geneid | 728780 |
---|---|
ensemblid | ENSG00000189045.15 |
hgncid | 32525 |
symbol | ANKDD1B |
name | ankyrin repeat and death domain containing 1B |
refseq_nuc | NM_001276713.2 |
refseq_prot | NP_001263642.1 |
ensembl_nuc | ENST00000601380.4 |
ensembl_prot | ENSP00000471417.1 |
mane_status | MANE Select |
chr | chr5 |
start | 75611453 |
end | 75671846 |
strand | + |
ver | v1.2 |
region | chr5:75611453-75671846 |
region5000 | chr5:75606453-75676846 |
regionname0 | ANKDD1B_chr5_75611453_75671846 |
regionname5000 | ANKDD1B_chr5_75606453_75676846 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 479 | 105 | 14 | 20 | 56 | 4 | 10 | 44 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002 | 0/0 | 528 | 89 | 9 | 8 | 60 | 1 | 11 | 49 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0003 | 0/0 | 528 | 49 | 5 | 4 | 39 | 0 | 1 | 30 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004 | 1/0 | 528 | 29 | 6 | 13 | 5 | 2 | 2 | 4 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0005 | 0/0 | 528 | 26 | 0 | 2 | 15 | 1 | 8 | 14 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006 | 0/0 | 260 | 12 | 9 | 3 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0007 | 0/0 | 479 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0008 | 0/0 | 528 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0009 | 0/0 | 462 | 6 | 0 | 0 | 6 | 0 | 0 | 2 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0010 | 0/0 | 479 | 5 | 3 | 1 | 1 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0011 | 0/0 | 528 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0012 | 0/0 | 528 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0013 | 0/0 | 92 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0014 | 0/0 | 528 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0015 | 0/0 | 260 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0016 | 0/0 | 528 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0017 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0018 | 0/0 | 461 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0019 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0020 | 0/0 | 260 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0021 | 0/0 | 479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0022 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0023 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0024 | 0/0 | 479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0025 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0026 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0027 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0028 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1587 | 102 | 12 | 20 | 55 | 4 | 10 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0002 | 0/0 | 1587 | 86 | 7 | 8 | 60 | 1 | 10 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0003 | 0/0 | 1587 | 46 | 5 | 4 | 36 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0004 | 0/0 | 1587 | 26 | 0 | 2 | 15 | 1 | 8 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0005 | 1/0 | 1587 | 17 | 3 | 10 | 0 | 2 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0006 | 0/0 | 1587 | 12 | 3 | 3 | 5 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0007 | 0/0 | 1587 | 11 | 9 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0008 | 0/0 | 1587 | 10 | 9 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0009 | 0/0 | 1582 | 8 | 7 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0010 | 0/0 | 1587 | 6 | 0 | 0 | 6 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0011 | 0/0 | 1587 | 5 | 3 | 1 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0012 | 0/0 | 1587 | 5 | 2 | 3 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0013 | 0/0 | 1587 | 4 | 1 | 2 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0014 | 0/0 | 1587 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0015 | 0/0 | 1582 | 3 | 1 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0016 | 0/0 | 1574 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0017 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0018 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0019 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0020 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0021 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0022 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0023 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0024 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0025 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0026 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0027 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0028 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0029 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0030 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0031 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0032 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0033 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0034 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0035 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0036 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0037 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0038 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
c0039 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 997 | 109 | 15 | 23 | 55 | 4 | 11 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0002 | 1/0 | 989 | 73 | 3 | 10 | 48 | 2 | 9 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0003 | 0/0 | 987 | 61 | 13 | 4 | 35 | 1 | 8 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0004 | 0/0 | 987 | 39 | 22 | 9 | 5 | 0 | 3 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0005 | 0/0 | 963 | 33 | 3 | 4 | 25 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0006 | 0/0 | 997 | 13 | 12 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0007 | 0/0 | 993 | 10 | 9 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0008 | 0/0 | 965 | 7 | 0 | 5 | 0 | 1 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0009 | 0/0 | 987 | 6 | 0 | 0 | 6 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0010 | 0/0 | 988 | 5 | 0 | 0 | 5 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0011 | 0/0 | 989 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0012 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0013 | 0/0 | 997 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0014 | 0/0 | 997 | 2 | 0 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0015 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0016 | 0/0 | 987 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0017 | 0/0 | 997 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0018 | 0/0 | 996 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0019 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0020 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0021 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
t0022 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 6 | 1 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0002 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1587 | 102 | 12 | 20 | 55 | 4 | 10 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0019 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0035 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0002 | 0/0 | 1587 | 86 | 7 | 8 | 60 | 1 | 10 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0028 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0029 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0036 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0003c0003 | 0/0 | 1587 | 46 | 5 | 4 | 36 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0003c0014 | 0/0 | 1587 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005 | 1/0 | 1587 | 17 | 3 | 10 | 0 | 2 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0006 | 0/0 | 1587 | 12 | 3 | 3 | 5 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0005c0004 | 0/0 | 1587 | 26 | 0 | 2 | 15 | 1 | 8 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006c0009 | 0/0 | 1582 | 8 | 7 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006c0015 | 0/0 | 1582 | 3 | 1 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006c0034 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0007c0007 | 0/0 | 1587 | 11 | 9 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0008c0008 | 0/0 | 1587 | 10 | 9 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0009c0010 | 0/0 | 1587 | 6 | 0 | 0 | 6 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0010c0011 | 0/0 | 1587 | 5 | 3 | 1 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0011c0012 | 0/0 | 1587 | 5 | 2 | 3 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0012c0013 | 0/0 | 1587 | 4 | 1 | 2 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0013c0016 | 0/0 | 1574 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0013c0024 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0014c0017 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0015c0025 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0015c0026 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0016c0018 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0017c0023 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0018c0022 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0019c0027 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0020c0030 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0021c0031 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0022c0032 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0023c0033 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0024c0020 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0025c0021 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0026c0037 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0027c0038 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0028c0039 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2583 | 94 | 7 | 19 | 53 | 4 | 10 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0001t0006 | 0/0 | 2583 | 5 | 5 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0001t0017 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0001t0018 | 0/0 | 2582 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0001t0021 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0019t0001 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0001c0035t0001 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0002t0002 | 0/0 | 2575 | 68 | 2 | 8 | 48 | 1 | 9 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0002t0003 | 0/0 | 2573 | 10 | 3 | 0 | 7 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0002t0004 | 0/0 | 2573 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0002t0010 | 0/0 | 2574 | 5 | 0 | 0 | 5 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0002t0016 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0028t0002 | 0/0 | 2575 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0029t0004 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0002c0036t0003 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0003c0003t0003 | 0/0 | 2573 | 13 | 2 | 0 | 11 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0003c0003t0005 | 0/0 | 2549 | 33 | 3 | 4 | 25 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0003c0014t0003 | 0/0 | 2573 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005t0002 | 1/0 | 2575 | 4 | 0 | 2 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005t0003 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005t0004 | 0/0 | 2573 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005t0008 | 0/0 | 2551 | 7 | 0 | 5 | 0 | 1 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005t0011 | 0/0 | 2575 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0005t0020 | 0/0 | 2550 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0004c0006t0004 | 0/0 | 2573 | 12 | 3 | 3 | 5 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0005c0004t0003 | 0/0 | 2573 | 24 | 0 | 2 | 14 | 1 | 7 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0005c0004t0004 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0005c0004t0015 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006c0009t0007 | 0/0 | 2574 | 8 | 7 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006c0015t0001 | 0/0 | 2578 | 3 | 1 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0006c0034t0003 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0007c0007t0006 | 0/0 | 2583 | 7 | 6 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0007c0007t0012 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0007c0007t0013 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0007c0007t0014 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0008c0008t0004 | 0/0 | 2573 | 10 | 9 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0009c0010t0009 | 0/0 | 2573 | 6 | 0 | 0 | 6 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0010c0011t0001 | 0/0 | 2583 | 5 | 3 | 1 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0011c0012t0004 | 0/0 | 2573 | 5 | 2 | 3 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0012c0013t0003 | 0/0 | 2573 | 4 | 1 | 2 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0013c0016t0001 | 0/0 | 2570 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0013c0024t0003 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0014c0017t0004 | 0/0 | 2573 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0015c0025t0007 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0015c0026t0004 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0016c0018t0003 | 0/0 | 2573 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0017c0023t0019 | 0/0 | 2567 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0018c0022t0001 | 0/0 | 2583 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0019c0027t0004 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0020c0030t0007 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0021c0031t0001 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0022c0032t0012 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0023c0033t0006 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0024c0020t0014 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0025c0021t0022 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0026c0037t0003 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0027c0038t0004 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
a0028c0039t0004 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | copy fasta | chr5 | 75606453 | 75676846 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 6 | 1 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0017g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0018g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0001t0021g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0019t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0019t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0001c0035t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0002 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0010g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0010g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0010g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0010g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0002t0016g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0028t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0029t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0002c0036t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0014t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0014t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0003c0014t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0002g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0008g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0008g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0011g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0005t0020g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0004c0006t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0005c0004t0015g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0009t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0015t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0015t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0006c0034t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0006g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0007c0007t0014g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0008c0008t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0009c0010t0009g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0009c0010t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0009c0010t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0009c0010t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0009c0010t0009g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0010c0011t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0010c0011t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0010c0011t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0010c0011t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0010c0011t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0011c0012t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0011c0012t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0011c0012t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0011c0012t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0011c0012t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0012c0013t0003g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0012c0013t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0012c0013t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0013c0016t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0013c0016t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0013c0024t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0014c0017t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0014c0017t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0015c0025t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0015c0026t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0016c0018t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0016c0018t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0017c0023t0019g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0018c0022t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0019c0027t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0020c0030t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0021c0031t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0022c0032t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0023c0033t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0024c0020t0014g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0025c0021t0022g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0026c0037t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0027c0038t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
a0028c0039t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0008 | g0219 | EUR | GBR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0290 | EUR | GBR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00408 | hp2 | a0004 | c0006 | t0004 | g0048 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00423 | hp1 | a0003 | c0003 | t0005 | g0232 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00609 | hp2 | a0003 | c0003 | t0003 | g0073 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00621 | hp1 | a0003 | c0003 | t0005 | g0231 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00639 | hp1 | a0004 | c0005 | t0008 | g0218 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00642 | hp1 | a0004 | c0005 | t0008 | g0143 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00642 | hp2 | a0007 | c0007 | t0006 | g0255 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00735 | hp1 | a0008 | c0008 | t0004 | g0165 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00738 | hp2 | a0004 | c0005 | t0002 | g0160 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00741 | hp1 | a0006 | c0015 | t0001 | g0020 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01069 | hp1 | a0012 | c0013 | t0003 | g0018 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01071 | hp1 | a0012 | c0013 | t0003 | g0179 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01081 | hp2 | a0021 | c0031 | t0001 | g0159 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01099 | hp2 | a0004 | c0006 | t0004 | g0072 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01106 | hp1 | a0010 | c0011 | t0001 | g0293 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01106 | hp2 | a0006 | c0015 | t0001 | g0208 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01109 | hp1 | a0004 | c0005 | t0020 | g0144 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01109 | hp2 | a0011 | c0012 | t0004 | g0302 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01167 | hp1 | a0011 | c0012 | t0004 | g0299 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01167 | hp2 | a0006 | c0009 | t0007 | g0212 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01168 | hp1 | a0004 | c0005 | t0008 | g0221 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01168 | hp2 | a0001 | c0001 | t0018 | g0123 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01169 | hp1 | a0011 | c0012 | t0004 | g0300 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01192 | hp2 | a0024 | c0020 | t0014 | g0254 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01243 | hp1 | a0015 | c0026 | t0004 | g0253 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01243 | hp2 | a0004 | c0005 | t0011 | g0007 | AMR | PUR | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01255 | hp1 | a0004 | c0005 | t0008 | g0021 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01255 | hp2 | a0004 | c0005 | t0004 | g0060 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0282 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01261 | hp2 | a0007 | c0007 | t0014 | g0155 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01358 | hp1 | a0004 | c0005 | t0008 | g0021 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01358 | hp2 | a0005 | c0004 | t0003 | g0192 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01361 | hp1 | a0004 | c0006 | t0004 | g0216 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01433 | hp2 | a0004 | c0005 | t0002 | g0094 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01516 | hp2 | a0005 | c0004 | t0003 | g0193 | EUR | IBS | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01884 | hp1 | a0008 | c0008 | t0004 | g0162 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01884 | hp2 | a0011 | c0012 | t0004 | g0303 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01891 | hp2 | a0008 | c0008 | t0004 | g0168 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01934 | hp1 | a0003 | c0003 | t0005 | g0239 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0289 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0314 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01943 | hp2 | a0003 | c0003 | t0005 | g0236 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01952 | hp2 | a0004 | c0006 | t0004 | g0205 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01975 | hp1 | a0003 | c0003 | t0005 | g0235 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0089 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02027 | hp2 | a0009 | c0010 | t0009 | g0040 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02040 | hp2 | a0002 | c0002 | t0003 | g0263 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02056 | hp1 | a0009 | c0010 | t0009 | g0041 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02056 | hp2 | a0003 | c0003 | t0003 | g0066 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02080 | hp2 | a0003 | c0003 | t0005 | g0230 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02132 | hp1 | a0009 | c0010 | t0009 | g0043 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02135 | hp2 | a0009 | c0010 | t0009 | g0008 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02145 | hp1 | a0004 | c0006 | t0004 | g0140 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02145 | hp2 | a0011 | c0012 | t0004 | g0301 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0313 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | CDX | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02257 | hp2 | a0008 | c0008 | t0004 | g0167 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02258 | hp1 | a0007 | c0007 | t0013 | g0038 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02258 | hp2 | a0008 | c0008 | t0004 | g0166 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02293 | hp2 | a0003 | c0003 | t0005 | g0238 | AMR | PEL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02451 | hp1 | a0004 | c0006 | t0004 | g0199 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02451 | hp2 | a0003 | c0003 | t0005 | g0174 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02523 | hp2 | a0003 | c0003 | t0005 | g0228 | EAS | KHV | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02572 | hp1 | a0019 | c0027 | t0004 | g0204 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02572 | hp2 | a0008 | c0008 | t0004 | g0161 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02602 | hp1 | a0005 | c0004 | t0003 | g0079 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02615 | hp1 | a0006 | c0009 | t0007 | g0141 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02615 | hp2 | a0013 | c0016 | t0001 | g0029 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02622 | hp1 | a0010 | c0011 | t0001 | g0164 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02622 | hp2 | a0001 | c0019 | t0001 | g0074 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02630 | hp1 | a0007 | c0007 | t0013 | g0039 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02630 | hp2 | a0007 | c0007 | t0006 | g0156 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02647 | hp2 | a0008 | c0008 | t0004 | g0170 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0318 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02698 | hp2 | a0005 | c0004 | t0003 | g0183 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02723 | hp1 | a0027 | c0038 | t0004 | g0247 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02723 | hp2 | a0013 | c0024 | t0003 | g0316 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02735 | hp1 | a0005 | c0004 | t0003 | g0184 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02738 | hp2 | a0018 | c0022 | t0001 | g0083 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02809 | hp1 | a0002 | c0028 | t0002 | g0323 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02809 | hp2 | a0006 | c0009 | t0007 | g0213 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02818 | hp1 | a0016 | c0018 | t0003 | g0251 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02886 | hp1 | a0003 | c0003 | t0005 | g0017 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02886 | hp2 | a0004 | c0005 | t0003 | g0034 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02895 | hp1 | a0006 | c0009 | t0007 | g0211 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02895 | hp2 | a0020 | c0030 | t0007 | g0163 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02896 | hp1 | a0014 | c0017 | t0004 | g0245 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02896 | hp2 | a0007 | c0007 | t0012 | g0256 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02897 | hp1 | a0006 | c0009 | t0007 | g0214 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02897 | hp2 | a0007 | c0007 | t0006 | g0004 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0277 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02970 | hp2 | a0008 | c0008 | t0004 | g0016 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03041 | hp1 | a0008 | c0008 | t0004 | g0169 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03041 | hp2 | a0007 | c0007 | t0006 | g0004 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03098 | hp1 | a0003 | c0003 | t0003 | g0036 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03098 | hp2 | a0006 | c0009 | t0007 | g0210 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03139 | hp1 | a0002 | c0002 | t0003 | g0175 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03139 | hp2 | a0023 | c0033 | t0006 | g0249 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03195 | hp1 | a0002 | c0002 | t0004 | g0173 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03195 | hp2 | a0013 | c0016 | t0001 | g0033 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03453 | hp1 | a0008 | c0008 | t0004 | g0016 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03453 | hp2 | a0003 | c0003 | t0003 | g0037 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03486 | hp1 | a0015 | c0025 | t0007 | g0252 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03486 | hp2 | a0017 | c0023 | t0019 | g0190 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03491 | hp1 | a0002 | c0002 | t0016 | g0171 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0281 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03516 | hp1 | a0025 | c0021 | t0022 | g0258 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03516 | hp2 | a0002 | c0002 | t0003 | g0076 | AFR | ESN | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03540 | hp1 | a0016 | c0018 | t0003 | g0250 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03540 | hp2 | a0007 | c0007 | t0006 | g0004 | AFR | GWD | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03579 | hp2 | a0010 | c0011 | t0001 | g0158 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0308 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0324 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03669 | hp2 | a0004 | c0005 | t0008 | g0220 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03688 | hp1 | a0005 | c0004 | t0003 | g0186 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03688 | hp2 | a0004 | c0006 | t0004 | g0217 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0291 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03704 | hp2 | a0005 | c0004 | t0003 | g0082 | SAS | PJL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03927 | hp2 | a0005 | c0004 | t0003 | g0078 | SAS | BEB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG04199 | hp2 | a0005 | c0004 | t0003 | g0080 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG04204 | hp1 | a0003 | c0003 | t0005 | g0150 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG04204 | hp2 | a0002 | c0029 | t0004 | g0272 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0276 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG04228 | hp2 | a0012 | c0013 | t0003 | g0176 | SAS | STU | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18522 | hp1 | a0006 | c0015 | t0001 | g0020 | AFR | YRI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18522 | hp2 | a0006 | c0034 | t0003 | g0215 | AFR | YRI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18612 | hp1 | a0003 | c0003 | t0005 | g0229 | EAS | CHB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | CHB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18747 | hp1 | a0005 | c0004 | t0015 | g0188 | EAS | CHB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18747 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | CHB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18906 | hp1 | a0014 | c0017 | t0004 | g0244 | AFR | YRI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18906 | hp2 | a0003 | c0003 | t0005 | g0017 | AFR | YRI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18940 | hp2 | a0003 | c0003 | t0005 | g0147 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18942 | hp2 | a0005 | c0004 | t0003 | g0189 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18944 | hp1 | a0003 | c0003 | t0005 | g0240 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18948 | hp1 | a0003 | c0003 | t0005 | g0223 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18948 | hp2 | a0005 | c0004 | t0003 | g0180 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18950 | hp1 | a0003 | c0003 | t0003 | g0152 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0306 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18953 | hp2 | a0003 | c0003 | t0005 | g0222 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18959 | hp2 | a0003 | c0003 | t0005 | g0241 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18960 | hp1 | a0010 | c0011 | t0001 | g0265 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18962 | hp1 | a0005 | c0004 | t0003 | g0177 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18962 | hp2 | a0009 | c0010 | t0009 | g0008 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18963 | hp2 | a0003 | c0014 | t0003 | g0071 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18964 | hp2 | a0002 | c0002 | t0010 | g0297 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18965 | hp1 | a0003 | c0003 | t0005 | g0225 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18967 | hp2 | a0002 | c0002 | t0003 | g0264 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18968 | hp1 | a0003 | c0003 | t0005 | g0149 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18968 | hp2 | a0005 | c0004 | t0003 | g0005 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18971 | hp1 | a0005 | c0004 | t0003 | g0178 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18972 | hp1 | a0003 | c0003 | t0005 | g0148 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18972 | hp2 | a0004 | c0006 | t0004 | g0027 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18973 | hp1 | a0001 | c0001 | t0021 | g0146 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18973 | hp2 | a0003 | c0003 | t0003 | g0151 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18974 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0266 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18975 | hp2 | a0005 | c0004 | t0003 | g0187 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18977 | hp1 | a0003 | c0014 | t0003 | g0131 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18978 | hp2 | a0003 | c0003 | t0005 | g0145 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18979 | hp1 | a0003 | c0003 | t0003 | g0102 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18985 | hp1 | a0005 | c0004 | t0003 | g0081 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18985 | hp2 | a0003 | c0003 | t0005 | g0022 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18986 | hp1 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18989 | hp2 | a0001 | c0035 | t0001 | g0070 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18992 | hp1 | a0003 | c0003 | t0005 | g0234 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18993 | hp2 | a0003 | c0003 | t0005 | g0242 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18995 | hp1 | a0003 | c0014 | t0003 | g0132 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18995 | hp2 | a0003 | c0003 | t0005 | g0198 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18998 | hp1 | a0003 | c0003 | t0005 | g0226 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19001 | hp1 | a0003 | c0003 | t0005 | g0142 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19002 | hp1 | a0005 | c0004 | t0003 | g0181 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19004 | hp1 | a0003 | c0003 | t0005 | g0227 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19005 | hp1 | a0003 | c0003 | t0005 | g0224 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19005 | hp2 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19006 | hp2 | a0003 | c0003 | t0005 | g0233 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19007 | hp2 | a0004 | c0006 | t0004 | g0028 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19009 | hp1 | a0005 | c0004 | t0003 | g0019 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19011 | hp1 | a0004 | c0006 | t0004 | g0027 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19030 | hp1 | a0004 | c0005 | t0011 | g0007 | AFR | LWK | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19030 | hp2 | a0010 | c0011 | t0001 | g0194 | AFR | LWK | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19043 | hp1 | a0004 | c0006 | t0004 | g0197 | AFR | LWK | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0288 | AFR | LWK | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19056 | hp1 | a0003 | c0003 | t0005 | g0237 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19058 | hp2 | a0005 | c0004 | t0003 | g0182 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19059 | hp1 | a0002 | c0002 | t0010 | g0292 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19060 | hp1 | a0005 | c0004 | t0003 | g0019 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19063 | hp1 | a0009 | c0010 | t0009 | g0042 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19064 | hp2 | a0003 | c0003 | t0005 | g0022 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19070 | hp1 | a0005 | c0004 | t0003 | g0005 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19074 | hp1 | a0005 | c0004 | t0003 | g0005 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19075 | hp1 | a0003 | c0003 | t0003 | g0054 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19076 | hp1 | a0002 | c0002 | t0010 | g0024 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19077 | hp2 | a0004 | c0006 | t0004 | g0028 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19078 | hp2 | a0005 | c0004 | t0003 | g0077 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0117 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0118 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19080 | hp2 | a0002 | c0002 | t0010 | g0319 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19081 | hp1 | a0001 | c0001 | t0017 | g0058 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19088 | hp2 | a0002 | c0002 | t0010 | g0320 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19240 | hp1 | a0007 | c0007 | t0006 | g0004 | AFR | YRI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA19240 | hp2 | a0028 | c0039 | t0004 | g0248 | AFR | YRI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20129 | hp1 | a0022 | c0032 | t0012 | g0195 | AFR | ASW | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20752 | hp1 | a0004 | c0005 | t0002 | g0096 | EUR | TSI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | GIH | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20905 | hp2 | a0005 | c0004 | t0004 | g0185 | SAS | GIH | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG01123 | hp2 | a0005 | c0004 | t0003 | g0191 | AMR | CLM | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02109 | hp2 | a0006 | c0009 | t0007 | g0209 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02486 | hp1 | a0002 | c0002 | t0004 | g0157 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02486 | hp2 | a0006 | c0009 | t0007 | g0207 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02559 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0196 | AFR | ACB | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03471 | hp1 | a0026 | c0037 | t0003 | g0153 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG03471 | hp2 | a0002 | c0036 | t0003 | g0298 | AFR | MSL | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
HG06807 | hp2 | a0012 | c0013 | t0003 | g0018 | AFR | USA | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20300 | hp1 | a0004 | c0005 | t0004 | g0030 | AFR | USA | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | USA | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA21309 | hp1 | a0001 | c0019 | t0001 | g0075 | AFR | LWK | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
NA21309 | hp2 | a0007 | c0007 | t0006 | g0257 | AFR | LWK | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0135 | REF | REF | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0002 | g0095 | REF | REF | ANKDD1B_chr5_75606453_75676846 | ANKDD1B | chr5 | 75606453 | 75676846 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75611640
|
C | G | 3 | a0026a0027a0028 | 3 | HG02723.hp1 HG03471.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.6C>G | p.Asp2Glu | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 188/2575 | 6/1587 | 2/528 | chr5 | 75611640 | ||
chr5:75611644
|
G | A | 3 | a0007a0024a0025 | 13 | HG00642.hp2 HG01192.hp2 HG01261.hp2 others(10): Show |
missense_variant | MODERATE | c.10G>A | p.Ala4Thr | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 192/2575 | 10/1587 | 4/528 | chr5 | 75611644 | ||
chr5:75611678
|
G | A | 4 | a0005a0012a0017others(1): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
missense_variant | MODERATE | c.44G>A | p.Gly15Glu | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 226/2575 | 44/1587 | 15/528 | chr5 | 75611678 | ||
chr5:75611679
|
GGGGCTGC others(6): Show |
G | 1 | a0013 | 3 | HG02615.hp2 HG02723.hp2 HG03195.hp2 |
frameshift_variant | HIGH | c.56_68delTCCGGGCTGC others(3): Show |
p.Leu19fs | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 238/2575 | 56/1587 | 19/528 | INFO_REALIGN_3_PRIME | chr5 | 75611679 | |
chr5:75611813
|
C | A | 3 | a0014a0015a0016 | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.179C>A | p.Ala60Asp | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 361/2575 | 179/1587 | 60/528 | chr5 | 75611813 | ||
chr5:75620396
|
G | A | 1 | a0019 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.379G>A | p.Val127Met | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/14 | 561/2575 | 379/1587 | 127/528 | chr5 | 75620396 | ||
chr5:75625861
|
G | A | 14 | a0002a0005a0008others(11): Show | 153 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(150): Show |
missense_variant | MODERATE | c.506G>A | p.Ser169Asn | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/14 | 688/2575 | 506/1587 | 169/528 | chr5 | 75625861 | ||
chr5:75625902
|
G | A | 1 | a0024 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.547G>A | p.Val183Met | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/14 | 729/2575 | 547/1587 | 183/528 | chr5 | 75625902 | ||
chr5:75635818
|
A | G | 3 | a0008a0014a0021 | 13 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
missense_variant | MODERATE | c.734A>G | p.His245Arg | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/14 | 916/2575 | 734/1587 | 245/528 | chr5 | 75635818 | ||
chr5:75635851
|
CCCAGT | C | 3 | a0006a0015a0020 | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
frameshift_variant | HIGH | c.768_772delCCAGT | p.Gln257fs | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/14 | 950/2575 | 768/1587 | 256/528 | chr5 | 75635851 | ||
chr5:75635857
|
G | T | 3 | a0006a0015a0020 | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
missense_variant | MODERATE | c.773G>T | p.Trp258Leu | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/14 | 955/2575 | 773/1587 | 258/528 | chr5 | 75635857 | ||
chr5:75653177
|
C | G | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.834C>G | p.Asn278Lys | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/14 | 1016/2575 | 834/1587 | 278/528 | chr5 | 75653177 | ||
chr5:75653218
|
T | C | 6 | a0008a0009a0014others(3): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
missense_variant | MODERATE | c.875T>C | p.Val292Ala | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/14 | 1057/2575 | 875/1587 | 292/528 | chr5 | 75653218 | ||
chr5:75656085
|
C | G | 2 | a0006a0017 | 9 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(6): Show |
missense_variant | MODERATE | c.954C>G | p.Asn318Lys | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/14 | 1136/2575 | 954/1587 | 318/528 | chr5 | 75656085 | ||
chr5:75663395
|
A | G | 7 | a0006a0008a0011others(4): Show | 28 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(25): Show |
missense_variant&splice_region_variant | MODERATE | c.1097A>G | p.Gln366Arg | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/14 | 1279/2575 | 1097/1587 | 366/528 | chr5 | 75663395 | ||
chr5:75666943
|
C | T | 2 | a0003a0012 | 53 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
missense_variant | MODERATE | c.1343C>T | p.Ser448Leu | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/14 | 1525/2575 | 1343/1587 | 448/528 | chr5 | 75666943 | ||
chr5:75666984
|
C | T | 1 | a0018 | 1 | HG02738.hp2 | stop_gained | HIGH | c.1384C>T | p.Gln462* | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/14 | 1566/2575 | 1384/1587 | 462/528 | chr5 | 75666984 | ||
chr5:75666988
|
G | A | 1 | a0009 | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
stop_gained | HIGH | c.1388G>A | p.Trp463* | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/14 | 1570/2575 | 1388/1587 | 463/528 | chr5 | 75666988 | ||
chr5:75669297
|
G | A | 13 | a0001a0006a0007others(10): Show | 142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
stop_gained | HIGH | c.1439G>A | p.Trp480* | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/14 | 1621/2575 | 1439/1587 | 480/528 | chr5 | 75669297 | ||
chr5:75669341
|
C | G | 1 | a0009 | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
missense_variant | MODERATE | c.1483C>G | p.Leu495Val | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/14 | 1665/2575 | 1483/1587 | 495/528 | chr5 | 75669341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75611742
|
C | T | 1 | a0002c0036 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.108C>T | p.Ala36Ala | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 290/2575 | 108/1587 | 36/528 | chr5 | 75611742 | ||
chr5:75634939
|
T | C | 1 | a0001c0019 | 2 | HG02622.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.642T>C | p.His214His | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/14 | 824/2575 | 642/1587 | 214/528 | chr5 | 75634939 | ||
chr5:75634984
|
A | G | 1 | a0001c0035 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.687A>G | p.Ser229Ser | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/14 | 869/2575 | 687/1587 | 229/528 | chr5 | 75634984 | ||
chr5:75635813
|
G | A | 1 | a0002c0028 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.729G>A | p.Ala243Ala | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/14 | 911/2575 | 729/1587 | 243/528 | chr5 | 75635813 | ||
chr5:75656076
|
G | A | 6 | a0002c0029a0003c0003a0004c0006others(3): Show | 65 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(62): Show |
synonymous_variant | LOW | c.945G>A | p.Thr315Thr | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/14 | 1127/2575 | 945/1587 | 315/528 | chr5 | 75656076 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75611509
|
C | T | 9 | a0001c0001t0006a0007c0007t0006a0007c0007t0012others(6): Show | 20 | HG00642.hp2 HG01192.hp2 HG01261.hp2 others(17): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-126C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | chr5 | 75611509 | ||||||
chr5:75611551
|
G | A | 1 | a0005c0004t0015 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 84 | chr5 | 75611551 | |||||
chr5:75611563
|
TGTCCGAG others(17): Show |
T | 4 | a0001c0001t0021a0003c0003t0005a0004c0005t0008others(1): Show | 42 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-30delATCTGGGT others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 30 | INFO_REALIGN_3_PRIME | chr5 | 75611563 | ||||
chr5:75611582
|
ATCTGGGT others(5): Show |
A | 1 | a0017c0023t0019 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44_-33delCGAGTCTG others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/14 | 33 | INFO_REALIGN_3_PRIME | chr5 | 75611582 | ||||
chr5:75671315
|
T | C | 1 | a0002c0002t0016 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 275 | chr5 | 75671315 | |||||
chr5:75671339
|
C | A | 13 | a0002c0002t0004a0002c0029t0004a0004c0005t0004others(10): Show | 41 | HG00408.hp2 HG00735.hp1 HG01099.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*299C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 299 | chr5 | 75671339 | |||||
chr5:75671374
|
G | C | 29 | a0002c0002t0003a0002c0002t0004a0002c0002t0016others(26): Show | 144 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*334G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 334 | chr5 | 75671374 | |||||
chr5:75671375
|
G | C | 1 | a0001c0001t0017 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 335 | chr5 | 75671375 | |||||
chr5:75671561
|
C | T | 23 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(20): Show | 142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 521 | chr5 | 75671561 | |||||
chr5:75671609
|
C | T | 2 | a0007c0007t0014a0024c0020t0014 | 2 | HG01192.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*569C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 569 | chr5 | 75671609 | |||||
chr5:75671697
|
AT | A | 5 | a0001c0001t0018a0002c0002t0010a0004c0005t0020others(2): Show | 9 | HG01109.hp1 HG01168.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*672delT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 672 | INFO_REALIGN_3_PRIME | chr5 | 75671697 | ||||
chr5:75671697
|
ATT | A | 28 | a0002c0002t0003a0002c0002t0004a0002c0002t0016others(25): Show | 142 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*671_*672delTT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 671 | INFO_REALIGN_3_PRIME | chr5 | 75671697 | ||||
chr5:75671713
|
A | T | 1 | a0007c0007t0013 | 2 | HG02258.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*673A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 673 | chr5 | 75671713 | |||||
chr5:75671744
|
A | T | 1 | a0009c0010t0009 | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*704A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 704 | chr5 | 75671744 | |||||
chr5:75671746
|
T | C | 1 | a0009c0010t0009 | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*706T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 706 | chr5 | 75671746 | |||||
chr5:75671775
|
CTT | C | 23 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(20): Show | 142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*741_*742delTT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 741 | INFO_REALIGN_3_PRIME | chr5 | 75671775 | ||||
chr5:75671837
|
T | TTATCAG | 4 | a0006c0009t0007a0015c0025t0007a0017c0023t0019others(1): Show | 11 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*798_*799insATCAGT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 799 | INFO_REALIGN_3_PRIME | chr5 | 75671837 | ||||
chr5:75671839
|
G | T | 4 | a0006c0009t0007a0015c0025t0007a0017c0023t0019others(1): Show | 11 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*799G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 799 | chr5 | 75671839 | |||||
chr5:75671840
|
A | AGTATCAG others(3): Show |
19 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(16): Show | 131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*802_*803insATCAGT others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 803 | INFO_REALIGN_3_PRIME | chr5 | 75671840 | ||||
chr5:75671840
|
A | T | 4 | a0006c0009t0007a0015c0025t0007a0017c0023t0019others(1): Show | 11 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*800A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 14/14 | 800 | chr5 | 75671840 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75611914
|
CCGGA | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0004c0005t0004g0030others(2): Show | 5 | HG01081.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+90_193+93delGA others(2): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75611914 | |||||
chr5:75611934
|
A | C | 1 | a0002c0002t0002g0328 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.193+107A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75611934 | ||||||
chr5:75611940
|
G | T | 3 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327 | 3 | NA18945.hp2 NA18986.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.193+113G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75611940 | ||||||
chr5:75611949
|
C | G | 2 | a0004c0006t0004g0027a0004c0006t0004g0028 | 4 | NA18972.hp2 NA19007.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+122C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75611949 | ||||||
chr5:75612142
|
T | C | 5 | a0001c0001t0001g0035a0003c0003t0003g0036a0003c0003t0003g0037others(2): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+315T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612142 | ||||||
chr5:75612207
|
T | G | 2 | a0007c0007t0013g0038a0007c0007t0013g0039 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.193+380T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612207 | ||||||
chr5:75612318
|
G | GC | 35 | a0001c0001t0001g0009a0001c0001t0001g0045a0001c0001t0001g0046others(32): Show | 36 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.193+500dupC | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612318 | |||||
chr5:75612318
|
GC | G | 94 | a0001c0001t0001g0035a0001c0001t0001g0200a0001c0001t0001g0201others(91): Show | 105 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.193+500delC | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612318 | |||||
chr5:75612318
|
GCCCCCCC others(12): Show |
G | 75 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(72): Show | 88 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.193+494_193+512del others(19): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612318 | |||||
chr5:75612322
|
C | CCCCCCCC others(13): Show |
4 | a0009c0010t0009g0040a0009c0010t0009g0041a0009c0010t0009g0042others(1): Show | 4 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+500_193+501ins others(20): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612322
|
C | CCCCCCCG others(12): Show |
1 | a0009c0010t0009g0008 | 2 | HG02135.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.193+500_193+501ins others(19): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612322
|
C | CCCCCCGC others(29): Show |
5 | a0005c0004t0003g0079a0005c0004t0003g0080a0005c0004t0003g0081others(2): Show | 5 | HG02602.hp1 HG02738.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+497_193+532dup others(36): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612322
|
C | CCCCCCGC others(47): Show |
1 | a0005c0004t0003g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.193+532_193+533ins others(54): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612322
|
C | CCCCCGCC others(28): Show |
11 | a0005c0004t0003g0183a0005c0004t0003g0184a0005c0004t0003g0186others(8): Show | 11 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+499_193+500ins others(35): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612322
|
C | CCCCCGCC others(46): Show |
7 | a0005c0004t0003g0005a0005c0004t0003g0019a0005c0004t0003g0180others(4): Show | 11 | HG01069.hp1 HG01071.hp1 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+499_193+500ins others(53): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612322
|
C | CCCCCGCC others(64): Show |
3 | a0005c0004t0003g0177a0005c0004t0003g0178a0012c0013t0003g0176 | 3 | HG04228.hp2 NA18962.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.193+499_193+500ins others(71): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612322 | |||||
chr5:75612324
|
CCCCGCCC others(9): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.193+501_193+516del others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612324 | |||||
chr5:75612335
|
G | GCCCCGCC others(48): Show |
1 | a0005c0004t0003g0077 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.193+532_193+533ins others(55): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612335 | |||||
chr5:75612350
|
T | TCCGCCCC others(13): Show |
14 | a0002c0002t0003g0076a0002c0002t0003g0172a0002c0002t0003g0175others(11): Show | 16 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+530_193+531ins others(20): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612350 | |||||
chr5:75612350
|
T | TCCGCCCC others(40): Show |
4 | a0008c0008t0004g0161a0008c0008t0004g0162a0010c0011t0001g0164others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+530_193+531ins others(47): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75612350 | |||||
chr5:75612360
|
G | A | 23 | a0002c0002t0003g0076a0002c0002t0003g0172a0002c0002t0003g0175others(20): Show | 26 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.193+533G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612360 | ||||||
chr5:75612556
|
A | T | 1 | a0004c0005t0002g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.193+729A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612556 | ||||||
chr5:75612594
|
G | T | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.193+767G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612594 | ||||||
chr5:75612621
|
G | C | 76 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(73): Show | 89 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.193+794G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612621 | ||||||
chr5:75612984
|
G | A | 3 | a0001c0001t0006g0084a0001c0001t0006g0196a0022c0032t0012g0195 | 3 | HG02559.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.193+1157G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75612984 | ||||||
chr5:75613364
|
A | G | 2 | a0002c0002t0003g0076a0002c0002t0003g0175 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.193+1537A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75613364 | ||||||
chr5:75613621
|
C | G | 168 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(165): Show | 192 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.193+1794C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75613621 | ||||||
chr5:75613975
|
G | C | 1 | a0001c0001t0006g0243 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193+2148G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75613975 | ||||||
chr5:75614100
|
T | G | 1 | a0004c0006t0004g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193+2273T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614100 | ||||||
chr5:75614147
|
C | T | 233 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(230): Show | 262 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.193+2320C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614147 | ||||||
chr5:75614208
|
TTG | T | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+2385_193+2386d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75614208 | |||||
chr5:75614316
|
C | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-2488C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614316 | ||||||
chr5:75614444
|
TC | T | 8 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(5): Show | 9 | HG02451.hp2 HG02559.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-2358delC | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75614444 | |||||
chr5:75614446
|
C | T | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.194-2358C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614446 | ||||||
chr5:75614699
|
T | C | 1 | a0002c0002t0002g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.194-2105T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614699 | ||||||
chr5:75614701
|
C | T | 2 | a0002c0002t0004g0157a0010c0011t0001g0158 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.194-2103C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614701 | ||||||
chr5:75614737
|
A | G | 4 | a0003c0003t0003g0073a0003c0003t0003g0151a0003c0003t0003g0152others(1): Show | 4 | HG00609.hp2 NA18950.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2067A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614737 | ||||||
chr5:75614765
|
A | G | 10 | a0007c0007t0006g0004a0007c0007t0006g0156a0007c0007t0006g0255others(7): Show | 13 | HG00642.hp2 HG01192.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.194-2039A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614765 | ||||||
chr5:75614899
|
G | C | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-1905G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75614899 | ||||||
chr5:75615009
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.194-1795A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615009 | ||||||
chr5:75615018
|
T | C | 28 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(25): Show | 31 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.194-1786T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615018 | ||||||
chr5:75615044
|
C | T | 2 | a0003c0003t0003g0036a0003c0003t0003g0037 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.194-1760C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615044 | ||||||
chr5:75615045
|
A | G | 237 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(234): Show | 266 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.194-1759A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615045 | ||||||
chr5:75615503
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 9 | HG02027.hp1 NA18942.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-1301G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615503 | ||||||
chr5:75615514
|
G | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-1290G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615514 | ||||||
chr5:75615668
|
C | CTG | 48 | a0001c0001t0001g0069a0001c0001t0001g0126a0001c0001t0001g0127others(45): Show | 50 | HG00621.hp2 HG00735.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.194-1102_194-1101d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75615668 | |||||
chr5:75615668
|
C | CTGTG | 19 | a0001c0001t0001g0035a0001c0001t0001g0133a0001c0001t0001g0134others(16): Show | 23 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-1104_194-1101d others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75615668 | |||||
chr5:75615668
|
CTG | C | 67 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(64): Show | 80 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.194-1102_194-1101d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75615668 | |||||
chr5:75615668
|
CTGTG | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0085a0002c0002t0002g0260others(2): Show | 5 | HG01081.hp2 NA18942.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-1104_194-1101d others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75615668 | |||||
chr5:75615668
|
CTGTGTGT others(5): Show |
C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-1112_194-1101d others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 75615668 | |||||
chr5:75615721
|
T | C | 2 | a0027c0038t0004g0247a0028c0039t0004g0248 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.194-1083T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615721 | ||||||
chr5:75615727
|
C | A | 2 | a0010c0011t0001g0194a0021c0031t0001g0159 | 2 | HG01081.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.194-1077C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615727 | ||||||
chr5:75615934
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.194-870G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615934 | ||||||
chr5:75615956
|
C | T | 9 | a0002c0002t0002g0026a0002c0002t0002g0309a0002c0002t0002g0310others(6): Show | 10 | HG00438.hp1 HG01943.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-848C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75615956 | ||||||
chr5:75616109
|
A | G | 1 | a0002c0002t0002g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.194-695A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616109 | ||||||
chr5:75616181
|
T | C | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.194-623T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616181 | ||||||
chr5:75616457
|
T | C | 1 | a0004c0006t0004g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-347T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616457 | ||||||
chr5:75616557
|
T | C | 1 | a0005c0004t0003g0178 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.194-247T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616557 | ||||||
chr5:75616613
|
G | T | 3 | a0002c0002t0002g0306a0002c0002t0002g0307a0002c0002t0002g0328 | 3 | NA18953.hp1 NA18977.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.194-191G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616613 | ||||||
chr5:75616636
|
C | A | 19 | a0002c0002t0003g0076a0002c0002t0003g0172a0002c0002t0003g0175others(16): Show | 20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.194-168C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616636 | ||||||
chr5:75616679
|
G | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.194-125G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 1/13 | chr5 | 75616679 | ||||||
chr5:75617044
|
G | T | 1 | a0004c0005t0003g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.297+137G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617044 | ||||||
chr5:75617149
|
C | A | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.297+242C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617149 | ||||||
chr5:75617184
|
G | T | 1 | a0002c0002t0002g0305 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.297+277G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617184 | ||||||
chr5:75617196
|
C | T | 1 | a0002c0002t0002g0304 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.297+289C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617196 | ||||||
chr5:75617324
|
C | T | 1 | a0002c0002t0003g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.297+417C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617324 | ||||||
chr5:75617937
|
G | C | 6 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+1030G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617937 | ||||||
chr5:75617971
|
G | A | 136 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(133): Show | 155 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.297+1064G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617971 | ||||||
chr5:75617994
|
T | C | 5 | a0001c0001t0001g0035a0003c0003t0003g0036a0003c0003t0003g0037others(2): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+1087T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75617994 | ||||||
chr5:75618059
|
A | G | 8 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(5): Show | 9 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+1152A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618059 | ||||||
chr5:75618087
|
C | T | 37 | a0001c0001t0021g0146a0003c0003t0005g0022a0003c0003t0005g0142others(34): Show | 39 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.297+1180C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618087 | ||||||
chr5:75618236
|
G | A | 136 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(133): Show | 156 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.297+1329G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618236 | ||||||
chr5:75618268
|
G | A | 116 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(113): Show | 134 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.297+1361G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618268 | ||||||
chr5:75618333
|
C | A | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297+1426C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618333 | ||||||
chr5:75618635
|
A | G | 1 | a0003c0003t0003g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.298-1680A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618635 | ||||||
chr5:75618691
|
T | A | 29 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(26): Show | 33 | HG01069.hp1 HG01071.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.298-1624T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618691 | ||||||
chr5:75618704
|
C | T | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1611C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618704 | ||||||
chr5:75618801
|
A | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1514A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618801 | ||||||
chr5:75618833
|
C | T | 1 | a0013c0016t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.298-1482C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75618833 | ||||||
chr5:75619046
|
A | G | 6 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1269A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619046 | ||||||
chr5:75619056
|
T | C | 1 | a0002c0036t0003g0298 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-1259T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619056 | ||||||
chr5:75619059
|
T | C | 22 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(19): Show | 24 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-1256T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619059 | ||||||
chr5:75619437
|
G | A | 1 | a0004c0006t0004g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.298-878G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619437 | ||||||
chr5:75619452
|
G | A | 2 | a0010c0011t0001g0194a0021c0031t0001g0159 | 2 | HG01081.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.298-863G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619452 | ||||||
chr5:75619627
|
G | A | 2 | a0001c0001t0001g0049a0004c0006t0004g0048 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.298-688G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619627 | ||||||
chr5:75619808
|
T | C | 23 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(20): Show | 25 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.298-507T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619808 | ||||||
chr5:75619905
|
A | G | 5 | a0002c0002t0002g0025a0002c0002t0002g0294a0002c0002t0002g0295others(2): Show | 6 | HG02165.hp2 NA18963.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-410A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75619905 | ||||||
chr5:75620158
|
C | T | 63 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(60): Show | 76 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.298-157C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75620158 | ||||||
chr5:75620175
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-140T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 2/13 | chr5 | 75620175 | ||||||
chr5:75620479
|
A | G | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.396+66A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75620479 | ||||||
chr5:75620857
|
C | T | 29 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(26): Show | 33 | HG01069.hp1 HG01071.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.396+444C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75620857 | ||||||
chr5:75620889
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.396+476G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75620889 | ||||||
chr5:75620993
|
A | G | 136 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(133): Show | 156 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.396+580A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75620993 | ||||||
chr5:75621047
|
G | A | 136 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(133): Show | 156 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.396+634G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621047 | ||||||
chr5:75621093
|
G | C | 1 | a0004c0006t0004g0048 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.396+680G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621093 | ||||||
chr5:75621147
|
G | A | 71 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(68): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.396+734G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621147 | ||||||
chr5:75621287
|
T | C | 1 | a0007c0007t0013g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.396+874T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621287 | ||||||
chr5:75621306
|
G | A | 2 | a0007c0007t0013g0038a0007c0007t0013g0039 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.396+893G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621306 | ||||||
chr5:75621333
|
C | G | 1 | a0017c0023t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.396+920C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621333 | ||||||
chr5:75621358
|
G | T | 2 | a0007c0007t0013g0038a0007c0007t0013g0039 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.396+945G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621358 | ||||||
chr5:75621573
|
G | C | 1 | a0013c0016t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.396+1160G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621573 | ||||||
chr5:75621613
|
C | T | 1 | a0002c0002t0003g0266 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.396+1200C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621613 | ||||||
chr5:75621924
|
G | T | 1 | a0018c0022t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.396+1511G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75621924 | ||||||
chr5:75622037
|
A | G | 78 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(75): Show | 91 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.396+1624A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75622037 | ||||||
chr5:75622060
|
C | G | 5 | a0007c0007t0006g0004a0007c0007t0006g0255a0007c0007t0006g0257others(2): Show | 8 | HG00642.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.396+1647C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75622060 | ||||||
chr5:75622103
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0019t0001g0074others(4): Show | 7 | HG01081.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.396+1690C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75622103 | ||||||
chr5:75622681
|
C | T | 1 | a0025c0021t0022g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.396+2268C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75622681 | ||||||
chr5:75622975
|
C | T | 1 | a0005c0004t0003g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.396+2562C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75622975 | ||||||
chr5:75623031
|
G | T | 33 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(30): Show | 37 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.397-2616G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623031 | ||||||
chr5:75623072
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.397-2575T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623072 | ||||||
chr5:75623080
|
G | T | 10 | a0007c0007t0006g0004a0007c0007t0006g0156a0007c0007t0006g0255others(7): Show | 13 | HG00642.hp2 HG01192.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.397-2567G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623080 | ||||||
chr5:75623136
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.397-2511C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623136 | ||||||
chr5:75623188
|
T | C | 144 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(141): Show | 166 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.397-2459T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623188 | ||||||
chr5:75623411
|
C | T | 1 | a0005c0004t0003g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.397-2236C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623411 | ||||||
chr5:75623508
|
C | T | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.397-2139C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623508 | ||||||
chr5:75623584
|
G | A | 134 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(131): Show | 153 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.397-2063G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623584 | ||||||
chr5:75623710
|
G | A | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397-1937G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623710 | ||||||
chr5:75623739
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-1908T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623739 | ||||||
chr5:75623998
|
A | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-1649A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75623998 | ||||||
chr5:75624161
|
A | G | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397-1486A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624161 | ||||||
chr5:75624172
|
G | A | 1 | a0005c0004t0003g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.397-1475G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624172 | ||||||
chr5:75624270
|
A | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-1377A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624270 | ||||||
chr5:75624434
|
A | G | 1 | a0001c0001t0006g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.397-1213A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624434 | ||||||
chr5:75624665
|
C | T | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-982C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624665 | ||||||
chr5:75624779
|
C | A | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397-868C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624779 | ||||||
chr5:75624810
|
A | G | 1 | a0010c0011t0001g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.397-837A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624810 | ||||||
chr5:75624831
|
A | T | 1 | a0004c0006t0004g0217 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.397-816A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624831 | ||||||
chr5:75624960
|
C | T | 1 | a0004c0006t0004g0216 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.397-687C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75624960 | ||||||
chr5:75625043
|
C | A | 2 | a0002c0002t0002g0267a0002c0002t0002g0268 | 2 | NA18954.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.397-604C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625043 | ||||||
chr5:75625075
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.397-572A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625075 | ||||||
chr5:75625233
|
G | T | 2 | a0002c0002t0002g0267a0002c0002t0002g0268 | 2 | NA18954.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.397-414G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625233 | ||||||
chr5:75625345
|
G | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.397-302G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625345 | ||||||
chr5:75625448
|
G | A | 1 | a0003c0003t0005g0142 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.397-199G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625448 | ||||||
chr5:75625517
|
T | A | 1 | a0002c0002t0002g0269 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.397-130T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625517 | ||||||
chr5:75625529
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.397-118A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 3/13 | chr5 | 75625529 | ||||||
chr5:75626058
|
C | T | 108 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(105): Show | 125 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.600+103C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75626058 | ||||||
chr5:75626071
|
G | A | 140 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(137): Show | 161 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.600+116G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75626071 | ||||||
chr5:75626235
|
A | G | 1 | a0015c0026t0004g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+280A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75626235 | ||||||
chr5:75626623
|
T | C | 1 | a0002c0002t0002g0309 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.600+668T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75626623 | ||||||
chr5:75626782
|
GT | G | 136 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(133): Show | 156 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.600+839delT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 75626782 | |||||
chr5:75626791
|
T | G | 115 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(112): Show | 133 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.600+836T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75626791 | ||||||
chr5:75626912
|
A | G | 24 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(21): Show | 26 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+957A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75626912 | ||||||
chr5:75627077
|
C | T | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+1122C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627077 | ||||||
chr5:75627153
|
A | G | 138 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(135): Show | 158 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.600+1198A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627153 | ||||||
chr5:75627158
|
C | A | 6 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(3): Show | 7 | HG01081.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+1203C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627158 | ||||||
chr5:75627193
|
T | G | 5 | a0001c0001t0001g0035a0003c0003t0003g0036a0003c0003t0003g0037others(2): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+1238T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627193 | ||||||
chr5:75627279
|
C | T | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+1324C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627279 | ||||||
chr5:75627349
|
T | C | 1 | a0001c0001t0006g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.600+1394T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627349 | ||||||
chr5:75627368
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0090 | 2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.600+1413T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627368 | ||||||
chr5:75627376
|
C | T | 40 | a0001c0001t0021g0146a0003c0003t0003g0073a0003c0003t0003g0151others(37): Show | 42 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.600+1421C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627376 | ||||||
chr5:75627398
|
T | C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+1443T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627398 | ||||||
chr5:75627496
|
G | A | 138 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(135): Show | 158 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.600+1541G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627496 | ||||||
chr5:75627573
|
A | G | 3 | a0003c0003t0003g0073a0003c0003t0003g0151a0003c0003t0003g0152 | 3 | HG00609.hp2 NA18950.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.600+1618A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627573 | ||||||
chr5:75627613
|
G | A | 2 | a0002c0002t0002g0269a0002c0002t0002g0270 | 2 | NA18949.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.600+1658G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627613 | ||||||
chr5:75627701
|
C | T | 22 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(19): Show | 24 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.600+1746C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627701 | ||||||
chr5:75627749
|
C | G | 2 | a0001c0001t0001g0049a0004c0006t0004g0048 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.600+1794C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627749 | ||||||
chr5:75627756
|
C | T | 108 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(105): Show | 125 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.600+1801C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627756 | ||||||
chr5:75627765
|
A | G | 138 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(135): Show | 158 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.600+1810A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627765 | ||||||
chr5:75627778
|
G | C | 75 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(72): Show | 88 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.600+1823G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627778 | ||||||
chr5:75627793
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.600+1838C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627793 | ||||||
chr5:75627894
|
A | G | 1 | a0008c0008t0004g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.600+1939A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627894 | ||||||
chr5:75627935
|
T | A | 2 | a0013c0016t0001g0029a0013c0016t0001g0033 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.600+1980T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75627935 | ||||||
chr5:75628107
|
C | T | 17 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(14): Show | 20 | HG00642.hp2 HG01192.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.600+2152C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628107 | ||||||
chr5:75628131
|
G | A | 136 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(133): Show | 156 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.600+2176G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628131 | ||||||
chr5:75628149
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+2194T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628149 | ||||||
chr5:75628159
|
G | A | 1 | a0013c0016t0001g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.600+2204G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628159 | ||||||
chr5:75628282
|
G | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+2327G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628282 | ||||||
chr5:75628364
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.600+2409G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628364 | ||||||
chr5:75628449
|
G | A | 1 | a0004c0005t0008g0021 | 2 | HG01255.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.600+2494G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628449 | ||||||
chr5:75628622
|
A | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0124a0001c0001t0018g0123 | 4 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+2667A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628622 | ||||||
chr5:75628724
|
T | A | 1 | a0004c0006t0004g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.600+2769T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628724 | ||||||
chr5:75628952
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.600+2997G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628952 | ||||||
chr5:75628967
|
G | T | 1 | a0002c0002t0002g0307 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.600+3012G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75628967 | ||||||
chr5:75629065
|
A | G | 138 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(135): Show | 158 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.600+3110A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629065 | ||||||
chr5:75629247
|
T | C | 2 | a0002c0002t0002g0317a0002c0002t0002g0318 | 2 | HG01257.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.600+3292T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629247 | ||||||
chr5:75629337
|
C | T | 107 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(104): Show | 124 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.600+3382C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629337 | ||||||
chr5:75629355
|
G | A | 1 | a0004c0006t0004g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.600+3400G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629355 | ||||||
chr5:75629370
|
G | T | 21 | a0002c0002t0003g0076a0002c0002t0003g0172a0002c0002t0003g0175others(18): Show | 23 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.600+3415G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629370 | ||||||
chr5:75629437
|
A | T | 1 | a0004c0005t0003g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.600+3482A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629437 | ||||||
chr5:75629476
|
C | T | 2 | a0002c0002t0002g0304a0002c0002t0010g0292 | 2 | NA18999.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.600+3521C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629476 | ||||||
chr5:75629548
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.600+3593T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629548 | ||||||
chr5:75629610
|
C | CAA | 22 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(19): Show | 24 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.600+3665_600+3666d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 75629610 | |||||
chr5:75629870
|
G | A | 2 | a0004c0005t0011g0007a0010c0011t0001g0158 | 3 | HG01243.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.600+3915G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75629870 | ||||||
chr5:75630017
|
C | T | 1 | a0002c0002t0002g0321 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.600+4062C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630017 | ||||||
chr5:75630138
|
G | T | 6 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+4183G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630138 | ||||||
chr5:75630143
|
A | G | 2 | a0003c0003t0005g0240a0003c0003t0005g0241 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.600+4188A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630143 | ||||||
chr5:75630276
|
C | G | 2 | a0010c0011t0001g0194a0015c0025t0007g0252 | 2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.600+4321C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630276 | ||||||
chr5:75630324
|
A | G | 36 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0084others(33): Show | 41 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.600+4369A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630324 | ||||||
chr5:75630375
|
A | T | 2 | a0003c0003t0005g0240a0003c0003t0005g0241 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.600+4420A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630375 | ||||||
chr5:75630421
|
C | T | 47 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(44): Show | 51 | HG00741.hp1 HG01106.hp2 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.600+4466C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630421 | ||||||
chr5:75630489
|
A | T | 4 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163others(1): Show | 4 | HG01081.hp2 HG01243.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-4409A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630489 | ||||||
chr5:75630516
|
G | A | 4 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163others(1): Show | 4 | HG01081.hp2 HG01243.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-4382G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630516 | ||||||
chr5:75630522
|
C | T | 1 | a0001c0001t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.601-4376C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630522 | ||||||
chr5:75630741
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.601-4157G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630741 | ||||||
chr5:75630953
|
A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.601-3945A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75630953 | ||||||
chr5:75631005
|
G | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.601-3893G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631005 | ||||||
chr5:75631065
|
T | C | 10 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(7): Show | 11 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.601-3833T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631065 | ||||||
chr5:75631214
|
G | A | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.601-3684G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631214 | ||||||
chr5:75631371
|
G | C | 11 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(8): Show | 12 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-3527G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631371 | ||||||
chr5:75631427
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-3471G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631427 | ||||||
chr5:75631464
|
C | T | 1 | a0024c0020t0014g0254 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.601-3434C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631464 | ||||||
chr5:75631570
|
G | A | 1 | a0015c0025t0007g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601-3328G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631570 | ||||||
chr5:75631571
|
C | G | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601-3327C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631571 | ||||||
chr5:75631587
|
G | A | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.601-3311G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631587 | ||||||
chr5:75631620
|
T | G | 11 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(8): Show | 12 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-3278T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631620 | ||||||
chr5:75631662
|
C | T | 14 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(11): Show | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-3236C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631662 | ||||||
chr5:75631694
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.601-3204A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631694 | ||||||
chr5:75631799
|
T | C | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-3099T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631799 | ||||||
chr5:75631825
|
G | T | 17 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(14): Show | 20 | HG03704.hp2 HG03927.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.601-3073G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631825 | ||||||
chr5:75631832
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601-3066G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631832 | ||||||
chr5:75631860
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 163 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.601-3038C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631860 | ||||||
chr5:75631934
|
C | T | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.601-2964C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75631934 | ||||||
chr5:75632010
|
C | T | 1 | a0002c0002t0002g0291 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.601-2888C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632010 | ||||||
chr5:75632106
|
C | CA | 8 | a0001c0001t0001g0133a0001c0001t0001g0200a0001c0001t0001g0201others(5): Show | 9 | HG01257.hp1 HG01952.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-2775dupA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 75632106 | |||||
chr5:75632106
|
CA | C | 15 | a0001c0001t0001g0087a0001c0001t0001g0122a0001c0001t0001g0139others(12): Show | 15 | HG01168.hp1 HG01516.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-2775delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 75632106 | |||||
chr5:75632244
|
C | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 166 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.601-2654C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632244 | ||||||
chr5:75632322
|
A | G | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.601-2576A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632322 | ||||||
chr5:75632451
|
A | G | 2 | a0001c0001t0001g0035a0027c0038t0004g0247 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.601-2447A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632451 | ||||||
chr5:75632468
|
A | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(252): Show | 283 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.601-2430A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632468 | ||||||
chr5:75632716
|
C | T | 4 | a0001c0001t0001g0035a0002c0002t0002g0289a0002c0002t0002g0290others(1): Show | 4 | HG00140.hp1 HG01106.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-2182C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632716 | ||||||
chr5:75632809
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0121 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.601-2089A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632809 | ||||||
chr5:75632850
|
G | A | 5 | a0002c0002t0002g0261a0002c0002t0003g0262a0002c0002t0003g0263others(2): Show | 5 | HG02040.hp2 HG03490.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-2048G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632850 | ||||||
chr5:75632863
|
C | T | 1 | a0005c0004t0003g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.601-2035C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632863 | ||||||
chr5:75632874
|
C | T | 1 | a0001c0001t0006g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.601-2024C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632874 | ||||||
chr5:75632881
|
G | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG00438.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.601-2017G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632881 | ||||||
chr5:75632906
|
A | T | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.601-1992A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632906 | ||||||
chr5:75632973
|
A | G | 7 | a0004c0005t0004g0030a0004c0005t0011g0007a0009c0010t0009g0008others(4): Show | 9 | HG01243.hp2 HG02027.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-1925A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632973 | ||||||
chr5:75632983
|
T | G | 1 | a0002c0002t0002g0271 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601-1915T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75632983 | ||||||
chr5:75633058
|
G | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 229 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.601-1840G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633058 | ||||||
chr5:75633072
|
A | G | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.601-1826A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633072 | ||||||
chr5:75633077
|
T | G | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0084others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.601-1821T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633077 | ||||||
chr5:75633147
|
C | T | 14 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(11): Show | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-1751C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633147 | ||||||
chr5:75633256
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.601-1642G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633256 | ||||||
chr5:75633315
|
G | A | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601-1583G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633315 | ||||||
chr5:75633367
|
A | T | 7 | a0002c0002t0002g0261a0002c0002t0003g0262a0002c0002t0003g0263others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-1531A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633367 | ||||||
chr5:75633446
|
G | A | 14 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(11): Show | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-1452G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633446 | ||||||
chr5:75633479
|
T | C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.601-1419T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633479 | ||||||
chr5:75633487
|
G | A | 43 | a0002c0002t0002g0261a0002c0002t0003g0076a0002c0002t0003g0136others(40): Show | 46 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-1411G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633487 | ||||||
chr5:75633490
|
G | A | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-1408G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633490 | ||||||
chr5:75633822
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 197 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.601-1076G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75633822 | ||||||
chr5:75634203
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.601-695G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75634203 | ||||||
chr5:75634259
|
C | T | 3 | a0003c0003t0003g0066a0003c0003t0003g0117a0003c0003t0003g0118 | 3 | HG02056.hp2 NA19079.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.601-639C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75634259 | ||||||
chr5:75634443
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-455T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75634443 | ||||||
chr5:75634602
|
G | A | 15 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(12): Show | 16 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.601-296G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75634602 | ||||||
chr5:75634627
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.601-271T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75634627 | ||||||
chr5:75634863
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.601-35G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 5/13 | chr5 | 75634863 | ||||||
chr5:75635093
|
G | A | 13 | a0001c0001t0001g0035a0008c0008t0004g0016a0008c0008t0004g0161others(10): Show | 14 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.699+97G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635093 | ||||||
chr5:75635148
|
A | G | 1 | a0004c0006t0004g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.699+152A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635148 | ||||||
chr5:75635178
|
G | C | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.699+182G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635178 | ||||||
chr5:75635246
|
C | T | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.699+250C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635246 | ||||||
chr5:75635266
|
T | G | 1 | a0002c0002t0003g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.699+270T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635266 | ||||||
chr5:75635361
|
T | A | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0084others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.699+365T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635361 | ||||||
chr5:75635373
|
TA | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 163 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.699+378delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635373 | ||||||
chr5:75635443
|
A | G | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.700-341A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635443 | ||||||
chr5:75635508
|
G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(252): Show | 283 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.700-276G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635508 | ||||||
chr5:75635672
|
C | T | 36 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0136others(33): Show | 39 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.700-112C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 6/13 | chr5 | 75635672 | ||||||
chr5:75635898
|
C | T | 1 | a0001c0001t0006g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.798+16C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75635898 | ||||||
chr5:75635921
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0099 | 2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.798+39G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75635921 | ||||||
chr5:75635956
|
G | A | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.798+74G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75635956 | ||||||
chr5:75636073
|
G | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+191G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75636073 | ||||||
chr5:75636092
|
G | A | 2 | a0011c0012t0004g0299a0011c0012t0004g0300 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.798+210G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75636092 | ||||||
chr5:75636247
|
T | C | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0084others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+365T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75636247 | ||||||
chr5:75636274
|
G | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(166): Show | 190 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.798+392G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75636274 | ||||||
chr5:75636543
|
G | T | 14 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(11): Show | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.798+661G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75636543 | ||||||
chr5:75636927
|
T | C | 1 | a0002c0029t0004g0272 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.798+1045T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75636927 | ||||||
chr5:75637090
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | NA18950.hp2 NA18984.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.798+1208A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637090 | ||||||
chr5:75637217
|
C | T | 1 | a0004c0005t0011g0007 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.798+1335C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637217 | ||||||
chr5:75637240
|
C | A | 1 | a0005c0004t0003g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.798+1358C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637240 | ||||||
chr5:75637240
|
C | CA | 20 | a0002c0002t0002g0023a0002c0002t0002g0024a0002c0002t0002g0268others(17): Show | 22 | HG01255.hp1 HG01358.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.798+1391dupA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAA | 7 | a0002c0002t0002g0025a0002c0002t0002g0267a0002c0002t0002g0273others(4): Show | 8 | HG01433.hp2 HG02165.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+1390_798+1391d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAA | 9 | a0002c0002t0002g0295a0002c0002t0002g0305a0002c0002t0002g0317others(6): Show | 11 | HG01257.hp1 HG02683.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+1389_798+1391d others(5): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAA | 12 | a0002c0002t0003g0136a0002c0002t0003g0138a0005c0004t0003g0077others(9): Show | 12 | HG01516.hp2 HG02698.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.798+1388_798+1391d others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAA | 10 | a0002c0002t0002g0261a0002c0002t0002g0294a0002c0002t0003g0266others(7): Show | 10 | HG01123.hp2 HG01358.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.798+1387_798+1391d others(7): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(1): Show |
20 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(17): Show | 21 | HG00609.hp2 HG01952.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.798+1384_798+1391d others(10): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0126a0001c0001t0001g0202a0002c0002t0003g0172others(9): Show | 13 | HG00423.hp1 HG00621.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.798+1383_798+1391d others(11): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(3): Show |
7 | a0002c0002t0003g0076a0003c0003t0005g0147a0003c0003t0005g0228others(4): Show | 7 | HG01071.hp1 HG02523.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.798+1382_798+1391d others(12): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0021g0146a0003c0003t0003g0151a0003c0003t0005g0227others(3): Show | 7 | HG01361.hp1 NA18948.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+1381_798+1391d others(13): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(5): Show |
2 | a0003c0003t0005g0225a0003c0003t0005g0226 | 2 | NA18965.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.798+1380_798+1391d others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(6): Show |
4 | a0003c0003t0005g0022a0003c0003t0005g0145a0003c0003t0005g0198others(1): Show | 5 | NA18978.hp2 NA18985.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+1379_798+1391d others(15): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(7): Show |
2 | a0002c0002t0016g0171a0012c0013t0003g0176 | 2 | HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.798+1378_798+1391d others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(8): Show |
1 | a0003c0003t0005g0223 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.798+1377_798+1391d others(17): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(12): Show |
1 | a0002c0002t0002g0324 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.798+1373_798+1391d others(21): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
C | CAAAAAAA others(13): Show |
1 | a0003c0003t0005g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.798+1372_798+1391d others(22): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAA | C | 7 | a0001c0019t0001g0075a0004c0005t0011g0007a0011c0012t0004g0299others(4): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+1389_798+1391d others(5): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAA | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0243others(10): Show | 13 | HG01081.hp1 HG01891.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.798+1388_798+1391d others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAA | C | 13 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(10): Show | 14 | HG00735.hp1 HG01261.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.798+1387_798+1391d others(7): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAAA | C | 12 | a0005c0004t0003g0186a0008c0008t0004g0016a0008c0008t0004g0162others(9): Show | 13 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.798+1386_798+1391d others(8): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAAAA others(3): Show |
C | 3 | a0013c0024t0003g0316a0016c0018t0003g0250a0016c0018t0003g0251 | 3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.798+1382_798+1391d others(12): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0100others(3): Show | 7 | HG00423.hp2 HG02738.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+1379_798+1391d others(15): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAAAA others(7): Show |
C | 82 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 95 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.798+1378_798+1391d others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.798+1377_798+1391d others(17): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637240
|
CAAAAAAA others(9): Show |
C | 7 | a0007c0007t0006g0004a0007c0007t0006g0255a0007c0007t0006g0257others(4): Show | 10 | HG00642.hp2 HG01243.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.798+1376_798+1391d others(18): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637240 | |||||
chr5:75637268
|
AAAAAAG | A | 9 | a0006c0009t0007g0209a0006c0009t0007g0210a0006c0009t0007g0211others(6): Show | 10 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.798+1390_798+1395d others(8): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637268 | |||||
chr5:75637271
|
A | AAAAAAAA others(6): Show |
1 | a0003c0003t0005g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.798+1391_798+1392i others(15): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75637271 | |||||
chr5:75637274
|
G | A | 1 | a0003c0003t0005g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.798+1392G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637274 | ||||||
chr5:75637335
|
G | A | 1 | a0017c0023t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.798+1453G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637335 | ||||||
chr5:75637353
|
C | T | 1 | a0004c0006t0004g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.798+1471C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637353 | ||||||
chr5:75637440
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.798+1558C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637440 | ||||||
chr5:75637454
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.798+1572C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637454 | ||||||
chr5:75637492
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.798+1610C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637492 | ||||||
chr5:75637515
|
A | T | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+1633A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637515 | ||||||
chr5:75637530
|
C | A | 1 | a0003c0003t0003g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.798+1648C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637530 | ||||||
chr5:75637781
|
A | G | 44 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(41): Show | 48 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.798+1899A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637781 | ||||||
chr5:75637849
|
G | C | 1 | a0001c0001t0006g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.798+1967G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637849 | ||||||
chr5:75637862
|
C | T | 37 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(34): Show | 41 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.798+1980C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637862 | ||||||
chr5:75637987
|
G | C | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+2105G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75637987 | ||||||
chr5:75638045
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.798+2163T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638045 | ||||||
chr5:75638184
|
A | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(86): Show | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.798+2302A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638184 | ||||||
chr5:75638190
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01081.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.798+2308T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638190 | ||||||
chr5:75638388
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.798+2506T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638388 | ||||||
chr5:75638417
|
A | G | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.798+2535A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638417 | ||||||
chr5:75638447
|
T | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(35): Show | 42 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.798+2565T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638447 | ||||||
chr5:75638516
|
A | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+2634A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638516 | ||||||
chr5:75638538
|
A | G | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+2656A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638538 | ||||||
chr5:75638625
|
A | G | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(21): Show | 27 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+2743A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638625 | ||||||
chr5:75638676
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.798+2794G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638676 | ||||||
chr5:75638781
|
G | A | 3 | a0001c0001t0006g0246a0013c0016t0001g0029a0013c0016t0001g0033 | 3 | HG02615.hp2 HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.798+2899G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638781 | ||||||
chr5:75638834
|
T | G | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(35): Show | 42 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.798+2952T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75638834 | ||||||
chr5:75639155
|
A | T | 1 | a0004c0005t0011g0007 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.798+3273A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639155 | ||||||
chr5:75639202
|
T | G | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+3320T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639202 | ||||||
chr5:75639218
|
C | T | 1 | a0002c0002t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.798+3336C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639218 | ||||||
chr5:75639244
|
G | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(253): Show | 285 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.798+3362G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639244 | ||||||
chr5:75639284
|
C | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+3402C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639284 | ||||||
chr5:75639288
|
C | G | 1 | a0004c0006t0004g0048 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.798+3406C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639288 | ||||||
chr5:75639342
|
G | A | 1 | a0003c0003t0005g0147 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.798+3460G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639342 | ||||||
chr5:75639347
|
C | T | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.798+3465C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639347 | ||||||
chr5:75639350
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.798+3468C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639350 | ||||||
chr5:75639466
|
G | A | 2 | a0006c0015t0001g0020a0006c0015t0001g0208 | 3 | HG00741.hp1 HG01106.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.798+3584G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639466 | ||||||
chr5:75639745
|
A | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+3863A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639745 | ||||||
chr5:75639766
|
A | G | 7 | a0004c0005t0004g0030a0004c0005t0011g0007a0009c0010t0009g0008others(4): Show | 9 | HG01243.hp2 HG02027.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+3884A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639766 | ||||||
chr5:75639854
|
T | C | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 12 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.798+3972T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639854 | ||||||
chr5:75639984
|
G | A | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.798+4102G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75639984 | ||||||
chr5:75640000
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.798+4118A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640000 | ||||||
chr5:75640045
|
C | CT | 8 | a0002c0036t0003g0298a0004c0005t0004g0030a0011c0012t0004g0299others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+4174dupT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75640045 | |||||
chr5:75640045
|
CT | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+4174delT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75640045 | |||||
chr5:75640074
|
C | T | 22 | a0001c0001t0001g0035a0001c0001t0006g0084a0001c0001t0006g0154others(19): Show | 25 | HG00642.hp2 HG01192.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.798+4192C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640074 | ||||||
chr5:75640178
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.798+4296G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640178 | ||||||
chr5:75640204
|
C | T | 4 | a0007c0007t0006g0156a0007c0007t0014g0155a0010c0011t0001g0158others(1): Show | 4 | HG01192.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+4322C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640204 | ||||||
chr5:75640207
|
T | C | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.798+4325T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640207 | ||||||
chr5:75640247
|
G | A | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+4365G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640247 | ||||||
chr5:75640445
|
A | G | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 12 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.798+4563A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640445 | ||||||
chr5:75640505
|
G | A | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.798+4623G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640505 | ||||||
chr5:75640545
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.798+4663C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640545 | ||||||
chr5:75640571
|
G | A | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+4689G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640571 | ||||||
chr5:75640615
|
C | G | 3 | a0003c0014t0003g0071a0003c0014t0003g0131a0003c0014t0003g0132 | 3 | NA18963.hp2 NA18977.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.798+4733C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640615 | ||||||
chr5:75640628
|
G | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+4746G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640628 | ||||||
chr5:75640785
|
C | G | 1 | a0017c0023t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.798+4903C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640785 | ||||||
chr5:75640973
|
C | T | 1 | a0003c0003t0005g0238 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.798+5091C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75640973 | ||||||
chr5:75641163
|
T | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+5281T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641163 | ||||||
chr5:75641216
|
G | A | 2 | a0002c0002t0002g0269a0002c0002t0002g0270 | 2 | NA18949.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.798+5334G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641216 | ||||||
chr5:75641265
|
C | CAAAG | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+5385_798+5386i others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75641265 | |||||
chr5:75641304
|
T | C | 3 | a0009c0010t0009g0008a0009c0010t0009g0042a0009c0010t0009g0043 | 4 | HG02132.hp1 HG02135.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+5422T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641304 | ||||||
chr5:75641315
|
C | A | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+5433C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641315 | ||||||
chr5:75641410
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0046others(7): Show | 11 | HG02027.hp1 NA18942.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+5528G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641410 | ||||||
chr5:75641413
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+5531A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641413 | ||||||
chr5:75641448
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.798+5566C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641448 | ||||||
chr5:75641576
|
G | C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+5694G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641576 | ||||||
chr5:75641600
|
C | T | 18 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(15): Show | 20 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.798+5718C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641600 | ||||||
chr5:75641710
|
T | C | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+5828T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641710 | ||||||
chr5:75641832
|
A | C | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.798+5950A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641832 | ||||||
chr5:75641899
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+6017G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75641899 | ||||||
chr5:75642088
|
T | G | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.798+6206T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642088 | ||||||
chr5:75642138
|
TGA | T | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+6262_798+6263d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75642138 | |||||
chr5:75642253
|
C | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+6371C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642253 | ||||||
chr5:75642255
|
G | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0006c0015t0001g0020others(1): Show | 5 | HG00741.hp1 HG01081.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+6373G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642255 | ||||||
chr5:75642270
|
C | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+6388C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642270 | ||||||
chr5:75642294
|
G | C | 3 | a0001c0001t0001g0068a0004c0005t0004g0030a0004c0005t0011g0007 | 4 | HG01243.hp2 HG03834.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+6412G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642294 | ||||||
chr5:75642377
|
C | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+6495C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642377 | ||||||
chr5:75642379
|
A | G | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+6497A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642379 | ||||||
chr5:75642387
|
C | T | 1 | a0004c0005t0011g0007 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.798+6505C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642387 | ||||||
chr5:75642388
|
G | A | 2 | a0003c0003t0003g0117a0004c0005t0003g0034 | 2 | HG02886.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.798+6506G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642388 | ||||||
chr5:75642395
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.798+6513G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642395 | ||||||
chr5:75642405
|
C | T | 1 | a0005c0004t0015g0188 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.798+6523C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642405 | ||||||
chr5:75642430
|
C | T | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.798+6548C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642430 | ||||||
chr5:75642439
|
C | T | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.798+6557C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642439 | ||||||
chr5:75642466
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+6584G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642466 | ||||||
chr5:75642466
|
G | T | 9 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(6): Show | 11 | HG03927.hp2 NA18962.hp1 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+6584G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642466 | ||||||
chr5:75642469
|
T | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+6587T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642469 | ||||||
chr5:75642485
|
C | T | 18 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(15): Show | 21 | HG01361.hp1 HG01952.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.798+6603C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642485 | ||||||
chr5:75642486
|
G | A | 49 | a0001c0001t0001g0126a0001c0001t0001g0203a0001c0001t0021g0146others(46): Show | 53 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.798+6604G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642486 | ||||||
chr5:75642528
|
G | A | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+6646G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642528 | ||||||
chr5:75642554
|
C | T | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+6672C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642554 | ||||||
chr5:75642607
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+6725A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642607 | ||||||
chr5:75642639
|
T | TCA | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.798+6758_798+6759d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75642639 | |||||
chr5:75642652
|
C | T | 20 | a0002c0002t0002g0274a0008c0008t0004g0016a0008c0008t0004g0161others(17): Show | 22 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.798+6770C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642652 | ||||||
chr5:75642657
|
G | A | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.798+6775G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642657 | ||||||
chr5:75642695
|
T | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(26): Show | 34 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.798+6813T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642695 | ||||||
chr5:75642717
|
G | C | 6 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+6835G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642717 | ||||||
chr5:75642725
|
C | A | 2 | a0003c0003t0005g0017a0003c0003t0005g0174 | 3 | HG02451.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.798+6843C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642725 | ||||||
chr5:75642746
|
T | C | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+6864T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642746 | ||||||
chr5:75642782
|
C | T | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+6900C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642782 | ||||||
chr5:75642814
|
A | T | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+6932A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642814 | ||||||
chr5:75642839
|
G | A | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.798+6957G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642839 | ||||||
chr5:75642879
|
C | T | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 11 | HG01167.hp2 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+6997C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642879 | ||||||
chr5:75642905
|
C | T | 2 | a0002c0002t0002g0288a0004c0006t0004g0199 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.798+7023C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642905 | ||||||
chr5:75642925
|
G | T | 1 | a0002c0002t0002g0294 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.798+7043G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642925 | ||||||
chr5:75642994
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(82): Show | 98 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.798+7112C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75642994 | ||||||
chr5:75643003
|
G | A | 1 | a0003c0003t0005g0233 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.798+7121G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643003 | ||||||
chr5:75643031
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+7149A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643031 | ||||||
chr5:75643033
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+7151G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643033 | ||||||
chr5:75643097
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.798+7215A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643097 | ||||||
chr5:75643187
|
C | T | 18 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(15): Show | 20 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.798+7305C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643187 | ||||||
chr5:75643209
|
T | C | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.798+7327T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643209 | ||||||
chr5:75643229
|
G | A | 30 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(27): Show | 35 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.798+7347G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643229 | ||||||
chr5:75643239
|
T | C | 1 | a0005c0004t0003g0193 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.798+7357T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643239 | ||||||
chr5:75643284
|
C | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0196 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.798+7402C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643284 | ||||||
chr5:75643431
|
CAAGAACT others(2): Show |
C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+7550_798+7558d others(11): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643431 | ||||||
chr5:75643432
|
A | G | 14 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(11): Show | 15 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.798+7550A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643432 | ||||||
chr5:75643438
|
T | G | 1 | a0005c0004t0003g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.798+7556T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643438 | ||||||
chr5:75643440
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(249): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.798+7558T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643440 | ||||||
chr5:75643441
|
G | A | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.798+7559G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643441 | ||||||
chr5:75643442
|
T | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+7560T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643442 | ||||||
chr5:75643446
|
G | C | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+7564G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643446 | ||||||
chr5:75643453
|
GA | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+7573delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75643453 | |||||
chr5:75643467
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.798+7585T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643467 | ||||||
chr5:75643513
|
T | A | 1 | a0004c0005t0008g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.798+7631T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643513 | ||||||
chr5:75643528
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+7646G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643528 | ||||||
chr5:75643535
|
G | A | 1 | a0005c0004t0003g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.798+7653G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643535 | ||||||
chr5:75643537
|
A | C | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.798+7655A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643537 | ||||||
chr5:75643565
|
T | C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.798+7683T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643565 | ||||||
chr5:75643568
|
G | A | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+7686G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643568 | ||||||
chr5:75643582
|
A | G | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+7700A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643582 | ||||||
chr5:75643595
|
T | C | 14 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(11): Show | 18 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.798+7713T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643595 | ||||||
chr5:75643600
|
A | G | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.798+7718A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643600 | ||||||
chr5:75643613
|
A | G | 15 | a0001c0001t0001g0098a0001c0001t0001g0101a0008c0008t0004g0016others(12): Show | 16 | HG00423.hp2 HG00735.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+7731A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643613 | ||||||
chr5:75643618
|
G | T | 67 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(64): Show | 74 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.798+7736G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643618 | ||||||
chr5:75643658
|
G | C | 1 | a0006c0009t0007g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.798+7776G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643658 | ||||||
chr5:75643668
|
ACT | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+7789_798+7790d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75643668 | |||||
chr5:75643704
|
C | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 166 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.798+7822C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643704 | ||||||
chr5:75643740
|
C | G | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+7858C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643740 | ||||||
chr5:75643744
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.798+7862T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643744 | ||||||
chr5:75643746
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.798+7864A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643746 | ||||||
chr5:75643748
|
A | G | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.798+7866A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643748 | ||||||
chr5:75643766
|
G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(26): Show | 34 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.798+7884G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643766 | ||||||
chr5:75643901
|
G | A | 8 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(5): Show | 8 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+8019G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643901 | ||||||
chr5:75643913
|
A | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+8031A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643913 | ||||||
chr5:75643937
|
A | G | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.798+8055A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643937 | ||||||
chr5:75643977
|
A | T | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 11 | HG01167.hp2 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+8095A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643977 | ||||||
chr5:75643984
|
A | G | 2 | a0001c0001t0001g0112a0001c0035t0001g0070 | 2 | NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.798+8102A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75643984 | ||||||
chr5:75644116
|
A | G | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.798+8234A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644116 | ||||||
chr5:75644121
|
T | C | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.798+8239T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644121 | ||||||
chr5:75644131
|
C | T | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 35 | HG00597.hp2 HG00642.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.798+8249C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644131 | ||||||
chr5:75644132
|
G | T | 1 | a0002c0002t0002g0271 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.798+8250G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644132 | ||||||
chr5:75644163
|
T | C | 5 | a0002c0002t0002g0261a0002c0002t0003g0262a0002c0002t0003g0263others(2): Show | 5 | HG02040.hp2 HG03490.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+8281T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644163 | ||||||
chr5:75644164
|
C | T | 5 | a0002c0002t0002g0261a0002c0002t0003g0262a0002c0002t0003g0263others(2): Show | 5 | HG02040.hp2 HG03490.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+8282C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644164 | ||||||
chr5:75644165
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0018g0123 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.798+8283G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644165 | ||||||
chr5:75644266
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.798+8384A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644266 | ||||||
chr5:75644277
|
T | A | 3 | a0012c0013t0003g0018a0012c0013t0003g0176a0012c0013t0003g0179 | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+8395T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644277 | ||||||
chr5:75644278
|
C | A | 3 | a0012c0013t0003g0018a0012c0013t0003g0176a0012c0013t0003g0179 | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+8396C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644278 | ||||||
chr5:75644359
|
T | C | 52 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(49): Show | 58 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.798+8477T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644359 | ||||||
chr5:75644360
|
G | A | 14 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(11): Show | 15 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.798+8478G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644360 | ||||||
chr5:75644387
|
A | G | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+8505A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644387 | ||||||
chr5:75644587
|
G | A | 1 | a0005c0004t0003g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.799-8555G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644587 | ||||||
chr5:75644587
|
G | C | 1 | a0004c0005t0004g0030 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.799-8555G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644587 | ||||||
chr5:75644649
|
G | T | 1 | a0004c0005t0011g0007 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.799-8493G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644649 | ||||||
chr5:75644743
|
C | T | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-8399C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644743 | ||||||
chr5:75644744
|
G | A | 3 | a0001c0001t0001g0112a0001c0035t0001g0070a0002c0002t0002g0260 | 3 | NA18989.hp2 NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.799-8398G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644744 | ||||||
chr5:75644818
|
G | C | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.799-8324G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644818 | ||||||
chr5:75644841
|
G | C | 3 | a0007c0007t0014g0155a0021c0031t0001g0159a0024c0020t0014g0254 | 3 | HG01081.hp2 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.799-8301G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644841 | ||||||
chr5:75644953
|
G | A | 1 | a0011c0012t0004g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.799-8189G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644953 | ||||||
chr5:75644955
|
C | T | 1 | a0011c0012t0004g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.799-8187C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644955 | ||||||
chr5:75644960
|
A | G | 1 | a0011c0012t0004g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.799-8182A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644960 | ||||||
chr5:75644972
|
A | C | 5 | a0002c0002t0002g0261a0002c0002t0003g0262a0002c0002t0003g0263others(2): Show | 5 | HG02040.hp2 HG03490.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-8170A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644972 | ||||||
chr5:75644973
|
C | G | 1 | a0008c0008t0004g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.799-8169C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644973 | ||||||
chr5:75644999
|
T | C | 20 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(17): Show | 22 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.799-8143T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75644999 | ||||||
chr5:75645011
|
T | C | 65 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(62): Show | 72 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.799-8131T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645011 | ||||||
chr5:75645087
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0325others(2): Show | 5 | HG00408.hp1 HG00621.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-8055G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645087 | ||||||
chr5:75645134
|
C | G | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-8008C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645134 | ||||||
chr5:75645137
|
G | A | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.799-8005G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645137 | ||||||
chr5:75645168
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.799-7974C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645168 | ||||||
chr5:75645173
|
A | T | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-7969A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645173 | ||||||
chr5:75645225
|
A | G | 1 | a0005c0004t0003g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.799-7917A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645225 | ||||||
chr5:75645278
|
G | A | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.799-7864G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645278 | ||||||
chr5:75645346
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-7796C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645346 | ||||||
chr5:75645426
|
A | G | 54 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(51): Show | 61 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.799-7716A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645426 | ||||||
chr5:75645445
|
C | G | 1 | a0003c0003t0005g0223 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.799-7697C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645445 | ||||||
chr5:75645450
|
A | G | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-7692A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645450 | ||||||
chr5:75645456
|
G | A | 8 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(5): Show | 8 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-7686G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645456 | ||||||
chr5:75645497
|
A | G | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.799-7645A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645497 | ||||||
chr5:75645511
|
C | A | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799-7631C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645511 | ||||||
chr5:75645518
|
C | T | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-7624C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645518 | ||||||
chr5:75645519
|
G | A | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799-7623G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645519 | ||||||
chr5:75645570
|
A | C | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799-7572A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645570 | ||||||
chr5:75645673
|
A | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.799-7469A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645673 | ||||||
chr5:75645674
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 229 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.799-7468T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645674 | ||||||
chr5:75645689
|
A | G | 1 | a0008c0008t0004g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.799-7453A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645689 | ||||||
chr5:75645761
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.799-7381A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645761 | ||||||
chr5:75645779
|
G | A | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799-7363G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645779 | ||||||
chr5:75645948
|
C | A | 3 | a0003c0014t0003g0071a0003c0014t0003g0131a0003c0014t0003g0132 | 3 | NA18963.hp2 NA18977.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.799-7194C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75645948 | ||||||
chr5:75646028
|
A | G | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.799-7114A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646028 | ||||||
chr5:75646065
|
A | T | 6 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-7077A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646065 | ||||||
chr5:75646074
|
A | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-7068A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646074 | ||||||
chr5:75646094
|
G | A | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.799-7048G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646094 | ||||||
chr5:75646102
|
A | T | 1 | a0007c0007t0006g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.799-7040A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646102 | ||||||
chr5:75646103
|
A | AATAATAA others(5): Show |
1 | a0001c0019t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.799-7036_799-7025d others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75646103 | |||||
chr5:75646116
|
A | G | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-7026A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646116 | ||||||
chr5:75646151
|
T | G | 2 | a0002c0002t0003g0262a0002c0002t0003g0263 | 2 | HG02040.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.799-6991T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646151 | ||||||
chr5:75646174
|
C | G | 1 | a0005c0004t0003g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.799-6968C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646174 | ||||||
chr5:75646213
|
C | T | 6 | a0007c0007t0013g0039a0009c0010t0009g0008a0009c0010t0009g0040others(3): Show | 7 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-6929C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646213 | ||||||
chr5:75646214
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(146): Show | 168 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.799-6928G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646214 | ||||||
chr5:75646217
|
C | G | 1 | a0002c0002t0002g0289 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.799-6925C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646217 | ||||||
chr5:75646220
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-6922A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646220 | ||||||
chr5:75646252
|
C | A | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.799-6890C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646252 | ||||||
chr5:75646258
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.799-6884G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646258 | ||||||
chr5:75646273
|
T | C | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-6869T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646273 | ||||||
chr5:75646310
|
G | C | 2 | a0002c0002t0002g0261a0003c0014t0003g0131 | 2 | HG03490.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.799-6832G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646310 | ||||||
chr5:75646465
|
CAG | C | 2 | a0004c0005t0011g0007a0021c0031t0001g0159 | 3 | HG01081.hp2 HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.799-6672_799-6671d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75646465 | |||||
chr5:75646495
|
T | G | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.799-6647T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646495 | ||||||
chr5:75646498
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.799-6644C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646498 | ||||||
chr5:75646527
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.799-6615A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646527 | ||||||
chr5:75646576
|
A | G | 1 | a0003c0003t0003g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799-6566A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646576 | ||||||
chr5:75646604
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-6538C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646604 | ||||||
chr5:75646635
|
T | G | 2 | a0004c0005t0002g0094a0004c0005t0002g0160 | 2 | HG00738.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.799-6507T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646635 | ||||||
chr5:75646650
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.799-6492A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646650 | ||||||
chr5:75646656
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.799-6486G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646656 | ||||||
chr5:75646688
|
C | T | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-6454C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646688 | ||||||
chr5:75646750
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.799-6392C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646750 | ||||||
chr5:75646753
|
T | G | 8 | a0002c0036t0003g0298a0006c0034t0003g0215a0011c0012t0004g0299others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.799-6389T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646753 | ||||||
chr5:75646760
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(187): Show | 212 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.799-6382C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646760 | ||||||
chr5:75646777
|
C | G | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(63): Show | 73 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.799-6365C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646777 | ||||||
chr5:75646780
|
T | C | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(63): Show | 73 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.799-6362T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646780 | ||||||
chr5:75646782
|
C | T | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-6360C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646782 | ||||||
chr5:75646855
|
G | A | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-6287G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646855 | ||||||
chr5:75646910
|
T | G | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-6232T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646910 | ||||||
chr5:75646935
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.799-6207A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646935 | ||||||
chr5:75646948
|
A | T | 2 | a0003c0003t0005g0174a0006c0034t0003g0215 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.799-6194A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646948 | ||||||
chr5:75646992
|
CA | C | 48 | a0001c0001t0001g0126a0001c0001t0021g0146a0003c0003t0003g0012others(45): Show | 52 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.799-6148delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75646992 | |||||
chr5:75646997
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-6145G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75646997 | ||||||
chr5:75647051
|
T | TAGAAAGC others(1225): Show |
2 | a0011c0012t0004g0299a0011c0012t0004g0300 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.799-5914_799-5913i others(1234): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75647051 | |||||
chr5:75647051
|
T | TAGAAAGC others(1227): Show |
1 | a0011c0012t0004g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.799-5914_799-5913i others(1236): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75647051 | |||||
chr5:75647051
|
T | TAGAAAGC others(1228): Show |
4 | a0002c0036t0003g0298a0011c0012t0004g0301a0011c0012t0004g0302others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-5914_799-5913i others(1237): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75647051 | |||||
chr5:75647072
|
C | T | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-6070C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647072 | ||||||
chr5:75647115
|
G | T | 1 | a0002c0002t0002g0290 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.799-6027G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647115 | ||||||
chr5:75647117
|
T | C | 1 | a0008c0008t0004g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.799-6025T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647117 | ||||||
chr5:75647118
|
T | A | 1 | a0008c0008t0004g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.799-6024T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647118 | ||||||
chr5:75647129
|
A | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-6013A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647129 | ||||||
chr5:75647229
|
G | A | 27 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(24): Show | 29 | HG00735.hp1 HG01081.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.799-5913G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647229 | ||||||
chr5:75647244
|
G | T | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-5898G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647244 | ||||||
chr5:75647245
|
A | G | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-5897A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647245 | ||||||
chr5:75647258
|
A | C | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.799-5884A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647258 | ||||||
chr5:75647265
|
C | G | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.799-5877C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647265 | ||||||
chr5:75647289
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.799-5853G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647289 | ||||||
chr5:75647313
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.799-5829C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647313 | ||||||
chr5:75647329
|
A | G | 1 | a0013c0016t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.799-5813A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647329 | ||||||
chr5:75647339
|
C | T | 29 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 34 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.799-5803C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647339 | ||||||
chr5:75647340
|
A | G | 48 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0032others(45): Show | 55 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.799-5802A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647340 | ||||||
chr5:75647388
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-5754T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647388 | ||||||
chr5:75647438
|
A | G | 53 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(50): Show | 59 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.799-5704A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647438 | ||||||
chr5:75647508
|
T | C | 2 | a0001c0001t0006g0246a0013c0016t0001g0029 | 2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.799-5634T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647508 | ||||||
chr5:75647546
|
A | T | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-5596A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647546 | ||||||
chr5:75647555
|
C | T | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-5587C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647555 | ||||||
chr5:75647565
|
C | G | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-5577C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647565 | ||||||
chr5:75647594
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.799-5548A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647594 | ||||||
chr5:75647681
|
G | T | 1 | a0004c0006t0004g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.799-5461G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647681 | ||||||
chr5:75647707
|
A | T | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-5435A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647707 | ||||||
chr5:75647718
|
G | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(188): Show | 213 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.799-5424G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647718 | ||||||
chr5:75647802
|
C | T | 1 | a0017c0023t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.799-5340C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647802 | ||||||
chr5:75647816
|
G | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.799-5326G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647816 | ||||||
chr5:75647888
|
G | T | 1 | a0004c0005t0004g0030 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.799-5254G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647888 | ||||||
chr5:75647897
|
G | A | 44 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0136others(41): Show | 47 | HG01123.hp2 HG01167.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.799-5245G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647897 | ||||||
chr5:75647925
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-5217A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647925 | ||||||
chr5:75647996
|
A | G | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.799-5146A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75647996 | ||||||
chr5:75648015
|
C | T | 1 | a0001c0001t0006g0243 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.799-5127C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648015 | ||||||
chr5:75648100
|
G | T | 13 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(10): Show | 14 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-5042G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648100 | ||||||
chr5:75648108
|
G | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(241): Show | 272 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.799-5034G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648108 | ||||||
chr5:75648115
|
G | A | 3 | a0008c0008t0004g0162a0014c0017t0004g0244a0014c0017t0004g0245 | 3 | HG01884.hp1 HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.799-5027G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648115 | ||||||
chr5:75648131
|
T | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA19065.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.799-5011T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648131 | ||||||
chr5:75648160
|
T | C | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-4982T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648160 | ||||||
chr5:75648173
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.799-4969G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648173 | ||||||
chr5:75648176
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-4966G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648176 | ||||||
chr5:75648191
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.799-4951A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648191 | ||||||
chr5:75648195
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-4947A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648195 | ||||||
chr5:75648208
|
T | C | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4934T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648208 | ||||||
chr5:75648219
|
A | T | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.799-4923A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648219 | ||||||
chr5:75648253
|
TAAAAAAA others(8): Show |
T | 6 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0301others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-4876_799-4862d others(17): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648253 | |||||
chr5:75648253
|
TAAAAAAA others(9): Show |
T | 1 | a0011c0012t0004g0300 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.799-4876_799-4861d others(18): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648253 | |||||
chr5:75648264
|
A | AC | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 36 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.799-4878_799-4877i others(3): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648264 | ||||||
chr5:75648265
|
A | AC | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0165others(9): Show | 13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4877_799-4876i others(3): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648265 | ||||||
chr5:75648265
|
A | C | 1 | a0008c0008t0004g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.799-4877A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648265 | ||||||
chr5:75648265
|
A | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0110 | 3 | HG00735.hp2 NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-4877A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648265 | ||||||
chr5:75648266
|
T | A | 15 | a0006c0034t0003g0215a0008c0008t0004g0016a0008c0008t0004g0161others(12): Show | 16 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-4876T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648266 | ||||||
chr5:75648267
|
T | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0110others(1): Show | 4 | HG00735.hp2 HG01081.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4875T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648267 | ||||||
chr5:75648267
|
TA | T | 69 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0006others(66): Show | 83 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.799-4859delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648267 | |||||
chr5:75648267
|
TAA | T | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(28): Show | 36 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.799-4860_799-4859d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648267 | |||||
chr5:75648268
|
A | AAAAAAAA others(7): Show |
1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.799-4862_799-4861i others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648268 | |||||
chr5:75648268
|
A | C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.799-4874A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648268 | ||||||
chr5:75648268
|
A | T | 14 | a0002c0002t0002g0268a0008c0008t0004g0016a0008c0008t0004g0161others(11): Show | 15 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.799-4874A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648268 | ||||||
chr5:75648269
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.799-4862_799-4861i others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648269 | |||||
chr5:75648269
|
A | AAAAAAAA others(6): Show |
27 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(24): Show | 31 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.799-4862_799-4861i others(15): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648269 | |||||
chr5:75648269
|
A | AAAAAAAA others(5): Show |
45 | a0001c0001t0001g0126a0001c0001t0001g0203a0001c0001t0021g0146others(42): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.799-4863_799-4862i others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648269 | |||||
chr5:75648269
|
A | AAAAAAAA others(4): Show |
1 | a0003c0003t0005g0233 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.799-4864_799-4863i others(13): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648269 | |||||
chr5:75648269
|
A | T | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-4873A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648269 | ||||||
chr5:75648270
|
A | AAAAAAAA others(5): Show |
76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 89 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.799-4862_799-4861i others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648270 | |||||
chr5:75648270
|
A | AAAAAAAA others(4): Show |
4 | a0001c0001t0001g0069a0001c0001t0001g0100a0001c0001t0001g0110others(1): Show | 4 | HG00621.hp2 HG00735.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4863_799-4862i others(13): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648270 | |||||
chr5:75648271
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0062 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.799-4862_799-4861i others(13): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648271 | |||||
chr5:75648271
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0116 | 2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.799-4863_799-4862i others(12): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648271 | |||||
chr5:75648274
|
A | AAAAAAAT others(1): Show |
11 | a0002c0002t0002g0324a0002c0002t0003g0076a0002c0002t0003g0172others(8): Show | 11 | HG02559.hp1 HG02818.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-4862_799-4861i others(10): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648274 | |||||
chr5:75648274
|
A | AAAAAATT | 22 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0004g0173others(19): Show | 25 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.799-4863_799-4862i others(9): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75648274 | |||||
chr5:75648280
|
A | T | 8 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(5): Show | 8 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-4862A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648280 | ||||||
chr5:75648299
|
A | G | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.799-4843A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648299 | ||||||
chr5:75648371
|
C | T | 2 | a0002c0002t0004g0157a0017c0023t0019g0190 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-4771C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648371 | ||||||
chr5:75648376
|
C | T | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-4766C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648376 | ||||||
chr5:75648441
|
A | G | 1 | a0004c0005t0004g0030 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.799-4701A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648441 | ||||||
chr5:75648504
|
A | G | 3 | a0009c0010t0009g0008a0009c0010t0009g0042a0009c0010t0009g0043 | 4 | HG02132.hp1 HG02135.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4638A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648504 | ||||||
chr5:75648547
|
T | G | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-4595T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648547 | ||||||
chr5:75648616
|
G | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-4526G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648616 | ||||||
chr5:75648652
|
T | C | 1 | a0002c0028t0002g0323 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.799-4490T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648652 | ||||||
chr5:75648726
|
C | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-4416C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648726 | ||||||
chr5:75648837
|
G | C | 1 | a0001c0019t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.799-4305G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648837 | ||||||
chr5:75648890
|
A | C | 1 | a0003c0003t0003g0102 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.799-4252A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75648890 | ||||||
chr5:75649012
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-4130C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649012 | ||||||
chr5:75649033
|
G | C | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-4109G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649033 | ||||||
chr5:75649043
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.799-4099A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649043 | ||||||
chr5:75649049
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-4093G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649049 | ||||||
chr5:75649069
|
C | T | 1 | a0015c0026t0004g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.799-4073C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649069 | ||||||
chr5:75649078
|
C | T | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799-4064C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649078 | ||||||
chr5:75649109
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.799-4033T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649109 | ||||||
chr5:75649115
|
A | G | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(63): Show | 73 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.799-4027A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649115 | ||||||
chr5:75649121
|
A | G | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-4021A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649121 | ||||||
chr5:75649184
|
C | CT | 44 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(41): Show | 48 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.799-3941dupT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75649184 | |||||
chr5:75649184
|
CT | C | 6 | a0001c0001t0001g0090a0003c0003t0005g0149a0004c0005t0004g0030others(3): Show | 7 | HG01243.hp2 HG02723.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-3941delT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75649184 | |||||
chr5:75649184
|
CTT | C | 25 | a0002c0036t0003g0298a0008c0008t0004g0016a0008c0008t0004g0161others(22): Show | 27 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.799-3942_799-3941d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75649184 | |||||
chr5:75649282
|
T | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-3860T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649282 | ||||||
chr5:75649283
|
G | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.799-3859G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649283 | ||||||
chr5:75649323
|
T | C | 1 | a0006c0009t0007g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.799-3819T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649323 | ||||||
chr5:75649365
|
T | TATA | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-3775_799-3774i others(5): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75649365 | |||||
chr5:75649462
|
G | A | 1 | a0010c0011t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.799-3680G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649462 | ||||||
chr5:75649531
|
C | T | 2 | a0002c0002t0004g0157a0017c0023t0019g0190 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-3611C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649531 | ||||||
chr5:75649542
|
G | A | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-3600G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649542 | ||||||
chr5:75649551
|
G | A | 4 | a0012c0013t0003g0018a0012c0013t0003g0176a0012c0013t0003g0179others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-3591G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649551 | ||||||
chr5:75649599
|
G | A | 1 | a0026c0037t0003g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.799-3543G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649599 | ||||||
chr5:75649665
|
T | C | 1 | a0005c0004t0003g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.799-3477T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649665 | ||||||
chr5:75649720
|
T | G | 55 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(52): Show | 62 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.799-3422T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649720 | ||||||
chr5:75649752
|
G | C | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 11 | HG01167.hp2 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-3390G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649752 | ||||||
chr5:75649800
|
T | C | 2 | a0003c0003t0005g0017a0003c0003t0005g0174 | 3 | HG02451.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.799-3342T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649800 | ||||||
chr5:75649816
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-3326C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649816 | ||||||
chr5:75649975
|
A | T | 8 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(5): Show | 8 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-3167A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649975 | ||||||
chr5:75649985
|
A | C | 1 | a0001c0001t0001g0047 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.799-3157A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75649985 | ||||||
chr5:75650035
|
T | C | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-3107T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650035 | ||||||
chr5:75650125
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.799-3017A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650125 | ||||||
chr5:75650131
|
A | C | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.799-3011A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650131 | ||||||
chr5:75650136
|
G | C | 66 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(63): Show | 73 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.799-3006G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650136 | ||||||
chr5:75650199
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0124a0001c0001t0018g0123 | 4 | HG00099.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-2943G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650199 | ||||||
chr5:75650263
|
T | C | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.799-2879T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650263 | ||||||
chr5:75650365
|
G | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0125 | 2 | NA18978.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.799-2777G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650365 | ||||||
chr5:75650425
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-2717A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650425 | ||||||
chr5:75650485
|
C | T | 1 | a0004c0006t0004g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799-2657C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650485 | ||||||
chr5:75650532
|
A | T | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-2610A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650532 | ||||||
chr5:75650568
|
C | T | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.799-2574C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650568 | ||||||
chr5:75650630
|
G | A | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-2512G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650630 | ||||||
chr5:75650693
|
G | A | 24 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(21): Show | 27 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-2449G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650693 | ||||||
chr5:75650741
|
C | T | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-2401C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650741 | ||||||
chr5:75650837
|
G | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-2305G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75650837 | ||||||
chr5:75651052
|
A | C | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(23): Show | 30 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-2090A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651052 | ||||||
chr5:75651056
|
G | A | 1 | a0003c0003t0005g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.799-2086G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651056 | ||||||
chr5:75651074
|
C | G | 1 | a0002c0002t0010g0320 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.799-2068C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651074 | ||||||
chr5:75651147
|
A | T | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.799-1995A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651147 | ||||||
chr5:75651364
|
A | G | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-1778A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651364 | ||||||
chr5:75651444
|
C | T | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-1698C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651444 | ||||||
chr5:75651445
|
G | A | 2 | a0002c0002t0004g0157a0017c0023t0019g0190 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-1697G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651445 | ||||||
chr5:75651559
|
T | TGTCTGCC others(37): Show |
1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.799-1582_799-1539d others(46): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 75651559 | |||||
chr5:75651610
|
T | G | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-1532T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651610 | ||||||
chr5:75651669
|
T | C | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-1473T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651669 | ||||||
chr5:75651862
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(22): Show | 29 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.799-1280G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75651862 | ||||||
chr5:75652158
|
T | A | 19 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(16): Show | 21 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-984T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652158 | ||||||
chr5:75652420
|
G | A | 3 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0034t0003g0215 | 4 | HG01243.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-722G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652420 | ||||||
chr5:75652474
|
C | G | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-668C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652474 | ||||||
chr5:75652602
|
C | G | 1 | a0005c0004t0003g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.799-540C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652602 | ||||||
chr5:75652650
|
G | A | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 11 | HG01167.hp2 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-492G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652650 | ||||||
chr5:75652713
|
G | A | 45 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-429G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652713 | ||||||
chr5:75652782
|
G | A | 2 | a0002c0002t0004g0157a0017c0023t0019g0190 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-360G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652782 | ||||||
chr5:75652809
|
C | G | 2 | a0002c0002t0004g0157a0017c0023t0019g0190 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-333C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652809 | ||||||
chr5:75652909
|
A | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-233A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652909 | ||||||
chr5:75652932
|
A | G | 9 | a0003c0003t0005g0022a0003c0003t0005g0145a0003c0003t0005g0148others(6): Show | 10 | NA18948.hp1 NA18953.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-210A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652932 | ||||||
chr5:75652934
|
T | A | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-208T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75652934 | ||||||
chr5:75653070
|
T | C | 1 | a0003c0003t0005g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.799-72T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75653070 | ||||||
chr5:75653120
|
C | T | 25 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(22): Show | 29 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.799-22C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 7/13 | chr5 | 75653120 | ||||||
chr5:75653552
|
G | A | 14 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(11): Show | 15 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.897+312G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653552 | ||||||
chr5:75653650
|
C | A | 2 | a0007c0007t0013g0038a0007c0007t0013g0039 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.897+410C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653650 | ||||||
chr5:75653705
|
T | C | 44 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(41): Show | 50 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.897+465T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653705 | ||||||
chr5:75653775
|
A | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG01952.hp1 HG01975.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+535A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653775 | ||||||
chr5:75653880
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.897+640G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653880 | ||||||
chr5:75653968
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.897+728C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653968 | ||||||
chr5:75653994
|
T | C | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.897+754T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75653994 | ||||||
chr5:75654034
|
T | C | 20 | a0002c0002t0004g0157a0008c0008t0004g0016a0008c0008t0004g0161others(17): Show | 22 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.897+794T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654034 | ||||||
chr5:75654042
|
G | T | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0006g0246others(10): Show | 17 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.897+802G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654042 | ||||||
chr5:75654098
|
A | G | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.897+858A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654098 | ||||||
chr5:75654145
|
G | C | 1 | a0001c0019t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.897+905G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654145 | ||||||
chr5:75654145
|
G | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(21): Show | 28 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.897+905G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654145 | ||||||
chr5:75654190
|
G | A | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.897+950G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654190 | ||||||
chr5:75654312
|
G | T | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.897+1072G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654312 | ||||||
chr5:75654330
|
C | T | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.897+1090C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654330 | ||||||
chr5:75654348
|
G | A | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.897+1108G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654348 | ||||||
chr5:75654387
|
T | G | 2 | a0007c0007t0013g0038a0007c0007t0013g0039 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.897+1147T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654387 | ||||||
chr5:75654427
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0062a0004c0006t0004g0048 | 3 | HG00408.hp2 HG02015.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.897+1187C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654427 | ||||||
chr5:75654547
|
G | A | 3 | a0004c0005t0008g0021a0004c0005t0008g0219a0004c0005t0008g0221 | 4 | HG00099.hp1 HG01168.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+1307G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654547 | ||||||
chr5:75654560
|
G | T | 1 | a0006c0009t0007g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.897+1320G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654560 | ||||||
chr5:75654594
|
C | T | 10 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(7): Show | 10 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.897+1354C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654594 | ||||||
chr5:75654595
|
G | A | 5 | a0002c0002t0002g0261a0002c0002t0003g0262a0002c0002t0003g0263others(2): Show | 5 | HG02040.hp2 HG03490.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+1355G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654595 | ||||||
chr5:75654757
|
C | G | 2 | a0007c0007t0014g0155a0024c0020t0014g0254 | 2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.898-1272C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654757 | ||||||
chr5:75654764
|
G | A | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.898-1265G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654764 | ||||||
chr5:75654852
|
C | A | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.898-1177C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654852 | ||||||
chr5:75654868
|
C | T | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.898-1161C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654868 | ||||||
chr5:75654920
|
C | G | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.898-1109C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654920 | ||||||
chr5:75654929
|
C | G | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.898-1100C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654929 | ||||||
chr5:75654944
|
C | T | 1 | a0007c0007t0013g0039 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.898-1085C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75654944 | ||||||
chr5:75655021
|
C | G | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.898-1008C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655021 | ||||||
chr5:75655022
|
T | A | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-1007T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655022 | ||||||
chr5:75655025
|
G | A | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.898-1004G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655025 | ||||||
chr5:75655127
|
T | C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.898-902T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655127 | ||||||
chr5:75655160
|
G | A | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.898-869G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655160 | ||||||
chr5:75655229
|
G | T | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-800G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655229 | ||||||
chr5:75655260
|
G | A | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-769G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655260 | ||||||
chr5:75655262
|
A | G | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-767A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655262 | ||||||
chr5:75655340
|
G | A | 1 | a0002c0002t0003g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.898-689G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655340 | ||||||
chr5:75655420
|
G | C | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.898-609G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655420 | ||||||
chr5:75655579
|
C | G | 1 | a0003c0003t0005g0238 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.898-450C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655579 | ||||||
chr5:75655735
|
A | T | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-294A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655735 | ||||||
chr5:75655912
|
T | G | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-117T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655912 | ||||||
chr5:75655922
|
C | T | 35 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(32): Show | 38 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.898-107C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 8/13 | chr5 | 75655922 | ||||||
chr5:75656372
|
G | A | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.996+245G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656372 | ||||||
chr5:75656469
|
G | A | 2 | a0003c0003t0003g0036a0003c0003t0003g0037 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.996+342G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656469 | ||||||
chr5:75656572
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.996+445A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656572 | ||||||
chr5:75656573
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.996+446G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656573 | ||||||
chr5:75656600
|
G | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.996+473G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656600 | ||||||
chr5:75656679
|
T | G | 1 | a0002c0002t0010g0297 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.996+552T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656679 | ||||||
chr5:75656706
|
CTCTGGGG others(4): Show |
C | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.996+589_996+599del others(11): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 75656706 | |||||
chr5:75656793
|
A | T | 2 | a0003c0003t0005g0240a0003c0003t0005g0241 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.996+666A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656793 | ||||||
chr5:75656935
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.996+808C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75656935 | ||||||
chr5:75657036
|
C | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(124): Show | 145 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.996+909C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657036 | ||||||
chr5:75657138
|
A | G | 9 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.996+1011A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657138 | ||||||
chr5:75657176
|
G | A | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.996+1049G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657176 | ||||||
chr5:75657310
|
TA | T | 9 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.996+1189delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 75657310 | |||||
chr5:75657372
|
TA | T | 12 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0009t0007g0141others(9): Show | 13 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.996+1252delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 75657372 | |||||
chr5:75657416
|
CTCT | C | 9 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.996+1294_996+1296d others(5): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 75657416 | |||||
chr5:75657593
|
A | G | 1 | a0001c0001t0017g0058 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.996+1466A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657593 | ||||||
chr5:75657635
|
G | C | 1 | a0003c0003t0005g0147 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.996+1508G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657635 | ||||||
chr5:75657645
|
A | G | 2 | a0005c0004t0003g0080a0005c0004t0003g0193 | 2 | HG01516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.996+1518A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657645 | ||||||
chr5:75657679
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 135 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.996+1552C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657679 | ||||||
chr5:75657691
|
G | A | 1 | a0002c0002t0002g0275 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.996+1564G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657691 | ||||||
chr5:75657924
|
T | C | 1 | a0002c0002t0004g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.997-1359T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75657924 | ||||||
chr5:75658132
|
G | C | 3 | a0015c0025t0007g0252a0015c0026t0004g0253a0020c0030t0007g0163 | 3 | HG01243.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.997-1151G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658132 | ||||||
chr5:75658200
|
GA | G | 105 | a0002c0002t0002g0261a0002c0002t0003g0076a0002c0002t0003g0136others(102): Show | 114 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.997-1076delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 75658200 | |||||
chr5:75658455
|
T | G | 1 | a0003c0003t0005g0237 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.997-828T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658455 | ||||||
chr5:75658541
|
T | C | 39 | a0003c0003t0003g0012a0003c0003t0003g0054a0003c0003t0003g0066others(36): Show | 41 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.997-742T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658541 | ||||||
chr5:75658554
|
G | A | 35 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(32): Show | 38 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.997-729G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658554 | ||||||
chr5:75658808
|
A | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(124): Show | 145 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.997-475A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658808 | ||||||
chr5:75658812
|
T | A | 1 | a0002c0002t0002g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.997-471T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658812 | ||||||
chr5:75658906
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.997-377A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658906 | ||||||
chr5:75658930
|
C | T | 1 | a0020c0030t0007g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.997-353C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75658930 | ||||||
chr5:75659032
|
A | T | 1 | a0005c0004t0003g0187 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.997-251A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75659032 | ||||||
chr5:75659076
|
T | TG | 258 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(255): Show | 287 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.997-207_997-206ins others(1): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75659076 | ||||||
chr5:75659199
|
T | C | 1 | a0018c0022t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.997-84T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75659199 | ||||||
chr5:75659266
|
C | A | 1 | a0002c0002t0010g0320 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.997-17C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 9/13 | chr5 | 75659266 | ||||||
chr5:75659394
|
A | G | 2 | a0002c0002t0002g0294a0002c0002t0002g0296 | 2 | NA18963.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1095+13A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659394 | ||||||
chr5:75659416
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+35T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659416 | ||||||
chr5:75659539
|
G | A | 2 | a0006c0009t0007g0207a0006c0009t0007g0210 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1095+158G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659539 | ||||||
chr5:75659620
|
C | T | 12 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0009t0007g0141others(9): Show | 13 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+239C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659620 | ||||||
chr5:75659717
|
C | A | 38 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(35): Show | 41 | HG01123.hp2 HG01243.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.1095+336C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659717 | ||||||
chr5:75659724
|
T | C | 12 | a0004c0005t0004g0030a0004c0005t0011g0007a0006c0009t0007g0141others(9): Show | 13 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+343T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659724 | ||||||
chr5:75659877
|
T | A | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1095+496T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75659877 | ||||||
chr5:75660016
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1095+635G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660016 | ||||||
chr5:75660098
|
T | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(177): Show | 203 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1095+717T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660098 | ||||||
chr5:75660227
|
T | C | 12 | a0002c0002t0004g0157a0006c0009t0007g0141a0006c0009t0007g0207others(9): Show | 12 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+846T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660227 | ||||||
chr5:75660231
|
C | T | 1 | a0002c0002t0002g0287 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1095+850C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660231 | ||||||
chr5:75660234
|
A | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(324): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1095+853A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660234 | ||||||
chr5:75660526
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1095+1145T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660526 | ||||||
chr5:75660622
|
G | C | 7 | a0002c0036t0003g0298a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095+1241G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660622 | ||||||
chr5:75660692
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 134 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1095+1311C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660692 | ||||||
chr5:75660770
|
G | C | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1095+1389G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660770 | ||||||
chr5:75660887
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1095+1506C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660887 | ||||||
chr5:75660888
|
G | A | 2 | a0004c0005t0004g0030a0004c0005t0011g0007 | 3 | HG01243.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1095+1507G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75660888 | ||||||
chr5:75661078
|
G | GT | 54 | a0001c0001t0001g0052a0001c0001t0001g0202a0002c0002t0002g0269others(51): Show | 58 | HG00544.hp1 HG00735.hp1 HG01358.hp2 others(55): Show |
intron_variant | MODIFIER | c.1095+1708dupT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661078 | |||||
chr5:75661082
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1095+1701T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661082 | ||||||
chr5:75661104
|
A | C | 6 | a0011c0012t0004g0299a0011c0012t0004g0300a0011c0012t0004g0301others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+1723A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661104 | ||||||
chr5:75661234
|
T | A | 1 | a0002c0002t0002g0280 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1095+1853T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661234 | ||||||
chr5:75661255
|
G | A | 43 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(40): Show | 47 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(44): Show |
intron_variant | MODIFIER | c.1095+1874G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661255 | ||||||
chr5:75661290
|
C | G | 43 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(40): Show | 47 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(44): Show |
intron_variant | MODIFIER | c.1095+1909C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661290 | ||||||
chr5:75661296
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(176): Show | 202 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1095+1915C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661296 | ||||||
chr5:75661350
|
C | T | 5 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+1969C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661350 | ||||||
chr5:75661361
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1095+1980C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661361 | ||||||
chr5:75661374
|
G | A | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+1993G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661374 | ||||||
chr5:75661396
|
GA | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(157): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1096-1969delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661396 | |||||
chr5:75661396
|
GAA | G | 46 | a0001c0001t0001g0062a0001c0001t0001g0122a0001c0001t0001g0139others(43): Show | 55 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1096-1970_1096-196 others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661396 | |||||
chr5:75661396
|
GAAAAAAA others(3): Show |
G | 1 | a0011c0012t0004g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1096-1978_1096-196 others(14): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661396 | |||||
chr5:75661396
|
GAAAAAAA others(4): Show |
G | 8 | a0008c0008t0004g0168a0011c0012t0004g0299a0011c0012t0004g0300others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1096-1979_1096-196 others(15): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661396 | |||||
chr5:75661396
|
GAAAAAAA others(5): Show |
G | 26 | a0002c0002t0004g0157a0004c0005t0004g0030a0004c0005t0011g0007others(23): Show | 28 | HG00735.hp1 HG01081.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1096-1980_1096-196 others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661396 | |||||
chr5:75661414
|
A | AAAAAAAA others(7): Show |
7 | a0002c0002t0003g0264a0004c0005t0003g0034a0005c0004t0003g0080others(4): Show | 7 | HG01123.hp2 HG01358.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-1969_1096-196 others(18): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661414 | |||||
chr5:75661414
|
A | AAAAAAAA others(6): Show |
28 | a0002c0002t0003g0076a0002c0002t0003g0137a0002c0002t0003g0138others(25): Show | 31 | HG01516.hp2 HG02559.hp1 HG02602.hp1 others(28): Show |
intron_variant | MODIFIER | c.1096-1969_1096-196 others(17): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661414 | |||||
chr5:75661414
|
A | AAAAAAAA others(5): Show |
3 | a0002c0002t0003g0136a0002c0002t0016g0171a0005c0004t0003g0081 | 3 | HG03491.hp1 NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1096-1979_1096-196 others(16): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661414 | |||||
chr5:75661448
|
G | A | 43 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(40): Show | 47 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(44): Show |
intron_variant | MODIFIER | c.1096-1946G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661448 | ||||||
chr5:75661489
|
A | G | 30 | a0002c0002t0004g0157a0006c0009t0007g0141a0006c0009t0007g0207others(27): Show | 31 | HG00735.hp1 HG01081.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1096-1905A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661489 | ||||||
chr5:75661570
|
T | A | 2 | a0015c0025t0007g0252a0020c0030t0007g0163 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1096-1824T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661570 | ||||||
chr5:75661573
|
T | C | 43 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(40): Show | 47 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(44): Show |
intron_variant | MODIFIER | c.1096-1821T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661573 | ||||||
chr5:75661789
|
C | T | 42 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(39): Show | 46 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.1096-1605C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661789 | ||||||
chr5:75661865
|
T | C | 1 | a0002c0029t0004g0272 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1096-1529T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661865 | ||||||
chr5:75661899
|
A | AT | 69 | a0001c0001t0001g0064a0001c0001t0001g0114a0001c0001t0001g0129others(66): Show | 76 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1096-1470dupT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661899 | |||||
chr5:75661899
|
A | ATT | 101 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(98): Show | 114 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1096-1471_1096-147 others(6): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661899 | |||||
chr5:75661899
|
A | ATTT | 23 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0049others(20): Show | 27 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1096-1472_1096-147 others(7): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661899 | |||||
chr5:75661899
|
AT | A | 51 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0025others(48): Show | 60 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1096-1470delT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661899 | |||||
chr5:75661899
|
ATTTT | A | 35 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(32): Show | 38 | HG01123.hp2 HG01358.hp2 HG02559.hp1 others(35): Show |
intron_variant | MODIFIER | c.1096-1473_1096-147 others(8): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661899 | |||||
chr5:75661899
|
ATTTTTTT | A | 7 | a0001c0019t0001g0074a0011c0012t0004g0299a0011c0012t0004g0300others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-1476_1096-147 others(11): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 75661899 | |||||
chr5:75661925
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1096-1469G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661925 | ||||||
chr5:75661956
|
G | A | 10 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(7): Show | 10 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-1438G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661956 | ||||||
chr5:75661977
|
A | C | 4 | a0011c0012t0004g0299a0011c0012t0004g0300a0011c0012t0004g0302others(1): Show | 4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-1417A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661977 | ||||||
chr5:75661994
|
A | C | 42 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(39): Show | 46 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.1096-1400A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75661994 | ||||||
chr5:75662151
|
T | C | 2 | a0002c0002t0002g0269a0002c0002t0002g0270 | 2 | NA18949.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1096-1243T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662151 | ||||||
chr5:75662358
|
G | A | 5 | a0011c0012t0004g0299a0011c0012t0004g0300a0011c0012t0004g0301others(2): Show | 5 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-1036G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662358 | ||||||
chr5:75662454
|
T | C | 1 | a0003c0003t0005g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1096-940T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662454 | ||||||
chr5:75662458
|
T | A | 42 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(39): Show | 46 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.1096-936T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662458 | ||||||
chr5:75662471
|
G | T | 37 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(34): Show | 40 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.1096-923G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662471 | ||||||
chr5:75662517
|
A | C | 1 | a0004c0006t0004g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096-877A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662517 | ||||||
chr5:75662609
|
T | C | 1 | a0004c0005t0011g0007 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1096-785T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662609 | ||||||
chr5:75662717
|
A | G | 42 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(39): Show | 46 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.1096-677A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662717 | ||||||
chr5:75662995
|
C | T | 26 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(23): Show | 27 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1096-399C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75662995 | ||||||
chr5:75663123
|
C | G | 5 | a0011c0012t0004g0299a0011c0012t0004g0300a0011c0012t0004g0301others(2): Show | 5 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-271C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 10/13 | chr5 | 75663123 | ||||||
chr5:75663558
|
G | C | 1 | a0002c0002t0003g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1191+69G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75663558 | ||||||
chr5:75663584
|
A | C | 3 | a0002c0002t0002g0273a0002c0002t0002g0304a0002c0002t0010g0292 | 3 | NA18999.hp2 NA19059.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1191+95A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75663584 | ||||||
chr5:75663646
|
C | T | 1 | a0007c0007t0013g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1191+157C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75663646 | ||||||
chr5:75663653
|
T | C | 2 | a0015c0025t0007g0252a0020c0030t0007g0163 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1191+164T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75663653 | ||||||
chr5:75664135
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1191+646T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664135 | ||||||
chr5:75664145
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(253): Show | 285 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1191+656G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664145 | ||||||
chr5:75664242
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1191+753G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664242 | ||||||
chr5:75664368
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1191+879C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664368 | ||||||
chr5:75664408
|
A | G | 12 | a0008c0008t0004g0016a0008c0008t0004g0161a0008c0008t0004g0162others(9): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+919A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664408 | ||||||
chr5:75664533
|
A | G | 26 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(23): Show | 27 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1191+1044A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664533 | ||||||
chr5:75664845
|
T | C | 1 | a0002c0002t0002g0283 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1191+1356T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664845 | ||||||
chr5:75664980
|
C | T | 1 | a0002c0002t0002g0279 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1191+1491C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75664980 | ||||||
chr5:75665257
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1192-1535C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665257 | ||||||
chr5:75665281
|
A | G | 1 | a0004c0005t0011g0007 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1192-1511A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665281 | ||||||
chr5:75665442
|
G | A | 1 | a0002c0002t0002g0284 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1192-1350G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665442 | ||||||
chr5:75665444
|
A | G | 1 | a0004c0006t0004g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1192-1348A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665444 | ||||||
chr5:75665460
|
C | T | 1 | a0013c0024t0003g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1192-1332C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665460 | ||||||
chr5:75665466
|
G | C | 9 | a0003c0003t0005g0022a0003c0003t0005g0145a0003c0003t0005g0148others(6): Show | 10 | NA18948.hp1 NA18953.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192-1326G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665466 | ||||||
chr5:75665512
|
TCTTA | T | 51 | a0003c0003t0003g0012a0003c0003t0003g0036a0003c0003t0003g0037others(48): Show | 56 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1192-1276_1192-127 others(8): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 75665512 | |||||
chr5:75665788
|
GTTC | G | 5 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192-999_1192-997d others(5): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 75665788 | |||||
chr5:75665789
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1192-1003T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665789 | ||||||
chr5:75665971
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(255): Show | 287 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.1192-821T>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75665971 | ||||||
chr5:75666027
|
C | T | 1 | a0022c0032t0012g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1192-765C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666027 | ||||||
chr5:75666078
|
T | C | 2 | a0004c0006t0004g0205a0004c0006t0004g0216 | 2 | HG01361.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1192-714T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666078 | ||||||
chr5:75666096
|
C | T | 2 | a0006c0009t0007g0141a0023c0033t0006g0249 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1192-696C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666096 | ||||||
chr5:75666234
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1192-558G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666234 | ||||||
chr5:75666417
|
A | G | 15 | a0002c0002t0004g0173a0002c0029t0004g0272a0004c0005t0004g0060others(12): Show | 17 | HG00408.hp2 HG01099.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1192-375A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666417 | ||||||
chr5:75666569
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1192-223T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666569 | ||||||
chr5:75666585
|
C | T | 1 | a0007c0007t0014g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1192-207C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666585 | ||||||
chr5:75666615
|
A | C | 3 | a0007c0007t0006g0004a0007c0007t0006g0257a0007c0007t0012g0256 | 6 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1192-177A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666615 | ||||||
chr5:75666631
|
G | T | 52 | a0003c0003t0003g0012a0003c0003t0003g0036a0003c0003t0003g0037others(49): Show | 57 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1192-161G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666631 | ||||||
chr5:75666632
|
CA | C | 73 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0124others(70): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1192-148delA | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 75666632 | |||||
chr5:75666643
|
A | T | 1 | a0002c0002t0002g0280 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1192-149A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666643 | ||||||
chr5:75666643
|
AAT | A | 54 | a0001c0001t0001g0032a0003c0003t0003g0012a0003c0003t0003g0036others(51): Show | 59 | HG00423.hp1 HG00609.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.1192-140_1192-139d others(4): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 75666643 | |||||
chr5:75666644
|
AT | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 211 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1192-147delT | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666644 | ||||||
chr5:75666645
|
T | A | 2 | a0015c0025t0007g0252a0020c0030t0007g0163 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1192-147T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666645 | ||||||
chr5:75666647
|
T | A | 1 | a0004c0005t0004g0030 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1192-145T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666647 | ||||||
chr5:75666689
|
G | A | 8 | a0001c0001t0001g0325a0002c0002t0002g0261a0002c0002t0003g0262others(5): Show | 8 | HG01243.hp1 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192-103G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666689 | ||||||
chr5:75666721
|
A | G | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-71A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666721 | ||||||
chr5:75666737
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0135 | 3 | HG01192.hp1 HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1192-55A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 11/13 | chr5 | 75666737 | ||||||
chr5:75667079
|
G | A | 9 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1393+86G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667079 | ||||||
chr5:75667087
|
C | G | 3 | a0007c0007t0006g0004a0007c0007t0006g0257a0007c0007t0012g0256 | 6 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393+94C>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667087 | ||||||
chr5:75667312
|
A | G | 3 | a0012c0013t0003g0018a0012c0013t0003g0176a0012c0013t0003g0179 | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1393+319A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667312 | ||||||
chr5:75667452
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(166): Show | 190 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1393+459G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667452 | ||||||
chr5:75667464
|
A | G | 75 | a0002c0002t0004g0173a0002c0029t0004g0272a0003c0003t0003g0012others(72): Show | 82 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1393+471A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667464 | ||||||
chr5:75667521
|
G | A | 1 | a0017c0023t0019g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1393+528G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667521 | ||||||
chr5:75667775
|
T | C | 15 | a0002c0002t0004g0173a0002c0029t0004g0272a0004c0005t0004g0060others(12): Show | 17 | HG00408.hp2 HG01099.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1393+782T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667775 | ||||||
chr5:75667860
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1393+867G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75667860 | ||||||
chr5:75668159
|
A | C | 1 | a0018c0022t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1394-1093A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668159 | ||||||
chr5:75668185
|
A | G | 6 | a0001c0001t0006g0084a0001c0001t0006g0154a0001c0001t0006g0196others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394-1067A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668185 | ||||||
chr5:75668282
|
G | A | 27 | a0002c0002t0004g0173a0002c0029t0004g0272a0004c0005t0004g0060others(24): Show | 30 | HG00408.hp2 HG00735.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1394-970G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668282 | ||||||
chr5:75668303
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 285 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1394-949C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668303 | ||||||
chr5:75668370
|
T | C | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394-882T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668370 | ||||||
chr5:75668402
|
AG | A | 5 | a0011c0012t0004g0299a0011c0012t0004g0300a0011c0012t0004g0301others(2): Show | 5 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1394-849delG | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668402 | ||||||
chr5:75668494
|
A | G | 49 | a0003c0003t0003g0012a0003c0003t0003g0036a0003c0003t0003g0037others(46): Show | 53 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1394-758A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668494 | ||||||
chr5:75668501
|
G | A | 1 | a0002c0002t0002g0324 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1394-751G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668501 | ||||||
chr5:75668610
|
G | C | 1 | a0013c0016t0001g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1394-642G>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668610 | ||||||
chr5:75668633
|
A | T | 5 | a0009c0010t0009g0008a0009c0010t0009g0040a0009c0010t0009g0041others(2): Show | 6 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394-619A>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668633 | ||||||
chr5:75668755
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1394-497G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668755 | ||||||
chr5:75668757
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(211): Show | 238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1394-495A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668757 | ||||||
chr5:75668809
|
A | C | 1 | a0007c0007t0013g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1394-443A>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75668809 | ||||||
chr5:75669029
|
C | A | 1 | a0003c0003t0005g0234 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1394-223C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 12/13 | chr5 | 75669029 | ||||||
chr5:75669555
|
G | T | 2 | a0002c0002t0002g0277a0002c0002t0002g0288 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1525+172G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75669555 | ||||||
chr5:75669729
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1525+346A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75669729 | ||||||
chr5:75670048
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1525+665G>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670048 | ||||||
chr5:75670114
|
A | G | 1 | a0006c0034t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1525+731A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670114 | ||||||
chr5:75670117
|
T | C | 2 | a0019c0027t0004g0204a0028c0039t0004g0248 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1525+734T>C | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670117 | ||||||
chr5:75670152
|
T | A | 143 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(140): Show | 155 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.1525+769T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670152 | ||||||
chr5:75670421
|
C | T | 11 | a0006c0009t0007g0141a0006c0009t0007g0207a0006c0009t0007g0209others(8): Show | 11 | HG01167.hp2 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1526-558C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670421 | ||||||
chr5:75670517
|
G | T | 1 | a0005c0004t0003g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1526-462G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670517 | ||||||
chr5:75670527
|
CAAG | C | 37 | a0002c0002t0004g0157a0002c0002t0004g0173a0002c0029t0004g0272others(34): Show | 41 | HG00408.hp2 HG00735.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.1526-448_1526-446d others(5): Show |
ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 75670527 | |||||
chr5:75670537
|
G | T | 143 | a0002c0002t0003g0076a0002c0002t0003g0136a0002c0002t0003g0137others(140): Show | 155 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.1526-442G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670537 | ||||||
chr5:75670653
|
G | T | 1 | a0021c0031t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1526-326G>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670653 | ||||||
chr5:75670669
|
C | T | 1 | a0027c0038t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1526-310C>T | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670669 | ||||||
chr5:75670760
|
T | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG00438.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1526-219T>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670760 | ||||||
chr5:75670833
|
C | A | 5 | a0003c0003t0005g0229a0003c0003t0005g0235a0003c0003t0005g0236others(2): Show | 5 | HG01934.hp1 HG01943.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-146C>A | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670833 | ||||||
chr5:75670857
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A | G | 1 | a0001c0001t0001g0050 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1526-122A>G | ANKDD1B | ENSG00000189045.15 | transcript | ENST00000601380.4 | protein_coding | 13/13 | chr5 | 75670857 |