Item | Value |
---|---|
geneid | 23253 |
ensemblid | ENSG00000101745.17 |
hgncid | 29135 |
symbol | ANKRD12 |
name | ankyrin repeat domain 12 |
refseq_nuc | NM_015208.5 |
refseq_prot | NP_056023.3 |
ensembl_nuc | ENST00000262126.9 |
ensembl_prot | ENSP00000262126.3 |
mane_status | MANE Select |
chr | chr18 |
start | 9136781 |
end | 9285985 |
strand | + |
ver | v1.2 |
region | chr18:9136781-9285985 |
region5000 | chr18:9131781-9290985 |
regionname0 | ANKRD12_chr18_9136781_9285985 |
regionname5000 | ANKRD12_chr18_9131781_9290985 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2062 | 139 | 32 | 24 | 57 | 8 | 17 | 44 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0002 | 1/0 | 2062 | 81 | 37 | 17 | 16 | 3 | 7 | 13 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0003 | 0/0 | 2062 | 44 | 1 | 3 | 36 | 1 | 3 | 33 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0004 | 0/0 | 2062 | 34 | 7 | 2 | 23 | 1 | 1 | 20 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0005 | 0/0 | 2062 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0006 | 0/0 | 2062 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0007 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0008 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0009 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0010 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0011 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0012 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0013 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0014 | 0/0 | 2062 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0015 | 0/0 | 2062 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
a0016 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | MPKSG others(2057): Show |
chr18 | 9131781 | 9290985 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 6186 | 129 | 25 | 24 | 57 | 8 | 14 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0001c0007 | 0/0 | 6186 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0001c0009 | 0/0 | 6186 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0001c0010 | 0/0 | 6186 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0001c0012 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0001c0024 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0001c0029 | 0/0 | 6186 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0002 | 1/0 | 6186 | 74 | 34 | 13 | 16 | 3 | 7 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0008 | 0/0 | 6186 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0013 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0015 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0018 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0022 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0002c0025 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0003c0003 | 0/0 | 6186 | 44 | 1 | 3 | 36 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0004c0004 | 0/0 | 6186 | 33 | 7 | 2 | 22 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0004c0028 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0005c0006 | 0/0 | 6186 | 5 | 0 | 4 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0006c0005 | 0/0 | 6186 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0007c0027 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0008c0016 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0009c0021 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0010c0011 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0011c0019 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0012c0023 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0013c0026 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0014c0014 | 0/0 | 6186 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0015c0020 | 0/0 | 6186 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 | ||
a0016c0017 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | ATGCC others(6181): Show |
chr18 | 9131781 | 9290985 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 11284 | 27 | 4 | 6 | 13 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0003 | 0/0 | 11285 | 21 | 0 | 3 | 14 | 0 | 4 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0005 | 0/0 | 11286 | 20 | 4 | 1 | 13 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0007 | 0/1 | 11285 | 9 | 1 | 3 | 0 | 4 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0008 | 0/0 | 11284 | 4 | 0 | 3 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0010 | 0/0 | 11284 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0011 | 0/0 | 11287 | 6 | 0 | 0 | 6 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11282): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0015 | 0/0 | 11284 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0018 | 0/0 | 11284 | 3 | 0 | 2 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0019 | 0/0 | 11284 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0020 | 0/0 | 11285 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0025 | 0/0 | 11285 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0027 | 0/0 | 11284 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0028 | 0/0 | 11284 | 2 | 0 | 1 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0029 | 0/0 | 11284 | 2 | 0 | 0 | 0 | 2 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0033 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0040 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0043 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0044 | 0/0 | 11286 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0045 | 0/0 | 11287 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11282): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0046 | 0/0 | 11286 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0047 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0048 | 0/0 | 11286 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0049 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0050 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0052 | 0/0 | 11286 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0053 | 0/0 | 11286 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0054 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0055 | 0/0 | 11283 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11278): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0056 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0062 | 0/0 | 11286 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0001t0070 | 0/0 | 11286 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11281): Show |
chr18 | 9131781 | 9290985 |
a0001c0007t0026 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0007t0051 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0009t0032 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0010t0003 | 0/0 | 11285 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0001c0012t0002 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0024t0069 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0001c0029t0003 | 0/0 | 11285 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0001 | 1/0 | 11284 | 32 | 8 | 6 | 12 | 2 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0006 | 0/0 | 11284 | 13 | 6 | 4 | 0 | 1 | 2 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0009 | 0/0 | 11285 | 5 | 1 | 1 | 2 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0010 | 0/0 | 11284 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0012 | 0/0 | 11284 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0017 | 0/0 | 11284 | 3 | 2 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0023 | 0/0 | 11285 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0024 | 0/0 | 11284 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0030 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0031 | 0/0 | 11285 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0042 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0057 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0059 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0063 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0064 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0002t0067 | 0/0 | 11284 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0008t0006 | 0/0 | 11284 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0013t0066 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0015t0006 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0018t0041 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0022t0030 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0002c0025t0001 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0001 | 0/0 | 11284 | 33 | 1 | 3 | 25 | 1 | 3 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0009 | 0/0 | 11285 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0021 | 0/0 | 11284 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0058 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0060 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0061 | 0/0 | 11284 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0003c0003t0068 | 0/0 | 11285 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0004 | 0/0 | 11281 | 21 | 1 | 1 | 19 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11276): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0013 | 0/0 | 11282 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11277): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0016 | 0/0 | 11282 | 3 | 1 | 0 | 2 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11277): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0022 | 0/0 | 11283 | 2 | 0 | 0 | 0 | 1 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11278): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0035 | 0/0 | 11281 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11276): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0036 | 0/0 | 11282 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11277): Show |
chr18 | 9131781 | 9290985 |
a0004c0004t0037 | 0/0 | 11282 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11277): Show |
chr18 | 9131781 | 9290985 |
a0004c0028t0004 | 0/0 | 11281 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11276): Show |
chr18 | 9131781 | 9290985 |
a0005c0006t0008 | 0/0 | 11284 | 5 | 0 | 4 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0006c0005t0014 | 0/0 | 11284 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0006c0005t0039 | 0/0 | 11285 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11280): Show |
chr18 | 9131781 | 9290985 |
a0007c0027t0004 | 0/0 | 11281 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11276): Show |
chr18 | 9131781 | 9290985 |
a0008c0016t0001 | 0/0 | 11284 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0009c0021t0002 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0010c0011t0012 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0011c0019t0065 | 0/0 | 11283 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11278): Show |
chr18 | 9131781 | 9290985 |
a0012c0023t0034 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0013c0026t0038 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0014c0014t0001 | 0/0 | 11284 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0015c0020t0002 | 0/0 | 11284 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
a0016c0017t0012 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | GCGGG others(11279): Show |
chr18 | 9131781 | 9290985 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0007g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0008g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0011g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0015g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0018g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0018g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0018g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0019g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0019g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0019g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0020g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0020g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0020g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0025g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0025g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0027g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0027g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0028g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0028g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0029g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0029g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0033g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0033g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0040g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0043g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0044g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0045g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0046g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0047g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0048g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0049g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0050g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0052g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0053g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0054g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0055g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0056g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0062g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0001t0070g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0007t0026g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0007t0026g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0007t0051g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0009t0032g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0009t0032g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0010t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0010t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0012t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0024t0069g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0001c0029t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0009g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0017g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0017g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0023g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0023g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0024g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0024g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0030g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0031g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0031g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0042g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0057g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0059g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0063g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0064g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0002t0067g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0008t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0008t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0013t0066g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0015t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0018t0041g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0022t0030g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0002c0025t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0009g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0021g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0021g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0058g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0060g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0061g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0003c0003t0068g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0013g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0013g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0013g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0013g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0016g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0016g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0016g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0022g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0022g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0035g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0036g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0004t0037g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0004c0028t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0005c0006t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0005c0006t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0005c0006t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0005c0006t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0005c0006t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0006c0005t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0006c0005t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0006c0005t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0006c0005t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0006c0005t0039g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0007c0027t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0008c0016t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0009c0021t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0010c0011t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0011c0019t0065g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0012c0023t0034g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0013c0026t0038g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0014c0014t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0015c0020t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
a0016c0017t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0008 | g0179 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00099 | hp2 | a0001 | c0001 | t0044 | g0207 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00140 | hp1 | a0004 | c0004 | t0022 | g0307 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00140 | hp2 | a0002 | c0002 | t0006 | g0053 | EUR | GBR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0101 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0184 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0083 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0209 | EUR | FIN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0108 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00639 | hp1 | a0007 | c0027 | t0004 | g0309 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00639 | hp2 | a0001 | c0001 | t0052 | g0003 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0240 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00733 | hp2 | a0002 | c0002 | t0006 | g0051 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG00735 | hp2 | a0002 | c0002 | t0030 | g0143 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01069 | hp1 | a0001 | c0001 | t0007 | g0212 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01069 | hp2 | a0002 | c0002 | t0009 | g0155 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01070 | hp2 | a0002 | c0002 | t0017 | g0057 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0213 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01081 | hp2 | a0002 | c0008 | t0006 | g0049 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01106 | hp1 | a0001 | c0001 | t0018 | g0182 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01106 | hp2 | a0002 | c0018 | t0041 | g0315 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01109 | hp1 | a0008 | c0016 | t0001 | g0079 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0187 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01167 | hp1 | a0002 | c0022 | t0030 | g0316 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01167 | hp2 | a0002 | c0025 | t0001 | g0120 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01168 | hp2 | a0001 | c0001 | t0055 | g0244 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01243 | hp1 | a0002 | c0002 | t0006 | g0038 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01255 | hp1 | a0005 | c0006 | t0008 | g0178 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01255 | hp2 | a0002 | c0002 | t0006 | g0039 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01256 | hp1 | a0005 | c0006 | t0008 | g0202 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0177 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0066 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01433 | hp1 | a0001 | c0001 | t0018 | g0183 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0074 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0317 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01515 | hp2 | a0001 | c0001 | t0029 | g0248 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0192 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0198 | EUR | IBS | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01884 | hp1 | a0006 | c0005 | t0014 | g0008 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01884 | hp2 | a0009 | c0021 | t0002 | g0168 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01891 | hp2 | a0002 | c0002 | t0031 | g0160 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01928 | hp2 | a0005 | c0006 | t0008 | g0270 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01934 | hp1 | a0001 | c0001 | t0025 | g0065 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01934 | hp2 | a0004 | c0004 | t0004 | g0286 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0189 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0076 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01952 | hp2 | a0004 | c0004 | t0013 | g0312 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02004 | hp1 | a0005 | c0006 | t0008 | g0176 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02004 | hp2 | a0002 | c0002 | t0006 | g0050 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02015 | hp1 | a0004 | c0004 | t0004 | g0283 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0029 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02055 | hp2 | a0001 | c0001 | t0020 | g0002 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02071 | hp1 | a0002 | c0002 | t0009 | g0134 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02129 | hp1 | a0001 | c0001 | t0047 | g0180 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02132 | hp1 | a0001 | c0001 | t0019 | g0191 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02132 | hp2 | a0004 | c0004 | t0004 | g0288 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02135 | hp2 | a0004 | c0004 | t0004 | g0284 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02148 | hp2 | a0001 | c0001 | t0028 | g0276 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02300 | hp2 | a0001 | c0001 | t0020 | g0170 | AMR | PEL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02451 | hp1 | a0002 | c0002 | t0006 | g0042 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0111 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0208 | EAS | KHV | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02572 | hp1 | a0002 | c0002 | t0017 | g0056 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02572 | hp2 | a0001 | c0007 | t0051 | g0027 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02615 | hp2 | a0004 | c0004 | t0037 | g0310 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02622 | hp1 | a0004 | c0004 | t0013 | g0313 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02622 | hp2 | a0002 | c0002 | t0023 | g0060 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02630 | hp2 | a0006 | c0005 | t0039 | g0166 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02647 | hp1 | a0006 | c0005 | t0014 | g0007 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02647 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0099 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02683 | hp2 | a0001 | c0010 | t0003 | g0175 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02717 | hp1 | a0002 | c0002 | t0010 | g0147 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02717 | hp2 | a0002 | c0002 | t0006 | g0041 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02723 | hp1 | a0004 | c0004 | t0013 | g0311 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02723 | hp2 | a0002 | c0002 | t0006 | g0052 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02809 | hp1 | a0006 | c0005 | t0014 | g0009 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02809 | hp2 | a0004 | c0004 | t0004 | g0308 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02886 | hp1 | a0002 | c0002 | t0063 | g0165 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02895 | hp1 | a0001 | c0001 | t0053 | g0001 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02895 | hp2 | a0010 | c0011 | t0012 | g0140 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02922 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02965 | hp1 | a0002 | c0002 | t0010 | g0164 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02965 | hp2 | a0011 | c0019 | t0065 | g0266 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02970 | hp1 | a0002 | c0002 | t0012 | g0114 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02970 | hp2 | a0001 | c0001 | t0070 | g0004 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02976 | hp1 | a0004 | c0004 | t0013 | g0314 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02976 | hp2 | a0012 | c0023 | t0034 | g0061 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03017 | hp1 | a0001 | c0001 | t0046 | g0232 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03041 | hp1 | a0001 | c0001 | t0054 | g0174 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03041 | hp2 | a0002 | c0002 | t0012 | g0069 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03098 | hp2 | a0001 | c0001 | t0020 | g0005 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03130 | hp1 | a0001 | c0007 | t0026 | g0026 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03130 | hp2 | a0001 | c0001 | t0040 | g0169 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03139 | hp1 | a0006 | c0005 | t0014 | g0006 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03139 | hp2 | a0002 | c0002 | t0010 | g0118 | AFR | ESN | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03209 | hp1 | a0001 | c0024 | t0069 | g0018 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03209 | hp2 | a0004 | c0004 | t0036 | g0289 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03225 | hp1 | a0002 | c0002 | t0042 | g0040 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03225 | hp2 | a0002 | c0002 | t0012 | g0115 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03239 | hp1 | a0001 | c0029 | t0003 | g0229 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03453 | hp1 | a0001 | c0009 | t0032 | g0019 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03453 | hp2 | a0002 | c0002 | t0024 | g0046 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03486 | hp2 | a0001 | c0001 | t0033 | g0030 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03490 | hp2 | a0014 | c0014 | t0001 | g0078 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03540 | hp2 | a0002 | c0002 | t0006 | g0059 | AFR | GWD | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03579 | hp1 | a0002 | c0002 | t0006 | g0037 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03579 | hp2 | a0002 | c0013 | t0066 | g0162 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03654 | hp1 | a0002 | c0002 | t0006 | g0055 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03654 | hp2 | a0004 | c0004 | t0022 | g0272 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03669 | hp1 | a0001 | c0001 | t0008 | g0255 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03688 | hp1 | a0015 | c0020 | t0002 | g0265 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03688 | hp2 | a0002 | c0002 | t0067 | g0141 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03704 | hp1 | a0001 | c0001 | t0045 | g0190 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03704 | hp2 | a0002 | c0002 | t0006 | g0062 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03710 | hp1 | a0001 | c0001 | t0062 | g0102 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03710 | hp2 | a0001 | c0010 | t0003 | g0185 | SAS | PJL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03831 | hp1 | a0001 | c0001 | t0018 | g0197 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0090 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03942 | hp2 | a0002 | c0002 | t0009 | g0126 | SAS | BEB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0089 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0278 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0222 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | STU | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18522 | hp2 | a0002 | c0002 | t0010 | g0086 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | CHB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18612 | hp2 | a0001 | c0001 | t0027 | g0269 | EAS | CHB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18906 | hp1 | a0002 | c0002 | t0024 | g0043 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18906 | hp2 | a0002 | c0002 | t0009 | g0149 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18942 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18948 | hp2 | a0003 | c0003 | t0021 | g0012 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0088 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0109 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0104 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18959 | hp1 | a0003 | c0003 | t0021 | g0097 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18960 | hp1 | a0004 | c0004 | t0004 | g0287 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18960 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18963 | hp1 | a0004 | c0004 | t0016 | g0291 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18967 | hp1 | a0004 | c0028 | t0004 | g0282 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18967 | hp2 | a0003 | c0003 | t0009 | g0084 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18969 | hp1 | a0004 | c0004 | t0004 | g0298 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18969 | hp2 | a0001 | c0001 | t0019 | g0267 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18973 | hp1 | a0004 | c0004 | t0004 | g0292 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18977 | hp2 | a0003 | c0003 | t0058 | g0098 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18979 | hp2 | a0002 | c0002 | t0009 | g0159 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18980 | hp1 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18981 | hp1 | a0001 | c0001 | t0011 | g0226 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18982 | hp1 | a0001 | c0001 | t0049 | g0230 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18982 | hp2 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18983 | hp1 | a0002 | c0002 | t0059 | g0130 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18983 | hp2 | a0001 | c0001 | t0028 | g0243 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18984 | hp1 | a0003 | c0003 | t0009 | g0105 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18984 | hp2 | a0004 | c0004 | t0004 | g0295 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18985 | hp1 | a0003 | c0003 | t0068 | g0011 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18986 | hp1 | a0004 | c0004 | t0004 | g0281 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18986 | hp2 | a0001 | c0001 | t0027 | g0252 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18990 | hp2 | a0003 | c0003 | t0009 | g0075 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18991 | hp2 | a0004 | c0004 | t0004 | g0301 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18992 | hp1 | a0004 | c0004 | t0004 | g0302 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18994 | hp2 | a0001 | c0001 | t0011 | g0227 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18997 | hp2 | a0004 | c0004 | t0004 | g0290 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19003 | hp2 | a0003 | c0003 | t0009 | g0112 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19005 | hp1 | a0004 | c0004 | t0035 | g0293 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19005 | hp2 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19006 | hp1 | a0001 | c0001 | t0011 | g0224 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19009 | hp1 | a0001 | c0001 | t0050 | g0256 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19009 | hp2 | a0004 | c0004 | t0004 | g0297 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19010 | hp1 | a0004 | c0004 | t0004 | g0296 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19012 | hp1 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19012 | hp2 | a0001 | c0001 | t0056 | g0253 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19030 | hp1 | a0004 | c0004 | t0016 | g0306 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19030 | hp2 | a0002 | c0002 | t0010 | g0163 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19043 | hp1 | a0016 | c0017 | t0012 | g0145 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19043 | hp2 | a0002 | c0015 | t0006 | g0047 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19055 | hp2 | a0004 | c0004 | t0004 | g0294 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19057 | hp2 | a0003 | c0003 | t0061 | g0071 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19064 | hp1 | a0002 | c0002 | t0057 | g0129 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19064 | hp2 | a0004 | c0004 | t0004 | g0305 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19065 | hp1 | a0001 | c0001 | t0048 | g0221 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19070 | hp2 | a0004 | c0004 | t0004 | g0300 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19077 | hp1 | a0003 | c0003 | t0021 | g0010 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19077 | hp2 | a0001 | c0001 | t0019 | g0257 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19079 | hp2 | a0004 | c0004 | t0004 | g0304 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19081 | hp2 | a0004 | c0004 | t0004 | g0303 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19082 | hp2 | a0001 | c0001 | t0011 | g0264 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19083 | hp1 | a0003 | c0003 | t0060 | g0072 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19089 | hp1 | a0003 | c0003 | t0001 | g0234 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19089 | hp2 | a0001 | c0001 | t0011 | g0238 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19090 | hp1 | a0004 | c0004 | t0016 | g0299 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19240 | hp1 | a0002 | c0002 | t0031 | g0161 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA19240 | hp2 | a0001 | c0009 | t0032 | g0020 | AFR | YRI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA20129 | hp1 | a0002 | c0002 | t0017 | g0058 | AFR | ASW | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA20129 | hp2 | a0001 | c0001 | t0015 | g0028 | AFR | ASW | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0196 | EUR | TSI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | TSI | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG01123 | hp2 | a0001 | c0001 | t0025 | g0131 | AMR | CLM | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02109 | hp1 | a0001 | c0007 | t0026 | g0025 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02486 | hp1 | a0002 | c0002 | t0023 | g0036 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02559 | hp1 | a0002 | c0002 | t0006 | g0054 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG02559 | hp2 | a0001 | c0012 | t0002 | g0280 | AFR | ACB | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03471 | hp1 | a0013 | c0026 | t0038 | g0016 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG03471 | hp2 | a0002 | c0008 | t0006 | g0048 | AFR | MSL | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG06807 | hp1 | a0001 | c0001 | t0043 | g0258 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA18955 | hp2 | a0004 | c0004 | t0004 | g0285 | EAS | JPT | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0122 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA20300 | hp2 | a0001 | c0001 | t0033 | g0031 | AFR | USA | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA21309 | hp1 | a0002 | c0002 | t0064 | g0063 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | LWK | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0277 | REF | REF | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0156 | REF | REF | ANKRD12_chr18_9131781_9290985 | ANKRD12 | chr18 | 9131781 | 9290985 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9221885 | C | G | 2 | a0004 a0007 |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
missense_variant | MODERATE | c.829C>G | p.Pro277Ala | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/13 | 1065/11284 | 829/6189 | 277/2062 | chr18 | 9221885 | |||
chr18:9254391 | T | C | 1 | a0010 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.1124T>C | p.Ile375Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1360/11284 | 1124/6189 | 375/2062 | chr18 | 9254391 | |||
chr18:9254449 | A | C | 1 | a0013 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1182A>C | p.Glu394Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1418/11284 | 1182/6189 | 394/2062 | chr18 | 9254449 | |||
chr18:9254787 | C | T | 2 | a0004 a0007 |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
missense_variant | MODERATE | c.1520C>T | p.Thr507Ile | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1756/11284 | 1520/6189 | 507/2062 | chr18 | 9254787 | |||
chr18:9254859 | C | G | 1 | a0005 | 5 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
missense_variant | MODERATE | c.1592C>G | p.Thr531Ser | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1828/11284 | 1592/6189 | 531/2062 | chr18 | 9254859 | |||
chr18:9255473 | A | G | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2206A>G | p.Thr736Ala | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2442/11284 | 2206/6189 | 736/2062 | chr18 | 9255473 | |||
chr18:9255720 | G | A | 2 | a0003 a0014 |
45 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(42): Show |
missense_variant | MODERATE | c.2453G>A | p.Ser818Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2689/11284 | 2453/6189 | 818/2062 | chr18 | 9255720 | |||
chr18:9255786 | C | A | 3 | a0004 a0006 a0007 |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
missense_variant | MODERATE | c.2519C>A | p.Thr840Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2755/11284 | 2519/6189 | 840/2062 | chr18 | 9255786 | |||
chr18:9255867 | T | G | 1 | a0014 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.2600T>G | p.Ile867Arg | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2836/11284 | 2600/6189 | 867/2062 | chr18 | 9255867 | |||
chr18:9255891 | C | T | 1 | a0012 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2624C>T | p.Ser875Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2860/11284 | 2624/6189 | 875/2062 | chr18 | 9255891 | |||
chr18:9255984 | A | G | 6 | a0001 a0005 a0009 others(3): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
missense_variant | MODERATE | c.2717A>G | p.Lys906Arg | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2953/11284 | 2717/6189 | 906/2062 | chr18 | 9255984 | |||
chr18:9256048 | A | C | 1 | a0006 | 5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
missense_variant | MODERATE | c.2781A>C | p.Glu927Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3017/11284 | 2781/6189 | 927/2062 | chr18 | 9256048 | |||
chr18:9256232 | G | A | 1 | a0011 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2965G>A | p.Gly989Ser | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3201/11284 | 2965/6189 | 989/2062 | chr18 | 9256232 | |||
chr18:9256635 | A | C | 1 | a0010 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.3368A>C | p.Lys1123Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3604/11284 | 3368/6189 | 1123/2062 | chr18 | 9256635 | |||
chr18:9256857 | C | T | 1 | a0016 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3590C>T | p.Pro1197Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3826/11284 | 3590/6189 | 1197/2062 | chr18 | 9256857 | |||
chr18:9257061 | G | A | 1 | a0015 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3794G>A | p.Ser1265Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 4030/11284 | 3794/6189 | 1265/2062 | chr18 | 9257061 | |||
chr18:9257579 | A | G | 1 | a0009 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.4312A>G | p.Asn1438Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 4548/11284 | 4312/6189 | 1438/2062 | chr18 | 9257579 | |||
chr18:9258090 | A | G | 1 | a0008 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.4823A>G | p.Lys1608Arg | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5059/11284 | 4823/6189 | 1608/2062 | chr18 | 9258090 | |||
chr18:9258539 | T | C | 4 | a0004 a0006 a0007 others(1): Show |
41 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(38): Show |
missense_variant | MODERATE | c.5272T>C | p.Ser1758Pro | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5508/11284 | 5272/6189 | 1758/2062 | chr18 | 9258539 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9204537 | A | G | 1 | a0001c0029 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.297A>G | p.Thr99Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/13 | 533/11284 | 297/6189 | 99/2062 | chr18 | 9204537 | |||
chr18:9254722 | C | T | 1 | a0001c0007 | 3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1455C>T | p.Asn485Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1691/11284 | 1455/6189 | 485/2062 | chr18 | 9254722 | |||
chr18:9254887 | T | G | 1 | a0002c0008 | 2 | HG01081.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.1620T>G | p.Thr540Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 1856/11284 | 1620/6189 | 540/2062 | chr18 | 9254887 | |||
chr18:9255124 | A | G | 1 | a0004c0028 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1857A>G | p.Lys619Lys | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2093/11284 | 1857/6189 | 619/2062 | chr18 | 9255124 | |||
chr18:9255214 | A | G | 1 | a0002c0025 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.1947A>G | p.Thr649Thr | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2183/11284 | 1947/6189 | 649/2062 | chr18 | 9255214 | |||
chr18:9255304 | G | A | 1 | a0001c0012 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2037G>A | p.Lys679Lys | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2273/11284 | 2037/6189 | 679/2062 | chr18 | 9255304 | |||
chr18:9255541 | C | T | 1 | a0001c0010 | 2 | HG02683.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.2274C>T | p.Ser758Ser | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2510/11284 | 2274/6189 | 758/2062 | chr18 | 9255541 | |||
chr18:9255574 | T | C | 1 | a0002c0013 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2307T>C | p.Asp769Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2543/11284 | 2307/6189 | 769/2062 | chr18 | 9255574 | |||
chr18:9255577 | A | G | 1 | a0001c0024 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2310A>G | p.Leu770Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2546/11284 | 2310/6189 | 770/2062 | chr18 | 9255577 | |||
chr18:9255961 | C | T | 2 | a0002c0013 a0002c0022 |
2 | HG01167.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2694C>T | p.Asp898Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 2930/11284 | 2694/6189 | 898/2062 | chr18 | 9255961 | |||
chr18:9256132 | C | T | 1 | a0002c0018 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.2865C>T | p.Asp955Asp | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 3101/11284 | 2865/6189 | 955/2062 | chr18 | 9256132 | |||
chr18:9257153 | C | T | 1 | a0001c0009 | 2 | HG03453.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.3886C>T | p.Leu1296Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 4122/11284 | 3886/6189 | 1296/2062 | chr18 | 9257153 | |||
chr18:9258533 | C | T | 5 | a0004c0004 a0004c0028 a0006c0005 others(2): Show |
41 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(38): Show |
synonymous_variant | LOW | c.5266C>T | p.Leu1756Leu | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5502/11284 | 5266/6189 | 1756/2062 | chr18 | 9258533 | |||
chr18:9258904 | C | T | 2 | a0002c0008 a0002c0015 |
3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.5637C>T | p.Asn1879Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/13 | 5873/11284 | 5637/6189 | 1879/2062 | chr18 | 9258904 | |||
chr18:9275544 | C | T | 3 | a0004c0004 a0004c0028 a0007c0027 |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
synonymous_variant | LOW | c.5784C>T | p.Asn1928Asn | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/13 | 6020/11284 | 5784/6189 | 1928/2062 | chr18 | 9275544 | |||
chr18:9275565 | T | G | 3 | a0004c0004 a0004c0028 a0007c0027 |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
synonymous_variant | LOW | c.5805T>G | p.Val1935Val | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/13 | 6041/11284 | 5805/6189 | 1935/2062 | chr18 | 9275565 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9281317 | G | C | 1 | a0012c0023t0034 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 191 | chr18 | 9281317 | ||||||
chr18:9281325 | T | A | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0016 others(6): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*199T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 199 | chr18 | 9281325 | ||||||
chr18:9281550 | G | A | 1 | a0013c0026t0038 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 424 | chr18 | 9281550 | ||||||
chr18:9281569 | T | C | 11 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0016 others(8): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*443T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 443 | chr18 | 9281569 | ||||||
chr18:9281782 | T | A | 1 | a0001c0001t0040 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 656 | chr18 | 9281782 | ||||||
chr18:9282144 | T | C | 6 | a0002c0002t0006 a0002c0002t0017 a0002c0002t0023 others(3): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1018T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1018 | chr18 | 9282144 | ||||||
chr18:9282482 | G | A | 1 | a0002c0018t0041 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1356 | chr18 | 9282482 | ||||||
chr18:9282585 | G | A | 1 | a0002c0002t0042 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1459G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1459 | chr18 | 9282585 | ||||||
chr18:9282857 | T | TA | 15 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(12): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1741dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 1742 | INFO_REALIGN_3_PRIME | chr18 | 9282857 | |||||
chr18:9283160 | T | G | 1 | a0001c0001t0025 | 2 | HG01123.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2034 | chr18 | 9283160 | ||||||
chr18:9283181 | A | G | 1 | a0002c0002t0024 | 2 | HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2055A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2055 | chr18 | 9283181 | ||||||
chr18:9283219 | A | G | 1 | a0001c0001t0070 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2093 | chr18 | 9283219 | ||||||
chr18:9283699 | T | C | 2 | a0001c0001t0019 a0001c0001t0050 |
4 | HG02132.hp1 NA18969.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2573T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2573 | chr18 | 9283699 | ||||||
chr18:9283785 | C | T | 1 | a0001c0001t0033 | 2 | HG03486.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2659C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2659 | chr18 | 9283785 | ||||||
chr18:9284084 | G | A | 2 | a0001c0007t0026 a0001c0007t0051 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2958G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2958 | chr18 | 9284084 | ||||||
chr18:9284087 | C | T | 1 | a0001c0009t0032 | 2 | HG03453.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2961C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 2961 | chr18 | 9284087 | ||||||
chr18:9284202 | A | G | 1 | a0012c0023t0034 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3076A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3076 | chr18 | 9284202 | ||||||
chr18:9284402 | TTG | T | 9 | a0004c0004t0004 a0004c0004t0013 a0004c0004t0016 others(6): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3278_*3279delGT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3278 | INFO_REALIGN_3_PRIME | chr18 | 9284402 | |||||
chr18:9284428 | A | G | 1 | a0004c0004t0037 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3302A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3302 | chr18 | 9284428 | ||||||
chr18:9284604 | T | C | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(31): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*3478T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3478 | chr18 | 9284604 | ||||||
chr18:9284829 | A | G | 3 | a0001c0024t0069 a0002c0002t0031 a0012c0023t0034 |
4 | HG01891.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3703A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3703 | chr18 | 9284829 | ||||||
chr18:9284935 | A | G | 1 | a0001c0001t0049 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3809A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3809 | chr18 | 9284935 | ||||||
chr18:9284943 | G | A | 2 | a0001c0001t0018 a0001c0001t0043 |
4 | HG01106.hp1 HG01433.hp1 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3817G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3817 | chr18 | 9284943 | ||||||
chr18:9284944 | C | T | 2 | a0001c0001t0018 a0001c0001t0043 |
4 | HG01106.hp1 HG01433.hp1 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3818C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3818 | chr18 | 9284944 | ||||||
chr18:9284953 | T | C | 1 | a0002c0018t0041 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3827T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3827 | chr18 | 9284953 | ||||||
chr18:9284972 | C | T | 1 | a0001c0001t0029 | 2 | HG01515.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3846C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3846 | chr18 | 9284972 | ||||||
chr18:9284973 | A | G | 2 | a0001c0001t0029 a0004c0004t0036 |
3 | HG01515.hp1 HG01515.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3847A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3847 | chr18 | 9284973 | ||||||
chr18:9284978 | G | A | 1 | a0001c0009t0032 | 2 | HG03453.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3852G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3852 | chr18 | 9284978 | ||||||
chr18:9284988 | C | T | 6 | a0002c0002t0006 a0002c0002t0017 a0002c0002t0023 others(3): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3862C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3862 | chr18 | 9284988 | ||||||
chr18:9285017 | T | C | 1 | a0002c0002t0057 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3891T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3891 | chr18 | 9285017 | ||||||
chr18:9285019 | A | G | 1 | a0001c0001t0048 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3893A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3893 | chr18 | 9285019 | ||||||
chr18:9285030 | C | A | 3 | a0002c0002t0012 a0010c0011t0012 a0016c0017t0012 |
5 | HG02895.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3904C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3904 | chr18 | 9285030 | ||||||
chr18:9285034 | G | A | 2 | a0004c0004t0013 a0004c0004t0037 |
5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3908G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3908 | chr18 | 9285034 | ||||||
chr18:9285125 | C | T | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(14): Show |
68 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3999C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 3999 | chr18 | 9285125 | ||||||
chr18:9285130 | G | A | 18 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(15): Show |
69 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4004G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4004 | chr18 | 9285130 | ||||||
chr18:9285133 | T | C | 18 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(15): Show |
69 | HG01099.hp1 HG01106.hp1 HG01123.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4007T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4007 | chr18 | 9285133 | ||||||
chr18:9285141 | G | A | 2 | a0002c0002t0057 a0002c0002t0059 |
2 | NA18983.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4015G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4015 | chr18 | 9285141 | ||||||
chr18:9285163 | C | T | 1 | a0004c0004t0035 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4037C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4037 | chr18 | 9285163 | ||||||
chr18:9285165 | T | C | 3 | a0003c0003t0060 a0003c0003t0061 a0004c0004t0035 |
3 | NA19005.hp1 NA19057.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4039T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4039 | chr18 | 9285165 | ||||||
chr18:9285208 | C | CA | 8 | a0001c0001t0020 a0001c0001t0045 a0001c0001t0052 others(5): Show |
14 | HG00140.hp1 HG00639.hp2 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4097dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4098 | INFO_REALIGN_3_PRIME | chr18 | 9285208 | |||||
chr18:9285220 | AAAAG | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(3): Show |
15 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4102_*4105delGAAA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4102 | INFO_REALIGN_3_PRIME | chr18 | 9285220 | |||||
chr18:9285234 | A | T | 1 | a0002c0002t0067 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4108A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4108 | chr18 | 9285234 | ||||||
chr18:9285245 | A | G | 1 | a0002c0002t0031 | 2 | HG01891.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4119A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4119 | chr18 | 9285245 | ||||||
chr18:9285296 | C | T | 3 | a0002c0013t0066 a0006c0005t0014 a0006c0005t0039 |
6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4170C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4170 | chr18 | 9285296 | ||||||
chr18:9285302 | C | T | 1 | a0013c0026t0038 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4176C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4176 | chr18 | 9285302 | ||||||
chr18:9285427 | C | CA | 19 | a0001c0001t0005 a0001c0001t0044 a0001c0001t0045 others(16): Show |
47 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4324dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4325 | INFO_REALIGN_3_PRIME | chr18 | 9285427 | |||||
chr18:9285427 | C | CAA | 3 | a0001c0001t0011 a0001c0001t0053 a0001c0001t0062 |
8 | HG02895.hp1 HG03710.hp1 NA18980.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4323_*4324dupAA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4325 | INFO_REALIGN_3_PRIME | chr18 | 9285427 | |||||
chr18:9285427 | CA | C | 11 | a0001c0001t0018 a0001c0001t0047 a0001c0001t0055 others(8): Show |
36 | HG00639.hp1 HG01106.hp1 HG01106.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4324delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4324 | INFO_REALIGN_3_PRIME | chr18 | 9285427 | |||||
chr18:9285428 | A | C | 4 | a0001c0001t0015 a0001c0001t0033 a0001c0024t0069 others(1): Show |
8 | HG02055.hp1 HG02922.hp2 HG03098.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4302A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4302 | chr18 | 9285428 | ||||||
chr18:9285511 | C | T | 1 | a0002c0002t0031 | 2 | HG01891.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4385C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4385 | chr18 | 9285511 | ||||||
chr18:9285540 | T | G | 1 | a0001c0001t0027 | 2 | NA18612.hp2 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4414T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4414 | chr18 | 9285540 | ||||||
chr18:9285724 | C | G | 5 | a0002c0002t0006 a0002c0002t0023 a0002c0002t0024 others(2): Show |
20 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4598C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4598 | chr18 | 9285724 | ||||||
chr18:9285826 | T | C | 24 | a0001c0001t0046 a0001c0009t0032 a0002c0002t0006 others(21): Show |
70 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4700T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4700 | chr18 | 9285826 | ||||||
chr18:9285889 | G | C | 1 | a0002c0002t0064 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4763G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4763 | chr18 | 9285889 | ||||||
chr18:9285894 | T | G | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(34): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*4768T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 13/13 | 4768 | chr18 | 9285894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9137220 | C | CCCGCCCG others(11): Show |
1 | a0001c0001t0029g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-52+258_-52+275dup others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9137220 | ||||||
chr18:9137251 | A | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+286A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137251 | |||||||
chr18:9137280 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+315A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137280 | |||||||
chr18:9137308 | G | A | 4 | a0001c0001t0020g0002 a0001c0001t0020g0005 a0001c0001t0052g0003 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+343G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137308 | |||||||
chr18:9137333 | G | A | 4 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+368G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137333 | |||||||
chr18:9137406 | G | T | 34 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.-52+441G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137406 | |||||||
chr18:9137456 | G | C | 3 | a0003c0003t0021g0010 a0003c0003t0021g0012 a0003c0003t0068g0011 |
3 | NA18948.hp2 NA18985.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-52+491G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137456 | |||||||
chr18:9137507 | G | T | 1 | a0001c0012t0002g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-52+542G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137507 | |||||||
chr18:9137518 | C | T | 5 | a0004c0004t0013g0311 a0004c0004t0013g0312 a0004c0004t0013g0313 others(2): Show |
5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+553C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137518 | |||||||
chr18:9137564 | G | T | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-52+599G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137564 | |||||||
chr18:9137583 | G | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-52+618G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137583 | |||||||
chr18:9137612 | G | A | 1 | a0002c0002t0001g0013 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-52+647G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137612 | |||||||
chr18:9137612 | G | C | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-52+647G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137612 | |||||||
chr18:9137620 | T | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-52+655T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137620 | |||||||
chr18:9137808 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+843A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137808 | |||||||
chr18:9137843 | C | G | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-52+878C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137843 | |||||||
chr18:9137858 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+893A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137858 | |||||||
chr18:9137866 | A | G | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-52+901A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137866 | |||||||
chr18:9137952 | G | C | 1 | a0002c0002t0064g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-52+987G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9137952 | |||||||
chr18:9138092 | A | G | 1 | a0004c0004t0004g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-52+1127A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138092 | |||||||
chr18:9138121 | G | T | 1 | a0004c0004t0022g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-52+1156G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138121 | |||||||
chr18:9138222 | CAT | C | 3 | a0002c0002t0010g0163 a0002c0002t0010g0164 a0002c0002t0063g0165 |
3 | HG02886.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-52+1260_-52+1261d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9138222 | ||||||
chr18:9138247 | T | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-52+1282T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138247 | |||||||
chr18:9138324 | C | A | 1 | a0001c0001t0025g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-52+1359C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138324 | |||||||
chr18:9138360 | A | G | 2 | a0001c0001t0002g0279 a0001c0001t0003g0278 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-52+1395A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138360 | |||||||
chr18:9138372 | G | C | 138 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-52+1407G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138372 | |||||||
chr18:9138408 | G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-52+1443G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138408 | |||||||
chr18:9138481 | C | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+1516C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138481 | |||||||
chr18:9138525 | AAAAC | A | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+1580_-52+1583d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9138525 | ||||||
chr18:9138549 | A | C | 1 | a0004c0004t0016g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-52+1584A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138549 | |||||||
chr18:9138663 | A | G | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+1698A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138663 | |||||||
chr18:9138684 | A | G | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-52+1719A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138684 | |||||||
chr18:9138841 | T | C | 4 | a0001c0001t0002g0001 a0001c0001t0040g0169 a0001c0001t0053g0001 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+1876T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138841 | |||||||
chr18:9138996 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-52+2031C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9138996 | |||||||
chr18:9139101 | A | T | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+2136A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139101 | |||||||
chr18:9139210 | C | CGT | 3 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0023g0036 |
3 | HG01243.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-52+2245_-52+2246i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139210 | |||||||
chr18:9139211 | T | C | 3 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0023g0036 |
3 | HG01243.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-52+2246T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139211 | |||||||
chr18:9139248 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+2283C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139248 | |||||||
chr18:9139358 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+2393A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139358 | |||||||
chr18:9139445 | A | T | 2 | a0001c0001t0002g0275 a0001c0001t0028g0276 |
2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-52+2480A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139445 | |||||||
chr18:9139534 | T | C | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+2569T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139534 | |||||||
chr18:9139592 | G | A | 1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-52+2627G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139592 | |||||||
chr18:9139605 | C | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+2640C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139605 | |||||||
chr18:9139607 | C | T | 4 | a0002c0002t0001g0013 a0002c0002t0001g0157 a0002c0002t0001g0158 others(1): Show |
4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+2642C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139607 | |||||||
chr18:9139613 | A | G | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | NA18941.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-52+2648A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139613 | |||||||
chr18:9139841 | C | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-52+2876C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139841 | |||||||
chr18:9139922 | C | A | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+2957C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139922 | |||||||
chr18:9139966 | C | T | 1 | a0003c0003t0021g0012 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-52+3001C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9139966 | |||||||
chr18:9140331 | T | C | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0020g0170 |
3 | HG01361.hp2 HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-52+3366T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9140331 | |||||||
chr18:9140479 | T | A | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+3514T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9140479 | |||||||
chr18:9140837 | A | AATC | 42 | a0001c0001t0002g0271 a0001c0001t0020g0005 a0004c0004t0004g0281 others(39): Show |
42 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.-52+3875_-52+3877d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9140837 | ||||||
chr18:9140953 | G | C | 315 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-52+3988G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9140953 | |||||||
chr18:9141025 | G | A | 3 | a0001c0001t0002g0173 a0001c0001t0054g0174 a0001c0012t0002g0280 |
3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52+4060G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141025 | |||||||
chr18:9141042 | T | C | 1 | a0001c0010t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-52+4077T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141042 | |||||||
chr18:9141065 | C | T | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-52+4100C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141065 | |||||||
chr18:9141215 | TGTG | T | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-52+4268_-52+4270d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9141215 | ||||||
chr18:9141406 | G | A | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+4441G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141406 | |||||||
chr18:9141464 | G | T | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+4499G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141464 | |||||||
chr18:9141475 | C | T | 1 | a0005c0006t0008g0270 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-52+4510C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141475 | |||||||
chr18:9141815 | T | C | 5 | a0001c0001t0007g0177 a0005c0006t0008g0176 a0005c0006t0008g0178 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+4850T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141815 | |||||||
chr18:9141956 | A | G | 1 | a0001c0001t0015g0028 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+4991A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141956 | |||||||
chr18:9141992 | C | T | 5 | a0001c0001t0002g0173 a0001c0001t0033g0030 a0001c0001t0033g0031 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+5027C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9141992 | |||||||
chr18:9142033 | A | G | 1 | a0001c0001t0027g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-52+5068A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142033 | |||||||
chr18:9142137 | C | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+5172C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142137 | |||||||
chr18:9142200 | C | G | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-52+5235C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142200 | |||||||
chr18:9142213 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+5248A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142213 | |||||||
chr18:9142232 | C | G | 1 | a0003c0003t0001g0146 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-52+5267C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142232 | |||||||
chr18:9142317 | G | T | 1 | a0001c0001t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-52+5352G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142317 | |||||||
chr18:9142522 | C | CT | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52+5558dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9142522 | ||||||
chr18:9142717 | A | G | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+5752A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142717 | |||||||
chr18:9142723 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+5758G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142723 | |||||||
chr18:9142736 | T | C | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+5771T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142736 | |||||||
chr18:9142745 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+5780G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142745 | |||||||
chr18:9142753 | G | A | 119 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-52+5788G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9142753 | |||||||
chr18:9142882 | CA | C | 211 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-52+5928delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9142882 | ||||||
chr18:9143268 | T | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+6303T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143268 | |||||||
chr18:9143396 | C | G | 2 | a0002c0002t0042g0040 a0012c0023t0034g0061 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-52+6431C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143396 | |||||||
chr18:9143444 | A | C | 1 | a0016c0017t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-52+6479A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143444 | |||||||
chr18:9143708 | C | G | 1 | a0003c0003t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-52+6743C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143708 | |||||||
chr18:9143776 | C | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+6811C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143776 | |||||||
chr18:9143799 | C | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+6834C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143799 | |||||||
chr18:9143813 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+6848G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143813 | |||||||
chr18:9143822 | AGT | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+6862_-52+6863d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9143822 | ||||||
chr18:9143916 | C | G | 1 | a0002c0002t0023g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-52+6951C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143916 | |||||||
chr18:9143944 | A | G | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+6979A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9143944 | |||||||
chr18:9144223 | G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-52+7258G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144223 | |||||||
chr18:9144298 | T | G | 1 | a0001c0001t0047g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+7333T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144298 | |||||||
chr18:9144352 | C | A | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-52+7387C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144352 | |||||||
chr18:9144421 | A | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+7456A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144421 | |||||||
chr18:9144490 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+7525T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144490 | |||||||
chr18:9144571 | C | T | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-52+7606C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144571 | |||||||
chr18:9144871 | A | T | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+7906A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144871 | |||||||
chr18:9144877 | TTGTA | T | 4 | a0001c0001t0018g0182 a0001c0001t0018g0183 a0003c0003t0001g0066 others(1): Show |
4 | HG01106.hp1 HG01361.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+7921_-52+7924d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9144877 | ||||||
chr18:9144883 | G | A | 2 | a0005c0006t0008g0176 a0005c0006t0008g0270 |
2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-52+7918G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144883 | |||||||
chr18:9144980 | GT | G | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-52+8016delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9144980 | |||||||
chr18:9145080 | A | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+8115A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145080 | |||||||
chr18:9145091 | A | G | 1 | a0003c0003t0068g0011 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-52+8126A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145091 | |||||||
chr18:9145169 | C | T | 2 | a0001c0001t0052g0003 a0001c0001t0070g0004 |
2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-52+8204C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145169 | |||||||
chr18:9145262 | G | A | 1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-52+8297G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145262 | |||||||
chr18:9145440 | A | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+8475A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145440 | |||||||
chr18:9145527 | G | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+8562G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145527 | |||||||
chr18:9145584 | A | G | 1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52+8619A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145584 | |||||||
chr18:9145585 | C | T | 3 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0009g0149 |
3 | HG02258.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-52+8620C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145585 | |||||||
chr18:9145586 | G | A | 1 | a0004c0004t0037g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-52+8621G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145586 | |||||||
chr18:9145624 | A | AATC | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+8661_-52+8663d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9145624 | ||||||
chr18:9145778 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+8813T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145778 | |||||||
chr18:9145923 | G | T | 1 | a0001c0001t0003g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-52+8958G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9145923 | |||||||
chr18:9146872 | A | G | 1 | a0002c0002t0009g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-52+9907A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9146872 | |||||||
chr18:9146978 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10013C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9146978 | |||||||
chr18:9146979 | G | A | 1 | a0001c0001t0007g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-52+10014G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9146979 | |||||||
chr18:9147314 | G | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+10349G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147314 | |||||||
chr18:9147546 | T | A | 1 | a0001c0010t0003g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-52+10581T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147546 | |||||||
chr18:9147622 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10657C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147622 | |||||||
chr18:9147637 | G | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10672G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147637 | |||||||
chr18:9147721 | A | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52+10756A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147721 | |||||||
chr18:9147800 | C | T | 1 | a0001c0001t0018g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-52+10835C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147800 | |||||||
chr18:9147914 | A | G | 3 | a0002c0002t0001g0142 a0002c0002t0030g0143 a0002c0002t0067g0141 |
3 | HG00735.hp2 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-52+10949A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147914 | |||||||
chr18:9147966 | A | G | 1 | a0001c0001t0019g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-52+11001A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9147966 | |||||||
chr18:9148166 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-52+11201T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148166 | |||||||
chr18:9148323 | T | C | 1 | a0002c0002t0012g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-52+11358T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148323 | |||||||
chr18:9148333 | C | CAT | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+11368_-52+1136 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148333 | |||||||
chr18:9148417 | A | G | 1 | a0010c0011t0012g0140 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-52+11452A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148417 | |||||||
chr18:9148631 | C | T | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52+11666C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148631 | |||||||
chr18:9148668 | C | T | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+11703C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148668 | |||||||
chr18:9148674 | C | T | 1 | a0001c0001t0003g0274 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-52+11709C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148674 | |||||||
chr18:9148863 | A | T | 139 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-52+11898A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148863 | |||||||
chr18:9148912 | A | AT | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+11951dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9148912 | ||||||
chr18:9148954 | T | C | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-52+11989T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9148954 | |||||||
chr18:9149109 | G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-52+12144G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149109 | |||||||
chr18:9149176 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+12211T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149176 | |||||||
chr18:9149415 | G | A | 2 | a0002c0002t0042g0040 a0012c0023t0034g0061 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-52+12450G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149415 | |||||||
chr18:9149417 | A | G | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52+12452A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149417 | |||||||
chr18:9149439 | A | T | 139 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-52+12474A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149439 | |||||||
chr18:9149515 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-52+12550G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149515 | |||||||
chr18:9149636 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12671G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149636 | |||||||
chr18:9149719 | A | G | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+12754A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149719 | |||||||
chr18:9149771 | G | GATTT | 158 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.-52+12822_-52+1282 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149771 | ||||||
chr18:9149771 | G | GATTTATT others(5): Show |
5 | a0004c0004t0013g0311 a0004c0004t0013g0312 a0004c0004t0013g0313 others(2): Show |
5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12814_-52+1282 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149771 | ||||||
chr18:9149788 | A | ATTTAT | 4 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0285 others(1): Show |
4 | HG02015.hp1 HG02135.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+12825_-52+1282 others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149788 | ||||||
chr18:9149791 | A | T | 207 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(204): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-52+12826A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149791 | |||||||
chr18:9149792 | A | ATTT | 34 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0005g0167 others(31): Show |
34 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-52+12827_-52+1282 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | |||||||
chr18:9149792 | A | ATTTT | 5 | a0004c0004t0004g0281 a0004c0004t0004g0304 a0004c0004t0004g0305 others(2): Show |
5 | HG00639.hp1 HG02809.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12827_-52+1282 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | |||||||
chr18:9149792 | A | C | 3 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0285 |
3 | HG02015.hp1 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-52+12827A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | |||||||
chr18:9149792 | A | T | 1 | a0004c0004t0016g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-52+12827A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149792 | |||||||
chr18:9149793 | A | T | 177 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-52+12828A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149793 | |||||||
chr18:9149796 | T | TA | 5 | a0004c0004t0004g0286 a0004c0004t0004g0287 a0004c0004t0004g0288 others(2): Show |
5 | HG01934.hp2 HG02132.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+12831_-52+1283 others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149796 | |||||||
chr18:9149796 | T | TTTTA | 3 | a0004c0004t0004g0301 a0004c0004t0004g0302 a0004c0004t0004g0303 |
3 | NA18991.hp2 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-52+12832_-52+1283 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9149796 | ||||||
chr18:9149797 | T | TTA | 27 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0005g0167 others(24): Show |
27 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52+12832_-52+1283 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149797 | |||||||
chr18:9149798 | A | T | 55 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0005g0167 others(52): Show |
55 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-52+12833A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149798 | |||||||
chr18:9149799 | T | A | 1 | a0001c0001t0008g0189 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-52+12834T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149799 | |||||||
chr18:9149801 | T | A | 1 | a0001c0001t0008g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-52+12836T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149801 | |||||||
chr18:9149802 | T | A | 4 | a0002c0002t0010g0163 a0002c0002t0010g0164 a0004c0004t0013g0311 others(1): Show |
4 | HG02723.hp1 HG02965.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+12837T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149802 | |||||||
chr18:9149804 | T | A | 4 | a0001c0001t0003g0188 a0001c0001t0003g0273 a0001c0001t0003g0274 others(1): Show |
4 | HG03486.hp2 NA18612.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+12839T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149804 | |||||||
chr18:9149806 | T | A | 2 | a0004c0004t0022g0272 a0004c0004t0022g0307 |
2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-52+12841T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149806 | |||||||
chr18:9149953 | C | T | 3 | a0002c0002t0001g0137 a0003c0003t0001g0138 a0003c0003t0001g0139 |
3 | HG00609.hp1 NA18981.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-52+12988C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9149953 | |||||||
chr18:9150017 | G | C | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+13052G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150017 | |||||||
chr18:9150091 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+13126G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150091 | |||||||
chr18:9150143 | T | A | 215 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-52+13178T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150143 | |||||||
chr18:9150153 | G | C | 1 | a0001c0001t0003g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-52+13188G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150153 | |||||||
chr18:9150235 | C | A | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+13270C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150235 | |||||||
chr18:9150497 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52+13532A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150497 | |||||||
chr18:9150637 | T | A | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+13672T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150637 | |||||||
chr18:9150638 | T | A | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(1): Show |
4 | HG01167.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+13673T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150638 | |||||||
chr18:9150639 | A | T | 19 | a0001c0001t0025g0065 a0001c0001t0025g0131 a0002c0002t0001g0013 others(16): Show |
19 | HG00423.hp1 HG01123.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.-52+13674A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150639 | |||||||
chr18:9150656 | T | A | 1 | a0001c0001t0045g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-52+13691T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150656 | |||||||
chr18:9150740 | G | A | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(1): Show |
4 | HG01167.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+13775G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150740 | |||||||
chr18:9150754 | G | A | 219 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-52+13789G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150754 | |||||||
chr18:9150897 | C | T | 1 | a0003c0003t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-52+13932C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150897 | |||||||
chr18:9150920 | T | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+13955T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9150920 | |||||||
chr18:9150964 | T | TA | 147 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-52+14009dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9150964 | ||||||
chr18:9151030 | A | G | 2 | a0002c0002t0042g0040 a0012c0023t0034g0061 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-52+14065A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151030 | |||||||
chr18:9151092 | A | C | 1 | a0001c0001t0070g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-52+14127A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151092 | |||||||
chr18:9151211 | C | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+14246C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151211 | |||||||
chr18:9151277 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52+14312G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151277 | |||||||
chr18:9151316 | A | G | 1 | a0004c0004t0036g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-52+14351A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151316 | |||||||
chr18:9151351 | A | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+14386A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151351 | |||||||
chr18:9151465 | T | C | 1 | a0001c0001t0019g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-52+14500T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151465 | |||||||
chr18:9151493 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+14528G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151493 | |||||||
chr18:9151624 | C | G | 130 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-52+14659C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151624 | |||||||
chr18:9151683 | C | G | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-52+14718C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151683 | |||||||
chr18:9151714 | G | A | 3 | a0001c0001t0002g0173 a0001c0001t0054g0174 a0001c0012t0002g0280 |
3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52+14749G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151714 | |||||||
chr18:9151983 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0068 |
2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-52+15018G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9151983 | |||||||
chr18:9152086 | A | G | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+15121A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152086 | |||||||
chr18:9152117 | A | G | 1 | a0001c0001t0033g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-52+15152A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152117 | |||||||
chr18:9152579 | A | G | 1 | a0003c0003t0001g0121 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-52+15614A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152579 | |||||||
chr18:9152636 | C | T | 139 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-52+15671C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152636 | |||||||
chr18:9152664 | A | T | 2 | a0002c0002t0001g0119 a0002c0025t0001g0120 |
2 | HG01167.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-52+15699A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152664 | |||||||
chr18:9152695 | A | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+15730A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152695 | |||||||
chr18:9152716 | C | T | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+15751C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152716 | |||||||
chr18:9152748 | A | G | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-52+15783A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152748 | |||||||
chr18:9152848 | C | T | 12 | a0002c0002t0001g0116 a0002c0002t0001g0117 a0002c0002t0001g0119 others(9): Show |
12 | HG01167.hp2 HG01891.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+15883C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152848 | |||||||
chr18:9152877 | T | A | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52+15912T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152877 | |||||||
chr18:9152948 | A | ATAAACTC others(316): Show |
3 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0005g0017 |
3 | HG03490.hp1 NA19058.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-52+15996_-52+1599 others(327): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9152948 | ||||||
chr18:9152948 | A | ATAAACTC others(317): Show |
1 | a0001c0001t0005g0262 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-52+15996_-52+1599 others(328): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9152948 | ||||||
chr18:9152958 | T | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+15993T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9152958 | |||||||
chr18:9153195 | A | G | 2 | a0001c0001t0002g0259 a0001c0001t0002g0263 |
2 | HG00735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-52+16230A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153195 | |||||||
chr18:9153237 | G | A | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+16272G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153237 | |||||||
chr18:9153542 | A | G | 4 | a0004c0004t0013g0311 a0004c0004t0013g0313 a0004c0004t0013g0314 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+16577A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153542 | |||||||
chr18:9153714 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+16749T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153714 | |||||||
chr18:9153787 | G | T | 26 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(23): Show |
26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52+16822G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9153787 | |||||||
chr18:9154215 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+17250A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154215 | |||||||
chr18:9154241 | G | A | 1 | a0001c0001t0007g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-52+17276G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154241 | |||||||
chr18:9154275 | A | G | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-52+17310A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154275 | |||||||
chr18:9154363 | G | A | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+17398G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154363 | |||||||
chr18:9154572 | A | C | 1 | a0002c0002t0023g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-52+17607A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154572 | |||||||
chr18:9154682 | AGAGAT | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+17720_-52+1772 others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9154682 | ||||||
chr18:9154777 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+17812T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154777 | |||||||
chr18:9154822 | G | A | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+17857G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9154822 | |||||||
chr18:9155098 | A | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+18133A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155098 | |||||||
chr18:9155148 | C | T | 1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-52+18183C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155148 | |||||||
chr18:9155344 | C | T | 1 | a0001c0001t0043g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-52+18379C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155344 | |||||||
chr18:9155515 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+18550G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155515 | |||||||
chr18:9155529 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-52+18564G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155529 | |||||||
chr18:9155668 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-52+18703T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155668 | |||||||
chr18:9155675 | T | C | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0041 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+18710T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9155675 | |||||||
chr18:9156119 | C | G | 1 | a0001c0001t0047g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+19154C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156119 | |||||||
chr18:9156137 | C | CA | 67 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0009t0032g0019 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-52+19190dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | ||||||
chr18:9156137 | C | CAA | 6 | a0001c0001t0010g0023 a0002c0018t0041g0315 a0004c0004t0016g0299 others(3): Show |
6 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+19189_-52+1919 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | ||||||
chr18:9156137 | C | CAAA | 123 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-52+19188_-52+1919 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | ||||||
chr18:9156137 | C | CAAAA | 12 | a0001c0001t0002g0173 a0001c0001t0002g0193 a0001c0001t0002g0263 others(9): Show |
12 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52+19187_-52+1919 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156137 | ||||||
chr18:9156160 | A | G | 1 | a0001c0010t0003g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-52+19195A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156160 | |||||||
chr18:9156205 | C | A | 5 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(2): Show |
5 | HG01106.hp2 HG01167.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+19240C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156205 | |||||||
chr18:9156316 | T | C | 1 | a0001c0001t0011g0264 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-52+19351T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156316 | |||||||
chr18:9156319 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-52+19354A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156319 | |||||||
chr18:9156344 | T | C | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-52+19379T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156344 | |||||||
chr18:9156352 | G | A | 61 | a0001c0001t0002g0198 a0001c0001t0003g0067 a0001c0001t0003g0068 others(58): Show |
61 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.-52+19387G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156352 | |||||||
chr18:9156534 | G | A | 3 | a0002c0002t0001g0070 a0002c0002t0001g0080 a0008c0016t0001g0079 |
3 | HG01109.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-52+19569G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156534 | |||||||
chr18:9156600 | A | G | 2 | a0003c0003t0001g0113 a0003c0003t0009g0112 |
2 | NA19003.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-52+19635A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156600 | |||||||
chr18:9156685 | A | G | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+19720A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156685 | |||||||
chr18:9156748 | C | T | 6 | a0002c0002t0006g0053 a0002c0002t0006g0054 a0002c0002t0006g0055 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+19783C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156748 | |||||||
chr18:9156926 | T | TAGAGTAG others(14): Show |
1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-52+19963_-52+1998 others(25): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9156926 | ||||||
chr18:9156932 | A | G | 1 | a0002c0002t0009g0134 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-52+19967A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156932 | |||||||
chr18:9156973 | G | A | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+20008G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9156973 | |||||||
chr18:9157141 | A | G | 122 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-52+20176A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157141 | |||||||
chr18:9157159 | A | G | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+20194A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157159 | |||||||
chr18:9157241 | T | TA | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-52+20277dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157241 | ||||||
chr18:9157255 | G | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-52+20290G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157255 | |||||||
chr18:9157426 | T | C | 1 | a0002c0002t0001g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-52+20461T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157426 | |||||||
chr18:9157437 | C | T | 7 | a0002c0002t0001g0116 a0002c0002t0001g0117 a0002c0002t0001g0119 others(4): Show |
7 | HG01167.hp2 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+20472C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157437 | |||||||
chr18:9157480 | C | T | 2 | a0001c0001t0010g0022 a0001c0001t0010g0023 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+20515C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157480 | |||||||
chr18:9157550 | G | GGT | 4 | a0003c0003t0001g0103 a0003c0003t0001g0104 a0003c0003t0009g0105 others(1): Show |
4 | NA18943.hp2 NA18957.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20620_-52+2062 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGT | 3 | a0003c0003t0001g0014 a0003c0003t0001g0138 a0003c0003t0001g0139 |
3 | HG00609.hp1 NA18960.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-52+20618_-52+2062 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGT | 3 | a0003c0003t0001g0107 a0003c0003t0001g0108 a0003c0003t0001g0109 |
3 | HG00621.hp1 NA18956.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-52+20616_-52+2062 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(3): Show |
2 | a0001c0001t0015g0015 a0013c0026t0038g0016 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(7): Show |
2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(7): Show |
4 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(9): Show |
1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(39): Show |
1 | a0001c0007t0026g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(50): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(41): Show |
1 | a0001c0007t0026g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(52): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | GGTGTGTA others(45): Show |
1 | a0001c0007t0051g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(56): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157550 | G | T | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+20585G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157550 | |||||||
chr18:9157550 | GGT | G | 3 | a0001c0001t0005g0181 a0002c0002t0001g0013 a0002c0002t0001g0158 |
3 | NA18941.hp1 NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-52+20620_-52+2062 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157550 | ||||||
chr18:9157551 | G | GTGTGTAT others(5): Show |
20 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(17): Show |
20 | HG00733.hp2 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157551 | ||||||
chr18:9157552 | T | G | 1 | a0004c0004t0016g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-52+20587T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157552 | |||||||
chr18:9157553 | G | GTGTATGT others(3): Show |
5 | a0002c0002t0006g0053 a0002c0002t0006g0059 a0002c0008t0006g0048 others(2): Show |
5 | HG00140.hp2 HG01081.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+20591_-52+2059 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157553 | ||||||
chr18:9157555 | G | GTATGTGT others(9): Show |
1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-52+20591_-52+2059 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157555 | ||||||
chr18:9157557 | G | A | 132 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-52+20592G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157557 | |||||||
chr18:9157559 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-52+20594G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157559 | |||||||
chr18:9157571 | G | A | 6 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+20606G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157571 | |||||||
chr18:9157575 | G | GTATATAT others(9): Show |
2 | a0004c0004t0004g0283 a0004c0004t0004g0284 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-52+20611_-52+2061 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157575 | ||||||
chr18:9157577 | G | A | 2 | a0004c0004t0004g0283 a0004c0004t0004g0284 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-52+20612G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157577 | |||||||
chr18:9157577 | G | GTATATAT others(3): Show |
1 | a0004c0004t0022g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-52+20613_-52+2061 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157577 | ||||||
chr18:9157577 | G | GTATATAT others(5): Show |
1 | a0004c0004t0022g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-52+20613_-52+2061 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157577 | ||||||
chr18:9157577 | G | GTATATAT others(11): Show |
1 | a0004c0004t0004g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-52+20613_-52+2061 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157577 | ||||||
chr18:9157579 | G | A | 5 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0286 others(2): Show |
5 | HG00140.hp1 HG01934.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+20614G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157579 | |||||||
chr18:9157579 | G | GTATATAT others(3): Show |
1 | a0004c0004t0016g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-52+20615_-52+2061 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(5): Show |
4 | a0004c0004t0013g0311 a0004c0004t0013g0312 a0004c0004t0013g0313 others(1): Show |
4 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(11): Show |
2 | a0004c0004t0004g0285 a0004c0004t0004g0300 |
2 | NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(13): Show |
6 | a0004c0004t0004g0294 a0004c0004t0004g0295 a0004c0004t0004g0296 others(3): Show |
6 | HG00639.hp1 NA18969.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(24): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(15): Show |
2 | a0004c0004t0004g0303 a0004c0004t0035g0293 |
2 | NA19005.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(26): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(17): Show |
1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-52+20615_-52+2061 others(28): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(19): Show |
4 | a0004c0004t0004g0292 a0004c0004t0004g0301 a0004c0004t0004g0302 others(1): Show |
4 | NA18973.hp1 NA18991.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+20615_-52+2061 others(30): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157579 | G | GTATATAT others(21): Show |
1 | a0004c0004t0016g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-52+20615_-52+2061 others(32): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157579 | ||||||
chr18:9157581 | G | A | 27 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(24): Show |
27 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52+20616G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157581 | |||||||
chr18:9157581 | G | GTATATAT others(5): Show |
1 | a0004c0004t0004g0305 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | ||||||
chr18:9157581 | G | GTATATAT others(7): Show |
1 | a0004c0004t0013g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | ||||||
chr18:9157581 | G | GTATATAT others(9): Show |
1 | a0004c0004t0036g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | ||||||
chr18:9157581 | G | GTATATAT others(11): Show |
1 | a0004c0004t0004g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | ||||||
chr18:9157581 | G | GTATATAT others(19): Show |
1 | a0004c0004t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-52+20617_-52+2061 others(30): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157581 | ||||||
chr18:9157583 | G | A | 143 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52+20618G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157583 | |||||||
chr18:9157583 | G | GTATATAT others(7): Show |
1 | a0001c0001t0015g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+20619_-52+2062 others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157583 | ||||||
chr18:9157585 | G | A | 187 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-52+20620G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157585 | |||||||
chr18:9157585 | G | GTA | 14 | a0002c0002t0001g0070 a0002c0002t0001g0080 a0002c0002t0001g0152 others(11): Show |
14 | HG00323.hp1 HG01168.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52+20634_-52+2063 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTATA | 3 | a0002c0002t0006g0039 a0002c0002t0023g0060 a0002c0022t0030g0316 |
3 | HG01167.hp1 HG01255.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-52+20632_-52+2063 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTATATA | 19 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0041 others(16): Show |
19 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-52+20630_-52+2063 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTATATAT others(3): Show |
3 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0023g0036 |
3 | HG01243.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-52+20626_-52+2063 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTATATAT others(9): Show |
1 | a0001c0001t0015g0028 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+20635_-52+2063 others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTATATAT others(15): Show |
1 | a0004c0004t0004g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-52+20635_-52+2063 others(26): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTA | 42 | a0001c0001t0062g0102 a0002c0002t0001g0094 a0002c0002t0001g0095 others(39): Show |
42 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-52+20621_-52+2062 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTA | 11 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0035 others(8): Show |
11 | HG00735.hp2 HG01243.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-52+20621_-52+2062 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTAT others(3): Show |
1 | a0001c0001t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(3): Show |
1 | a0003c0003t0021g0010 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(17): Show |
1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(28): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0033g0030 a0001c0001t0033g0031 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+20621_-52+2062 others(22): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(17): Show |
1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(28): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(19): Show |
1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(30): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(23): Show |
1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(34): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(25): Show |
1 | a0002c0002t0031g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(36): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157585 | G | GTGTGTGT others(25): Show |
1 | a0002c0002t0031g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-52+20621_-52+2062 others(36): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157585 | ||||||
chr18:9157587 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+20622A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157587 | |||||||
chr18:9157597 | A | ATATATAT others(21): Show |
1 | a0004c0004t0004g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-52+20635_-52+2063 others(32): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157597 | ||||||
chr18:9157601 | G | A | 13 | a0001c0001t0002g0198 a0001c0001t0002g0259 a0001c0001t0003g0261 others(10): Show |
13 | HG00735.hp1 HG01106.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52+20636G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157601 | |||||||
chr18:9157603 | A | ATATATAT others(20): Show |
1 | a0004c0004t0004g0304 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-52+20639_-52+2064 others(31): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157603 | ||||||
chr18:9157603 | A | ATATATAT others(12): Show |
1 | a0004c0028t0004g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-52+20639_-52+2064 others(23): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157603 | ||||||
chr18:9157603 | A | G | 11 | a0001c0001t0002g0198 a0001c0001t0002g0259 a0001c0001t0003g0261 others(8): Show |
11 | HG00735.hp1 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+20638A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157603 | |||||||
chr18:9157603 | AT | A | 106 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-52+20655delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9157603 | ||||||
chr18:9157604 | T | TA | 11 | a0001c0001t0002g0198 a0001c0001t0002g0259 a0001c0001t0003g0261 others(8): Show |
11 | HG00735.hp1 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+20639_-52+2064 others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157604 | |||||||
chr18:9157635 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52+20670C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157635 | |||||||
chr18:9157955 | G | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+20990G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9157955 | |||||||
chr18:9158314 | C | G | 5 | a0001c0001t0007g0177 a0005c0006t0008g0176 a0005c0006t0008g0178 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+21349C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158314 | |||||||
chr18:9158328 | G | A | 1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52+21363G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158328 | |||||||
chr18:9158364 | G | A | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+21399G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158364 | |||||||
chr18:9158512 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-52+21547T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158512 | |||||||
chr18:9158645 | G | A | 7 | a0003c0003t0001g0077 a0003c0003t0001g0081 a0003c0003t0001g0082 others(4): Show |
7 | NA18943.hp2 NA18957.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+21680G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158645 | |||||||
chr18:9158783 | G | C | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-52+21818G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158783 | |||||||
chr18:9158983 | T | C | 1 | a0002c0002t0010g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-52+22018T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9158983 | |||||||
chr18:9159196 | A | T | 1 | a0002c0002t0064g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-52+22231A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159196 | |||||||
chr18:9159225 | ATATGTG | A | 4 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+22264_-52+2226 others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9159225 | ||||||
chr18:9159229 | G | A | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+22264G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159229 | |||||||
chr18:9159349 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52+22384A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159349 | |||||||
chr18:9159443 | A | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52+22478A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159443 | |||||||
chr18:9159492 | C | T | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52+22527C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159492 | |||||||
chr18:9159599 | A | AT | 200 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-52+22647dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9159599 | ||||||
chr18:9159599 | A | ATT | 9 | a0002c0002t0006g0038 a0002c0002t0042g0040 a0004c0004t0016g0299 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-52+22646_-52+2264 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9159599 | ||||||
chr18:9159963 | C | T | 2 | a0004c0004t0004g0308 a0007c0027t0004g0309 |
2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-51-22419C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159963 | |||||||
chr18:9159971 | A | G | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-51-22411A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159971 | |||||||
chr18:9159998 | G | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-22384G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9159998 | |||||||
chr18:9160070 | G | C | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-51-22312G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160070 | |||||||
chr18:9160191 | G | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-22191G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160191 | |||||||
chr18:9160441 | G | GT | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-21934dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9160441 | ||||||
chr18:9160491 | C | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-21891C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160491 | |||||||
chr18:9160577 | T | C | 1 | a0001c0001t0003g0194 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-51-21805T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160577 | |||||||
chr18:9160648 | C | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-21734C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160648 | |||||||
chr18:9160668 | T | A | 2 | a0003c0003t0060g0072 a0003c0003t0061g0071 |
2 | NA19057.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-51-21714T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160668 | |||||||
chr18:9160709 | C | T | 2 | a0002c0002t0042g0040 a0012c0023t0034g0061 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-21673C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160709 | |||||||
chr18:9160915 | G | T | 1 | a0001c0001t0020g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-51-21467G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160915 | |||||||
chr18:9160942 | T | C | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-21440T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9160942 | |||||||
chr18:9161069 | G | A | 1 | a0001c0012t0002g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-51-21313G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161069 | |||||||
chr18:9161106 | G | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-21276G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161106 | |||||||
chr18:9161180 | A | G | 1 | a0003c0003t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-51-21202A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161180 | |||||||
chr18:9161354 | TTTTTA | T | 3 | a0001c0001t0002g0173 a0001c0001t0054g0174 a0001c0012t0002g0280 |
3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-51-21014_-51-2101 others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161354 | ||||||
chr18:9161534 | C | T | 2 | a0002c0002t0010g0163 a0002c0002t0010g0164 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-51-20848C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161534 | |||||||
chr18:9161577 | G | A | 1 | a0002c0002t0006g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-51-20805G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161577 | |||||||
chr18:9161622 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-20760C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161622 | |||||||
chr18:9161623 | G | A | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-20759G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161623 | |||||||
chr18:9161637 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-20745A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161637 | |||||||
chr18:9161655 | T | C | 315 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-51-20727T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161655 | |||||||
chr18:9161726 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-20656T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161726 | |||||||
chr18:9161738 | A | ATG | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-20630_-51-2062 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161738 | ||||||
chr18:9161740 | G | A | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-20642G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161740 | |||||||
chr18:9161750 | G | GTA | 3 | a0002c0008t0006g0048 a0002c0008t0006g0049 a0002c0015t0006g0047 |
3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-20631_-51-2063 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161750 | ||||||
chr18:9161752 | G | A | 3 | a0002c0008t0006g0048 a0002c0008t0006g0049 a0002c0015t0006g0047 |
3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-20630G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161752 | |||||||
chr18:9161752 | G | GTA | 22 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(19): Show |
22 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-51-20619_-51-2061 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9161752 | ||||||
chr18:9161754 | A | G | 8 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0285 others(5): Show |
8 | HG02015.hp1 HG02132.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-20628A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161754 | |||||||
chr18:9161873 | C | T | 213 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-51-20509C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9161873 | |||||||
chr18:9162016 | C | T | 1 | a0003c0003t0060g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-51-20366C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162016 | |||||||
chr18:9162197 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-20185C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162197 | |||||||
chr18:9162224 | T | G | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-20158T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162224 | |||||||
chr18:9162422 | T | C | 2 | a0002c0002t0042g0040 a0012c0023t0034g0061 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-19960T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162422 | |||||||
chr18:9162444 | C | T | 1 | a0014c0014t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-51-19938C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162444 | |||||||
chr18:9162620 | C | T | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-51-19762C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162620 | |||||||
chr18:9162710 | C | T | 1 | a0001c0001t0008g0255 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-51-19672C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162710 | |||||||
chr18:9162804 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-51-19578T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162804 | |||||||
chr18:9162808 | G | GT | 137 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-51-19566dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9162808 | ||||||
chr18:9162818 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-19564A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162818 | |||||||
chr18:9162914 | T | C | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-19468T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9162914 | |||||||
chr18:9163142 | C | G | 26 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(23): Show |
26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-19240C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163142 | |||||||
chr18:9163148 | T | C | 3 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0285 |
3 | HG02015.hp1 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-51-19234T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163148 | |||||||
chr18:9163261 | G | A | 2 | a0001c0001t0003g0199 a0001c0001t0011g0264 |
2 | NA18953.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-51-19121G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163261 | |||||||
chr18:9163387 | G | T | 137 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-51-18995G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163387 | |||||||
chr18:9163477 | T | C | 137 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-51-18905T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163477 | |||||||
chr18:9163511 | C | T | 4 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-18871C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9163511 | |||||||
chr18:9164011 | G | A | 211 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-51-18371G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164011 | |||||||
chr18:9164101 | G | C | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-18281G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164101 | |||||||
chr18:9164209 | T | C | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-18173T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164209 | |||||||
chr18:9164357 | C | G | 3 | a0002c0002t0017g0056 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | HG01070.hp2 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-51-18025C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164357 | |||||||
chr18:9164599 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-17783C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164599 | |||||||
chr18:9164756 | G | A | 1 | a0001c0001t0015g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51-17626G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164756 | |||||||
chr18:9164761 | T | G | 127 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-51-17621T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164761 | |||||||
chr18:9164890 | C | T | 1 | a0004c0004t0016g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-51-17492C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9164890 | |||||||
chr18:9165215 | G | A | 1 | a0003c0003t0021g0012 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-51-17167G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165215 | |||||||
chr18:9165249 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-17133A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165249 | |||||||
chr18:9165382 | G | A | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-17000G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165382 | |||||||
chr18:9165678 | G | A | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(1): Show |
4 | HG01167.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16704G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165678 | |||||||
chr18:9165681 | T | C | 1 | a0001c0001t0005g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-51-16701T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165681 | |||||||
chr18:9165720 | T | A | 51 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(48): Show |
51 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-51-16662T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165720 | |||||||
chr18:9165743 | A | T | 2 | a0001c0001t0003g0067 a0001c0001t0003g0068 |
2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-51-16639A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165743 | |||||||
chr18:9165815 | T | C | 215 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-51-16567T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165815 | |||||||
chr18:9165863 | T | TC | 9 | a0001c0001t0002g0271 a0001c0001t0005g0200 a0001c0001t0005g0262 others(6): Show |
9 | HG02647.hp1 HG02738.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-16512dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9165863 | ||||||
chr18:9165871 | T | C | 39 | a0001c0001t0003g0204 a0001c0001t0003g0210 a0004c0004t0004g0283 others(36): Show |
39 | HG00140.hp1 HG00639.hp1 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.-51-16511T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165871 | |||||||
chr18:9165877 | C | T | 90 | a0001c0001t0002g0001 a0001c0001t0002g0173 a0001c0001t0002g0198 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-51-16505C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165877 | |||||||
chr18:9165878 | A | C | 7 | a0004c0004t0004g0281 a0004c0004t0004g0290 a0004c0004t0004g0301 others(4): Show |
7 | NA18986.hp1 NA18991.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-16504A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9165878 | |||||||
chr18:9166065 | G | A | 2 | a0004c0004t0004g0294 a0004c0004t0004g0295 |
2 | NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-51-16317G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166065 | |||||||
chr18:9166169 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-16213C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166169 | |||||||
chr18:9166170 | G | A | 4 | a0002c0002t0010g0086 a0002c0002t0010g0163 a0002c0002t0010g0164 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16212G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166170 | |||||||
chr18:9166236 | A | G | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-16146A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166236 | |||||||
chr18:9166244 | G | A | 4 | a0002c0002t0001g0013 a0002c0002t0001g0157 a0002c0002t0001g0158 others(1): Show |
4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16138G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166244 | |||||||
chr18:9166283 | G | C | 1 | a0003c0003t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-51-16099G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166283 | |||||||
chr18:9166348 | G | A | 1 | a0006c0005t0014g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-51-16034G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166348 | |||||||
chr18:9166353 | C | T | 1 | a0016c0017t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-51-16029C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166353 | |||||||
chr18:9166380 | C | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-16002C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166380 | |||||||
chr18:9166406 | T | C | 43 | a0003c0003t0001g0103 a0003c0003t0001g0104 a0003c0003t0009g0105 others(40): Show |
43 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.-51-15976T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166406 | |||||||
chr18:9166415 | G | A | 1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-51-15967G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166415 | |||||||
chr18:9166450 | T | C | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-15932T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166450 | |||||||
chr18:9166459 | C | T | 1 | a0001c0001t0002g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-51-15923C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166459 | |||||||
chr18:9166497 | T | C | 1 | a0001c0001t0005g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-51-15885T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166497 | |||||||
chr18:9166934 | T | C | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-15448T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9166934 | |||||||
chr18:9167045 | C | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-15337C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167045 | |||||||
chr18:9167070 | GTC | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-15310_-51-1530 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9167070 | ||||||
chr18:9167074 | A | G | 139 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-51-15308A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167074 | |||||||
chr18:9167145 | C | T | 9 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-15237C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167145 | |||||||
chr18:9167225 | TTAAAGTA others(10): Show |
T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-15156_-51-1514 others(21): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167225 | |||||||
chr18:9167245 | TCTG | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-15136_-51-1513 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167245 | |||||||
chr18:9167249 | T | G | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-15133T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167249 | |||||||
chr18:9167349 | G | A | 1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-15033G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167349 | |||||||
chr18:9167370 | G | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-15012G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167370 | |||||||
chr18:9167423 | A | G | 6 | a0001c0001t0056g0253 a0006c0005t0014g0006 a0006c0005t0014g0007 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-14959A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167423 | |||||||
chr18:9167440 | G | T | 1 | a0002c0002t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-51-14942G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167440 | |||||||
chr18:9167649 | C | T | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-14733C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167649 | |||||||
chr18:9167773 | G | C | 2 | a0001c0001t0052g0003 a0001c0001t0070g0004 |
2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-51-14609G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167773 | |||||||
chr18:9167796 | A | G | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-14586A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167796 | |||||||
chr18:9167875 | G | A | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-51-14507G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167875 | |||||||
chr18:9167887 | G | A | 6 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0031g0160 others(3): Show |
6 | HG01167.hp1 HG01891.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-14495G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167887 | |||||||
chr18:9167893 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-14489T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167893 | |||||||
chr18:9167921 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-14461G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9167921 | |||||||
chr18:9167927 | AG | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-14452delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9167927 | ||||||
chr18:9168045 | G | T | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-14337G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168045 | |||||||
chr18:9168053 | T | C | 1 | a0006c0005t0014g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-51-14329T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168053 | |||||||
chr18:9168376 | G | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-14006G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168376 | |||||||
chr18:9168589 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-13793G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168589 | |||||||
chr18:9168591 | C | T | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-13791C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168591 | |||||||
chr18:9168596 | T | C | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-13786T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168596 | |||||||
chr18:9168614 | T | C | 1 | a0002c0002t0009g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-51-13768T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168614 | |||||||
chr18:9168626 | C | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-13756C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168626 | |||||||
chr18:9168662 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-51-13720G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168662 | |||||||
chr18:9168747 | C | T | 2 | a0001c0001t0027g0252 a0001c0001t0027g0269 |
2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-51-13635C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168747 | |||||||
chr18:9168809 | G | C | 1 | a0001c0001t0056g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-51-13573G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168809 | |||||||
chr18:9168821 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-13561A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168821 | |||||||
chr18:9168949 | C | T | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-13433C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168949 | |||||||
chr18:9168975 | T | G | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-13407T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168975 | |||||||
chr18:9168985 | G | A | 1 | a0002c0002t0001g0135 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-51-13397G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9168985 | |||||||
chr18:9169020 | C | T | 213 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-51-13362C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169020 | |||||||
chr18:9169088 | T | C | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-51-13294T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169088 | |||||||
chr18:9169217 | G | A | 7 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0002g0236 others(4): Show |
7 | HG00609.hp2 HG02080.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-13165G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169217 | |||||||
chr18:9169517 | C | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-12865C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169517 | |||||||
chr18:9169588 | T | C | 3 | a0001c0001t0008g0187 a0001c0001t0008g0189 a0001c0001t0008g0240 |
3 | HG00733.hp1 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-51-12794T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169588 | |||||||
chr18:9169793 | G | A | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-12589G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169793 | |||||||
chr18:9169824 | T | G | 1 | a0003c0003t0001g0138 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-51-12558T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9169824 | |||||||
chr18:9170001 | G | T | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-12381G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170001 | |||||||
chr18:9170012 | A | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-12370A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170012 | |||||||
chr18:9170030 | G | A | 3 | a0001c0001t0002g0173 a0001c0001t0054g0174 a0001c0012t0002g0280 |
3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-51-12352G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170030 | |||||||
chr18:9170089 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0198 a0001c0001t0003g0064 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-51-12293G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170089 | |||||||
chr18:9170173 | T | A | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-12209T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170173 | |||||||
chr18:9170246 | T | C | 1 | a0001c0001t0011g0201 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-51-12136T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170246 | |||||||
chr18:9170467 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-11915G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170467 | |||||||
chr18:9170527 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-11855T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170527 | |||||||
chr18:9170675 | A | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-51-11707A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170675 | |||||||
chr18:9170740 | G | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-51-11642G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9170740 | |||||||
chr18:9171002 | A | G | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-11380A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171002 | |||||||
chr18:9171009 | G | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-11373G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171009 | |||||||
chr18:9171034 | G | A | 4 | a0004c0004t0013g0311 a0004c0004t0013g0313 a0004c0004t0013g0314 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-11348G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171034 | |||||||
chr18:9171109 | G | A | 1 | a0003c0003t0009g0112 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-51-11273G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171109 | |||||||
chr18:9171134 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-51-11248T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171134 | |||||||
chr18:9171163 | G | A | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-11219G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171163 | |||||||
chr18:9171179 | C | T | 50 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(47): Show |
50 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-51-11203C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171179 | |||||||
chr18:9171228 | A | T | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-11154A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171228 | |||||||
chr18:9171403 | T | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.-51-10979T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171403 | |||||||
chr18:9171536 | T | C | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-10846T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171536 | |||||||
chr18:9171589 | A | G | 3 | a0001c0001t0008g0187 a0001c0001t0008g0189 a0001c0001t0008g0240 |
3 | HG00733.hp1 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-51-10793A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171589 | |||||||
chr18:9171600 | C | G | 1 | a0001c0010t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-51-10782C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171600 | |||||||
chr18:9171758 | C | T | 1 | a0002c0002t0030g0143 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-51-10624C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171758 | |||||||
chr18:9171855 | A | T | 4 | a0001c0001t0005g0186 a0001c0001t0005g0225 a0001c0001t0011g0226 others(1): Show |
4 | NA18957.hp2 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-10527A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171855 | |||||||
chr18:9171884 | G | T | 19 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(16): Show |
19 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51-10498G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171884 | |||||||
chr18:9171929 | A | G | 3 | a0002c0002t0006g0050 a0002c0002t0006g0051 a0002c0002t0006g0062 |
3 | HG00733.hp2 HG02004.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-51-10453A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9171929 | |||||||
chr18:9172025 | C | CA | 146 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-51-10342dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9172025 | ||||||
chr18:9172025 | C | CAA | 9 | a0001c0001t0002g0242 a0001c0001t0002g0254 a0001c0001t0005g0228 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-10343_-51-1034 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9172025 | ||||||
chr18:9172041 | C | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0173 a0001c0001t0002g0198 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-51-10341C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172041 | |||||||
chr18:9172084 | T | TCAAAAAA others(3): Show |
1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10298_-51-1029 others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172084 | |||||||
chr18:9172085 | T | G | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10297T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172085 | |||||||
chr18:9172088 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10294C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172088 | |||||||
chr18:9172089 | A | G | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-10293A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172089 | |||||||
chr18:9172339 | C | G | 26 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(23): Show |
26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-10043C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172339 | |||||||
chr18:9172587 | T | C | 1 | a0001c0001t0003g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-51-9795T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172587 | |||||||
chr18:9172620 | C | G | 1 | a0002c0002t0006g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-51-9762C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172620 | |||||||
chr18:9172702 | T | G | 1 | a0003c0003t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-51-9680T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172702 | |||||||
chr18:9172757 | C | T | 2 | a0001c0001t0019g0257 a0001c0001t0050g0256 |
2 | NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-51-9625C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172757 | |||||||
chr18:9172779 | A | C | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-9603A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172779 | |||||||
chr18:9172853 | T | C | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-9529T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172853 | |||||||
chr18:9172886 | T | A | 4 | a0002c0002t0001g0013 a0002c0002t0001g0157 a0002c0002t0001g0158 others(1): Show |
4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-9496T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172886 | |||||||
chr18:9172892 | G | T | 1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-9490G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172892 | |||||||
chr18:9172925 | A | G | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-51-9457A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172925 | |||||||
chr18:9172930 | C | CT | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-9451dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9172930 | ||||||
chr18:9172961 | G | A | 3 | a0001c0001t0008g0187 a0001c0001t0008g0189 a0001c0001t0008g0240 |
3 | HG00733.hp1 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-51-9421G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172961 | |||||||
chr18:9172993 | G | A | 2 | a0004c0004t0022g0272 a0004c0004t0022g0307 |
2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-51-9389G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172993 | |||||||
chr18:9172996 | A | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-9386A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9172996 | |||||||
chr18:9173067 | A | AT | 30 | a0001c0001t0002g0001 a0001c0001t0002g0250 a0001c0001t0002g0251 others(27): Show |
30 | HG00423.hp1 HG00639.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-51-9295dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173067 | ||||||
chr18:9173067 | AT | A | 43 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0005g0032 others(40): Show |
43 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-51-9295delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173067 | ||||||
chr18:9173106 | A | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-9276A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173106 | |||||||
chr18:9173162 | C | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-51-9220C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173162 | |||||||
chr18:9173293 | C | A | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-51-9089C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173293 | |||||||
chr18:9173449 | A | G | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-8933A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173449 | |||||||
chr18:9173538 | A | G | 34 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.-51-8844A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173538 | |||||||
chr18:9173558 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-51-8824G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173558 | |||||||
chr18:9173577 | T | C | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-8805T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173577 | |||||||
chr18:9173616 | T | TG | 48 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0001g0070 others(45): Show |
48 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-51-8756dupG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173616 | ||||||
chr18:9173616 | T | TGG | 21 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(18): Show |
21 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51-8757_-51-8756d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9173616 | ||||||
chr18:9173619 | G | C | 1 | a0004c0004t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-51-8763G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173619 | |||||||
chr18:9173619 | G | T | 2 | a0001c0001t0025g0131 a0002c0018t0041g0315 |
2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-51-8763G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173619 | |||||||
chr18:9173622 | G | GT | 142 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-51-8760_-51-8759i others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173622 | |||||||
chr18:9173623 | G | T | 1 | a0001c0001t0062g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51-8759G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173623 | |||||||
chr18:9173626 | G | C | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-8756G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173626 | |||||||
chr18:9173628 | A | G | 25 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-8754A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173628 | |||||||
chr18:9173790 | G | C | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-8592G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173790 | |||||||
chr18:9173828 | G | A | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-8554G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173828 | |||||||
chr18:9173836 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-8546G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173836 | |||||||
chr18:9173888 | T | G | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-8494T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173888 | |||||||
chr18:9173891 | T | G | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-51-8491T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173891 | |||||||
chr18:9173894 | G | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-51-8488G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173894 | |||||||
chr18:9173935 | G | C | 69 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0002c0002t0006g0037 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-51-8447G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9173935 | |||||||
chr18:9174033 | C | CA | 3 | a0003c0003t0001g0103 a0003c0003t0001g0104 a0003c0003t0009g0105 |
3 | NA18943.hp2 NA18957.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-51-8348dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9174033 | ||||||
chr18:9174046 | T | C | 34 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.-51-8336T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174046 | |||||||
chr18:9174123 | C | T | 13 | a0001c0001t0005g0186 a0001c0001t0005g0200 a0001c0001t0005g0219 others(10): Show |
13 | HG02135.hp1 HG03017.hp1 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-8259C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174123 | |||||||
chr18:9174206 | C | T | 1 | a0002c0002t0001g0158 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-51-8176C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174206 | |||||||
chr18:9174452 | C | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-7930C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174452 | |||||||
chr18:9174574 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-51-7808A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174574 | |||||||
chr18:9174582 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-7800C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174582 | |||||||
chr18:9174652 | C | T | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-51-7730C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174652 | |||||||
chr18:9174660 | T | C | 2 | a0001c0001t0028g0243 a0001c0001t0056g0253 |
2 | NA18983.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-51-7722T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174660 | |||||||
chr18:9174713 | G | T | 5 | a0002c0002t0006g0053 a0002c0002t0006g0055 a0002c0002t0017g0056 others(2): Show |
5 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-7669G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174713 | |||||||
chr18:9174723 | T | G | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-51-7659T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174723 | |||||||
chr18:9174741 | A | G | 122 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-51-7641A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174741 | |||||||
chr18:9174787 | C | A | 1 | a0001c0001t0055g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-51-7595C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174787 | |||||||
chr18:9174847 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-7535C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174847 | |||||||
chr18:9174851 | TG | T | 140 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-51-7530delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174851 | |||||||
chr18:9174852 | G | T | 2 | a0002c0002t0042g0040 a0012c0023t0034g0061 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-7530G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174852 | |||||||
chr18:9174887 | G | A | 189 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-51-7495G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9174887 | |||||||
chr18:9174929 | CATTT | C | 204 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-51-7427_-51-7424d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9174929 | ||||||
chr18:9175023 | C | T | 1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-7359C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175023 | |||||||
chr18:9175100 | G | A | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-7282G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175100 | |||||||
chr18:9175174 | A | C | 1 | a0001c0001t0003g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-51-7208A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175174 | |||||||
chr18:9175178 | A | C | 1 | a0002c0002t0001g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-51-7204A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175178 | |||||||
chr18:9175261 | G | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-7121G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175261 | |||||||
chr18:9175288 | G | A | 1 | a0002c0002t0006g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-51-7094G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175288 | |||||||
chr18:9175336 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-51-7046T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175336 | |||||||
chr18:9175448 | T | C | 24 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(21): Show |
24 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-51-6934T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175448 | |||||||
chr18:9175523 | C | CT | 17 | a0001c0001t0005g0032 a0001c0001t0005g0034 a0001c0001t0005g0035 others(14): Show |
17 | HG00733.hp2 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-51-6831dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTT | 9 | a0001c0001t0003g0064 a0001c0001t0003g0274 a0001c0001t0015g0028 others(6): Show |
9 | HG01106.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-6832_-51-6831d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTTT | 39 | a0001c0001t0003g0204 a0001c0001t0003g0206 a0001c0001t0003g0268 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.-51-6833_-51-6831d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTTTT | 45 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 others(42): Show |
45 | HG00323.hp2 HG01106.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.-51-6834_-51-6831d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTTTTT | 45 | a0001c0001t0002g0171 a0001c0001t0002g0193 a0001c0001t0002g0198 others(42): Show |
45 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-51-6835_-51-6831d others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTTTTTT | 19 | a0001c0001t0002g0172 a0001c0001t0002g0235 a0001c0001t0002g0239 others(16): Show |
19 | HG00423.hp2 HG00621.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51-6836_-51-6831d others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTTTTTTT | 9 | a0001c0001t0002g0001 a0001c0001t0002g0249 a0001c0001t0002g0259 others(6): Show |
9 | HG00735.hp1 HG01515.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-6837_-51-6831d others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0040g0169 a0005c0006t0008g0178 a0005c0006t0008g0179 |
3 | HG00099.hp1 HG01255.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-51-6841_-51-6831d others(13): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175523 | CT | C | 84 | a0001c0001t0025g0065 a0001c0001t0025g0131 a0001c0001t0062g0102 others(81): Show |
84 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-51-6831delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175523 | ||||||
chr18:9175541 | T | TC | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-6841_-51-6840i others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175541 | |||||||
chr18:9175565 | T | C | 1 | a0006c0005t0014g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-51-6817T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175565 | |||||||
chr18:9175568 | T | C | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-6814T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175568 | |||||||
chr18:9175939 | C | A | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-6443C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9175939 | |||||||
chr18:9175940 | C | CA | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-6434dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9175940 | ||||||
chr18:9176049 | A | G | 140 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-51-6333A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176049 | |||||||
chr18:9176118 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-6264C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176118 | |||||||
chr18:9176232 | G | T | 3 | a0002c0002t0006g0050 a0002c0002t0006g0051 a0002c0002t0006g0062 |
3 | HG00733.hp2 HG02004.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-51-6150G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176232 | |||||||
chr18:9176274 | C | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-51-6108C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176274 | |||||||
chr18:9176524 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-5858C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9176524 | |||||||
chr18:9177129 | GC | G | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-5250delC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9177129 | ||||||
chr18:9177299 | C | T | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-5083C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177299 | |||||||
chr18:9177316 | C | T | 2 | a0002c0002t0001g0110 a0003c0003t0001g0066 |
2 | HG01361.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-51-5066C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177316 | |||||||
chr18:9177343 | T | C | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-5039T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177343 | |||||||
chr18:9177379 | T | C | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | NA18941.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-51-5003T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177379 | |||||||
chr18:9177433 | A | ATT | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-51-4948_-51-4947d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9177433 | ||||||
chr18:9177437 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-4945A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177437 | |||||||
chr18:9177571 | G | C | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-4811G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177571 | |||||||
chr18:9177870 | T | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-4512T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177870 | |||||||
chr18:9177896 | T | C | 58 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.-51-4486T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177896 | |||||||
chr18:9177966 | AAG | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-4413_-51-4412d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9177966 | ||||||
chr18:9177974 | T | C | 84 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(81): Show |
84 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.-51-4408T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9177974 | |||||||
chr18:9178073 | CT | C | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-4305delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178073 | ||||||
chr18:9178075 | T | C | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-4307T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178075 | |||||||
chr18:9178188 | A | G | 1 | a0004c0004t0016g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-51-4194A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178188 | |||||||
chr18:9178308 | G | A | 68 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(65): Show |
68 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.-51-4074G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178308 | |||||||
chr18:9178321 | T | TTC | 46 | a0001c0001t0062g0102 a0002c0002t0001g0137 a0003c0003t0001g0014 others(43): Show |
46 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-51-4040_-51-4039d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178321 | ||||||
chr18:9178321 | T | TTCTCTCT others(3): Show |
9 | a0004c0004t0013g0311 a0004c0004t0013g0312 a0004c0004t0013g0313 others(6): Show |
9 | HG00140.hp1 HG01952.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-4052_-51-4051i others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178321 | ||||||
chr18:9178321 | TTC | T | 6 | a0001c0001t0003g0199 a0001c0001t0005g0208 a0001c0001t0005g0225 others(3): Show |
6 | HG02523.hp2 NA18953.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-4040_-51-4039d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178321 | ||||||
chr18:9178325 | C | CTCTCTCT others(3): Show |
26 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(23): Show |
26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-4048_-51-4047i others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr18 | 9178325 | ||||||
chr18:9178343 | C | CTCTCTCT others(7): Show |
5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-4039_-51-4038i others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178343 | |||||||
chr18:9178343 | C | CTT | 162 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-51-4039_-51-4038i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178343 | |||||||
chr18:9178343 | C | T | 41 | a0001c0001t0003g0199 a0001c0001t0005g0208 a0001c0001t0005g0225 others(38): Show |
41 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.-51-4039C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178343 | |||||||
chr18:9178360 | T | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-4022T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178360 | |||||||
chr18:9178454 | G | A | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51-3928G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178454 | |||||||
chr18:9178485 | G | A | 1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-51-3897G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178485 | |||||||
chr18:9178503 | A | G | 4 | a0001c0001t0002g0001 a0001c0001t0040g0169 a0001c0001t0053g0001 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-3879A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178503 | |||||||
chr18:9178624 | A | G | 1 | a0015c0020t0002g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-51-3758A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9178624 | |||||||
chr18:9179034 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-3348C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179034 | |||||||
chr18:9179130 | A | G | 4 | a0002c0002t0006g0039 a0002c0002t0006g0050 a0002c0002t0006g0051 others(1): Show |
4 | HG00733.hp2 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-3252A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179130 | |||||||
chr18:9179151 | A | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-3231A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179151 | |||||||
chr18:9179244 | T | C | 1 | a0001c0001t0007g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-51-3138T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179244 | |||||||
chr18:9179249 | T | C | 126 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-51-3133T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179249 | |||||||
chr18:9179349 | T | C | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-3033T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179349 | |||||||
chr18:9179473 | A | G | 5 | a0002c0002t0006g0053 a0002c0002t0006g0055 a0002c0002t0017g0056 others(2): Show |
5 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-2909A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179473 | |||||||
chr18:9179540 | G | C | 1 | a0001c0001t0062g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51-2842G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179540 | |||||||
chr18:9179635 | C | G | 4 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-2747C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179635 | |||||||
chr18:9179848 | A | G | 1 | a0006c0005t0014g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-51-2534A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179848 | |||||||
chr18:9179917 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-2465G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179917 | |||||||
chr18:9179929 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-2453C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9179929 | |||||||
chr18:9180067 | A | G | 1 | a0001c0001t0003g0274 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-51-2315A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180067 | |||||||
chr18:9180078 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-51-2304T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180078 | |||||||
chr18:9180099 | T | G | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-2283T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180099 | |||||||
chr18:9180108 | C | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-51-2274C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180108 | |||||||
chr18:9180156 | T | C | 1 | a0003c0003t0001g0091 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-51-2226T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180156 | |||||||
chr18:9180217 | C | T | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-2165C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180217 | |||||||
chr18:9180258 | T | C | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-51-2124T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180258 | |||||||
chr18:9180446 | T | C | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-1936T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180446 | |||||||
chr18:9180462 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-1920G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180462 | |||||||
chr18:9180467 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-1915A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9180467 | |||||||
chr18:9181119 | A | G | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-1263A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181119 | |||||||
chr18:9181329 | G | A | 3 | a0004c0004t0004g0287 a0004c0004t0004g0294 a0004c0004t0004g0295 |
3 | NA18960.hp1 NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-51-1053G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181329 | |||||||
chr18:9181548 | G | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-51-834G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181548 | |||||||
chr18:9181713 | G | C | 1 | a0001c0001t0018g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-51-669G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181713 | |||||||
chr18:9181716 | A | G | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-666A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181716 | |||||||
chr18:9181802 | A | G | 1 | a0003c0003t0001g0121 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-51-580A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181802 | |||||||
chr18:9181818 | A | C | 45 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(42): Show |
45 | HG00140.hp1 HG00639.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.-51-564A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181818 | |||||||
chr18:9181965 | T | C | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-51-417T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181965 | |||||||
chr18:9181976 | G | A | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-406G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9181976 | |||||||
chr18:9182178 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-204C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182178 | |||||||
chr18:9182193 | T | A | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-51-189T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182193 | |||||||
chr18:9182318 | T | G | 1 | a0009c0021t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-51-64T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182318 | |||||||
chr18:9182330 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51-52G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182330 | |||||||
chr18:9182333 | A | AACTTCAG others(6): Show |
210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-51-49_-51-48insAC others(11): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182333 | |||||||
chr18:9182334 | C | T | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-51-48C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182334 | |||||||
chr18:9182364 | T | C | 5 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 others(2): Show |
5 | HG01106.hp2 HG01167.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-18T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 1/12 | chr18 | 9182364 | |||||||
chr18:9182647 | C | T | 3 | a0001c0001t0005g0222 a0001c0001t0005g0228 a0001c0001t0046g0232 |
3 | HG03017.hp1 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.87+128C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9182647 | |||||||
chr18:9182998 | C | T | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.87+479C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9182998 | |||||||
chr18:9183047 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.87+528G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183047 | |||||||
chr18:9183110 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+591A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183110 | |||||||
chr18:9183262 | G | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+743G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183262 | |||||||
chr18:9183561 | T | G | 1 | a0001c0001t0020g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.87+1042T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183561 | |||||||
chr18:9183673 | ACTT | A | 47 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(44): Show |
47 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.87+1158_87+1160del others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9183673 | ||||||
chr18:9183689 | G | A | 11 | a0001c0001t0025g0065 a0001c0001t0025g0131 a0002c0002t0001g0124 others(8): Show |
11 | HG00423.hp1 HG01123.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+1170G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183689 | |||||||
chr18:9183744 | A | G | 63 | a0001c0001t0002g0198 a0001c0001t0003g0064 a0001c0001t0003g0067 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.87+1225A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183744 | |||||||
chr18:9183921 | G | A | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+1402G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9183921 | |||||||
chr18:9184135 | T | C | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.87+1616T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184135 | |||||||
chr18:9184214 | T | G | 1 | a0004c0004t0013g0312 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.87+1695T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184214 | |||||||
chr18:9184392 | A | AT | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.87+1882dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9184392 | ||||||
chr18:9184467 | A | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+1948A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184467 | |||||||
chr18:9184497 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.87+1978A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184497 | |||||||
chr18:9184611 | G | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.87+2092G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184611 | |||||||
chr18:9184672 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.87+2153G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184672 | |||||||
chr18:9184704 | A | C | 1 | a0001c0007t0026g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.87+2185A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184704 | |||||||
chr18:9184714 | C | T | 2 | a0001c0001t0007g0212 a0001c0001t0007g0213 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.87+2195C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184714 | |||||||
chr18:9184861 | T | C | 1 | a0001c0001t0020g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.87+2342T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184861 | |||||||
chr18:9184875 | C | T | 2 | a0001c0001t0005g0017 a0001c0001t0005g0262 |
2 | NA19058.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.87+2356C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184875 | |||||||
chr18:9184902 | C | T | 1 | a0003c0003t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.87+2383C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9184902 | |||||||
chr18:9185069 | A | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+2550A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185069 | |||||||
chr18:9185131 | C | G | 211 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.87+2612C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185131 | |||||||
chr18:9185304 | A | C | 1 | a0003c0003t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.87+2785A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185304 | |||||||
chr18:9185313 | A | G | 1 | a0005c0006t0008g0202 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.87+2794A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185313 | |||||||
chr18:9185478 | A | G | 1 | a0001c0001t0028g0243 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.87+2959A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185478 | |||||||
chr18:9185511 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.87+2992T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185511 | |||||||
chr18:9185740 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+3221A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185740 | |||||||
chr18:9185849 | A | G | 3 | a0001c0007t0026g0025 a0002c0002t0042g0040 a0012c0023t0034g0061 |
3 | HG02109.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.87+3330A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185849 | |||||||
chr18:9185986 | A | G | 1 | a0004c0004t0036g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.87+3467A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9185986 | |||||||
chr18:9186006 | G | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.87+3487G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186006 | |||||||
chr18:9186009 | A | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.87+3490A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186009 | |||||||
chr18:9186079 | T | C | 1 | a0002c0002t0064g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+3560T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186079 | |||||||
chr18:9186094 | C | T | 2 | a0001c0001t0003g0199 a0001c0001t0011g0264 |
2 | NA18953.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.87+3575C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186094 | |||||||
chr18:9186137 | A | AT | 37 | a0001c0001t0011g0201 a0001c0001t0015g0029 a0001c0001t0018g0183 others(34): Show |
37 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.87+3639dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186137 | ||||||
chr18:9186137 | AT | A | 14 | a0001c0001t0002g0250 a0001c0001t0003g0064 a0001c0001t0007g0212 others(11): Show |
14 | HG01069.hp1 HG01167.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.87+3639delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186137 | ||||||
chr18:9186204 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+3685G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186204 | |||||||
chr18:9186237 | A | G | 1 | a0003c0003t0001g0138 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.87+3718A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186237 | |||||||
chr18:9186486 | G | A | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.87+3967G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186486 | |||||||
chr18:9186545 | T | G | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.87+4026T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186545 | |||||||
chr18:9186686 | G | T | 22 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(19): Show |
22 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.87+4167G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186686 | |||||||
chr18:9186750 | C | CT | 26 | a0001c0001t0002g0263 a0001c0001t0005g0200 a0001c0001t0008g0255 others(23): Show |
26 | HG00609.hp1 HG00735.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.87+4251dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186750 | ||||||
chr18:9186750 | CT | C | 47 | a0001c0001t0005g0225 a0001c0001t0007g0212 a0002c0002t0001g0127 others(44): Show |
47 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.87+4251delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186750 | ||||||
chr18:9186791 | C | G | 211 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.87+4272C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186791 | |||||||
chr18:9186795 | G | A | 211 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.87+4276G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186795 | |||||||
chr18:9186799 | C | T | 35 | a0001c0001t0005g0225 a0004c0004t0004g0281 a0004c0004t0004g0283 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.87+4280C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186799 | |||||||
chr18:9186821 | A | G | 41 | a0001c0001t0005g0225 a0004c0004t0004g0281 a0004c0004t0004g0283 others(38): Show |
41 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.87+4302A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186821 | |||||||
chr18:9186876 | C | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.87+4357C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186876 | |||||||
chr18:9186901 | G | A | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.87+4382G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186901 | |||||||
chr18:9186952 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.87+4433C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9186952 | |||||||
chr18:9186973 | GAATGGTC others(3): Show |
G | 1 | a0003c0003t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.87+4456_87+4465del others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9186973 | ||||||
chr18:9187056 | T | C | 1 | a0003c0003t0021g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.87+4537T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187056 | |||||||
chr18:9187169 | A | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.87+4650A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187169 | |||||||
chr18:9187506 | A | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+4987A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187506 | |||||||
chr18:9187600 | A | G | 1 | a0001c0001t0019g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.87+5081A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187600 | |||||||
chr18:9187612 | T | C | 1 | a0001c0001t0045g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.87+5093T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187612 | |||||||
chr18:9187632 | G | A | 1 | a0004c0004t0004g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.87+5113G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187632 | |||||||
chr18:9187730 | G | T | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.87+5211G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187730 | |||||||
chr18:9187741 | G | C | 1 | a0003c0003t0001g0073 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.87+5222G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187741 | |||||||
chr18:9187793 | A | G | 1 | a0003c0003t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.87+5274A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187793 | |||||||
chr18:9187874 | C | T | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.87+5355C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187874 | |||||||
chr18:9187875 | G | A | 2 | a0005c0006t0008g0178 a0005c0006t0008g0179 |
2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.87+5356G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187875 | |||||||
chr18:9187922 | T | C | 1 | a0002c0002t0064g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+5403T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187922 | |||||||
chr18:9187991 | A | G | 8 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(5): Show |
8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+5472A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9187991 | |||||||
chr18:9188136 | A | C | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0013t0066g0162 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.87+5617A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188136 | |||||||
chr18:9188177 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.87+5658G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188177 | |||||||
chr18:9188190 | C | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+5671C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188190 | |||||||
chr18:9188229 | A | G | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.87+5710A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188229 | |||||||
chr18:9188365 | G | C | 4 | a0002c0002t0001g0123 a0002c0002t0001g0133 a0002c0002t0057g0129 others(1): Show |
4 | NA18983.hp1 NA19006.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+5846G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188365 | |||||||
chr18:9188369 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.87+5850G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188369 | |||||||
chr18:9188425 | T | A | 6 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0002g0236 others(3): Show |
6 | HG00609.hp2 HG02080.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+5906T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188425 | |||||||
chr18:9188432 | C | T | 1 | a0001c0001t0028g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.87+5913C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188432 | |||||||
chr18:9188856 | T | C | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.87+6337T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188856 | |||||||
chr18:9188870 | G | T | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.87+6351G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188870 | |||||||
chr18:9188929 | TG | T | 11 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 others(8): Show |
11 | HG02055.hp1 HG02647.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+6412delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9188929 | ||||||
chr18:9188947 | G | C | 4 | a0002c0002t0010g0086 a0002c0002t0010g0163 a0002c0002t0010g0164 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+6428G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9188947 | |||||||
chr18:9189013 | A | G | 4 | a0001c0001t0020g0002 a0001c0001t0020g0005 a0001c0001t0052g0003 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+6494A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189013 | |||||||
chr18:9189252 | A | G | 21 | a0002c0002t0006g0039 a0002c0002t0006g0041 a0002c0002t0006g0042 others(18): Show |
21 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.88-6299A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189252 | |||||||
chr18:9189308 | A | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.88-6243A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189308 | |||||||
chr18:9189486 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88-6065T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9189486 | |||||||
chr18:9190187 | G | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.88-5364G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190187 | |||||||
chr18:9190421 | G | T | 214 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.88-5130G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190421 | |||||||
chr18:9190470 | C | A | 8 | a0003c0003t0001g0087 a0003c0003t0001g0091 a0003c0003t0001g0092 others(5): Show |
8 | NA18939.hp2 NA18967.hp2 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-5081C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190470 | |||||||
chr18:9190595 | A | G | 28 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(25): Show |
28 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.88-4956A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190595 | |||||||
chr18:9190644 | A | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.88-4907A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190644 | |||||||
chr18:9190653 | T | A | 2 | a0002c0002t0001g0127 a0002c0002t0009g0126 |
2 | HG03942.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.88-4898T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190653 | |||||||
chr18:9190927 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-4624T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190927 | |||||||
chr18:9190930 | G | A | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88-4621G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9190930 | |||||||
chr18:9191023 | C | T | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.88-4528C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9191023 | |||||||
chr18:9191422 | A | G | 125 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.88-4129A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9191422 | |||||||
chr18:9191493 | T | G | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.88-4058T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9191493 | |||||||
chr18:9192130 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.88-3421C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192130 | |||||||
chr18:9192310 | A | G | 170 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.88-3241A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192310 | |||||||
chr18:9192397 | G | A | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.88-3154G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192397 | |||||||
chr18:9192419 | G | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.88-3132G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192419 | |||||||
chr18:9192649 | T | C | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88-2902T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192649 | |||||||
chr18:9192672 | C | T | 1 | a0001c0001t0008g0255 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.88-2879C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192672 | |||||||
chr18:9192705 | C | G | 11 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0203 others(8): Show |
11 | HG02015.hp2 HG02129.hp1 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-2846C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192705 | |||||||
chr18:9192709 | C | CT | 140 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.88-2833dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9192709 | ||||||
chr18:9192722 | G | A | 1 | a0001c0001t0007g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.88-2829G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192722 | |||||||
chr18:9192809 | G | A | 1 | a0004c0004t0004g0301 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.88-2742G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192809 | |||||||
chr18:9192812 | G | A | 5 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-2739G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192812 | |||||||
chr18:9192931 | G | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.88-2620G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9192931 | |||||||
chr18:9193094 | A | G | 1 | a0003c0003t0009g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.88-2457A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193094 | |||||||
chr18:9193135 | A | AT | 48 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 others(45): Show |
48 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.88-2397dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9193135 | ||||||
chr18:9193135 | AT | A | 7 | a0001c0001t0003g0064 a0001c0009t0032g0019 a0001c0009t0032g0020 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-2397delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9193135 | ||||||
chr18:9193173 | T | A | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.88-2378T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193173 | |||||||
chr18:9193265 | A | G | 6 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0249 others(3): Show |
6 | HG01168.hp2 HG01361.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.88-2286A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193265 | |||||||
chr18:9193516 | T | G | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-2035T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193516 | |||||||
chr18:9193525 | T | G | 4 | a0001c0001t0002g0001 a0001c0001t0040g0169 a0001c0001t0053g0001 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-2026T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193525 | |||||||
chr18:9193529 | G | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-2022G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193529 | |||||||
chr18:9193569 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-1982C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193569 | |||||||
chr18:9193640 | C | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88-1911C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193640 | |||||||
chr18:9193729 | A | G | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.88-1822A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193729 | |||||||
chr18:9193909 | A | G | 1 | a0004c0004t0004g0285 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.88-1642A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9193909 | |||||||
chr18:9194107 | A | G | 2 | a0004c0004t0004g0283 a0004c0004t0004g0284 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.88-1444A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194107 | |||||||
chr18:9194172 | G | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.88-1379G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194172 | |||||||
chr18:9194216 | C | A | 142 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.88-1335C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194216 | |||||||
chr18:9194327 | T | TTTTA | 71 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(68): Show |
71 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.88-1181_88-1178dup others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | ||||||
chr18:9194327 | T | TTTTATTT others(1): Show |
11 | a0002c0002t0001g0013 a0002c0002t0001g0124 a0002c0002t0001g0125 others(8): Show |
11 | HG00621.hp1 HG02886.hp1 NA18906.hp2 others(8): Show |
intron_variant | MODIFIER | c.88-1185_88-1178dup others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | ||||||
chr18:9194327 | TTTTA | T | 39 | a0001c0001t0002g0001 a0001c0001t0002g0254 a0001c0001t0003g0215 others(36): Show |
39 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(36): Show |
intron_variant | MODIFIER | c.88-1181_88-1178del others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | ||||||
chr18:9194327 | TTTTATTT others(1): Show |
T | 137 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0171 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.88-1185_88-1178del others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | ||||||
chr18:9194327 | TTTTATTT others(13): Show |
T | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.88-1197_88-1178del others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | ||||||
chr18:9194327 | TTTTATTT others(17): Show |
T | 6 | a0001c0001t0015g0015 a0006c0005t0014g0006 a0006c0005t0014g0007 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.88-1201_88-1178del others(24): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr18 | 9194327 | ||||||
chr18:9194433 | T | C | 1 | a0001c0001t0027g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.88-1118T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194433 | |||||||
chr18:9194734 | C | T | 2 | a0001c0001t0003g0199 a0001c0001t0011g0264 |
2 | NA18953.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.88-817C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194734 | |||||||
chr18:9194749 | T | C | 6 | a0001c0001t0015g0015 a0006c0005t0014g0006 a0006c0005t0014g0007 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.88-802T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194749 | |||||||
chr18:9194778 | A | G | 2 | a0005c0006t0008g0178 a0005c0006t0008g0179 |
2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.88-773A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194778 | |||||||
chr18:9194854 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-697A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9194854 | |||||||
chr18:9195165 | C | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.88-386C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195165 | |||||||
chr18:9195183 | G | C | 65 | a0001c0001t0002g0198 a0001c0001t0003g0064 a0001c0001t0003g0067 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.88-368G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195183 | |||||||
chr18:9195368 | A | G | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-183A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195368 | |||||||
chr18:9195534 | A | G | 2 | a0001c0001t0033g0030 a0001c0001t0033g0031 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88-17A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 2/12 | chr18 | 9195534 | |||||||
chr18:9196108 | A | AAC | 9 | a0002c0002t0001g0096 a0002c0002t0001g0100 a0002c0002t0001g0137 others(6): Show |
9 | HG01099.hp2 HG02148.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+452_235+453dup others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | ||||||
chr18:9196108 | A | AACAC | 10 | a0001c0001t0005g0032 a0001c0001t0005g0034 a0001c0001t0005g0035 others(7): Show |
10 | HG01106.hp2 HG01243.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+450_235+453dup others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | ||||||
chr18:9196108 | AAC | A | 17 | a0002c0002t0001g0124 a0002c0002t0001g0125 a0002c0002t0001g0127 others(14): Show |
17 | HG01361.hp1 HG01433.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+452_235+453del others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | ||||||
chr18:9196108 | AACAC | A | 12 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(9): Show |
12 | HG02071.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+450_235+453del others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | ||||||
chr18:9196108 | AACACACA others(3): Show |
A | 1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+444_235+453del others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | ||||||
chr18:9196108 | AACACACA others(11): Show |
A | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235+436_235+453del others(18): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196108 | ||||||
chr18:9196110 | C | CACACACA others(60): Show |
2 | a0004c0004t0004g0287 a0004c0028t0004g0282 |
2 | NA18960.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.235+441_235+442ins others(67): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196110 | ||||||
chr18:9196112 | C | CACACACA others(58): Show |
4 | a0004c0004t0004g0285 a0004c0004t0004g0292 a0004c0004t0004g0300 others(1): Show |
4 | NA18955.hp2 NA18973.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196112 | ||||||
chr18:9196114 | C | CACACACA others(58): Show |
2 | a0004c0004t0004g0286 a0004c0004t0013g0312 |
2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.235+443_235+444ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196114 | ||||||
chr18:9196114 | C | CACACACA others(56): Show |
7 | a0004c0004t0004g0288 a0004c0004t0004g0296 a0004c0004t0004g0297 others(4): Show |
7 | HG02132.hp2 HG03209.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(63): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196114 | ||||||
chr18:9196116 | C | CACACACA others(56): Show |
2 | a0004c0004t0016g0291 a0004c0004t0022g0272 |
2 | HG03654.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.235+443_235+444ins others(63): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196116 | ||||||
chr18:9196116 | C | CACACACA others(54): Show |
18 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(15): Show |
18 | HG00140.hp1 HG00639.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196116 | ||||||
chr18:9196118 | C | CACACACA others(54): Show |
2 | a0001c0001t0033g0031 a0013c0026t0038g0016 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.235+443_235+444ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196118 | ||||||
chr18:9196120 | C | CACACACA others(58): Show |
1 | a0009c0021t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235+449_235+450ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | ||||||
chr18:9196120 | C | CACACACA others(54): Show |
4 | a0001c0001t0015g0015 a0001c0007t0026g0025 a0001c0007t0026g0026 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+445_235+446ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | ||||||
chr18:9196120 | C | CACACACA others(52): Show |
8 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 others(5): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+443_235+444ins others(59): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | ||||||
chr18:9196120 | C | CACACACA others(50): Show |
5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+441_235+442ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | ||||||
chr18:9196120 | C | CACACACA others(48): Show |
2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.235+439_235+440ins others(55): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196120 | ||||||
chr18:9196122 | C | CACACACA others(58): Show |
1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.235+451_235+452ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196122 | C | CACACACA others(56): Show |
4 | a0001c0001t0002g0271 a0002c0002t0006g0041 a0002c0002t0024g0043 others(1): Show |
4 | HG02717.hp2 HG02738.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+449_235+450ins others(63): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196122 | C | CACACACA others(54): Show |
19 | a0001c0001t0003g0268 a0001c0001t0005g0217 a0002c0002t0006g0037 others(16): Show |
19 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.235+447_235+448ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196122 | C | CACACACA others(52): Show |
4 | a0001c0001t0003g0064 a0001c0001t0003g0203 a0001c0001t0049g0230 others(1): Show |
4 | HG03239.hp1 HG04199.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+445_235+446ins others(59): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196122 | C | CACACACA others(50): Show |
1 | a0001c0001t0003g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.235+443_235+444ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196122 | C | CACACACA others(44): Show |
2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235+437_235+438ins others(51): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196122 | C | CACACACA others(40): Show |
1 | a0002c0002t0023g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.235+434_235+435ins others(47): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196122 | ||||||
chr18:9196124 | C | CACACACA others(54): Show |
1 | a0001c0012t0002g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.235+449_235+450ins others(61): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | ||||||
chr18:9196124 | C | CACACACA others(52): Show |
18 | a0001c0001t0002g0241 a0001c0001t0002g0245 a0001c0001t0002g0246 others(15): Show |
18 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+447_235+448ins others(59): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | ||||||
chr18:9196124 | C | CACACACA others(50): Show |
88 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.235+445_235+446ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | ||||||
chr18:9196124 | C | CACACACA others(42): Show |
1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235+437_235+438ins others(49): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196124 | ||||||
chr18:9196126 | C | CACACACA others(50): Show |
1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.235+447_235+448ins others(57): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196126 | ||||||
chr18:9196126 | C | CACACACA others(48): Show |
1 | a0001c0001t0003g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.235+445_235+446ins others(55): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196126 | ||||||
chr18:9196189 | T | TAC | 36 | a0001c0001t0002g0275 a0001c0001t0005g0032 a0001c0001t0005g0033 others(33): Show |
36 | HG00639.hp1 HG00733.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.235+524_235+525dup others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACAC | 12 | a0001c0001t0002g0241 a0001c0001t0003g0195 a0001c0001t0005g0167 others(9): Show |
12 | HG00140.hp1 HG00621.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+522_235+525dup others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACAC | 89 | a0001c0001t0002g0193 a0001c0001t0002g0233 a0001c0001t0002g0235 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.235+520_235+525dup others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(1): Show |
29 | a0001c0001t0002g0279 a0001c0001t0003g0064 a0001c0001t0003g0067 others(26): Show |
29 | HG00140.hp2 HG00639.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.235+518_235+525dup others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(3): Show |
18 | a0001c0001t0002g0198 a0001c0001t0002g0271 a0001c0001t0015g0021 others(15): Show |
18 | HG01081.hp2 HG01255.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+516_235+525dup others(10): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(5): Show |
8 | a0001c0001t0010g0024 a0001c0001t0029g0248 a0001c0001t0070g0004 others(5): Show |
8 | HG00733.hp2 HG01243.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+514_235+525dup others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(7): Show |
6 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0002c0002t0006g0052 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+512_235+525dup others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(9): Show |
1 | a0002c0002t0023g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.235+510_235+525dup others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(70): Show |
1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+525_235+526ins others(77): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(78): Show |
1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.235+522_235+523ins others(85): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(64): Show |
4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 others(1): Show |
4 | HG02109.hp2 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+518_235+519ins others(71): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(66): Show |
3 | a0001c0001t0002g0001 a0001c0001t0040g0169 a0001c0001t0053g0001 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.235+518_235+519ins others(73): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(74): Show |
1 | a0002c0002t0006g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235+518_235+519ins others(81): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(66): Show |
1 | a0001c0001t0003g0204 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.235+516_235+517ins others(73): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | T | TACACACA others(72): Show |
1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235+514_235+515ins others(79): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | TAC | T | 76 | a0001c0001t0062g0102 a0002c0002t0001g0013 a0002c0002t0001g0094 others(73): Show |
76 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.235+524_235+525del others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196189 | TACACAC | T | 6 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0249 others(3): Show |
6 | HG01168.hp2 HG01361.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+520_235+525del others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196189 | ||||||
chr18:9196193 | C | CACACACA others(58): Show |
1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.235+522_235+523ins others(65): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9196193 | ||||||
chr18:9196222 | A | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 others(1): Show |
4 | HG02109.hp2 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+524A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196222 | |||||||
chr18:9196326 | C | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.235+628C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196326 | |||||||
chr18:9196530 | T | C | 170 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.235+832T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196530 | |||||||
chr18:9196606 | T | A | 1 | a0003c0003t0001g0088 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.235+908T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196606 | |||||||
chr18:9196652 | T | G | 63 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.235+954T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196652 | |||||||
chr18:9196773 | C | T | 1 | a0001c0001t0005g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.235+1075C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196773 | |||||||
chr18:9196786 | C | T | 1 | a0002c0002t0064g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235+1088C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196786 | |||||||
chr18:9196873 | T | C | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.235+1175T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196873 | |||||||
chr18:9196900 | G | A | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.235+1202G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196900 | |||||||
chr18:9196957 | C | T | 2 | a0001c0001t0007g0223 a0001c0001t0044g0207 |
2 | HG00099.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.235+1259C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9196957 | |||||||
chr18:9197004 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.235+1306C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197004 | |||||||
chr18:9197069 | A | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.235+1371A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197069 | |||||||
chr18:9197176 | T | A | 1 | a0002c0002t0012g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.235+1478T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197176 | |||||||
chr18:9197214 | A | G | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.235+1516A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197214 | |||||||
chr18:9197220 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+1522G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197220 | |||||||
chr18:9197295 | C | T | 1 | a0002c0002t0006g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.235+1597C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197295 | |||||||
chr18:9197306 | T | C | 1 | a0003c0003t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.235+1608T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197306 | |||||||
chr18:9197374 | A | G | 63 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.235+1676A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197374 | |||||||
chr18:9197460 | T | C | 1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+1762T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197460 | |||||||
chr18:9197515 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0007g0192 |
2 | HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.235+1817C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197515 | |||||||
chr18:9197528 | T | G | 217 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.235+1830T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197528 | |||||||
chr18:9197553 | TAAAC | T | 58 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.235+1857_235+1860d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9197553 | ||||||
chr18:9197723 | T | C | 1 | a0003c0003t0021g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.235+2025T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197723 | |||||||
chr18:9197817 | G | T | 2 | a0001c0001t0002g0275 a0001c0001t0028g0276 |
2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.235+2119G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9197817 | |||||||
chr18:9198042 | T | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+2344T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198042 | |||||||
chr18:9198355 | C | CA | 63 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.235+2659dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9198355 | ||||||
chr18:9198406 | C | A | 46 | a0001c0001t0062g0102 a0003c0003t0001g0014 a0003c0003t0001g0066 others(43): Show |
46 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.235+2708C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198406 | |||||||
chr18:9198544 | A | G | 4 | a0002c0002t0001g0013 a0002c0002t0001g0157 a0002c0002t0001g0158 others(1): Show |
4 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+2846A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198544 | |||||||
chr18:9198549 | AATG | A | 6 | a0002c0002t0006g0053 a0002c0002t0006g0054 a0002c0002t0006g0055 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+2854_235+2856d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9198549 | ||||||
chr18:9198625 | C | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+2927C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198625 | |||||||
chr18:9198684 | G | A | 1 | a0001c0010t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235+2986G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198684 | |||||||
chr18:9198697 | C | T | 1 | a0003c0003t0021g0010 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.235+2999C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198697 | |||||||
chr18:9198774 | G | A | 1 | a0001c0001t0033g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.235+3076G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198774 | |||||||
chr18:9198950 | G | A | 5 | a0001c0001t0002g0198 a0001c0001t0007g0196 a0001c0001t0007g0209 others(2): Show |
5 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+3252G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9198950 | |||||||
chr18:9199117 | A | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+3419A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199117 | |||||||
chr18:9199319 | T | G | 1 | a0001c0001t0003g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.235+3621T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199319 | |||||||
chr18:9199388 | T | C | 5 | a0004c0004t0013g0311 a0004c0004t0013g0312 a0004c0004t0013g0313 others(2): Show |
5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+3690T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199388 | |||||||
chr18:9199419 | T | C | 1 | a0001c0001t0044g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.235+3721T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199419 | |||||||
chr18:9199831 | G | T | 1 | a0001c0001t0028g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.235+4133G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9199831 | |||||||
chr18:9200097 | T | A | 4 | a0004c0004t0013g0311 a0004c0004t0013g0313 a0004c0004t0013g0314 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-4379T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200097 | |||||||
chr18:9200103 | G | A | 1 | a0002c0002t0023g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236-4373G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200103 | |||||||
chr18:9200114 | G | A | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.236-4362G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200114 | |||||||
chr18:9200296 | G | C | 1 | a0001c0001t0007g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.236-4180G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200296 | |||||||
chr18:9200594 | G | T | 1 | a0001c0001t0007g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.236-3882G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200594 | |||||||
chr18:9200611 | C | T | 140 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.236-3865C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200611 | |||||||
chr18:9200616 | G | A | 142 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.236-3860G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200616 | |||||||
chr18:9200812 | T | C | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.236-3664T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200812 | |||||||
chr18:9200840 | G | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.236-3636G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9200840 | |||||||
chr18:9201080 | G | A | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.236-3396G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201080 | |||||||
chr18:9201369 | A | G | 3 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 |
3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.236-3107A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201369 | |||||||
chr18:9201432 | T | C | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.236-3044T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201432 | |||||||
chr18:9201641 | T | C | 1 | a0002c0002t0030g0143 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.236-2835T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201641 | |||||||
chr18:9201658 | C | T | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.236-2818C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201658 | |||||||
chr18:9201809 | GT | G | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.236-2664delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9201809 | ||||||
chr18:9201827 | CT | C | 46 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(43): Show |
46 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.236-2636delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9201827 | ||||||
chr18:9201897 | G | A | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 |
3 | HG01891.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.236-2579G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201897 | |||||||
chr18:9201936 | T | C | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.236-2540T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9201936 | |||||||
chr18:9202101 | C | G | 5 | a0002c0002t0001g0116 a0002c0002t0001g0117 a0002c0002t0001g0148 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-2375C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202101 | |||||||
chr18:9202216 | A | C | 2 | a0001c0001t0002g0242 a0001c0001t0002g0246 |
2 | NA18990.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.236-2260A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202216 | |||||||
chr18:9202289 | A | G | 1 | a0001c0001t0056g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.236-2187A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202289 | |||||||
chr18:9202470 | A | T | 142 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.236-2006A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202470 | |||||||
chr18:9202499 | A | G | 142 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.236-1977A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202499 | |||||||
chr18:9202571 | A | T | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.236-1905A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202571 | |||||||
chr18:9202573 | C | T | 1 | a0003c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.236-1903C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202573 | |||||||
chr18:9202632 | C | T | 1 | a0003c0003t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.236-1844C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202632 | |||||||
chr18:9202657 | G | A | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.236-1819G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202657 | |||||||
chr18:9202730 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.236-1746G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202730 | |||||||
chr18:9202857 | A | G | 166 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.236-1619A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202857 | |||||||
chr18:9202935 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.236-1541G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9202935 | |||||||
chr18:9203124 | T | G | 3 | a0002c0002t0001g0070 a0002c0002t0001g0080 a0008c0016t0001g0079 |
3 | HG01109.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.236-1352T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203124 | |||||||
chr18:9203168 | T | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.236-1308T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203168 | |||||||
chr18:9203218 | G | A | 1 | a0004c0004t0004g0303 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.236-1258G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203218 | |||||||
chr18:9203525 | A | G | 1 | a0004c0004t0016g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236-951A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203525 | |||||||
chr18:9203583 | A | ATG | 25 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(22): Show |
25 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.236-881_236-880dup others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr18 | 9203583 | ||||||
chr18:9203597 | A | G | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.236-879A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203597 | |||||||
chr18:9203615 | A | T | 2 | a0001c0001t0005g0220 a0002c0002t0042g0040 |
2 | HG02135.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.236-861A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203615 | |||||||
chr18:9203654 | G | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-822G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203654 | |||||||
chr18:9203708 | G | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.236-768G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203708 | |||||||
chr18:9203718 | C | A | 6 | a0003c0003t0001g0066 a0003c0003t0001g0073 a0003c0003t0001g0074 others(3): Show |
6 | HG01361.hp1 HG01433.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-758C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203718 | |||||||
chr18:9203730 | A | G | 1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.236-746A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203730 | |||||||
chr18:9203890 | C | T | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.236-586C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203890 | |||||||
chr18:9203964 | C | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.236-512C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9203964 | |||||||
chr18:9204150 | C | A | 2 | a0004c0004t0004g0290 a0004c0004t0004g0304 |
2 | NA18997.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.236-326C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9204150 | |||||||
chr18:9204230 | A | G | 9 | a0002c0002t0001g0124 a0002c0002t0001g0125 a0002c0002t0001g0127 others(6): Show |
9 | HG00423.hp1 HG02071.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-246A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 3/12 | chr18 | 9204230 | |||||||
chr18:9204725 | T | G | 1 | a0001c0001t0005g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.304+181T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204725 | |||||||
chr18:9204738 | A | C | 2 | a0002c0002t0001g0096 a0002c0002t0001g0100 |
2 | HG02148.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.304+194A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204738 | |||||||
chr18:9204763 | C | T | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.304+219C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204763 | |||||||
chr18:9204890 | T | G | 1 | a0004c0004t0036g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.304+346T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204890 | |||||||
chr18:9204976 | A | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+432A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9204976 | |||||||
chr18:9205102 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.304+558T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205102 | |||||||
chr18:9205186 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+642T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205186 | |||||||
chr18:9205259 | G | GT | 315 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.304+720dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr18 | 9205259 | ||||||
chr18:9205322 | AT | A | 125 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.304+787delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr18 | 9205322 | ||||||
chr18:9205347 | A | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.304+803A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205347 | |||||||
chr18:9205378 | T | C | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.304+834T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205378 | |||||||
chr18:9205665 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.304+1121A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205665 | |||||||
chr18:9205753 | T | TC | 3 | a0002c0008t0006g0048 a0002c0008t0006g0049 a0002c0015t0006g0047 |
3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.304+1210dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr18 | 9205753 | ||||||
chr18:9205779 | A | G | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.304+1235A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205779 | |||||||
chr18:9205827 | T | C | 2 | a0001c0001t0002g0001 a0001c0001t0053g0001 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.304+1283T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9205827 | |||||||
chr18:9206687 | G | A | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 others(2): Show |
5 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1970G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206687 | |||||||
chr18:9206741 | A | T | 1 | a0004c0004t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.305-1916A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206741 | |||||||
chr18:9206759 | T | C | 1 | a0001c0001t0002g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.305-1898T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206759 | |||||||
chr18:9206931 | C | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.305-1726C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9206931 | |||||||
chr18:9207168 | T | C | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.305-1489T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207168 | |||||||
chr18:9207329 | A | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.305-1328A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207329 | |||||||
chr18:9207425 | T | A | 1 | a0002c0002t0001g0100 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.305-1232T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207425 | |||||||
chr18:9207426 | G | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.305-1231G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207426 | |||||||
chr18:9207556 | T | C | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.305-1101T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207556 | |||||||
chr18:9207621 | T | G | 7 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.305-1036T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207621 | |||||||
chr18:9207741 | A | C | 1 | a0001c0001t0033g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.305-916A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9207741 | |||||||
chr18:9208046 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-611A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208046 | |||||||
chr18:9208210 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-447T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208210 | |||||||
chr18:9208235 | G | A | 1 | a0002c0002t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.305-422G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208235 | |||||||
chr18:9208548 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.305-109T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 4/12 | chr18 | 9208548 | |||||||
chr18:9208821 | T | C | 1 | a0002c0002t0006g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.451+18T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9208821 | |||||||
chr18:9208974 | A | G | 55 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.451+171A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9208974 | |||||||
chr18:9209155 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+352T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209155 | |||||||
chr18:9209162 | A | G | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+359A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209162 | |||||||
chr18:9209240 | G | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.451+437G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209240 | |||||||
chr18:9209456 | G | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.451+653G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209456 | |||||||
chr18:9209476 | G | A | 1 | a0004c0004t0022g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.451+673G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209476 | |||||||
chr18:9209535 | G | A | 2 | a0002c0002t0010g0163 a0002c0002t0010g0164 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.451+732G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209535 | |||||||
chr18:9209665 | A | G | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.451+862A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209665 | |||||||
chr18:9209835 | G | T | 8 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0285 others(5): Show |
8 | HG02015.hp1 HG02132.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+1032G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209835 | |||||||
chr18:9209927 | T | G | 5 | a0001c0001t0002g0275 a0001c0001t0005g0181 a0001c0001t0027g0252 others(2): Show |
5 | HG01081.hp1 HG02148.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1124T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9209927 | |||||||
chr18:9210065 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.451+1262T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210065 | |||||||
chr18:9210095 | A | G | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.451+1292A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210095 | |||||||
chr18:9210223 | A | T | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.452-1361A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210223 | |||||||
chr18:9210262 | C | T | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.452-1322C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210262 | |||||||
chr18:9210381 | G | T | 1 | a0003c0003t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.452-1203G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210381 | |||||||
chr18:9210525 | A | G | 2 | a0001c0001t0007g0212 a0001c0001t0007g0213 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.452-1059A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210525 | |||||||
chr18:9210539 | G | T | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-1045G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210539 | |||||||
chr18:9210550 | G | A | 2 | a0001c0001t0010g0022 a0001c0001t0010g0023 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.452-1034G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210550 | |||||||
chr18:9210594 | C | T | 3 | a0002c0002t0017g0056 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | HG01070.hp2 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.452-990C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210594 | |||||||
chr18:9210725 | C | CAAAAAAA others(4): Show |
2 | a0004c0004t0004g0288 a0004c0004t0013g0314 |
2 | HG02132.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.452-855_452-845dup others(11): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | ||||||
chr18:9210725 | C | CAAAAAAA others(5): Show |
31 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(28): Show |
31 | HG00140.hp1 HG00639.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.452-856_452-845dup others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | ||||||
chr18:9210725 | C | CAAAAAAA others(6): Show |
29 | a0001c0001t0005g0017 a0001c0001t0015g0028 a0002c0002t0006g0037 others(26): Show |
29 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.452-857_452-845dup others(13): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | ||||||
chr18:9210725 | C | CAAAAAAA others(7): Show |
92 | a0001c0001t0002g0001 a0001c0001t0002g0045 a0001c0001t0002g0171 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.452-858_452-845dup others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | ||||||
chr18:9210725 | C | CAAAAAAA others(8): Show |
53 | a0001c0001t0002g0044 a0001c0001t0002g0173 a0001c0001t0002g0241 others(50): Show |
53 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.452-845_452-844ins others(15): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | ||||||
chr18:9210725 | C | CAAAAAAA others(9): Show |
5 | a0001c0001t0005g0220 a0001c0001t0011g0226 a0001c0001t0011g0227 others(2): Show |
5 | HG02135.hp1 HG02809.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-845_452-844ins others(16): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9210725 | ||||||
chr18:9210746 | A | T | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-838A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210746 | |||||||
chr18:9210782 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-802G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9210782 | |||||||
chr18:9211015 | T | A | 142 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.452-569T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211015 | |||||||
chr18:9211088 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.452-496A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211088 | |||||||
chr18:9211157 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.452-427A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211157 | |||||||
chr18:9211271 | A | G | 165 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.452-313A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | chr18 | 9211271 | |||||||
chr18:9211368 | AT | A | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-208delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9211368 | ||||||
chr18:9211406 | A | AG | 17 | a0002c0002t0001g0013 a0002c0002t0001g0123 a0002c0002t0001g0124 others(14): Show |
17 | HG00423.hp1 HG02071.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-175dupG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr18 | 9211406 | ||||||
chr18:9211928 | G | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.652+144G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9211928 | |||||||
chr18:9211937 | A | G | 3 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 |
3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.652+153A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9211937 | |||||||
chr18:9212323 | T | C | 1 | a0002c0002t0006g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.652+539T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212323 | |||||||
chr18:9212477 | A | G | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.652+693A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212477 | |||||||
chr18:9212478 | TATATTCT others(2): Show |
T | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.652+695_652+703del others(9): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212478 | |||||||
chr18:9212537 | AT | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.652+757delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9212537 | ||||||
chr18:9212557 | G | A | 1 | a0001c0001t0005g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.652+773G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212557 | |||||||
chr18:9212606 | T | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.652+822T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212606 | |||||||
chr18:9212641 | A | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+857A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212641 | |||||||
chr18:9212685 | G | GC | 35 | a0002c0022t0030g0316 a0004c0004t0004g0281 a0004c0004t0004g0283 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.652+909dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9212685 | ||||||
chr18:9212693 | CAAAATTC others(13): Show |
C | 1 | a0003c0003t0001g0234 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.652+911_652+930del others(20): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9212693 | ||||||
chr18:9212773 | T | G | 3 | a0001c0001t0018g0182 a0001c0001t0018g0183 a0001c0001t0018g0197 |
3 | HG01106.hp1 HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.652+989T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212773 | |||||||
chr18:9212837 | C | G | 1 | a0004c0004t0036g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.652+1053C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212837 | |||||||
chr18:9212928 | G | T | 1 | a0001c0010t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.652+1144G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9212928 | |||||||
chr18:9213067 | T | C | 1 | a0002c0002t0001g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.652+1283T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213067 | |||||||
chr18:9213159 | A | G | 1 | a0001c0001t0005g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.652+1375A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213159 | |||||||
chr18:9213276 | T | C | 2 | a0004c0004t0004g0283 a0004c0004t0004g0284 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.652+1492T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213276 | |||||||
chr18:9213418 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.652+1634G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213418 | |||||||
chr18:9213751 | T | C | 1 | a0001c0001t0056g0253 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.652+1967T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213751 | |||||||
chr18:9213805 | T | C | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.652+2021T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213805 | |||||||
chr18:9213934 | A | G | 1 | a0003c0003t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.652+2150A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9213934 | |||||||
chr18:9214103 | T | C | 1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.652+2319T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214103 | |||||||
chr18:9214137 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.652+2353C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214137 | |||||||
chr18:9214138 | A | G | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.652+2354A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214138 | |||||||
chr18:9214150 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+2366T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214150 | |||||||
chr18:9214245 | A | G | 1 | a0001c0001t0020g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652+2461A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214245 | |||||||
chr18:9214360 | TA | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.653-2394delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9214360 | ||||||
chr18:9214371 | G | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.653-2387G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214371 | |||||||
chr18:9214510 | G | GT | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.653-2247dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9214510 | ||||||
chr18:9214668 | G | GA | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.653-2084dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9214668 | ||||||
chr18:9214724 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653-2034C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214724 | |||||||
chr18:9214820 | G | A | 1 | a0002c0002t0006g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.653-1938G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9214820 | |||||||
chr18:9215054 | G | A | 1 | a0001c0001t0062g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.653-1704G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215054 | |||||||
chr18:9215667 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.653-1091A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215667 | |||||||
chr18:9215717 | C | T | 1 | a0003c0003t0009g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.653-1041C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215717 | |||||||
chr18:9215743 | T | TA | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.653-1015_653-1014i others(3): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215743 | |||||||
chr18:9215762 | A | G | 1 | a0001c0001t0002g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.653-996A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215762 | |||||||
chr18:9215976 | T | C | 2 | a0002c0002t0001g0127 a0003c0003t0001g0234 |
2 | NA18948.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.653-782T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9215976 | |||||||
chr18:9216015 | C | CT | 215 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0171 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.653-726dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr18 | 9216015 | ||||||
chr18:9216116 | T | C | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.653-642T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216116 | |||||||
chr18:9216223 | T | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653-535T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216223 | |||||||
chr18:9216601 | T | C | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.653-157T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216601 | |||||||
chr18:9216610 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.653-148T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 6/12 | chr18 | 9216610 | |||||||
chr18:9217208 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.795+308T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217208 | |||||||
chr18:9217236 | G | A | 315 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.795+336G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217236 | |||||||
chr18:9217340 | T | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.795+440T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217340 | |||||||
chr18:9217413 | T | C | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+513T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217413 | |||||||
chr18:9217437 | A | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 |
3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.795+537A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217437 | |||||||
chr18:9217449 | A | C | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.795+549A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217449 | |||||||
chr18:9217473 | G | A | 210 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.795+573G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217473 | |||||||
chr18:9217484 | A | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.795+584A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217484 | |||||||
chr18:9217539 | A | C | 170 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.795+639A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217539 | |||||||
chr18:9217551 | A | G | 1 | a0001c0010t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.795+651A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217551 | |||||||
chr18:9217743 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.795+843T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217743 | |||||||
chr18:9217903 | A | G | 1 | a0001c0001t0029g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.795+1003A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217903 | |||||||
chr18:9217989 | C | T | 1 | a0001c0001t0015g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.795+1089C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9217989 | |||||||
chr18:9218017 | C | T | 3 | a0003c0003t0001g0103 a0003c0003t0001g0104 a0003c0003t0009g0105 |
3 | NA18943.hp2 NA18957.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+1117C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218017 | |||||||
chr18:9218116 | G | A | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.795+1216G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218116 | |||||||
chr18:9218247 | A | G | 1 | a0002c0002t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.795+1347A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218247 | |||||||
chr18:9218390 | G | A | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.795+1490G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218390 | |||||||
chr18:9218557 | T | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.795+1657T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218557 | |||||||
chr18:9218568 | A | G | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.795+1668A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218568 | |||||||
chr18:9218600 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.795+1700T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218600 | |||||||
chr18:9218665 | CT | C | 49 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(46): Show |
49 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.795+1778delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr18 | 9218665 | ||||||
chr18:9218927 | T | C | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.795+2027T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218927 | |||||||
chr18:9218935 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.795+2035A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9218935 | |||||||
chr18:9219258 | G | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.795+2358G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219258 | |||||||
chr18:9219319 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.795+2419C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219319 | |||||||
chr18:9219463 | G | A | 51 | a0001c0001t0002g0198 a0001c0001t0003g0064 a0001c0001t0003g0067 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.796-2389G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219463 | |||||||
chr18:9219478 | A | T | 1 | a0001c0001t0033g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.796-2374A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219478 | |||||||
chr18:9219664 | G | A | 212 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.796-2188G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219664 | |||||||
chr18:9219719 | G | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.796-2133G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219719 | |||||||
chr18:9219758 | GA | G | 18 | a0001c0001t0045g0190 a0002c0002t0006g0037 a0002c0002t0006g0038 others(15): Show |
18 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.796-2080delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr18 | 9219758 | ||||||
chr18:9219918 | T | G | 315 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.796-1934T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9219918 | |||||||
chr18:9220464 | A | G | 1 | a0004c0004t0016g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.796-1388A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220464 | |||||||
chr18:9220537 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.796-1315G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220537 | |||||||
chr18:9220732 | G | A | 1 | a0002c0002t0017g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.796-1120G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220732 | |||||||
chr18:9220754 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.796-1098G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220754 | |||||||
chr18:9220814 | A | G | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.796-1038A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9220814 | |||||||
chr18:9221029 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.796-823T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221029 | |||||||
chr18:9221285 | T | C | 1 | a0001c0001t0018g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.796-567T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221285 | |||||||
chr18:9221302 | C | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.796-550C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221302 | |||||||
chr18:9221333 | G | A | 6 | a0002c0002t0006g0041 a0002c0002t0006g0042 a0002c0002t0006g0059 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-519G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221333 | |||||||
chr18:9221490 | G | A | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.796-362G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221490 | |||||||
chr18:9221605 | A | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.796-247A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221605 | |||||||
chr18:9221842 | A | G | 64 | a0001c0001t0062g0102 a0002c0002t0001g0013 a0002c0002t0001g0123 others(61): Show |
64 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.796-10A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 7/12 | chr18 | 9221842 | |||||||
chr18:9222018 | ACATT | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 |
3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.943+23_943+26delTC others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9222018 | ||||||
chr18:9222490 | A | G | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+491A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222490 | |||||||
chr18:9222509 | A | G | 1 | a0001c0001t0003g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.943+510A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222509 | |||||||
chr18:9222657 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+658G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222657 | |||||||
chr18:9222679 | C | T | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.943+680C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222679 | |||||||
chr18:9222877 | A | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.943+878A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9222877 | |||||||
chr18:9223111 | T | G | 8 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(5): Show |
8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.943+1112T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223111 | |||||||
chr18:9223259 | C | CT | 29 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(26): Show |
29 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.943+1272dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9223259 | ||||||
chr18:9223269 | T | G | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.943+1270T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223269 | |||||||
chr18:9223314 | C | T | 3 | a0001c0001t0003g0204 a0001c0001t0003g0206 a0001c0001t0003g0210 |
3 | HG01099.hp1 HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.943+1315C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223314 | |||||||
chr18:9223373 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.943+1374C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223373 | |||||||
chr18:9223376 | C | A | 1 | a0002c0002t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.943+1377C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223376 | |||||||
chr18:9223399 | G | A | 2 | a0005c0006t0008g0176 a0005c0006t0008g0270 |
2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.943+1400G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223399 | |||||||
chr18:9223437 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0053g0001 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.943+1438C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223437 | |||||||
chr18:9223923 | A | C | 1 | a0003c0003t0009g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.943+1924A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223923 | |||||||
chr18:9223992 | A | T | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+1993A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9223992 | |||||||
chr18:9224074 | A | G | 8 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 others(5): Show |
8 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.943+2075A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224074 | |||||||
chr18:9224093 | A | T | 1 | a0003c0003t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.943+2094A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224093 | |||||||
chr18:9224153 | A | T | 2 | a0001c0001t0019g0257 a0001c0001t0050g0256 |
2 | NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.943+2154A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224153 | |||||||
chr18:9224267 | A | G | 1 | a0001c0001t0062g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.943+2268A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224267 | |||||||
chr18:9224405 | C | T | 4 | a0001c0001t0019g0191 a0001c0001t0019g0257 a0001c0001t0019g0267 others(1): Show |
4 | HG02132.hp1 NA18969.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+2406C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224405 | |||||||
chr18:9224441 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.943+2442T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224441 | |||||||
chr18:9224596 | C | G | 1 | a0001c0001t0029g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.943+2597C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224596 | |||||||
chr18:9224638 | A | G | 3 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0009g0149 |
3 | HG02258.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.943+2639A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224638 | |||||||
chr18:9224746 | T | C | 3 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0018t0041g0315 |
3 | HG01106.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+2747T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224746 | |||||||
chr18:9224826 | T | C | 3 | a0004c0004t0004g0283 a0004c0004t0004g0284 a0004c0004t0004g0285 |
3 | HG02015.hp1 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.943+2827T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224826 | |||||||
chr18:9224827 | G | A | 26 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(23): Show |
26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.943+2828G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9224827 | |||||||
chr18:9225120 | AAGGCTTG others(328): Show |
A | 144 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.943+3124_943+3458d others(2): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225120 | ||||||
chr18:9225325 | T | G | 1 | a0003c0003t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.943+3326T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9225325 | |||||||
chr18:9225472 | T | TA | 196 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.943+3490dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225472 | ||||||
chr18:9225472 | T | TAA | 7 | a0001c0001t0002g0249 a0001c0001t0008g0255 a0001c0007t0026g0025 others(4): Show |
7 | HG02109.hp1 HG02273.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.943+3489_943+3490d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225472 | ||||||
chr18:9225472 | TA | T | 6 | a0001c0001t0062g0102 a0002c0002t0001g0095 a0002c0002t0001g0154 others(3): Show |
6 | HG01070.hp1 HG01099.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.943+3490delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225472 | ||||||
chr18:9225612 | G | A | 1 | a0003c0003t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.943+3613G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9225612 | |||||||
chr18:9225955 | T | TGG | 63 | a0001c0001t0062g0102 a0002c0002t0001g0013 a0002c0002t0001g0123 others(60): Show |
63 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.943+3957_943+3958i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9225955 | ||||||
chr18:9226057 | A | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+4058A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226057 | |||||||
chr18:9226063 | T | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+4064T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226063 | |||||||
chr18:9226161 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+4162C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226161 | |||||||
chr18:9226191 | A | G | 1 | a0002c0002t0012g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.943+4192A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226191 | |||||||
chr18:9226229 | G | A | 2 | a0002c0002t0001g0132 a0002c0002t0009g0134 |
2 | HG00423.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.943+4230G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226229 | |||||||
chr18:9226235 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0053g0001 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.943+4236G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226235 | |||||||
chr18:9226427 | A | G | 5 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+4428A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226427 | |||||||
chr18:9226433 | G | GA | 170 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.943+4443dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9226433 | ||||||
chr18:9226510 | T | C | 150 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.943+4511T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226510 | |||||||
chr18:9226678 | G | A | 1 | a0004c0004t0016g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.943+4679G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226678 | |||||||
chr18:9226697 | T | TC | 58 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.943+4700dupC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9226697 | ||||||
chr18:9226699 | C | T | 1 | a0001c0001t0019g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.943+4700C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226699 | |||||||
chr18:9226726 | T | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+4727T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226726 | |||||||
chr18:9226731 | A | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.943+4732A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226731 | |||||||
chr18:9226743 | A | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+4744A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226743 | |||||||
chr18:9226921 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.943+4922G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226921 | |||||||
chr18:9226997 | C | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+4998C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9226997 | |||||||
chr18:9227015 | C | T | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+5016C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227015 | |||||||
chr18:9227160 | A | G | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.943+5161A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227160 | |||||||
chr18:9227525 | G | A | 1 | a0001c0001t0025g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.943+5526G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227525 | |||||||
chr18:9227545 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+5546G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227545 | |||||||
chr18:9227664 | G | T | 1 | a0001c0001t0033g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.943+5665G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227664 | |||||||
chr18:9227937 | G | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+5938G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227937 | |||||||
chr18:9227962 | C | G | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.943+5963C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227962 | |||||||
chr18:9227997 | C | T | 4 | a0004c0004t0004g0292 a0004c0004t0004g0300 a0004c0004t0035g0293 others(1): Show |
4 | NA18967.hp1 NA18973.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+5998C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9227997 | |||||||
chr18:9228005 | A | C | 1 | a0015c0020t0002g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.943+6006A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228005 | |||||||
chr18:9228073 | G | GGA | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+6074_943+6075i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228073 | |||||||
chr18:9228075 | C | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+6076C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228075 | |||||||
chr18:9228277 | A | G | 1 | a0001c0001t0033g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.943+6278A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228277 | |||||||
chr18:9228308 | G | C | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.943+6309G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228308 | |||||||
chr18:9228454 | C | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+6455C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228454 | |||||||
chr18:9228576 | C | T | 149 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.943+6577C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9228576 | |||||||
chr18:9228911 | CT | C | 199 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.943+6924delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9228911 | ||||||
chr18:9229111 | A | G | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.943+7112A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229111 | |||||||
chr18:9229170 | G | C | 1 | a0001c0001t0046g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.943+7171G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229170 | |||||||
chr18:9229200 | C | T | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.943+7201C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229200 | |||||||
chr18:9229225 | G | A | 2 | a0001c0001t0011g0224 a0001c0001t0048g0221 |
2 | NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.943+7226G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229225 | |||||||
chr18:9229382 | G | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+7383G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229382 | |||||||
chr18:9229484 | A | G | 1 | a0001c0010t0003g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.943+7485A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229484 | |||||||
chr18:9229533 | T | C | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+7534T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229533 | |||||||
chr18:9229878 | T | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+7879T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9229878 | |||||||
chr18:9230161 | T | A | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+8162T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230161 | |||||||
chr18:9230200 | G | A | 47 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(44): Show |
47 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.943+8201G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230200 | |||||||
chr18:9230206 | T | G | 1 | a0001c0001t0002g0237 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.943+8207T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230206 | |||||||
chr18:9230280 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+8281A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230280 | |||||||
chr18:9230355 | A | G | 1 | a0001c0001t0045g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.943+8356A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230355 | |||||||
chr18:9230518 | T | C | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+8519T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230518 | |||||||
chr18:9230645 | C | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+8646C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230645 | |||||||
chr18:9230655 | CT | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.943+8670delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9230655 | ||||||
chr18:9230658 | T | C | 129 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.943+8659T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230658 | |||||||
chr18:9230721 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+8722C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230721 | |||||||
chr18:9230783 | C | T | 6 | a0004c0004t0004g0290 a0004c0004t0004g0301 a0004c0004t0004g0302 others(3): Show |
6 | NA18991.hp2 NA18992.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+8784C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230783 | |||||||
chr18:9230835 | T | A | 126 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.943+8836T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230835 | |||||||
chr18:9230836 | T | A | 1 | a0001c0001t0003g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.943+8837T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230836 | |||||||
chr18:9230852 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+8853G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230852 | |||||||
chr18:9230870 | G | T | 3 | a0001c0001t0003g0204 a0001c0001t0003g0206 a0001c0001t0003g0210 |
3 | HG01099.hp1 HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.943+8871G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230870 | |||||||
chr18:9230937 | G | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.943+8938G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9230937 | |||||||
chr18:9231252 | T | C | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+9253T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231252 | |||||||
chr18:9231330 | G | A | 3 | a0001c0001t0015g0021 a0001c0001t0015g0028 a0011c0019t0065g0266 |
3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.943+9331G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231330 | |||||||
chr18:9231368 | A | G | 5 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(2): Show |
5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+9369A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231368 | |||||||
chr18:9231374 | G | A | 3 | a0002c0002t0001g0117 a0002c0002t0001g0148 a0002c0002t0010g0147 |
3 | HG01891.hp1 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.943+9375G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231374 | |||||||
chr18:9231417 | A | G | 144 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.943+9418A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231417 | |||||||
chr18:9231579 | G | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943+9580G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231579 | |||||||
chr18:9231756 | C | T | 1 | a0001c0001t0011g0226 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.943+9757C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9231756 | |||||||
chr18:9231824 | C | CA | 180 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.943+9844dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231824 | ||||||
chr18:9231824 | C | CAA | 21 | a0001c0001t0002g0279 a0001c0001t0005g0219 a0002c0002t0001g0125 others(18): Show |
21 | HG00733.hp2 HG01081.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.943+9843_943+9844d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231824 | ||||||
chr18:9231824 | C | CAAA | 6 | a0002c0002t0001g0124 a0002c0002t0006g0053 a0002c0002t0006g0055 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.943+9842_943+9844d others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231824 | ||||||
chr18:9231914 | T | TTTTCCAT others(4): Show |
68 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(65): Show |
68 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.943+9917_943+9918i others(13): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9231914 | ||||||
chr18:9232009 | G | T | 1 | a0002c0025t0001g0120 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.943+10010G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232009 | |||||||
chr18:9232113 | C | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+10114C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232113 | |||||||
chr18:9232560 | G | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.943+10561G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232560 | |||||||
chr18:9232564 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.943+10565T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232564 | |||||||
chr18:9232676 | A | G | 1 | a0002c0008t0006g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.943+10677A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232676 | |||||||
chr18:9232849 | T | TTTG | 215 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.943+10865_943+1086 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9232849 | ||||||
chr18:9232868 | A | G | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.943+10869A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232868 | |||||||
chr18:9232918 | C | T | 8 | a0002c0002t0001g0116 a0002c0002t0001g0117 a0002c0002t0001g0119 others(5): Show |
8 | HG01106.hp2 HG01167.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.943+10919C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232918 | |||||||
chr18:9232932 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.943+10933C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9232932 | |||||||
chr18:9233007 | G | A | 1 | a0001c0001t0029g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.943+11008G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233007 | |||||||
chr18:9233009 | C | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.943+11010C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233009 | |||||||
chr18:9233166 | A | G | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+11167A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233166 | |||||||
chr18:9233602 | TGTTA | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+11607_943+1161 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9233602 | ||||||
chr18:9233638 | G | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.943+11639G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233638 | |||||||
chr18:9233643 | C | T | 4 | a0001c0001t0005g0200 a0001c0001t0005g0219 a0001c0001t0011g0224 others(1): Show |
4 | NA18991.hp1 NA18992.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+11644C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233643 | |||||||
chr18:9233912 | A | T | 1 | a0001c0001t0045g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.943+11913A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9233912 | |||||||
chr18:9234049 | G | A | 2 | a0002c0002t0001g0124 a0002c0002t0001g0125 |
2 | NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.943+12050G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234049 | |||||||
chr18:9234070 | C | CA | 146 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.943+12072dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9234070 | ||||||
chr18:9234108 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+12109G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234108 | |||||||
chr18:9234177 | G | A | 1 | a0001c0001t0003g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.943+12178G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234177 | |||||||
chr18:9234398 | G | A | 4 | a0001c0001t0005g0186 a0001c0001t0005g0225 a0001c0001t0011g0226 others(1): Show |
4 | NA18957.hp2 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+12399G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234398 | |||||||
chr18:9234480 | T | G | 1 | a0003c0003t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.943+12481T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234480 | |||||||
chr18:9234591 | G | A | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | HG01099.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.943+12592G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234591 | |||||||
chr18:9234592 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.943+12593G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234592 | |||||||
chr18:9234681 | G | A | 1 | a0001c0001t0046g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.943+12682G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234681 | |||||||
chr18:9234730 | C | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+12731C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234730 | |||||||
chr18:9234753 | G | A | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.943+12754G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234753 | |||||||
chr18:9234776 | A | G | 147 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.943+12777A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234776 | |||||||
chr18:9234858 | T | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.943+12859T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234858 | |||||||
chr18:9234921 | A | G | 144 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.943+12922A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9234921 | |||||||
chr18:9235075 | A | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.943+13076A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235075 | |||||||
chr18:9235084 | C | T | 2 | a0004c0004t0016g0306 a0004c0004t0036g0289 |
2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.943+13085C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235084 | |||||||
chr18:9235114 | CTA | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.943+13118_943+1311 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9235114 | ||||||
chr18:9235274 | G | A | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.943+13275G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235274 | |||||||
chr18:9235482 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+13483A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235482 | |||||||
chr18:9235676 | G | A | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+13677G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235676 | |||||||
chr18:9235950 | CT | C | 9 | a0001c0001t0005g0225 a0001c0001t0008g0189 a0001c0001t0054g0174 others(6): Show |
9 | HG01884.hp1 HG01943.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.943+13965delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9235950 | ||||||
chr18:9235953 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+13954T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9235953 | |||||||
chr18:9236077 | A | G | 1 | a0004c0004t0004g0284 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.943+14078A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236077 | |||||||
chr18:9236097 | A | G | 1 | a0002c0002t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.943+14098A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236097 | |||||||
chr18:9236227 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.943+14228A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236227 | |||||||
chr18:9236416 | CA | C | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.943+14423delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9236416 | ||||||
chr18:9236527 | C | T | 8 | a0003c0003t0001g0066 a0003c0003t0001g0073 a0003c0003t0001g0074 others(5): Show |
8 | HG01361.hp1 HG01433.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.943+14528C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236527 | |||||||
chr18:9236587 | A | AT | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(1): Show |
4 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+14590dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9236587 | ||||||
chr18:9236629 | A | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.943+14630A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236629 | |||||||
chr18:9236657 | C | CAT | 215 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.943+14658_943+1465 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236657 | |||||||
chr18:9236749 | G | A | 3 | a0002c0002t0017g0056 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | HG01070.hp2 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.943+14750G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236749 | |||||||
chr18:9236821 | C | T | 1 | a0002c0002t0009g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.943+14822C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9236821 | |||||||
chr18:9237258 | A | G | 4 | a0001c0001t0005g0186 a0001c0001t0005g0225 a0001c0001t0011g0226 others(1): Show |
4 | NA18957.hp2 NA18981.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+15259A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237258 | |||||||
chr18:9237277 | T | G | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.943+15278T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237277 | |||||||
chr18:9237481 | G | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.943+15482G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237481 | |||||||
chr18:9237575 | G | T | 2 | a0002c0013t0066g0162 a0002c0022t0030g0316 |
2 | HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.943+15576G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237575 | |||||||
chr18:9237811 | G | T | 1 | a0001c0001t0003g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.943+15812G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237811 | |||||||
chr18:9237918 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.943+15919C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9237918 | |||||||
chr18:9238011 | A | T | 20 | a0001c0001t0002g0198 a0001c0001t0002g0241 a0001c0001t0002g0242 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.943+16012A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238011 | |||||||
chr18:9238062 | C | G | 1 | a0001c0001t0044g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.943+16063C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238062 | |||||||
chr18:9238207 | C | T | 2 | a0002c0018t0041g0315 a0003c0003t0001g0014 |
2 | HG01106.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.944-16004C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238207 | |||||||
chr18:9238228 | C | G | 5 | a0005c0006t0008g0176 a0005c0006t0008g0178 a0005c0006t0008g0179 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-15983C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238228 | |||||||
chr18:9238486 | C | T | 2 | a0003c0003t0001g0144 a0013c0026t0038g0016 |
2 | HG03471.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.944-15725C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238486 | |||||||
chr18:9238487 | G | A | 5 | a0002c0002t0001g0124 a0002c0002t0001g0125 a0002c0002t0001g0128 others(2): Show |
5 | HG02129.hp2 NA18963.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-15724G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238487 | |||||||
chr18:9238606 | G | T | 2 | a0001c0001t0008g0189 a0001c0001t0008g0240 |
2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.944-15605G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238606 | |||||||
chr18:9238876 | C | G | 8 | a0001c0001t0002g0198 a0001c0001t0007g0177 a0001c0001t0007g0184 others(5): Show |
8 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.944-15335C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9238876 | |||||||
chr18:9239015 | G | A | 1 | a0001c0001t0005g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.944-15196G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239015 | |||||||
chr18:9239284 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-14927G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239284 | |||||||
chr18:9239823 | A | G | 4 | a0002c0002t0001g0127 a0002c0002t0001g0132 a0002c0002t0009g0126 others(1): Show |
4 | HG00423.hp1 HG02071.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-14388A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239823 | |||||||
chr18:9239841 | T | G | 5 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(2): Show |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-14370T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9239841 | |||||||
chr18:9240091 | C | A | 5 | a0004c0004t0013g0311 a0004c0004t0013g0312 a0004c0004t0013g0313 others(2): Show |
5 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-14120C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240091 | |||||||
chr18:9240102 | A | G | 3 | a0001c0001t0018g0182 a0001c0001t0018g0183 a0001c0001t0018g0197 |
3 | HG01106.hp1 HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.944-14109A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240102 | |||||||
chr18:9240147 | G | A | 4 | a0001c0001t0020g0002 a0001c0001t0020g0005 a0001c0001t0052g0003 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-14064G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240147 | |||||||
chr18:9240208 | T | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-14003T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240208 | |||||||
chr18:9240415 | C | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-13796C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240415 | |||||||
chr18:9240635 | C | G | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-13576C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240635 | |||||||
chr18:9240720 | C | G | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-13491C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240720 | |||||||
chr18:9240796 | G | C | 2 | a0001c0001t0002g0193 a0001c0001t0007g0192 |
2 | HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.944-13415G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240796 | |||||||
chr18:9240832 | T | C | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-13379T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240832 | |||||||
chr18:9240901 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-13310T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9240901 | |||||||
chr18:9241122 | G | A | 1 | a0001c0007t0026g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.944-13089G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241122 | |||||||
chr18:9241317 | C | G | 1 | a0001c0001t0007g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.944-12894C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241317 | |||||||
chr18:9241373 | C | T | 3 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 |
3 | HG02109.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.944-12838C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241373 | |||||||
chr18:9241388 | C | T | 129 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.944-12823C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241388 | |||||||
chr18:9241463 | T | C | 2 | a0004c0004t0004g0283 a0004c0004t0004g0284 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.944-12748T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241463 | |||||||
chr18:9241524 | G | A | 2 | a0002c0013t0066g0162 a0002c0022t0030g0316 |
2 | HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-12687G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241524 | |||||||
chr18:9241526 | A | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-12685A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241526 | |||||||
chr18:9241672 | A | C | 1 | a0001c0001t0005g0017 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.944-12539A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241672 | |||||||
chr18:9241783 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.944-12428A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241783 | |||||||
chr18:9241891 | G | GT | 51 | a0001c0001t0005g0181 a0001c0001t0005g0200 a0001c0001t0005g0219 others(48): Show |
51 | HG00140.hp1 HG00639.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.944-12306dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9241891 | ||||||
chr18:9241891 | GT | G | 8 | a0001c0001t0002g0242 a0001c0001t0002g0246 a0003c0003t0001g0085 others(5): Show |
8 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.944-12306delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9241891 | ||||||
chr18:9241958 | C | T | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-12253C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241958 | |||||||
chr18:9241965 | C | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-12246C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241965 | |||||||
chr18:9241989 | A | G | 2 | a0003c0003t0001g0138 a0003c0003t0001g0139 |
2 | HG00609.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.944-12222A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9241989 | |||||||
chr18:9242056 | C | A | 1 | a0001c0001t0005g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.944-12155C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242056 | |||||||
chr18:9242335 | G | A | 1 | a0004c0004t0016g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.944-11876G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242335 | |||||||
chr18:9242463 | C | CA | 138 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.944-11739dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9242463 | ||||||
chr18:9242463 | C | CAA | 9 | a0001c0001t0002g0198 a0001c0001t0002g0271 a0001c0001t0007g0177 others(6): Show |
9 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.944-11740_944-1173 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9242463 | ||||||
chr18:9242495 | A | T | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-11716A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242495 | |||||||
chr18:9242504 | G | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-11707G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242504 | |||||||
chr18:9242540 | A | T | 1 | a0001c0001t0005g0225 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.944-11671A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242540 | |||||||
chr18:9242577 | G | A | 1 | a0002c0002t0006g0039 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.944-11634G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9242577 | |||||||
chr18:9243138 | A | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.944-11073A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243138 | |||||||
chr18:9243556 | C | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-10655C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243556 | |||||||
chr18:9243619 | G | A | 2 | a0001c0001t0003g0216 a0001c0001t0003g0218 |
2 | NA18971.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.944-10592G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243619 | |||||||
chr18:9243707 | C | T | 4 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0052 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-10504C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243707 | |||||||
chr18:9243963 | G | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-10248G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9243963 | |||||||
chr18:9244036 | A | C | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.944-10175A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244036 | |||||||
chr18:9244066 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.944-10145G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244066 | |||||||
chr18:9244082 | C | T | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-10129C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244082 | |||||||
chr18:9244185 | T | C | 1 | a0001c0001t0005g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.944-10026T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244185 | |||||||
chr18:9244196 | G | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-10015G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244196 | |||||||
chr18:9244263 | C | A | 1 | a0001c0010t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.944-9948C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244263 | |||||||
chr18:9244316 | T | G | 1 | a0001c0001t0033g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.944-9895T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244316 | |||||||
chr18:9244532 | C | G | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-9679C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244532 | |||||||
chr18:9244548 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-9663G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244548 | |||||||
chr18:9244713 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.944-9498C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244713 | |||||||
chr18:9244830 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-9381A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244830 | |||||||
chr18:9244888 | T | C | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.944-9323T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244888 | |||||||
chr18:9244939 | G | T | 1 | a0015c0020t0002g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.944-9272G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244939 | |||||||
chr18:9244991 | A | G | 1 | a0001c0001t0011g0227 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.944-9220A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9244991 | |||||||
chr18:9245048 | A | C | 1 | a0006c0005t0039g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.944-9163A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245048 | |||||||
chr18:9245440 | A | G | 4 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-8771A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245440 | |||||||
chr18:9245514 | G | A | 2 | a0004c0004t0022g0272 a0004c0004t0022g0307 |
2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.944-8697G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245514 | |||||||
chr18:9245623 | A | G | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.944-8588A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245623 | |||||||
chr18:9245707 | T | C | 5 | a0002c0002t0001g0101 a0002c0002t0001g0142 a0002c0002t0009g0155 others(2): Show |
5 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.944-8504T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245707 | |||||||
chr18:9245883 | C | T | 1 | a0002c0002t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.944-8328C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245883 | |||||||
chr18:9245960 | CTT | C | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-8250_944-8249d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245960 | |||||||
chr18:9245983 | G | C | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.944-8228G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9245983 | |||||||
chr18:9246060 | A | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-8151A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246060 | |||||||
chr18:9246098 | A | G | 1 | a0002c0002t0023g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.944-8113A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246098 | |||||||
chr18:9246164 | CTT | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-8044_944-8043d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9246164 | ||||||
chr18:9246326 | T | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.944-7885T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246326 | |||||||
chr18:9246334 | T | C | 1 | a0004c0004t0013g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.944-7877T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246334 | |||||||
chr18:9246380 | C | T | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.944-7831C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246380 | |||||||
chr18:9246570 | G | A | 1 | a0001c0001t0005g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.944-7641G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246570 | |||||||
chr18:9246665 | T | G | 1 | a0002c0002t0063g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.944-7546T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246665 | |||||||
chr18:9246666 | G | A | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.944-7545G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246666 | |||||||
chr18:9246713 | A | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-7498A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246713 | |||||||
chr18:9246737 | A | G | 44 | a0001c0001t0002g0198 a0001c0001t0003g0064 a0001c0001t0003g0067 others(41): Show |
44 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.944-7474A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246737 | |||||||
chr18:9246752 | G | A | 1 | a0001c0001t0033g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.944-7459G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246752 | |||||||
chr18:9246860 | C | A | 1 | a0003c0003t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.944-7351C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246860 | |||||||
chr18:9246898 | G | A | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.944-7313G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9246898 | |||||||
chr18:9246961 | T | TAC | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-7249_944-7248d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9246961 | ||||||
chr18:9247144 | TTTTG | T | 27 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(24): Show |
27 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.944-7043_944-7040d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247144 | ||||||
chr18:9247222 | TAATCCC | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-6986_944-6981d others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247222 | ||||||
chr18:9247270 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.944-6941C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247270 | |||||||
chr18:9247313 | C | CA | 42 | a0001c0001t0005g0262 a0001c0001t0011g0227 a0004c0004t0004g0281 others(39): Show |
42 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.944-6882dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247313 | ||||||
chr18:9247329 | A | G | 1 | a0003c0003t0001g0093 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.944-6882A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247329 | |||||||
chr18:9247411 | C | T | 1 | a0001c0012t0002g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.944-6800C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247411 | |||||||
chr18:9247459 | A | G | 1 | a0001c0010t0003g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.944-6752A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247459 | |||||||
chr18:9247487 | T | A | 8 | a0002c0002t0001g0013 a0002c0002t0001g0123 a0002c0002t0001g0133 others(5): Show |
8 | NA18941.hp1 NA18971.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.944-6724T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247487 | |||||||
chr18:9247494 | A | T | 3 | a0002c0013t0066g0162 a0002c0018t0041g0315 a0002c0022t0030g0316 |
3 | HG01106.hp2 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-6717A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247494 | |||||||
chr18:9247562 | T | G | 1 | a0001c0001t0005g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.944-6649T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247562 | |||||||
chr18:9247604 | A | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-6607A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247604 | |||||||
chr18:9247782 | T | TTTTTGTT others(3): Show |
4 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-6404_944-6395d others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247782 | ||||||
chr18:9247782 | TTTTTG | T | 38 | a0002c0013t0066g0162 a0004c0004t0004g0281 a0004c0004t0004g0283 others(35): Show |
38 | HG00639.hp1 HG01884.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.944-6399_944-6395d others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9247782 | ||||||
chr18:9247851 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-6360G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247851 | |||||||
chr18:9247944 | G | A | 3 | a0002c0013t0066g0162 a0002c0018t0041g0315 a0002c0022t0030g0316 |
3 | HG01106.hp2 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-6267G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9247944 | |||||||
chr18:9248152 | T | C | 169 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.944-6059T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248152 | |||||||
chr18:9248224 | G | A | 1 | a0015c0020t0002g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.944-5987G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248224 | |||||||
chr18:9248297 | C | T | 1 | a0001c0001t0046g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.944-5914C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248297 | |||||||
chr18:9248312 | G | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.944-5899G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248312 | |||||||
chr18:9248359 | A | G | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-5852A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248359 | |||||||
chr18:9248466 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.944-5745C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248466 | |||||||
chr18:9248522 | G | A | 1 | a0001c0024t0069g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.944-5689G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248522 | |||||||
chr18:9248584 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-5627T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248584 | |||||||
chr18:9248616 | A | G | 3 | a0002c0013t0066g0162 a0002c0018t0041g0315 a0002c0022t0030g0316 |
3 | HG01106.hp2 HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.944-5595A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248616 | |||||||
chr18:9248648 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-5563A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248648 | |||||||
chr18:9248727 | A | AAGAC | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-5481_944-5478d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9248727 | ||||||
chr18:9248806 | A | G | 1 | a0003c0003t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.944-5405A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248806 | |||||||
chr18:9248929 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-5282T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9248929 | |||||||
chr18:9249001 | C | T | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.944-5210C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249001 | |||||||
chr18:9249110 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.944-5101G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249110 | |||||||
chr18:9249119 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-5092G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249119 | |||||||
chr18:9249269 | A | C | 2 | a0001c0001t0002g0279 a0001c0001t0003g0278 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.944-4942A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249269 | |||||||
chr18:9249468 | G | T | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-4743G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249468 | |||||||
chr18:9249591 | C | T | 1 | a0003c0003t0001g0146 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.944-4620C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249591 | |||||||
chr18:9249660 | T | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.944-4551T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249660 | |||||||
chr18:9249844 | T | C | 43 | a0002c0013t0066g0162 a0002c0018t0041g0315 a0002c0022t0030g0316 others(40): Show |
43 | HG00140.hp1 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.944-4367T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9249844 | |||||||
chr18:9249945 | CTG | C | 4 | a0004c0004t0004g0292 a0004c0004t0004g0300 a0004c0004t0035g0293 others(1): Show |
4 | NA18967.hp1 NA18973.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-4263_944-4262d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9249945 | ||||||
chr18:9250011 | G | A | 2 | a0001c0001t0025g0065 a0001c0001t0025g0131 |
2 | HG01123.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.944-4200G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250011 | |||||||
chr18:9250057 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-4154A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250057 | |||||||
chr18:9250377 | A | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-3834A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250377 | |||||||
chr18:9250382 | G | A | 1 | a0004c0004t0016g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.944-3829G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250382 | |||||||
chr18:9250418 | G | A | 1 | a0001c0001t0045g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.944-3793G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250418 | |||||||
chr18:9250499 | A | G | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.944-3712A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250499 | |||||||
chr18:9250538 | G | A | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-3673G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250538 | |||||||
chr18:9250545 | C | G | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.944-3666C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250545 | |||||||
chr18:9250743 | C | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-3468C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250743 | |||||||
chr18:9250915 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-3296T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250915 | |||||||
chr18:9250918 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-3293T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250918 | |||||||
chr18:9250970 | G | C | 2 | a0002c0002t0001g0127 a0002c0002t0009g0126 |
2 | HG03942.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.944-3241G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9250970 | |||||||
chr18:9251025 | T | C | 1 | a0002c0002t0006g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944-3186T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251025 | |||||||
chr18:9251027 | T | A | 1 | a0002c0002t0006g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944-3184T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251027 | |||||||
chr18:9251080 | A | G | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.944-3131A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251080 | |||||||
chr18:9251113 | A | G | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-3098A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251113 | |||||||
chr18:9251221 | G | A | 2 | a0004c0004t0004g0290 a0004c0004t0004g0304 |
2 | NA18997.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.944-2990G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251221 | |||||||
chr18:9251238 | C | T | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.944-2973C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251238 | |||||||
chr18:9251259 | C | A | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.944-2952C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251259 | |||||||
chr18:9251569 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-2642G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251569 | |||||||
chr18:9251613 | G | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-2598G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251613 | |||||||
chr18:9251666 | C | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0263 |
2 | HG00735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.944-2545C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251666 | |||||||
chr18:9251803 | A | T | 2 | a0004c0004t0004g0292 a0004c0004t0035g0293 |
2 | NA18973.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.944-2408A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251803 | |||||||
chr18:9251817 | C | T | 2 | a0001c0001t0025g0065 a0001c0001t0025g0131 |
2 | HG01123.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.944-2394C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9251817 | |||||||
chr18:9252260 | G | A | 8 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(5): Show |
8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.944-1951G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252260 | |||||||
chr18:9252498 | A | G | 1 | a0003c0003t0009g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.944-1713A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252498 | |||||||
chr18:9252499 | T | C | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02129.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.944-1712T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252499 | |||||||
chr18:9252539 | G | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-1672G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252539 | |||||||
chr18:9252751 | G | A | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.944-1460G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252751 | |||||||
chr18:9252808 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-1403A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9252808 | |||||||
chr18:9253004 | T | TTA | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-1198_944-1197d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr18 | 9253004 | ||||||
chr18:9253084 | T | C | 1 | a0003c0003t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.944-1127T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253084 | |||||||
chr18:9253114 | G | A | 1 | a0001c0001t0007g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.944-1097G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253114 | |||||||
chr18:9253157 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.944-1054A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253157 | |||||||
chr18:9253298 | C | T | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.944-913C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253298 | |||||||
chr18:9253415 | A | G | 1 | a0003c0003t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.944-796A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253415 | |||||||
chr18:9253474 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0068 |
2 | NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.944-737G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253474 | |||||||
chr18:9253744 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.944-467G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253744 | |||||||
chr18:9253914 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.944-297A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253914 | |||||||
chr18:9253945 | T | C | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.944-266T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 8/12 | chr18 | 9253945 | |||||||
chr18:9259000 | C | T | 1 | a0004c0004t0004g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5664+69C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259000 | |||||||
chr18:9259142 | A | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5664+211A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259142 | |||||||
chr18:9259172 | G | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.5664+241G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259172 | |||||||
chr18:9259220 | T | TCC | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+290_5664+291i others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9259220 | ||||||
chr18:9259222 | A | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+291A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259222 | |||||||
chr18:9259290 | T | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5664+359T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259290 | |||||||
chr18:9259368 | T | C | 147 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.5664+437T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259368 | |||||||
chr18:9259370 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5664+439C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259370 | |||||||
chr18:9259386 | A | AACACATT others(16): Show |
3 | a0002c0002t0001g0110 a0002c0022t0030g0316 a0007c0027t0004g0309 |
3 | HG00639.hp1 HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.5664+496_5664+518d others(25): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9259386 | ||||||
chr18:9259386 | AACACATT others(16): Show |
A | 6 | a0002c0002t0009g0155 a0006c0005t0014g0006 a0006c0005t0014g0007 others(3): Show |
6 | HG01069.hp2 HG01884.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5664+496_5664+518d others(25): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9259386 | ||||||
chr18:9259396 | T | C | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.5664+465T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259396 | |||||||
chr18:9259434 | C | T | 3 | a0002c0002t0001g0070 a0002c0002t0001g0080 a0008c0016t0001g0079 |
3 | HG01109.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.5664+503C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259434 | |||||||
chr18:9259452 | A | G | 2 | a0002c0002t0001g0119 a0002c0025t0001g0120 |
2 | HG01167.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5664+521A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259452 | |||||||
chr18:9259549 | T | A | 1 | a0002c0002t0010g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5664+618T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259549 | |||||||
chr18:9259721 | A | G | 1 | a0002c0002t0012g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5664+790A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259721 | |||||||
chr18:9259805 | T | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5664+874T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259805 | |||||||
chr18:9259894 | A | G | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5664+963A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9259894 | |||||||
chr18:9260012 | C | T | 1 | a0003c0003t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5664+1081C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260012 | |||||||
chr18:9260171 | C | T | 1 | a0004c0004t0004g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5664+1240C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260171 | |||||||
chr18:9260212 | C | T | 1 | a0002c0015t0006g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5664+1281C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260212 | |||||||
chr18:9260218 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+1287A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260218 | |||||||
chr18:9260248 | G | A | 5 | a0001c0001t0003g0188 a0001c0001t0003g0273 a0001c0001t0003g0274 others(2): Show |
5 | HG01123.hp2 HG01934.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.5664+1317G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260248 | |||||||
chr18:9260855 | T | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5664+1924T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260855 | |||||||
chr18:9260870 | C | T | 26 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(23): Show |
26 | HG00639.hp1 HG01934.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.5664+1939C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260870 | |||||||
chr18:9260877 | C | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5664+1946C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260877 | |||||||
chr18:9260994 | C | T | 2 | a0003c0003t0060g0072 a0003c0003t0061g0071 |
2 | NA19057.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.5664+2063C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9260994 | |||||||
chr18:9261021 | T | C | 7 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0006c0005t0014g0006 others(4): Show |
7 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.5664+2090T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261021 | |||||||
chr18:9261715 | T | G | 2 | a0001c0001t0033g0030 a0001c0001t0033g0031 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5665-2075T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261715 | |||||||
chr18:9261720 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5665-2070C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261720 | |||||||
chr18:9261781 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5665-2009G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261781 | |||||||
chr18:9261806 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5665-1984T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261806 | |||||||
chr18:9261991 | G | A | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5665-1799G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9261991 | |||||||
chr18:9262055 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5665-1735G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262055 | |||||||
chr18:9262103 | T | C | 2 | a0004c0004t0022g0272 a0004c0004t0022g0307 |
2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.5665-1687T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262103 | |||||||
chr18:9262110 | T | G | 1 | a0004c0004t0004g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.5665-1680T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262110 | |||||||
chr18:9262264 | G | A | 1 | a0001c0001t0003g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5665-1526G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262264 | |||||||
chr18:9262720 | A | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5665-1070A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262720 | |||||||
chr18:9262727 | T | G | 1 | a0003c0003t0058g0098 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.5665-1063T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262727 | |||||||
chr18:9262781 | A | T | 1 | a0001c0001t0003g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5665-1009A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262781 | |||||||
chr18:9262786 | C | CT | 66 | a0001c0001t0002g0198 a0001c0001t0002g0235 a0001c0001t0002g0236 others(63): Show |
66 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(5): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | |||||||
chr18:9262786 | C | CTT | 40 | a0001c0001t0002g0172 a0001c0001t0002g0193 a0001c0001t0002g0233 others(37): Show |
40 | HG00733.hp1 HG00735.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | |||||||
chr18:9262786 | C | CTTT | 7 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0028g0276 others(4): Show |
7 | HG01952.hp1 HG02148.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | |||||||
chr18:9262786 | C | CTTTT | 8 | a0001c0001t0002g0045 a0001c0001t0002g0173 a0001c0001t0002g0251 others(5): Show |
8 | HG01884.hp2 HG02300.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.5665-1004_5665-100 others(8): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262786 | |||||||
chr18:9262787 | C | CT | 91 | a0001c0001t0010g0023 a0001c0001t0010g0024 a0001c0001t0062g0102 others(88): Show |
91 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.5665-974dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | ||||||
chr18:9262787 | C | CTT | 25 | a0001c0001t0033g0031 a0002c0002t0001g0123 a0002c0002t0009g0126 others(22): Show |
25 | HG01361.hp1 HG01934.hp2 HG02523.hp1 others(22): Show |
intron_variant | MODIFIER | c.5665-975_5665-974d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | ||||||
chr18:9262787 | C | CTTTTTTT others(5): Show |
1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5665-985_5665-974d others(14): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | ||||||
chr18:9262787 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.5665-1003C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262787 | |||||||
chr18:9262787 | CT | C | 22 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(19): Show |
22 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.5665-974delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | ||||||
chr18:9262787 | CTTTTTTT others(3): Show |
C | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5665-983_5665-974d others(12): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr18 | 9262787 | ||||||
chr18:9262829 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5665-961C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262829 | |||||||
chr18:9262830 | G | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5665-960G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9262830 | |||||||
chr18:9263028 | C | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5665-762C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263028 | |||||||
chr18:9263156 | C | T | 1 | a0009c0021t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5665-634C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263156 | |||||||
chr18:9263399 | AC | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0171 a0001c0001t0002g0172 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5665-390delC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263399 | |||||||
chr18:9263414 | A | G | 2 | a0002c0002t0059g0130 a0012c0023t0034g0061 |
2 | HG02976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.5665-376A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263414 | |||||||
chr18:9263457 | A | G | 1 | a0001c0001t0047g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5665-333A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263457 | |||||||
chr18:9263580 | T | C | 5 | a0002c0002t0006g0053 a0002c0002t0006g0055 a0002c0002t0017g0056 others(2): Show |
5 | HG00140.hp2 HG01070.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5665-210T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 9/12 | chr18 | 9263580 | |||||||
chr18:9263943 | A | C | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5763+55A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9263943 | |||||||
chr18:9264265 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+377C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264265 | |||||||
chr18:9264290 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5763+402C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264290 | |||||||
chr18:9264349 | T | C | 3 | a0001c0001t0015g0021 a0001c0001t0015g0028 a0011c0019t0065g0266 |
3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+461T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264349 | |||||||
chr18:9264428 | G | T | 1 | a0002c0002t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5763+540G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264428 | |||||||
chr18:9264490 | G | A | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5763+602G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264490 | |||||||
chr18:9264517 | A | C | 2 | a0001c0001t0019g0257 a0001c0001t0050g0256 |
2 | NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.5763+629A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264517 | |||||||
chr18:9264521 | AT | A | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+637delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9264521 | ||||||
chr18:9264553 | T | A | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+665T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264553 | |||||||
chr18:9264595 | T | C | 1 | a0002c0002t0057g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5763+707T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264595 | |||||||
chr18:9264680 | C | G | 1 | a0002c0002t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5763+792C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264680 | |||||||
chr18:9264692 | A | G | 5 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0013t0066g0162 others(2): Show |
5 | HG01106.hp2 HG01167.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.5763+804A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264692 | |||||||
chr18:9264719 | C | T | 1 | a0004c0004t0016g0299 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.5763+831C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264719 | |||||||
chr18:9264766 | AT | A | 72 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0006g0037 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5763+880delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9264766 | ||||||
chr18:9264785 | C | T | 1 | a0002c0002t0006g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5763+897C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264785 | |||||||
chr18:9264900 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1012C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264900 | |||||||
chr18:9264984 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1096C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9264984 | |||||||
chr18:9265012 | G | A | 2 | a0001c0001t0008g0189 a0001c0001t0008g0240 |
2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.5763+1124G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265012 | |||||||
chr18:9265078 | AG | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+1194delG | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9265078 | ||||||
chr18:9265184 | A | G | 144 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.5763+1296A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265184 | |||||||
chr18:9265293 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+1405A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265293 | |||||||
chr18:9265372 | C | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5763+1484C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265372 | |||||||
chr18:9265430 | TC | T | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+1544delC | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9265430 | ||||||
chr18:9265474 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1586C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265474 | |||||||
chr18:9265560 | G | A | 1 | a0007c0027t0004g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5763+1672G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265560 | |||||||
chr18:9265727 | A | G | 1 | a0003c0003t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5763+1839A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265727 | |||||||
chr18:9265784 | G | A | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+1896G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265784 | |||||||
chr18:9265797 | A | G | 1 | a0001c0001t0005g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5763+1909A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265797 | |||||||
chr18:9265798 | A | C | 1 | a0001c0001t0005g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5763+1910A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265798 | |||||||
chr18:9265813 | A | C | 1 | a0003c0003t0009g0105 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5763+1925A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265813 | |||||||
chr18:9265822 | C | T | 38 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(35): Show |
38 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.5763+1934C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265822 | |||||||
chr18:9265823 | G | A | 3 | a0001c0001t0015g0021 a0001c0001t0015g0028 a0011c0019t0065g0266 |
3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+1935G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265823 | |||||||
chr18:9265955 | C | T | 4 | a0001c0001t0015g0029 a0001c0001t0029g0248 a0001c0001t0033g0030 others(1): Show |
4 | HG01515.hp2 HG02055.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.5763+2067C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9265955 | |||||||
chr18:9266081 | A | G | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5763+2193A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266081 | |||||||
chr18:9266084 | C | T | 2 | a0001c0001t0008g0189 a0001c0001t0008g0240 |
2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.5763+2196C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266084 | |||||||
chr18:9266177 | G | A | 1 | a0013c0026t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5763+2289G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266177 | |||||||
chr18:9266284 | T | C | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0020g0170 |
3 | HG01361.hp2 HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.5763+2396T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266284 | |||||||
chr18:9266373 | T | C | 1 | a0002c0002t0023g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5763+2485T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266373 | |||||||
chr18:9266378 | T | C | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5763+2490T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266378 | |||||||
chr18:9266439 | A | G | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+2551A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266439 | |||||||
chr18:9266506 | C | T | 1 | a0001c0001t0054g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5763+2618C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266506 | |||||||
chr18:9266627 | A | G | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+2739A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266627 | |||||||
chr18:9266640 | C | T | 42 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0004c0004t0004g0281 others(39): Show |
42 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.5763+2752C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266640 | |||||||
chr18:9266791 | T | C | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+2903T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266791 | |||||||
chr18:9266826 | T | G | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+2938T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266826 | |||||||
chr18:9266845 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+2957C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266845 | |||||||
chr18:9266860 | T | C | 2 | a0001c0001t0033g0030 a0001c0001t0033g0031 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+2972T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266860 | |||||||
chr18:9266946 | A | T | 1 | a0002c0002t0006g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5763+3058A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266946 | |||||||
chr18:9266975 | T | G | 1 | a0003c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5763+3087T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266975 | |||||||
chr18:9266990 | G | T | 8 | a0001c0001t0007g0177 a0001c0001t0007g0184 a0001c0001t0007g0192 others(5): Show |
8 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.5763+3102G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9266990 | |||||||
chr18:9267149 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+3261T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267149 | |||||||
chr18:9267214 | C | G | 3 | a0001c0001t0015g0021 a0001c0001t0015g0028 a0011c0019t0065g0266 |
3 | HG02965.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+3326C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267214 | |||||||
chr18:9267237 | C | A | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+3349C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267237 | |||||||
chr18:9267275 | T | C | 5 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(2): Show |
5 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5763+3387T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267275 | |||||||
chr18:9267329 | C | T | 1 | a0002c0022t0030g0316 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5763+3441C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267329 | |||||||
chr18:9267387 | G | C | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5763+3499G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267387 | |||||||
chr18:9267394 | G | A | 1 | a0001c0001t0015g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5763+3506G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267394 | |||||||
chr18:9267400 | A | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.5763+3512A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267400 | |||||||
chr18:9267501 | C | T | 3 | a0001c0001t0015g0029 a0001c0001t0033g0030 a0001c0001t0033g0031 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5763+3613C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267501 | |||||||
chr18:9267505 | C | T | 1 | a0004c0004t0013g0312 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5763+3617C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267505 | |||||||
chr18:9267593 | A | G | 5 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(2): Show |
5 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5763+3705A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267593 | |||||||
chr18:9267595 | C | T | 5 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(2): Show |
5 | HG01106.hp2 HG01891.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5763+3707C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267595 | |||||||
chr18:9267611 | C | T | 7 | a0003c0003t0001g0083 a0003c0003t0001g0088 a0003c0003t0021g0010 others(4): Show |
7 | HG00323.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.5763+3723C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267611 | |||||||
chr18:9267791 | T | G | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+3903T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267791 | |||||||
chr18:9267870 | A | G | 129 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.5763+3982A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267870 | |||||||
chr18:9267915 | C | T | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+4027C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267915 | |||||||
chr18:9267916 | G | A | 2 | a0001c0001t0015g0021 a0001c0001t0015g0028 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5763+4028G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9267916 | |||||||
chr18:9268083 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.5763+4195C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268083 | |||||||
chr18:9268173 | A | G | 72 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0006g0037 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5763+4285A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268173 | |||||||
chr18:9268174 | G | A | 72 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0006g0037 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5763+4286G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268174 | |||||||
chr18:9268224 | T | C | 6 | a0002c0002t0006g0053 a0002c0002t0006g0054 a0002c0002t0006g0055 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.5763+4336T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268224 | |||||||
chr18:9268252 | T | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5763+4364T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268252 | |||||||
chr18:9268471 | G | A | 1 | a0001c0001t0005g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5763+4583G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268471 | |||||||
chr18:9268497 | A | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+4609A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268497 | |||||||
chr18:9268573 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5763+4685C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268573 | |||||||
chr18:9268615 | T | C | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.5763+4727T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268615 | |||||||
chr18:9268616 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5763+4728G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268616 | |||||||
chr18:9268641 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+4753T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268641 | |||||||
chr18:9268642 | A | G | 1 | a0001c0001t0029g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5763+4754A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268642 | |||||||
chr18:9268700 | G | T | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5763+4812G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268700 | |||||||
chr18:9268701 | A | T | 1 | a0011c0019t0065g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5763+4813A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268701 | |||||||
chr18:9268725 | T | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+4837T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268725 | |||||||
chr18:9268764 | G | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5763+4876G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268764 | |||||||
chr18:9268884 | G | A | 1 | a0003c0003t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5763+4996G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268884 | |||||||
chr18:9268921 | A | G | 1 | a0003c0003t0001g0085 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.5763+5033A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268921 | |||||||
chr18:9268938 | A | G | 4 | a0001c0001t0020g0002 a0001c0001t0020g0005 a0001c0001t0052g0003 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5763+5050A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268938 | |||||||
chr18:9268957 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5763+5069G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9268957 | |||||||
chr18:9269068 | G | A | 1 | a0004c0004t0022g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5763+5180G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269068 | |||||||
chr18:9269077 | C | T | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5763+5189C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269077 | |||||||
chr18:9269135 | A | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5763+5247A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269135 | |||||||
chr18:9269162 | G | A | 3 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 |
3 | HG02109.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5763+5274G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269162 | |||||||
chr18:9269222 | C | T | 34 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.5763+5334C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269222 | |||||||
chr18:9269346 | A | G | 1 | a0004c0004t0004g0302 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5763+5458A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269346 | |||||||
chr18:9269390 | CA | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5763+5506delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9269390 | ||||||
chr18:9269484 | A | T | 4 | a0001c0001t0003g0215 a0001c0001t0003g0216 a0001c0001t0003g0218 others(1): Show |
4 | NA18971.hp2 NA18982.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.5763+5596A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269484 | |||||||
chr18:9269540 | A | C | 129 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.5763+5652A>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269540 | |||||||
chr18:9269591 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5763+5703C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269591 | |||||||
chr18:9269660 | A | G | 129 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.5763+5772A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269660 | |||||||
chr18:9269843 | ATGGGAGA others(4): Show |
A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5764-5679_5764-566 others(15): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9269843 | ||||||
chr18:9269907 | C | G | 2 | a0002c0002t0001g0157 a0002c0002t0009g0159 |
2 | NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.5764-5617C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9269907 | |||||||
chr18:9270090 | G | A | 8 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 others(5): Show |
8 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.5764-5434G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270090 | |||||||
chr18:9270243 | C | T | 1 | a0004c0004t0022g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5764-5281C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270243 | |||||||
chr18:9270409 | T | C | 1 | a0003c0003t0001g0014 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5764-5115T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270409 | |||||||
chr18:9270415 | G | A | 4 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5764-5109G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270415 | |||||||
chr18:9270604 | A | G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-4920A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270604 | |||||||
chr18:9270643 | C | T | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0173 others(2): Show |
5 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-4881C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270643 | |||||||
chr18:9270726 | C | T | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-4798C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270726 | |||||||
chr18:9270746 | C | T | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5764-4778C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270746 | |||||||
chr18:9270792 | T | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-4732T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270792 | |||||||
chr18:9270816 | A | T | 1 | a0001c0001t0054g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5764-4708A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270816 | |||||||
chr18:9270859 | T | C | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5764-4665T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9270859 | |||||||
chr18:9271381 | C | T | 1 | a0001c0001t0015g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5764-4143C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271381 | |||||||
chr18:9271400 | G | A | 1 | a0002c0002t0064g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5764-4124G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271400 | |||||||
chr18:9271532 | T | A | 311 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(308): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.5764-3992T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271532 | |||||||
chr18:9271666 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-3858T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271666 | |||||||
chr18:9271745 | T | G | 4 | a0002c0002t0006g0039 a0002c0002t0006g0050 a0002c0002t0006g0051 others(1): Show |
4 | HG00733.hp2 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.5764-3779T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271745 | |||||||
chr18:9271825 | T | C | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5764-3699T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9271825 | |||||||
chr18:9272022 | C | T | 5 | a0002c0002t0012g0069 a0002c0002t0012g0114 a0002c0002t0012g0115 others(2): Show |
5 | HG02895.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.5764-3502C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272022 | |||||||
chr18:9272066 | A | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5764-3458A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272066 | |||||||
chr18:9272101 | A | G | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5764-3423A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272101 | |||||||
chr18:9272301 | G | A | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5764-3223G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272301 | |||||||
chr18:9272430 | T | C | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5764-3094T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272430 | |||||||
chr18:9272494 | G | A | 1 | a0001c0001t0007g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5764-3030G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272494 | |||||||
chr18:9272644 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-2880G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272644 | |||||||
chr18:9272655 | A | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5764-2869A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272655 | |||||||
chr18:9272813 | A | G | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5764-2711A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272813 | |||||||
chr18:9272868 | A | G | 1 | a0003c0003t0060g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5764-2656A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272868 | |||||||
chr18:9272936 | G | A | 2 | a0001c0001t0010g0022 a0001c0001t0010g0023 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5764-2588G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272936 | |||||||
chr18:9272943 | G | A | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-2581G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272943 | |||||||
chr18:9272958 | C | CATG | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5764-2566_5764-256 others(7): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9272958 | |||||||
chr18:9273034 | G | A | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5764-2490G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273034 | |||||||
chr18:9273382 | C | G | 2 | a0001c0001t0015g0015 a0001c0024t0069g0018 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5764-2142C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273382 | |||||||
chr18:9273388 | G | T | 2 | a0001c0001t0015g0015 a0001c0024t0069g0018 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5764-2136G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273388 | |||||||
chr18:9273398 | A | G | 3 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0009g0149 |
3 | HG02258.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5764-2126A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273398 | |||||||
chr18:9273541 | G | T | 1 | a0001c0001t0005g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5764-1983G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273541 | |||||||
chr18:9273789 | C | G | 1 | a0001c0001t0002g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.5764-1735C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9273789 | |||||||
chr18:9274149 | G | A | 1 | a0001c0001t0005g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5764-1375G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274149 | |||||||
chr18:9274234 | A | G | 1 | a0006c0005t0014g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5764-1290A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274234 | |||||||
chr18:9274299 | A | G | 1 | a0003c0003t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5764-1225A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274299 | |||||||
chr18:9274577 | G | C | 1 | a0001c0001t0005g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5764-947G>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274577 | |||||||
chr18:9274638 | A | G | 216 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.5764-886A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274638 | |||||||
chr18:9274649 | A | G | 1 | a0004c0004t0004g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5764-875A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274649 | |||||||
chr18:9274923 | C | T | 1 | a0005c0006t0008g0202 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.5764-601C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9274923 | |||||||
chr18:9275173 | A | T | 1 | a0004c0004t0004g0304 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5764-351A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9275173 | |||||||
chr18:9275303 | A | AAT | 57 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0193 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.5764-208_5764-207d others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr18 | 9275303 | ||||||
chr18:9275316 | A | T | 9 | a0001c0001t0003g0194 a0001c0001t0003g0195 a0001c0001t0010g0022 others(6): Show |
9 | HG00639.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.5764-208A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9275316 | |||||||
chr18:9275366 | C | T | 8 | a0001c0001t0015g0015 a0001c0001t0015g0021 a0001c0001t0015g0028 others(5): Show |
8 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.5764-158C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 10/12 | chr18 | 9275366 | |||||||
chr18:9275744 | TAGAA | T | 15 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.5907+82_5907+85del others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9275744 | ||||||
chr18:9275844 | G | A | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5907+177G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9275844 | |||||||
chr18:9276191 | G | T | 72 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0006g0037 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5907+524G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276191 | |||||||
chr18:9276245 | TAAAC | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5907+580_5907+583d others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9276245 | ||||||
chr18:9276265 | C | G | 23 | a0002c0002t0006g0037 a0002c0002t0006g0038 a0002c0002t0006g0039 others(20): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.5907+598C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276265 | |||||||
chr18:9276408 | A | G | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5907+741A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276408 | |||||||
chr18:9276495 | C | T | 5 | a0003c0003t0001g0014 a0003c0003t0001g0085 a0003c0003t0001g0108 others(2): Show |
5 | HG00609.hp1 HG00621.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.5907+828C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276495 | |||||||
chr18:9276509 | T | G | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5907+842T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276509 | |||||||
chr18:9276617 | G | A | 1 | a0001c0001t0015g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5907+950G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276617 | |||||||
chr18:9276712 | C | CA | 15 | a0001c0001t0018g0182 a0001c0001t0018g0183 a0001c0001t0018g0197 others(12): Show |
15 | HG01106.hp1 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.5907+1054dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9276712 | ||||||
chr18:9276726 | A | G | 1 | a0001c0001t0005g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5907+1059A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276726 | |||||||
chr18:9276806 | G | T | 1 | a0001c0001t0062g0102 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5907+1139G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276806 | |||||||
chr18:9276936 | C | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5907+1269C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9276936 | |||||||
chr18:9277083 | C | T | 1 | a0004c0004t0004g0286 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.5907+1416C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277083 | |||||||
chr18:9277104 | T | C | 4 | a0001c0007t0026g0025 a0001c0007t0026g0026 a0001c0007t0051g0027 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5907+1437T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277104 | |||||||
chr18:9277116 | T | C | 2 | a0002c0002t0031g0160 a0002c0002t0031g0161 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5907+1449T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277116 | |||||||
chr18:9277181 | A | T | 4 | a0001c0001t0002g0241 a0001c0001t0002g0245 a0001c0001t0002g0247 others(1): Show |
4 | HG00423.hp2 HG00621.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.5907+1514A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277181 | |||||||
chr18:9277321 | C | CT | 41 | a0001c0001t0002g0251 a0001c0001t0002g0271 a0001c0001t0003g0268 others(38): Show |
41 | HG00733.hp2 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.5907+1679dupT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277321 | ||||||
chr18:9277321 | C | CTT | 34 | a0002c0002t0006g0052 a0002c0002t0023g0036 a0002c0002t0023g0060 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.5907+1678_5907+167 others(6): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277321 | ||||||
chr18:9277321 | CT | C | 6 | a0001c0001t0010g0023 a0001c0001t0054g0174 a0002c0002t0001g0094 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.5907+1679delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277321 | ||||||
chr18:9277527 | C | A | 145 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.5907+1860C>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277527 | |||||||
chr18:9277540 | G | T | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.5907+1873G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277540 | |||||||
chr18:9277549 | G | T | 1 | a0001c0001t0003g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5907+1882G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9277549 | |||||||
chr18:9277706 | GAGGTGGG others(105): Show |
G | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5908-1838_5908-172 others(4): Show |
ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9277706 | ||||||
chr18:9278180 | T | G | 2 | a0004c0004t0022g0272 a0004c0004t0022g0307 |
2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.5908-1369T>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278180 | |||||||
chr18:9278182 | T | C | 72 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0006g0037 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5908-1367T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278182 | |||||||
chr18:9278204 | A | T | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5908-1345A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278204 | |||||||
chr18:9278250 | GT | G | 72 | a0001c0009t0032g0019 a0001c0009t0032g0020 a0002c0002t0006g0037 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.5908-1297delT | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr18 | 9278250 | ||||||
chr18:9278482 | A | G | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5908-1067A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278482 | |||||||
chr18:9278556 | T | C | 40 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(37): Show |
40 | HG00140.hp1 HG00639.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.5908-993T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278556 | |||||||
chr18:9278744 | T | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5908-805T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278744 | |||||||
chr18:9278906 | T | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5908-643T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9278906 | |||||||
chr18:9279012 | C | T | 1 | a0002c0018t0041g0315 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5908-537C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279012 | |||||||
chr18:9279130 | T | C | 5 | a0005c0006t0008g0176 a0005c0006t0008g0178 a0005c0006t0008g0179 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.5908-419T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279130 | |||||||
chr18:9279344 | C | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 |
3 | HG01891.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5908-205C>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279344 | |||||||
chr18:9279526 | T | C | 35 | a0004c0004t0004g0281 a0004c0004t0004g0283 a0004c0004t0004g0284 others(32): Show |
35 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.5908-23T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 11/12 | chr18 | 9279526 | |||||||
chr18:9279690 | T | TA | 6 | a0001c0010t0003g0175 a0001c0010t0003g0185 a0002c0002t0031g0160 others(3): Show |
6 | HG01891.hp2 HG02683.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.6003+60dupA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | 9279690 | ||||||
chr18:9279690 | TA | T | 42 | a0001c0001t0003g0199 a0001c0001t0005g0225 a0001c0001t0005g0228 others(39): Show |
42 | HG00140.hp1 HG00639.hp1 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.6003+60delA | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | 9279690 | ||||||
chr18:9279706 | T | A | 1 | a0012c0023t0034g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6003+62T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279706 | |||||||
chr18:9279753 | A | G | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6003+109A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279753 | |||||||
chr18:9279763 | C | G | 2 | a0001c0009t0032g0019 a0001c0009t0032g0020 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6003+119C>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279763 | |||||||
chr18:9279860 | T | C | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6003+216T>C | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279860 | |||||||
chr18:9279970 | A | G | 3 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0024 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6003+326A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9279970 | |||||||
chr18:9280040 | T | A | 5 | a0006c0005t0014g0006 a0006c0005t0014g0007 a0006c0005t0014g0008 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.6003+396T>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280040 | |||||||
chr18:9280047 | A | T | 3 | a0002c0002t0031g0160 a0002c0002t0031g0161 a0002c0002t0042g0040 |
3 | HG01891.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6003+403A>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280047 | |||||||
chr18:9280133 | A | G | 1 | a0002c0002t0042g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6003+489A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280133 | |||||||
chr18:9280310 | G | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0198 |
2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.6004-631G>T | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280310 | |||||||
chr18:9280327 | A | G | 2 | a0001c0001t0003g0064 a0001c0001t0003g0268 |
2 | HG02738.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.6004-614A>G | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280327 | |||||||
chr18:9280356 | G | A | 1 | a0006c0005t0014g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6004-585G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280356 | |||||||
chr18:9280735 | G | A | 1 | a0002c0013t0066g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6004-206G>A | ANKRD12 | ENSG00000101745.17 | transcript | ENST00000262126.9 | protein_coding | 12/12 | chr18 | 9280735 |