g0268 others(1): Show |
4 | HG01891.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3562A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793950 | |||||||
chr8:41793996 | C | A | 9 | a0001c0001t0002g0106 a0001c0002t0002g0105 a0001c0004t0001g0108 others(6): Show |
9 | HG01192.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+3516G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41793996 | |||||||
chr8:41794083 | C | T | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+3429G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794083 | |||||||
chr8:41794208 | A | G | 23 | a0001c0001t0002g0023 a0001c0002t0001g0032 a0001c0002t0012g0031 others(20): Show |
23 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.27+3304T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794208 | |||||||
chr8:41794494 | C | T | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+3018G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794494 | |||||||
chr8:41794689 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.27+2823A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794689 | |||||||
chr8:41794783 | C | T | 23 | a0001c0001t0002g0023 a0001c0002t0001g0032 a0001c0002t0012g0031 others(20): Show |
23 | HG01243.hp2 HG01261.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.27+2729G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794783 | |||||||
chr8:41794865 | T | C | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2647A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794865 | |||||||
chr8:41794931 | C | G | 6 | a0001c0003t0001g0135 a0001c0003t0001g0137 a0001c0003t0001g0139 others(3): Show |
6 | HG01081.hp2 HG01099.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+2581G>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794931 | |||||||
chr8:41794948 | C | T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0005t0002g0019 others(9): Show |
12 | HG01106.hp2 HG02109.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+2564G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794948 | |||||||
chr8:41794965 | A | G | 1 | a0001c0005t0002g0189 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.27+2547T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41794965 | |||||||
chr8:41795047 | A | G | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2465T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795047 | |||||||
chr8:41795051 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2461G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795051 | |||||||
chr8:41795069 | T | C | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2443A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795069 | |||||||
chr8:41795130 | G | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2382C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795130 | |||||||
chr8:41795131 | C | T | 3 | a0001c0016t0002g0007 a0001c0016t0002g0008 a0001c0016t0002g0009 |
3 | HG01192.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.27+2381G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795131 | |||||||
chr8:41795202 | G | T | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2310C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795202 | |||||||
chr8:41795214 | G | A | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2298C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795214 | |||||||
chr8:41795215 | T | C | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2297A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795215 | |||||||
chr8:41795250 | C | A | 1 | a0001c0004t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+2262G>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795250 | |||||||
chr8:41795284 | G | A | 28 | a0001c0001t0002g0132 a0001c0002t0001g0121 a0001c0002t0001g0122 others(25): Show |
28 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.27+2228C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795284 | |||||||
chr8:41795284 | G | T | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2228C>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795284 | |||||||
chr8:41795288 | G | A | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+2224C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795288 | |||||||
chr8:41795311 | G | A | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+2201C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795311 | |||||||
chr8:41795361 | T | G | 21 | a0001c0001t0002g0132 a0001c0002t0001g0121 a0001c0002t0001g0122 others(18): Show |
21 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.27+2151A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795361 | |||||||
chr8:41795548 | A | G | 1 | a0001c0051t0008g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+1964T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795548 | |||||||
chr8:41795572 | C | T | 4 | a0001c0010t0003g0003 a0001c0023t0001g0274 a0001c0023t0001g0275 others(1): Show |
4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1940G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795572 | |||||||
chr8:41795646 | G | A | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+1866C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795646 | |||||||
chr8:41795678 | A | G | 1 | a0003c0015t0003g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.27+1834T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795678 | |||||||
chr8:41795738 | C | T | 1 | a0001c0003t0001g0135 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.27+1774G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795738 | |||||||
chr8:41795748 | G | A | 3 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0001g0184 |
3 | HG00735.hp2 HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.27+1764C>T | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795748 | |||||||
chr8:41795953 | T | G | 4 | a0001c0010t0003g0003 a0001c0023t0001g0274 a0001c0023t0001g0275 others(1): Show |
4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1559A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41795953 | |||||||
chr8:41796022 | T | G | 53 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(50): Show |
54 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.27+1490A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796022 | |||||||
chr8:41796073 | T | C | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+1439A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796073 | |||||||
chr8:41796297 | G | C | 2 | a0001c0023t0001g0274 a0001c0023t0001g0275 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+1215C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796297 | |||||||
chr8:41796549 | G | GA | 6 | a0001c0001t0002g0271 a0001c0010t0003g0188 a0003c0024t0001g0272 others(3): Show |
6 | HG02074.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+962dupT | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796549 | |||||||
chr8:41796686 | C | T | 1 | a0001c0006t0003g0006 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+826G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796686 | |||||||
chr8:41796940 | C | T | 192 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0151 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.27+572G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796940 | |||||||
chr8:41796956 | C | T | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+556G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796956 | |||||||
chr8:41796957 | C | T | 2 | a0001c0005t0002g0004 a0001c0005t0013g0005 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.27+555G>A | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796957 | |||||||
chr8:41796979 | A | G | 1 | a0001c0010t0003g0003 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27+533T>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796979 | |||||||
chr8:41796998 | T | C | 4 | a0001c0010t0003g0003 a0001c0023t0001g0274 a0001c0023t0001g0275 others(1): Show |
4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+514A>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796998 | |||||||
chr8:41796999 | A | C | 4 | a0001c0010t0003g0003 a0001c0023t0001g0274 a0001c0023t0001g0275 others(1): Show |
4 | HG00738.hp1 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+513T>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41796999 | |||||||
chr8:41797079 | T | G | 1 | a0003c0024t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.27+433A>C | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41797079 | |||||||
chr8:41797235 | G | C | 3 | a0001c0023t0001g0274 a0001c0023t0001g0275 a0001c0051t0008g0273 |
3 | HG00738.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.27+277C>G | ANK1 | ENSG00000029534.22 | transcript | ENST00000289734.13 | protein_coding | 1/42 | chr8 | 41797235 |