Item | Value |
---|---|
geneid | 540 |
ensemblid | ENSG00000123191.17 |
hgncid | 870 |
symbol | ATP7B |
name | ATPase copper transporting beta |
refseq_nuc | NM_000053.4 |
refseq_prot | NP_000044.2 |
ensembl_nuc | ENST00000242839.10 |
ensembl_prot | ENSP00000242839.5 |
mane_status | MANE Select |
chr | chr13 |
start | 51932669 |
end | 52011450 |
strand | - |
ver | v1.2 |
region | chr13:51932669-52011450 |
region5000 | chr13:51927669-52016450 |
regionname0 | ATP7B_chr13_51932669_52011450 |
regionname5000 | ATP7B_chr13_51927669_52016450 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1465 | 113 | 31 | 25 | 33 | 3 | 19 | 21 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002 | 0/0 | 1465 | 84 | 13 | 22 | 31 | 3 | 15 | 21 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003 | 0/0 | 1465 | 59 | 33 | 9 | 10 | 1 | 6 | 7 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0004 | 0/0 | 1465 | 12 | 1 | 0 | 11 | 0 | 0 | 6 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005 | 0/0 | 1465 | 11 | 4 | 7 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0006 | 0/0 | 1465 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0007 | 0/0 | 1465 | 4 | 3 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0008 | 0/0 | 1465 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0009 | 0/0 | 1465 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0010 | 0/0 | 1465 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0011 | 0/0 | 1465 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0012 | 0/0 | 1465 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0013 | 0/0 | 1465 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0014 | 0/0 | 1465 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0015 | 0/0 | 1465 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0016 | 0/0 | 1465 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0017 | 0/0 | 1465 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0018 | 0/0 | 1465 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 4398 | 102 | 30 | 24 | 31 | 3 | 13 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0002 | 0/0 | 4398 | 76 | 13 | 19 | 30 | 2 | 12 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0003 | 0/0 | 4398 | 44 | 29 | 7 | 6 | 1 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0004 | 0/0 | 4398 | 12 | 1 | 0 | 11 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0005 | 0/0 | 4398 | 11 | 1 | 1 | 4 | 0 | 5 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0006 | 0/0 | 4398 | 7 | 1 | 6 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0007 | 0/0 | 4398 | 4 | 0 | 0 | 4 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0008 | 0/0 | 4398 | 4 | 3 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0009 | 0/1 | 4398 | 4 | 0 | 0 | 0 | 0 | 3 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0010 | 0/0 | 4398 | 4 | 3 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0011 | 0/0 | 4398 | 3 | 0 | 0 | 0 | 1 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0012 | 0/0 | 4398 | 3 | 2 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0013 | 0/0 | 4398 | 3 | 0 | 0 | 0 | 0 | 3 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0014 | 0/0 | 4398 | 2 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0015 | 0/0 | 4398 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0016 | 0/0 | 4398 | 2 | 1 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0017 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0018 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0019 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0020 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0021 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0022 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0023 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0024 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0025 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0026 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0027 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0028 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0029 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0030 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0031 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0032 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0033 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0034 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
c0035 | 0/0 | 4398 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2201 | 101 | 33 | 16 | 33 | 1 | 16 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0002 | 0/0 | 2201 | 70 | 3 | 22 | 31 | 2 | 12 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0003 | 0/0 | 2201 | 31 | 4 | 7 | 16 | 2 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0004 | 0/0 | 2201 | 26 | 2 | 11 | 8 | 1 | 4 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0005 | 0/0 | 2201 | 16 | 13 | 2 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0006 | 0/0 | 2201 | 16 | 16 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0007 | 0/0 | 2201 | 8 | 7 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0008 | 0/0 | 2201 | 7 | 4 | 0 | 3 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0009 | 0/0 | 2201 | 4 | 4 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0010 | 0/0 | 2201 | 3 | 0 | 1 | 0 | 1 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0011 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0012 | 0/0 | 2201 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0013 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0014 | 0/0 | 2201 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0015 | 0/0 | 2201 | 2 | 0 | 0 | 0 | 1 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0016 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0017 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0018 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0019 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0020 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0021 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0022 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0023 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
t0024 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4398 | 102 | 30 | 24 | 31 | 3 | 13 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0001c0009 | 0/1 | 4398 | 4 | 0 | 0 | 0 | 0 | 3 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0001c0013 | 0/0 | 4398 | 3 | 0 | 0 | 0 | 0 | 3 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0001c0025 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0001c0028 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0001c0030 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0001c0031 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0002c0002 | 0/0 | 4398 | 76 | 13 | 19 | 30 | 2 | 12 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0002c0011 | 0/0 | 4398 | 3 | 0 | 0 | 0 | 1 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0002c0014 | 0/0 | 4398 | 2 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0002c0019 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0002c0020 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0002c0023 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0003c0003 | 0/0 | 4398 | 44 | 29 | 7 | 6 | 1 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0003c0005 | 0/0 | 4398 | 11 | 1 | 1 | 4 | 0 | 5 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0003c0015 | 0/0 | 4398 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0003c0032 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0003c0034 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0004c0004 | 0/0 | 4398 | 12 | 1 | 0 | 11 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0005c0006 | 0/0 | 4398 | 7 | 1 | 6 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0005c0012 | 0/0 | 4398 | 3 | 2 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0005c0026 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0006c0007 | 0/0 | 4398 | 4 | 0 | 0 | 4 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0007c0008 | 0/0 | 4398 | 4 | 3 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0008c0010 | 0/0 | 4398 | 4 | 3 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0009c0016 | 0/0 | 4398 | 2 | 1 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0010c0035 | 0/0 | 4398 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0011c0021 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0012c0018 | 0/0 | 4398 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0013c0022 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0014c0024 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0015c0029 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0016c0027 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0017c0033 | 0/0 | 4398 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 | |
a0018c0017 | 0/0 | 4398 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6598 | 83 | 30 | 15 | 27 | 0 | 10 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0001t0003 | 0/0 | 6598 | 14 | 0 | 6 | 4 | 2 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0001t0014 | 0/0 | 6598 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0001t0015 | 0/0 | 6598 | 2 | 0 | 0 | 0 | 1 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0001t0022 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0009t0001 | 0/1 | 6598 | 4 | 0 | 0 | 0 | 0 | 3 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0013t0001 | 0/0 | 6598 | 3 | 0 | 0 | 0 | 0 | 3 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0025t0003 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0028t0001 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0030t0001 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0001c0031t0001 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0002t0002 | 0/0 | 6598 | 62 | 3 | 18 | 28 | 2 | 11 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0002t0007 | 0/0 | 6598 | 8 | 7 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0002t0008 | 0/0 | 6598 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0002t0009 | 0/0 | 6598 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0002t0020 | 0/0 | 6598 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0002t0023 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0011t0010 | 0/0 | 6598 | 2 | 0 | 0 | 0 | 1 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0011t0018 | 0/0 | 6598 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0014t0002 | 0/0 | 6598 | 2 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0019t0002 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0020t0002 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0002c0023t0002 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0004 | 0/0 | 6598 | 12 | 0 | 6 | 5 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0005 | 0/0 | 6598 | 6 | 6 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0006 | 0/0 | 6598 | 15 | 15 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0008 | 0/0 | 6598 | 5 | 4 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0009 | 0/0 | 6598 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0013 | 0/0 | 6598 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0016 | 0/0 | 6598 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0003t0021 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0005t0004 | 0/0 | 6598 | 7 | 1 | 0 | 2 | 0 | 4 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0005t0005 | 0/0 | 6598 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0005t0010 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0005t0012 | 0/0 | 6598 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0015t0005 | 0/0 | 6598 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0032t0005 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0003c0034t0005 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0004c0004t0001 | 0/0 | 6598 | 3 | 1 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0004c0004t0003 | 0/0 | 6598 | 7 | 0 | 0 | 7 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0004c0004t0004 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0004c0004t0019 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005c0006t0004 | 0/0 | 6598 | 5 | 0 | 5 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005c0006t0005 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005c0006t0024 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005c0012t0001 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005c0012t0003 | 0/0 | 6598 | 2 | 1 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0005c0026t0004 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0006c0007t0003 | 0/0 | 6598 | 4 | 0 | 0 | 4 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0007c0008t0001 | 0/0 | 6598 | 2 | 1 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0007c0008t0003 | 0/0 | 6598 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0008c0010t0006 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0008c0010t0011 | 0/0 | 6598 | 3 | 2 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0009c0016t0005 | 0/0 | 6598 | 2 | 1 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0010c0035t0001 | 0/0 | 6598 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0011c0021t0002 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0012c0018t0002 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0013c0022t0017 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0014c0024t0005 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0015c0029t0001 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0016c0027t0003 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0017c0033t0005 | 0/0 | 6598 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
a0018c0017t0002 | 0/0 | 6598 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | copy fasta | chr13 | 51927669 | 52016450 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0014g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0015g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0015g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0001t0022g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0009t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0009t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0013t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0013t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0025t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0028t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0030t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0001c0031t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0009g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0020g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0002t0023g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0011t0010g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0011t0010g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0011t0018g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0014t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0014t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0019t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0020t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0002c0023t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0008g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0016g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0003t0021g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0012g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0005t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0015t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0015t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0032t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0003c0034t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0004c0004t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0006t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0006t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0006t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0006t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0006t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0006t0024g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0012t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0012t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0012t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0005c0026t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0006c0007t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0006c0007t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0006c0007t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0006c0007t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0007c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0007c0008t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0007c0008t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0007c0008t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0008c0010t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0008c0010t0011g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0008c0010t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0008c0010t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0009c0016t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0009c0016t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0010c0035t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0011c0021t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0012c0018t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0013c0022t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0014c0024t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0015c0029t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0016c0027t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0017c0033t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
a0018c0017t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0002 | c0011 | t0010 | g0082 | EUR | FIN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00323 | hp2 | a0003 | c0003 | t0004 | g0130 | EUR | FIN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00423 | hp2 | a0006 | c0007 | t0003 | g0045 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00544 | hp1 | a0015 | c0029 | t0001 | g0206 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00544 | hp2 | a0003 | c0005 | t0004 | g0025 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00621 | hp2 | a0006 | c0007 | t0003 | g0042 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00639 | hp1 | a0003 | c0003 | t0021 | g0146 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00639 | hp2 | a0012 | c0018 | t0002 | g0084 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00733 | hp1 | a0003 | c0003 | t0004 | g0134 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00733 | hp2 | a0001 | c0028 | t0001 | g0161 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01074 | hp1 | a0005 | c0012 | t0003 | g0128 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01081 | hp2 | a0003 | c0003 | t0004 | g0133 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01099 | hp1 | a0003 | c0005 | t0010 | g0020 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01106 | hp1 | a0002 | c0023 | t0002 | g0089 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01106 | hp2 | a0002 | c0002 | t0007 | g0099 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01109 | hp1 | a0005 | c0006 | t0004 | g0123 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01167 | hp2 | a0001 | c0001 | t0022 | g0142 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01168 | hp1 | a0002 | c0014 | t0002 | g0049 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01192 | hp1 | a0003 | c0032 | t0005 | g0272 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01243 | hp1 | a0008 | c0010 | t0011 | g0151 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01243 | hp2 | a0009 | c0016 | t0005 | g0270 | AMR | PUR | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01255 | hp2 | a0005 | c0006 | t0024 | g0124 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01256 | hp1 | a0005 | c0006 | t0004 | g0154 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0115 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01261 | hp2 | a0003 | c0003 | t0004 | g0131 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01346 | hp2 | a0001 | c0001 | t0014 | g0016 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0064 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01358 | hp2 | a0003 | c0003 | t0004 | g0132 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01361 | hp2 | a0005 | c0006 | t0004 | g0121 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01433 | hp1 | a0005 | c0006 | t0004 | g0009 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01433 | hp2 | a0002 | c0019 | t0002 | g0101 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01516 | hp1 | a0001 | c0001 | t0015 | g0196 | EUR | IBS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0114 | EUR | IBS | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01884 | hp1 | a0002 | c0002 | t0007 | g0096 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01891 | hp1 | a0003 | c0003 | t0006 | g0166 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01891 | hp2 | a0005 | c0012 | t0003 | g0129 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01934 | hp2 | a0005 | c0006 | t0004 | g0009 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01943 | hp1 | a0001 | c0001 | t0014 | g0016 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01978 | hp2 | a0003 | c0003 | t0004 | g0037 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02055 | hp1 | a0003 | c0003 | t0006 | g0181 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02055 | hp2 | a0002 | c0002 | t0023 | g0086 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02071 | hp1 | a0004 | c0004 | t0003 | g0004 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02071 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02074 | hp1 | a0004 | c0004 | t0003 | g0062 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02080 | hp2 | a0002 | c0020 | t0002 | g0051 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02083 | hp1 | a0001 | c0031 | t0001 | g0201 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02083 | hp2 | a0016 | c0027 | t0003 | g0060 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02129 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02135 | hp1 | a0004 | c0004 | t0004 | g0065 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02135 | hp2 | a0003 | c0003 | t0004 | g0125 | EAS | KHV | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CDX | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02165 | hp1 | a0003 | c0003 | t0008 | g0238 | EAS | CDX | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | CDX | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02257 | hp2 | a0003 | c0003 | t0013 | g0155 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02258 | hp1 | a0003 | c0034 | t0005 | g0279 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02280 | hp1 | a0002 | c0002 | t0007 | g0039 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02280 | hp2 | a0001 | c0025 | t0003 | g0147 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02293 | hp1 | a0003 | c0003 | t0004 | g0138 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | PEL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02451 | hp1 | a0003 | c0003 | t0006 | g0258 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02451 | hp2 | a0003 | c0003 | t0008 | g0228 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02572 | hp2 | a0003 | c0015 | t0005 | g0273 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02602 | hp1 | a0002 | c0011 | t0010 | g0080 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02615 | hp2 | a0003 | c0003 | t0006 | g0165 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02630 | hp1 | a0003 | c0003 | t0006 | g0259 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02647 | hp1 | a0002 | c0002 | t0007 | g0094 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02683 | hp1 | a0002 | c0014 | t0002 | g0052 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0069 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02717 | hp1 | a0003 | c0003 | t0005 | g0018 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02717 | hp2 | a0003 | c0003 | t0005 | g0157 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02723 | hp1 | a0003 | c0003 | t0006 | g0013 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02738 | hp1 | a0003 | c0003 | t0016 | g0127 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02738 | hp2 | a0003 | c0005 | t0005 | g0253 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02818 | hp1 | a0003 | c0003 | t0006 | g0167 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02886 | hp1 | a0003 | c0003 | t0005 | g0275 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0010 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02896 | hp1 | a0005 | c0026 | t0004 | g0120 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02896 | hp2 | a0002 | c0002 | t0007 | g0098 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02897 | hp1 | a0002 | c0002 | t0009 | g0010 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02897 | hp2 | a0002 | c0002 | t0007 | g0073 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02922 | hp1 | a0003 | c0003 | t0006 | g0271 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02922 | hp2 | a0007 | c0008 | t0001 | g0266 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02965 | hp1 | a0003 | c0003 | t0005 | g0274 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02965 | hp2 | a0005 | c0012 | t0001 | g0176 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02970 | hp2 | a0003 | c0003 | t0006 | g0164 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02976 | hp2 | a0007 | c0008 | t0003 | g0028 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03017 | hp1 | a0001 | c0009 | t0001 | g0220 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03017 | hp2 | a0003 | c0005 | t0004 | g0024 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03041 | hp2 | a0013 | c0022 | t0017 | g0034 | AFR | GWD | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03130 | hp1 | a0002 | c0002 | t0007 | g0095 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03139 | hp2 | a0003 | c0003 | t0006 | g0278 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03195 | hp1 | a0003 | c0003 | t0008 | g0017 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03195 | hp2 | a0007 | c0008 | t0003 | g0027 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03209 | hp1 | a0014 | c0024 | t0005 | g0169 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03225 | hp2 | a0003 | c0003 | t0008 | g0017 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03453 | hp2 | a0003 | c0003 | t0006 | g0182 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03486 | hp1 | a0009 | c0016 | t0005 | g0269 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03490 | hp1 | a0001 | c0013 | t0001 | g0011 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03490 | hp2 | a0001 | c0009 | t0001 | g0217 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03492 | hp2 | a0001 | c0013 | t0001 | g0011 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03516 | hp2 | a0003 | c0003 | t0006 | g0183 | AFR | ESN | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03579 | hp1 | a0003 | c0003 | t0009 | g0251 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03579 | hp2 | a0003 | c0003 | t0005 | g0018 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03654 | hp1 | a0002 | c0002 | t0020 | g0054 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03654 | hp2 | a0001 | c0009 | t0001 | g0219 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03688 | hp1 | a0003 | c0005 | t0004 | g0023 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0112 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03710 | hp1 | a0001 | c0013 | t0001 | g0189 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0113 | SAS | PJL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | BEB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0067 | SAS | BEB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03834 | hp2 | a0003 | c0005 | t0004 | g0074 | SAS | BEB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG04115 | hp1 | a0001 | c0001 | t0015 | g0198 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG04115 | hp2 | a0002 | c0011 | t0018 | g0035 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0085 | SAS | STU | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18522 | hp1 | a0008 | c0010 | t0006 | g0254 | AFR | YRI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18522 | hp2 | a0003 | c0003 | t0006 | g0013 | AFR | YRI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18906 | hp1 | a0002 | c0002 | t0007 | g0097 | AFR | YRI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18906 | hp2 | a0017 | c0033 | t0005 | g0240 | AFR | YRI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18942 | hp1 | a0001 | c0030 | t0001 | g0172 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18942 | hp2 | a0004 | c0004 | t0003 | g0057 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18951 | hp1 | a0006 | c0007 | t0003 | g0044 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18951 | hp2 | a0002 | c0002 | t0008 | g0267 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18954 | hp2 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18965 | hp1 | a0004 | c0004 | t0019 | g0081 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18967 | hp1 | a0004 | c0004 | t0003 | g0075 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18970 | hp2 | a0003 | c0003 | t0004 | g0139 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18978 | hp1 | a0018 | c0017 | t0002 | g0036 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18979 | hp1 | a0004 | c0004 | t0003 | g0040 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18984 | hp1 | a0003 | c0003 | t0004 | g0141 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18999 | hp1 | a0003 | c0003 | t0004 | g0140 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19000 | hp2 | a0004 | c0004 | t0003 | g0030 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19002 | hp2 | a0007 | c0008 | t0001 | g0214 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19003 | hp1 | a0011 | c0021 | t0002 | g0107 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19003 | hp2 | a0003 | c0005 | t0012 | g0058 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19030 | hp2 | a0003 | c0003 | t0006 | g0261 | AFR | LWK | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19043 | hp1 | a0003 | c0003 | t0005 | g0260 | AFR | LWK | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19055 | hp2 | a0003 | c0003 | t0004 | g0137 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19056 | hp1 | a0002 | c0002 | t0008 | g0276 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19080 | hp2 | a0003 | c0005 | t0004 | g0022 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19082 | hp1 | a0003 | c0005 | t0012 | g0021 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19082 | hp2 | a0006 | c0007 | t0003 | g0043 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19240 | hp1 | a0003 | c0003 | t0008 | g0236 | AFR | YRI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA19240 | hp2 | a0008 | c0010 | t0011 | g0152 | AFR | YRI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | ASW | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ASW | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20752 | hp1 | a0010 | c0035 | t0001 | g0212 | EUR | TSI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | GIH | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20905 | hp2 | a0003 | c0005 | t0004 | g0026 | SAS | GIH | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | CLM | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02109 | hp2 | a0003 | c0003 | t0013 | g0156 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02486 | hp1 | a0004 | c0004 | t0001 | g0160 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0068 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG02559 | hp2 | a0003 | c0003 | t0006 | g0184 | AFR | ACB | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG03471 | hp2 | a0003 | c0015 | t0005 | g0268 | AFR | MSL | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG06807 | hp1 | a0003 | c0005 | t0004 | g0029 | AFR | USA | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
HG06807 | hp2 | a0003 | c0003 | t0009 | g0248 | AFR | USA | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20300 | hp1 | a0008 | c0010 | t0011 | g0153 | AFR | USA | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | LWK | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
NA21309 | hp2 | a0005 | c0006 | t0005 | g0158 | AFR | LWK | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
homoSapiens_chm13v2 | hp1 | a0001 | c0009 | t0001 | g0218 | REF | REF | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | ATP7B_chr13_51927669_52016450 | ATP7B | chr13 | 51927669 | 52016450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51934941 | C | T | 1 | a0012 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.4213G>A | p.Gly1405Ser | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 4326/6598 | 4213/4398 | 1405/1465 | chr13 | 51934941 | ||
chr13:51937490 | C | T | 1 | a0016 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.3889G>A | p.Val1297Ile | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 18/21 | 4002/6598 | 3889/4398 | 1297/1465 | chr13 | 51937490 | ||
chr13:51937579 | T | G | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.3800A>C | p.Asp1267Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 18/21 | 3913/6598 | 3800/4398 | 1267/1465 | chr13 | 51937579 | ||
chr13:51937664 | C | A | 1 | a0015 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3715G>T | p.Val1239Phe | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 18/21 | 3828/6598 | 3715/4398 | 1239/1465 | chr13 | 51937664 | ||
chr13:51939130 | T | C | 1 | a0005 | 11 | HG01074.hp1 HG01109.hp1 HG01255.hp2 others(8): Show |
missense_variant | MODERATE | c.3620A>G | p.His1207Arg | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/21 | 3733/6598 | 3620/4398 | 1207/1465 | chr13 | 51939130 | ||
chr13:51941218 | A | G | 11 | a0002a0003a0005others(8): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
missense_variant | MODERATE | c.3419T>C | p.Val1140Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/21 | 3532/6598 | 3419/4398 | 1140/1465 | chr13 | 51941218 | ||
chr13:51944251 | T | C | 1 | a0017 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.3101A>G | p.His1034Arg | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/21 | 3214/6598 | 3101/4398 | 1034/1465 | chr13 | 51944251 | ||
chr13:51949672 | C | T | 10 | a0002a0003a0005others(7): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
missense_variant | MODERATE | c.2855G>A | p.Arg952Lys | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/21 | 2968/6598 | 2855/4398 | 952/1465 | chr13 | 51949672 | ||
chr13:51950352 | T | C | 9 | a0002a0003a0009others(6): Show | 151 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
missense_variant | MODERATE | c.2495A>G | p.Lys832Arg | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 10/21 | 2608/6598 | 2495/4398 | 832/1465 | chr13 | 51950352 | ||
chr13:51950368 | G | A | 1 | a0013 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.2479C>T | p.Arg827Trp | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 10/21 | 2592/6598 | 2479/4398 | 827/1465 | chr13 | 51950368 | ||
chr13:51970669 | C | G | 8 | a0002a0004a0007others(5): Show | 105 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
missense_variant | MODERATE | c.1366G>C | p.Val456Leu | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/21 | 1479/6598 | 1366/4398 | 456/1465 | chr13 | 51970669 | ||
chr13:51974004 | A | C | 7 | a0002a0004a0006others(4): Show | 104 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
missense_variant | MODERATE | c.1216T>G | p.Ser406Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/21 | 1329/6598 | 1216/4398 | 406/1465 | chr13 | 51974004 | ||
chr13:51974022 | T | C | 1 | a0009 | 2 | HG01243.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1198A>G | p.Thr400Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/21 | 1311/6598 | 1198/4398 | 400/1465 | chr13 | 51974022 | ||
chr13:51974223 | C | T | 1 | a0018 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.997G>A | p.Gly333Arg | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/21 | 1110/6598 | 997/4398 | 333/1465 | chr13 | 51974223 | ||
chr13:51974531 | G | C | 1 | a0010 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.689C>G | p.Thr230Ser | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/21 | 802/6598 | 689/4398 | 230/1465 | chr13 | 51974531 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51934759 | G | T | 1 | a0001c0028 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.4395C>A | p.Ile1465Ile | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 4508/6598 | 4395/4398 | 1465/1465 | chr13 | 51934759 | ||
chr13:51934843 | C | T | 1 | a0002c0019 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.4311G>A | p.Lys1437Lys | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 4424/6598 | 4311/4398 | 1437/1465 | chr13 | 51934843 | ||
chr13:51934852 | C | T | 2 | a0005c0012a0005c0026 | 4 | HG01074.hp1 HG01891.hp2 HG02896.hp1 others(1): Show |
synonymous_variant | LOW | c.4302G>A | p.Thr1434Thr | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 4415/6598 | 4302/4398 | 1434/1465 | chr13 | 51934852 | ||
chr13:51934903 | T | C | 1 | a0002c0020 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.4251A>G | p.Thr1417Thr | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 4364/6598 | 4251/4398 | 1417/1465 | chr13 | 51934903 | ||
chr13:51937488 | G | A | 1 | a0003c0015 | 2 | HG02572.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.3891C>T | p.Val1297Val | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 18/21 | 4004/6598 | 3891/4398 | 1297/1465 | chr13 | 51937488 | ||
chr13:51942432 | T | C | 1 | a0005c0012 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.3366A>G | p.Ala1122Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/21 | 3479/6598 | 3366/4398 | 1122/1465 | chr13 | 51942432 | ||
chr13:51946299 | C | T | 1 | a0002c0014 | 2 | HG01168.hp1 HG02683.hp1 |
synonymous_variant | LOW | c.3045G>A | p.Leu1015Leu | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/21 | 3158/6598 | 3045/4398 | 1015/1465 | chr13 | 51946299 | ||
chr13:51946329 | G | A | 1 | a0017c0033 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.3015C>T | p.Asn1005Asn | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/21 | 3128/6598 | 3015/4398 | 1005/1465 | chr13 | 51946329 | ||
chr13:51946335 | C | T | 2 | a0002c0011a0003c0005 | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
synonymous_variant | LOW | c.3009G>A | p.Ala1003Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/21 | 3122/6598 | 3009/4398 | 1003/1465 | chr13 | 51946335 | ||
chr13:51946338 | G | A | 1 | a0001c0030 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.3006C>T | p.Ala1002Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/21 | 3119/6598 | 3006/4398 | 1002/1465 | chr13 | 51946338 | ||
chr13:51946365 | C | T | 1 | a0003c0032 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.2979G>A | p.Thr993Thr | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/21 | 3092/6598 | 2979/4398 | 993/1465 | chr13 | 51946365 | ||
chr13:51946371 | C | T | 1 | a0001c0009 | 4 | HG03017.hp1 HG03490.hp2 HG03654.hp2 others(1): Show |
synonymous_variant | LOW | c.2973G>A | p.Thr991Thr | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/21 | 3086/6598 | 2973/4398 | 991/1465 | chr13 | 51946371 | ||
chr13:51950154 | G | A | 1 | a0001c0031 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.2583C>T | p.Ala861Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 11/21 | 2696/6598 | 2583/4398 | 861/1465 | chr13 | 51950154 | ||
chr13:51950363 | G | A | 1 | a0001c0013 | 3 | HG03490.hp1 HG03492.hp2 HG03710.hp1 |
synonymous_variant | LOW | c.2484C>T | p.Gly828Gly | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 10/21 | 2597/6598 | 2484/4398 | 828/1465 | chr13 | 51950363 | ||
chr13:51964911 | C | T | 1 | a0001c0025 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1830G>A | p.Pro610Pro | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/21 | 1943/6598 | 1830/4398 | 610/1465 | chr13 | 51964911 | ||
chr13:51968531 | G | A | 1 | a0002c0023 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.1620C>T | p.Leu540Leu | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/21 | 1733/6598 | 1620/4398 | 540/1465 | chr13 | 51968531 | ||
chr13:51974227 | G | A | 1 | a0003c0034 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.993C>T | p.Ala331Ala | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/21 | 1106/6598 | 993/4398 | 331/1465 | chr13 | 51974227 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51932974 | G | C | 40 | a0002c0002t0002a0002c0002t0007a0002c0002t0008others(37): Show | 161 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1782C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1782 | chr13 | 51932974 | |||||
chr13:51933012 | G | A | 3 | a0002c0011t0010a0002c0011t0018a0003c0005t0010 | 4 | HG00323.hp1 HG01099.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1744C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1744 | chr13 | 51933012 | |||||
chr13:51933039 | C | A | 2 | a0002c0002t0007a0013c0022t0017 | 9 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1717G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1717 | chr13 | 51933039 | |||||
chr13:51933048 | T | C | 3 | a0003c0003t0006a0003c0003t0013a0008c0010t0006 | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1708A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1708 | chr13 | 51933048 | |||||
chr13:51933234 | C | T | 1 | a0003c0003t0021 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1522G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1522 | chr13 | 51933234 | |||||
chr13:51933265 | T | C | 1 | a0001c0001t0015 | 2 | HG01516.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1491A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1491 | chr13 | 51933265 | |||||
chr13:51933347 | T | G | 1 | a0003c0005t0012 | 2 | NA19003.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1409A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1409 | chr13 | 51933347 | |||||
chr13:51933371 | C | T | 1 | a0002c0002t0020 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1385G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1385 | chr13 | 51933371 | |||||
chr13:51933574 | G | A | 4 | a0002c0002t0007a0002c0002t0009a0003c0003t0009others(1): Show | 13 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1182 | chr13 | 51933574 | |||||
chr13:51933584 | C | T | 12 | a0002c0002t0002a0002c0002t0008a0002c0002t0020others(9): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1172G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1172 | chr13 | 51933584 | |||||
chr13:51933628 | C | T | 1 | a0004c0004t0019 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1128G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1128 | chr13 | 51933628 | |||||
chr13:51933680 | T | A | 1 | a0001c0001t0022 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1076A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 1076 | chr13 | 51933680 | |||||
chr13:51933836 | C | T | 1 | a0002c0011t0018 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 920 | chr13 | 51933836 | |||||
chr13:51933913 | G | A | 1 | a0013c0022t0017 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*843C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 843 | chr13 | 51933913 | |||||
chr13:51933922 | C | T | 1 | a0001c0001t0014 | 2 | HG01346.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*834G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 834 | chr13 | 51933922 | |||||
chr13:51934025 | T | G | 1 | a0002c0002t0023 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 731 | chr13 | 51934025 | |||||
chr13:51934566 | G | T | 4 | a0002c0002t0007a0002c0002t0009a0003c0003t0009others(1): Show | 13 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*190C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 190 | chr13 | 51934566 | |||||
chr13:51934584 | C | A | 1 | a0005c0006t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 172 | chr13 | 51934584 | |||||
chr13:51934607 | C | T | 1 | a0003c0003t0016 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 149 | chr13 | 51934607 | |||||
chr13:51934741 | G | A | 1 | a0008c0010t0011 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 21/21 | 15 | chr13 | 51934741 | |||||
chr13:52011391 | C | A | 1 | a0003c0003t0013 | 2 | HG02109.hp2 HG02257.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/21 | chr13 | 52011391 | ||||||
chr13:52011412 | G | T | 35 | a0001c0001t0003a0001c0001t0022a0001c0025t0003others(32): Show | 154 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/21 | 75 | chr13 | 52011412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51935099 | T | C | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4125-70A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 20/20 | chr13 | 51935099 | ||||||
chr13:51935161 | A | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4125-132T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 20/20 | chr13 | 51935161 | ||||||
chr13:51935238 | G | C | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4125-209C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 20/20 | chr13 | 51935238 | ||||||
chr13:51935315 | A | T | 8 | a0003c0003t0006g0013a0003c0003t0006g0167a0003c0003t0006g0181others(5): Show | 9 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4124+278T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 20/20 | chr13 | 51935315 | ||||||
chr13:51935482 | T | G | 1 | a0018c0017t0002g0036 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4124+111A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 20/20 | chr13 | 51935482 | ||||||
chr13:51935772 | C | T | 2 | a0003c0003t0006g0258a0003c0003t0006g0259 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4022-77G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935772 | ||||||
chr13:51935849 | C | G | 1 | a0002c0002t0023g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4022-154G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935849 | ||||||
chr13:51935853 | C | G | 8 | a0003c0003t0005g0274a0003c0003t0005g0275a0003c0015t0005g0268others(5): Show | 8 | HG01192.hp1 HG01243.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4022-158G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935853 | ||||||
chr13:51935854 | C | G | 51 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(48): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.4022-159G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935854 | ||||||
chr13:51935854 | C | T | 1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4022-159G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935854 | ||||||
chr13:51935956 | C | G | 1 | a0002c0002t0008g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4022-261G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935956 | ||||||
chr13:51935983 | C | T | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4022-288G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51935983 | ||||||
chr13:51936024 | G | A | 135 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(132): Show | 143 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.4022-329C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936024 | ||||||
chr13:51936210 | G | A | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.4022-515C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936210 | ||||||
chr13:51936328 | A | T | 1 | a0001c0001t0001g0015 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4022-633T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936328 | ||||||
chr13:51936461 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4022-766C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936461 | ||||||
chr13:51936804 | G | A | 38 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(35): Show | 40 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.4021+472C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936804 | ||||||
chr13:51936804 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4021+472C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936804 | ||||||
chr13:51936909 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4021+367T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936909 | ||||||
chr13:51936960 | T | C | 1 | a0014c0024t0005g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4021+316A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51936960 | ||||||
chr13:51937139 | GA | G | 7 | a0003c0003t0005g0157a0003c0003t0005g0274a0003c0003t0008g0017others(4): Show | 8 | HG01192.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.4021+136delT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51937139 | ||||||
chr13:51937139 | GAA | G | 130 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(127): Show | 140 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.4021+135_4021+136d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51937139 | ||||||
chr13:51937154 | A | C | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4021+122T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51937154 | ||||||
chr13:51937169 | C | T | 1 | a0002c0002t0009g0010 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4021+107G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51937169 | ||||||
chr13:51937170 | G | A | 2 | a0001c0001t0003g0149a0001c0001t0003g0150 | 2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.4021+106C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51937170 | ||||||
chr13:51937226 | C | G | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.4021+50G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 19/20 | chr13 | 51937226 | ||||||
chr13:51937470 | G | A | 145 | a0001c0001t0001g0195a0001c0001t0001g0227a0002c0002t0002g0002others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
splice_region_variant&intron_variant | LOW | c.3903+6C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 18/20 | chr13 | 51937470 | ||||||
chr13:51937776 | G | A | 4 | a0004c0004t0003g0004a0004c0004t0003g0040a0004c0004t0003g0057others(1): Show | 5 | HG02071.hp1 NA18942.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.3700-97C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51937776 | ||||||
chr13:51938038 | T | C | 1 | a0003c0003t0004g0140 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3700-359A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938038 | ||||||
chr13:51938049 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3700-370C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938049 | ||||||
chr13:51938132 | T | C | 148 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(145): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.3700-453A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938132 | ||||||
chr13:51938356 | C | T | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.3700-677G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938356 | ||||||
chr13:51938382 | G | A | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.3699+669C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938382 | ||||||
chr13:51938505 | A | T | 3 | a0003c0034t0005g0279a0009c0016t0005g0269a0009c0016t0005g0270 | 3 | HG01243.hp2 HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3699+546T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938505 | ||||||
chr13:51938574 | T | C | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3699+477A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938574 | ||||||
chr13:51938581 | G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0227 | 2 | HG02155.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3699+470C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938581 | ||||||
chr13:51938624 | T | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3699+427A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938624 | ||||||
chr13:51938752 | C | T | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.3699+299G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938752 | ||||||
chr13:51938799 | C | T | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3699+252G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 17/20 | chr13 | 51938799 | ||||||
chr13:51939224 | C | A | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3557-31G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939224 | ||||||
chr13:51939288 | T | C | 6 | a0002c0002t0002g0068a0002c0002t0002g0069a0002c0002t0002g0070others(3): Show | 6 | HG00642.hp1 HG00741.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3557-95A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939288 | ||||||
chr13:51939427 | T | A | 2 | a0004c0004t0003g0062a0004c0004t0019g0081 | 2 | HG02074.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.3557-234A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939427 | ||||||
chr13:51939496 | T | C | 1 | a0011c0021t0002g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3557-303A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939496 | ||||||
chr13:51939501 | G | A | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.3557-308C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939501 | ||||||
chr13:51939595 | T | C | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.3557-402A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939595 | ||||||
chr13:51939642 | A | G | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3557-449T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939642 | ||||||
chr13:51939652 | G | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3557-459C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939652 | ||||||
chr13:51939660 | C | CT | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.3557-468dupA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939660 | ||||||
chr13:51939743 | C | T | 1 | a0002c0002t0002g0003 | 2 | NA18972.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3557-550G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939743 | ||||||
chr13:51939782 | G | A | 5 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0105others(2): Show | 5 | NA18956.hp2 NA18959.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.3557-589C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939782 | ||||||
chr13:51939874 | A | G | 5 | a0003c0003t0006g0181a0003c0003t0006g0182a0003c0003t0006g0183others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3557-681T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939874 | ||||||
chr13:51939893 | T | C | 51 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(48): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3557-700A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939893 | ||||||
chr13:51939941 | T | C | 5 | a0003c0003t0005g0274a0003c0003t0008g0017a0003c0003t0008g0228others(2): Show | 6 | HG01192.hp1 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3557-748A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939941 | ||||||
chr13:51939944 | A | C | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3557-751T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51939944 | ||||||
chr13:51940000 | CT | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(91): Show | 106 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.3557-808delA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940000 | ||||||
chr13:51940000 | CTT | C | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0221others(12): Show | 15 | HG01167.hp2 HG01243.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.3557-809_3557-808d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940000 | ||||||
chr13:51940000 | CTTT | C | 31 | a0002c0002t0002g0038a0002c0002t0002g0046a0002c0002t0002g0053others(28): Show | 34 | HG00544.hp2 HG01074.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.3557-810_3557-808d others(5): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940000 | ||||||
chr13:51940000 | CTTTT | C | 91 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(88): Show | 97 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.3557-811_3557-808d others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940000 | ||||||
chr13:51940000 | CTTTTT | C | 27 | a0002c0002t0002g0117a0002c0002t0002g0136a0002c0002t0007g0039others(24): Show | 29 | HG01106.hp2 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.3557-812_3557-808d others(7): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940000 | ||||||
chr13:51940148 | G | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0004c0004t0001g0160 | 3 | HG02486.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3556+933C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940148 | ||||||
chr13:51940174 | C | T | 18 | a0002c0002t0002g0078a0003c0003t0006g0013a0003c0003t0006g0164others(15): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.3556+907G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940174 | ||||||
chr13:51940212 | C | T | 3 | a0003c0034t0005g0279a0009c0016t0005g0269a0009c0016t0005g0270 | 3 | HG01243.hp2 HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3556+869G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940212 | ||||||
chr13:51940233 | G | A | 2 | a0002c0002t0002g0083a0002c0002t0002g0110 | 2 | HG00741.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3556+848C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940233 | ||||||
chr13:51940380 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3556+701C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940380 | ||||||
chr13:51940382 | G | A | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3556+699C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940382 | ||||||
chr13:51940392 | G | A | 1 | a0002c0002t0020g0054 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3556+689C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940392 | ||||||
chr13:51940423 | G | A | 72 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(69): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3556+658C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940423 | ||||||
chr13:51940475 | T | C | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3556+606A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940475 | ||||||
chr13:51940594 | A | G | 154 | a0001c0001t0015g0196a0001c0001t0015g0198a0002c0002t0002g0002others(151): Show | 165 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.3556+487T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940594 | ||||||
chr13:51940669 | T | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0252a0001c0001t0003g0122 | 3 | HG01952.hp1 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.3556+412A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940669 | ||||||
chr13:51940827 | T | C | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3556+254A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940827 | ||||||
chr13:51940902 | C | G | 4 | a0003c0003t0004g0125a0003c0003t0004g0137a0003c0003t0004g0139others(1): Show | 4 | HG02135.hp2 NA18970.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.3556+179G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51940902 | ||||||
chr13:51941080 | C | T | 1 | a0003c0005t0012g0021 | 1 | NA19082.hp1 | splice_donor_variant&intron_variant | HIGH | c.3556+1G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 16/20 | chr13 | 51941080 | ||||||
chr13:51941259 | T | C | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3413-35A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51941259 | ||||||
chr13:51941556 | T | C | 8 | a0003c0003t0006g0013a0003c0003t0006g0167a0003c0003t0006g0181others(5): Show | 9 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3413-332A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51941556 | ||||||
chr13:51941842 | T | C | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3412+544A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51941842 | ||||||
chr13:51941846 | A | AAC | 149 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(146): Show | 160 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.3412+538_3412+539d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51941846 | ||||||
chr13:51941944 | A | C | 1 | a0002c0002t0002g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3412+442T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51941944 | ||||||
chr13:51941966 | A | G | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3412+420T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51941966 | ||||||
chr13:51942023 | C | T | 3 | a0003c0003t0004g0037a0003c0003t0004g0138a0003c0003t0021g0146 | 3 | HG00639.hp1 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.3412+363G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51942023 | ||||||
chr13:51942094 | T | C | 177 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0174others(174): Show | 190 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.3412+292A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51942094 | ||||||
chr13:51942262 | C | T | 1 | a0002c0002t0007g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3412+124G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 15/20 | chr13 | 51942262 | ||||||
chr13:51942773 | T | C | 39 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(36): Show | 41 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.3244-219A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51942773 | ||||||
chr13:51942807 | C | T | 2 | a0004c0004t0003g0062a0004c0004t0019g0081 | 2 | HG02074.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.3244-253G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51942807 | ||||||
chr13:51943101 | C | G | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3244-547G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943101 | ||||||
chr13:51943392 | A | G | 19 | a0002c0002t0002g0006a0002c0002t0002g0038a0002c0002t0002g0068others(16): Show | 20 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.3243+717T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943392 | ||||||
chr13:51943462 | G | T | 72 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(69): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3243+647C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943462 | ||||||
chr13:51943469 | T | C | 2 | a0003c0003t0004g0131a0003c0003t0004g0134 | 2 | HG00733.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.3243+640A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943469 | ||||||
chr13:51943532 | T | C | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3243+577A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943532 | ||||||
chr13:51943545 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3243+564C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943545 | ||||||
chr13:51943819 | C | T | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.3243+290G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943819 | ||||||
chr13:51943820 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3243+289C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943820 | ||||||
chr13:51943926 | A | G | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3243+183T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943926 | ||||||
chr13:51943927 | A | G | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3243+182T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943927 | ||||||
chr13:51943929 | C | A | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3243+180G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943929 | ||||||
chr13:51943930 | T | A | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3243+179A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943930 | ||||||
chr13:51943933 | A | G | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3243+176T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943933 | ||||||
chr13:51943934 | ACT | A | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3243+173_3243+174d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943934 | ||||||
chr13:51943987 | C | T | 1 | a0001c0001t0003g0008 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3243+122G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 14/20 | chr13 | 51943987 | ||||||
chr13:51944556 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3061-265G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51944556 | ||||||
chr13:51944581 | C | G | 1 | a0003c0015t0005g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3061-290G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51944581 | ||||||
chr13:51944610 | C | T | 2 | a0003c0003t0006g0013a0008c0010t0006g0254 | 3 | HG02723.hp1 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3061-319G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51944610 | ||||||
chr13:51944717 | C | A | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3061-426G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51944717 | ||||||
chr13:51944786 | A | T | 6 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.3061-495T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51944786 | ||||||
chr13:51944981 | C | T | 19 | a0003c0003t0005g0157a0003c0003t0006g0013a0003c0003t0006g0164others(16): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3061-690G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51944981 | ||||||
chr13:51945073 | G | A | 92 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(89): Show | 100 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.3061-782C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945073 | ||||||
chr13:51945077 | G | GCCTT | 149 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(146): Show | 160 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.3061-790_3061-787d others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945077 | ||||||
chr13:51945178 | C | T | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3061-887G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945178 | ||||||
chr13:51945241 | A | C | 155 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(152): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.3061-950T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945241 | ||||||
chr13:51945401 | G | A | 1 | a0003c0003t0004g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3060+883C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945401 | ||||||
chr13:51945610 | G | A | 155 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(152): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.3060+674C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945610 | ||||||
chr13:51945710 | G | A | 4 | a0003c0003t0005g0275a0003c0034t0005g0279a0009c0016t0005g0269others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3060+574C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945710 | ||||||
chr13:51945819 | G | C | 51 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(48): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3060+465C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945819 | ||||||
chr13:51945877 | C | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0222 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3060+407G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945877 | ||||||
chr13:51945993 | T | A | 1 | a0003c0003t0006g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3060+291A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51945993 | ||||||
chr13:51946221 | T | A | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3060+63A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51946221 | ||||||
chr13:51946268 | C | A | 3 | a0003c0003t0006g0278a0003c0003t0013g0155a0003c0003t0013g0156 | 3 | HG02109.hp2 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3060+16G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 13/20 | chr13 | 51946268 | ||||||
chr13:51946491 | C | G | 37 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(34): Show | 39 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2866-13G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51946491 | ||||||
chr13:51946568 | C | A | 72 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(69): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.2866-90G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51946568 | ||||||
chr13:51946583 | C | T | 9 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(6): Show | 10 | HG00642.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2866-105G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51946583 | ||||||
chr13:51947069 | G | A | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2866-591C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51947069 | ||||||
chr13:51947071 | A | G | 151 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(148): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2866-593T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51947071 | ||||||
chr13:51947467 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2866-989G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51947467 | ||||||
chr13:51947541 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2866-1063C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51947541 | ||||||
chr13:51947568 | A | G | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2866-1090T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51947568 | ||||||
chr13:51947873 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2866-1395C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51947873 | ||||||
chr13:51948140 | G | C | 6 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2865+1522C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948140 | ||||||
chr13:51948292 | T | C | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2865+1370A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948292 | ||||||
chr13:51948679 | G | C | 141 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(138): Show | 151 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.2865+983C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948679 | ||||||
chr13:51948691 | T | C | 2 | a0002c0002t0002g0114a0002c0002t0002g0115 | 2 | HG01261.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2865+971A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948691 | ||||||
chr13:51948877 | C | T | 151 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(148): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2865+785G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948877 | ||||||
chr13:51948897 | C | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0199 | 2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.2865+765G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948897 | ||||||
chr13:51948981 | G | A | 1 | a0002c0002t0008g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2865+681C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51948981 | ||||||
chr13:51949049 | G | A | 20 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(17): Show | 22 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2865+613C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51949049 | ||||||
chr13:51949155 | G | A | 16 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(13): Show | 17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2865+507C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51949155 | ||||||
chr13:51949275 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2865+387T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51949275 | ||||||
chr13:51949413 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2865+249G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51949413 | ||||||
chr13:51949603 | T | A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2865+59A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51949603 | ||||||
chr13:51949640 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2865+22A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 12/20 | chr13 | 51949640 | ||||||
chr13:51950191 | T | C | 1 | a0007c0008t0001g0214 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2576-30A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 10/20 | chr13 | 51950191 | ||||||
chr13:51950424 | C | T | 72 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(69): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.2448-25G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51950424 | ||||||
chr13:51950544 | C | T | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2448-145G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51950544 | ||||||
chr13:51950613 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2448-214G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51950613 | ||||||
chr13:51950749 | GGGA | G | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2448-353_2448-351d others(5): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51950749 | ||||||
chr13:51951091 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2448-692A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951091 | ||||||
chr13:51951104 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2448-705A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951104 | ||||||
chr13:51951151 | C | A | 13 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(10): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2448-752G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951151 | ||||||
chr13:51951204 | T | C | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2448-805A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951204 | ||||||
chr13:51951327 | G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0246 | 3 | HG02735.hp2 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2448-928C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951327 | ||||||
chr13:51951416 | C | T | 1 | a0008c0010t0006g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2448-1017G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951416 | ||||||
chr13:51951417 | G | A | 6 | a0003c0003t0006g0167a0003c0003t0006g0181a0003c0003t0006g0182others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2448-1018C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951417 | ||||||
chr13:51951458 | C | T | 1 | a0003c0003t0006g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2448-1059G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951458 | ||||||
chr13:51951539 | T | C | 2 | a0003c0003t0004g0037a0003c0003t0004g0138 | 2 | HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2448-1140A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951539 | ||||||
chr13:51951584 | G | A | 35 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(32): Show | 37 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.2448-1185C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951584 | ||||||
chr13:51951703 | G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0265others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2448-1304C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951703 | ||||||
chr13:51951745 | C | T | 1 | a0005c0012t0003g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2448-1346G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951745 | ||||||
chr13:51951864 | A | T | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2448-1465T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951864 | ||||||
chr13:51951876 | C | A | 2 | a0003c0003t0006g0258a0003c0003t0006g0259 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2448-1477G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51951876 | ||||||
chr13:51952047 | C | T | 1 | a0002c0002t0008g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2448-1648G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952047 | ||||||
chr13:51952073 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2448-1674C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952073 | ||||||
chr13:51952290 | C | A | 6 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2448-1891G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952290 | ||||||
chr13:51952375 | G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2448-1976C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952375 | ||||||
chr13:51952433 | C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2448-2034G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952433 | ||||||
chr13:51952476 | C | T | 141 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(138): Show | 151 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.2448-2077G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952476 | ||||||
chr13:51952498 | G | A | 2 | a0003c0015t0005g0268a0003c0015t0005g0273 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2448-2099C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952498 | ||||||
chr13:51952514 | T | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2448-2115A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952514 | ||||||
chr13:51952751 | C | T | 151 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(148): Show | 162 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2448-2352G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952751 | ||||||
chr13:51952831 | A | G | 1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2448-2432T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952831 | ||||||
chr13:51952993 | A | C | 2 | a0007c0008t0003g0027a0007c0008t0003g0028 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2448-2594T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51952993 | ||||||
chr13:51953034 | A | G | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2448-2635T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953034 | ||||||
chr13:51953131 | A | T | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2448-2732T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953131 | ||||||
chr13:51953603 | T | C | 2 | a0001c0001t0003g0149a0001c0001t0003g0150 | 2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2448-3204A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953603 | ||||||
chr13:51953635 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2448-3236C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953635 | ||||||
chr13:51953766 | C | T | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2448-3367G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953766 | ||||||
chr13:51953804 | T | C | 1 | a0002c0002t0009g0010 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2448-3405A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953804 | ||||||
chr13:51953851 | T | TA | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0241others(3): Show | 6 | HG01981.hp2 HG02647.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2448-3453dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAA | 15 | a0003c0003t0004g0037a0003c0003t0004g0125a0003c0003t0004g0130others(12): Show | 15 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.2448-3455_2448-345 others(7): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(3): Show |
1 | a0003c0015t0005g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2448-3462_2448-345 others(14): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(4): Show |
2 | a0003c0015t0005g0273a0003c0034t0005g0279 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2448-3463_2448-345 others(15): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(5): Show |
7 | a0002c0002t0020g0054a0003c0003t0006g0164a0003c0003t0006g0165others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2448-3464_2448-345 others(16): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(6): Show |
20 | a0002c0002t0002g0048a0002c0002t0002g0066a0002c0002t0002g0105others(17): Show | 23 | HG00558.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.2448-3465_2448-345 others(17): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(7): Show |
36 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(33): Show | 41 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.2448-3466_2448-345 others(18): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(8): Show |
25 | a0002c0002t0002g0006a0002c0002t0002g0046a0002c0002t0002g0050others(22): Show | 26 | HG00438.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2448-3467_2448-345 others(19): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(9): Show |
8 | a0002c0002t0002g0070a0002c0002t0002g0072a0002c0002t0002g0087others(5): Show | 8 | HG00423.hp1 HG00642.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.2448-3468_2448-345 others(20): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(10): Show |
4 | a0002c0002t0002g0038a0002c0011t0010g0082a0003c0003t0005g0275others(1): Show | 4 | HG00323.hp1 HG01891.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2448-3469_2448-345 others(21): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(11): Show |
6 | a0002c0011t0010g0080a0003c0005t0004g0025a0003c0005t0004g0026others(3): Show | 6 | HG00544.hp2 HG02602.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448-3453_2448-345 others(22): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(12): Show |
12 | a0002c0002t0007g0039a0002c0002t0007g0095a0002c0002t0007g0096others(9): Show | 13 | HG01099.hp1 HG01106.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2448-3453_2448-345 others(23): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(13): Show |
6 | a0002c0002t0007g0073a0002c0002t0007g0094a0002c0002t0007g0097others(3): Show | 6 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448-3453_2448-345 others(24): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(14): Show |
4 | a0002c0002t0009g0010a0003c0003t0009g0251a0009c0016t0005g0270others(1): Show | 5 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2448-3453_2448-345 others(25): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(15): Show |
1 | a0003c0003t0009g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2448-3453_2448-345 others(26): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953851 | T | TAAAAAAA others(16): Show |
1 | a0009c0016t0005g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2448-3453_2448-345 others(27): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953851 | ||||||
chr13:51953868 | A | AAAAAAAA others(13): Show |
1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2448-3470_2448-346 others(24): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953868 | ||||||
chr13:51953868 | A | AAAAAAAA others(11): Show |
1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2448-3470_2448-346 others(22): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953868 | ||||||
chr13:51953899 | T | C | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2448-3500A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51953899 | ||||||
chr13:51954006 | G | A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2447+3510C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954006 | ||||||
chr13:51954119 | A | G | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2447+3397T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954119 | ||||||
chr13:51954120 | T | G | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2447+3396A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954120 | ||||||
chr13:51954316 | C | T | 2 | a0009c0016t0005g0269a0009c0016t0005g0270 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2447+3200G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954316 | ||||||
chr13:51954366 | C | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2447+3150G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954366 | ||||||
chr13:51954532 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2447+2984G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954532 | ||||||
chr13:51954569 | C | T | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2447+2947G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954569 | ||||||
chr13:51954647 | G | A | 1 | a0002c0011t0010g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2447+2869C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954647 | ||||||
chr13:51954673 | A | G | 155 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(152): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2447+2843T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954673 | ||||||
chr13:51954706 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2447+2810C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954706 | ||||||
chr13:51954721 | GA | G | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2447+2794delT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954721 | ||||||
chr13:51954727 | G | T | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2447+2789C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954727 | ||||||
chr13:51954828 | G | A | 78 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(75): Show | 84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2447+2688C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954828 | ||||||
chr13:51954852 | C | T | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2447+2664G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954852 | ||||||
chr13:51954870 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2447+2646C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954870 | ||||||
chr13:51954896 | G | A | 2 | a0003c0003t0009g0248a0003c0003t0009g0251 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2447+2620C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51954896 | ||||||
chr13:51955005 | G | A | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2447+2511C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955005 | ||||||
chr13:51955016 | G | A | 4 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(1): Show | 4 | HG00323.hp1 HG01099.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2447+2500C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955016 | ||||||
chr13:51955029 | C | A | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2447+2487G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955029 | ||||||
chr13:51955036 | A | G | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2447+2480T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955036 | ||||||
chr13:51955083 | T | C | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2447+2433A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955083 | ||||||
chr13:51955157 | G | A | 1 | a0002c0002t0002g0003 | 2 | NA18972.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2447+2359C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955157 | ||||||
chr13:51955207 | C | T | 36 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(33): Show | 38 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.2447+2309G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955207 | ||||||
chr13:51955225 | G | A | 1 | a0015c0029t0001g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2447+2291C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955225 | ||||||
chr13:51955418 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2447+2098T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955418 | ||||||
chr13:51955435 | T | C | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2447+2081A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955435 | ||||||
chr13:51955576 | G | A | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2447+1940C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955576 | ||||||
chr13:51955682 | T | C | 1 | a0001c0025t0003g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2447+1834A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955682 | ||||||
chr13:51955697 | G | A | 5 | a0003c0003t0005g0274a0003c0003t0008g0017a0003c0003t0008g0228others(2): Show | 6 | HG01192.hp1 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2447+1819C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955697 | ||||||
chr13:51955779 | T | C | 1 | a0003c0003t0009g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2447+1737A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955779 | ||||||
chr13:51955787 | G | A | 152 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(149): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2447+1729C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51955787 | ||||||
chr13:51956062 | C | T | 15 | a0003c0003t0004g0037a0003c0003t0004g0125a0003c0003t0004g0130others(12): Show | 15 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.2447+1454G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956062 | ||||||
chr13:51956138 | T | C | 13 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(10): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2447+1378A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956138 | ||||||
chr13:51956267 | AG | A | 5 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2447+1248delC | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956267 | ||||||
chr13:51956336 | G | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG00673.hp2 NA18941.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2447+1180C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956336 | ||||||
chr13:51956386 | T | C | 131 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(128): Show | 141 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2447+1130A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956386 | ||||||
chr13:51956422 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2447+1094C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956422 | ||||||
chr13:51956430 | A | C | 149 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(146): Show | 160 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2447+1086T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956430 | ||||||
chr13:51956520 | G | A | 1 | a0003c0003t0006g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2447+996C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956520 | ||||||
chr13:51956600 | G | A | 2 | a0002c0002t0002g0007a0002c0002t0002g0033 | 3 | HG01257.hp2 HG01346.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2447+916C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956600 | ||||||
chr13:51956601 | C | A | 2 | a0002c0002t0002g0007a0002c0002t0002g0033 | 3 | HG01257.hp2 HG01346.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2447+915G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956601 | ||||||
chr13:51956853 | T | C | 75 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(72): Show | 82 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2447+663A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956853 | ||||||
chr13:51956958 | T | C | 1 | a0002c0002t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2447+558A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956958 | ||||||
chr13:51956969 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2447+547T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51956969 | ||||||
chr13:51957098 | A | G | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2447+418T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51957098 | ||||||
chr13:51957105 | G | T | 1 | a0015c0029t0001g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2447+411C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51957105 | ||||||
chr13:51957109 | C | A | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2447+407G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51957109 | ||||||
chr13:51957227 | C | A | 72 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(69): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.2447+289G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51957227 | ||||||
chr13:51957442 | A | G | 1 | a0008c0010t0006g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2447+74T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51957442 | ||||||
chr13:51957476 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2447+40A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 9/20 | chr13 | 51957476 | ||||||
chr13:51957757 | T | C | 1 | a0002c0002t0002g0038 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2356-150A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 8/20 | chr13 | 51957757 | ||||||
chr13:51957824 | C | T | 155 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(152): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2356-217G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 8/20 | chr13 | 51957824 | ||||||
chr13:51957854 | A | C | 2 | a0002c0011t0010g0080a0002c0011t0018g0035 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2356-247T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 8/20 | chr13 | 51957854 | ||||||
chr13:51957903 | T | C | 78 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(75): Show | 86 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2356-296A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 8/20 | chr13 | 51957903 | ||||||
chr13:51958155 | T | G | 1 | a0002c0020t0002g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2355+156A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 8/20 | chr13 | 51958155 | ||||||
chr13:51958222 | T | C | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2355+89A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 8/20 | chr13 | 51958222 | ||||||
chr13:51958702 | C | T | 2 | a0003c0003t0004g0130a0003c0003t0004g0133 | 2 | HG00323.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2122-158G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51958702 | ||||||
chr13:51958910 | A | G | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2122-366T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51958910 | ||||||
chr13:51958982 | A | G | 2 | a0002c0002t0002g0076a0002c0002t0002g0077 | 2 | HG01978.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2122-438T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51958982 | ||||||
chr13:51959012 | T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0256 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2122-468A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959012 | ||||||
chr13:51959018 | C | T | 5 | a0003c0003t0005g0157a0008c0010t0011g0151a0008c0010t0011g0152others(2): Show | 5 | HG01243.hp1 HG02717.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2122-474G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959018 | ||||||
chr13:51959026 | C | T | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2122-482G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959026 | ||||||
chr13:51959094 | C | G | 1 | a0002c0002t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2122-550G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959094 | ||||||
chr13:51959178 | G | A | 16 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(13): Show | 17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2122-634C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959178 | ||||||
chr13:51959311 | T | C | 1 | a0002c0002t0002g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2122-767A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959311 | ||||||
chr13:51959330 | G | C | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2122-786C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959330 | ||||||
chr13:51959508 | C | CA | 18 | a0001c0001t0001g0187a0001c0001t0001g0208a0001c0001t0001g0226others(15): Show | 18 | HG01891.hp2 HG01978.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2121+639dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959508 | ||||||
chr13:51959508 | C | CAA | 6 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2121+638_2121+639d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959508 | ||||||
chr13:51959508 | CA | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0239a0001c0001t0001g0262others(18): Show | 23 | HG01106.hp2 HG01168.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2121+639delT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959508 | ||||||
chr13:51959678 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2121+470G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959678 | ||||||
chr13:51959679 | G | A | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2121+469C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51959679 | ||||||
chr13:51960021 | G | T | 6 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2121+127C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 7/20 | chr13 | 51960021 | ||||||
chr13:51960326 | G | A | 4 | a0004c0004t0003g0004a0004c0004t0003g0040a0004c0004t0003g0057others(1): Show | 5 | HG02071.hp1 NA18942.hp2 NA18954.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1947-4C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51960326 | ||||||
chr13:51960492 | T | A | 3 | a0003c0003t0006g0258a0003c0003t0006g0259a0003c0003t0006g0261 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1947-170A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51960492 | ||||||
chr13:51960747 | A | G | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1947-425T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51960747 | ||||||
chr13:51961157 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1946+680G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51961157 | ||||||
chr13:51961316 | T | C | 1 | a0003c0003t0006g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1946+521A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51961316 | ||||||
chr13:51961409 | G | T | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1946+428C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51961409 | ||||||
chr13:51961621 | C | T | 1 | a0003c0003t0004g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1946+216G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51961621 | ||||||
chr13:51961684 | A | G | 3 | a0003c0003t0005g0274a0003c0015t0005g0273a0003c0032t0005g0272 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1946+153T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 6/20 | chr13 | 51961684 | ||||||
chr13:51961978 | C | T | 72 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(69): Show | 76 | HG00323.hp1 HG00544.hp2 HG01074.hp1 others(73): Show |
intron_variant | MODIFIER | c.1870-65G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51961978 | ||||||
chr13:51962130 | T | C | 146 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(143): Show | 157 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1870-217A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962130 | ||||||
chr13:51962164 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1870-251G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962164 | ||||||
chr13:51962306 | G | T | 7 | a0003c0003t0004g0125a0003c0003t0004g0137a0003c0003t0004g0139others(4): Show | 7 | HG02135.hp2 HG02738.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1870-393C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962306 | ||||||
chr13:51962356 | C | A | 3 | a0003c0003t0005g0274a0003c0015t0005g0273a0003c0032t0005g0272 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1870-443G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962356 | ||||||
chr13:51962382 | A | G | 16 | a0003c0003t0004g0125a0003c0003t0004g0137a0003c0003t0004g0139others(13): Show | 17 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1870-469T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962382 | ||||||
chr13:51962406 | C | T | 9 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(6): Show | 10 | HG00642.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.1870-493G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962406 | ||||||
chr13:51962568 | T | C | 1 | a0001c0025t0003g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1870-655A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962568 | ||||||
chr13:51962808 | T | C | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1870-895A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962808 | ||||||
chr13:51962890 | G | A | 10 | a0003c0003t0004g0125a0003c0003t0004g0137a0003c0003t0004g0139others(7): Show | 10 | HG02135.hp2 HG02717.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1870-977C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962890 | ||||||
chr13:51962990 | G | C | 10 | a0003c0003t0006g0013a0003c0003t0006g0167a0003c0003t0006g0181others(7): Show | 11 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-1077C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51962990 | ||||||
chr13:51963017 | G | A | 8 | a0003c0003t0004g0125a0003c0003t0004g0137a0003c0003t0004g0139others(5): Show | 8 | HG02135.hp2 HG02738.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1870-1104C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963017 | ||||||
chr13:51963038 | G | A | 1 | a0002c0002t0002g0005 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1870-1125C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963038 | ||||||
chr13:51963040 | T | C | 1 | a0002c0002t0002g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1870-1127A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963040 | ||||||
chr13:51963196 | G | A | 3 | a0003c0003t0006g0278a0003c0003t0013g0155a0003c0003t0013g0156 | 3 | HG02109.hp2 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1870-1283C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963196 | ||||||
chr13:51963325 | T | G | 3 | a0003c0003t0006g0258a0003c0003t0006g0259a0003c0003t0006g0261 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1870-1412A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963325 | ||||||
chr13:51963430 | T | C | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+1442A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963430 | ||||||
chr13:51963636 | C | T | 1 | a0001c0009t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1869+1236G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963636 | ||||||
chr13:51963729 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1869+1143G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963729 | ||||||
chr13:51963736 | C | CA | 42 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0204others(39): Show | 42 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1869+1135dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963736 | ||||||
chr13:51963736 | C | CAA | 8 | a0002c0011t0010g0080a0003c0003t0009g0248a0003c0003t0009g0251others(5): Show | 8 | HG01192.hp1 HG02602.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1869+1134_1869+113 others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963736 | ||||||
chr13:51963736 | CAAA | C | 9 | a0002c0002t0009g0010a0003c0003t0004g0125a0003c0003t0004g0137others(6): Show | 10 | HG02135.hp2 HG02738.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1869+1133_1869+113 others(7): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963736 | ||||||
chr13:51963749 | A | AAC | 9 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(6): Show | 9 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1869+1122_1869+112 others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963749 | ||||||
chr13:51963771 | C | A | 1 | a0003c0003t0006g0184 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1869+1101G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963771 | ||||||
chr13:51963771 | C | G | 12 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(9): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1869+1101G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963771 | ||||||
chr13:51963838 | T | C | 7 | a0003c0003t0006g0013a0003c0003t0006g0167a0003c0003t0006g0181others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1869+1034A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963838 | ||||||
chr13:51963924 | C | A | 1 | a0003c0003t0009g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1869+948G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51963924 | ||||||
chr13:51964000 | A | G | 38 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(35): Show | 39 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1869+872T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964000 | ||||||
chr13:51964108 | A | AAC | 22 | a0001c0001t0001g0177a0001c0001t0001g0191a0001c0001t0001g0205others(19): Show | 22 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1869+762_1869+763d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964108 | ||||||
chr13:51964108 | A | AACAC | 26 | a0002c0002t0002g0088a0002c0002t0002g0091a0002c0011t0010g0080others(23): Show | 26 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1869+760_1869+763d others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964108 | ||||||
chr13:51964108 | A | AACACACA others(3): Show |
3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1869+754_1869+763d others(12): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964108 | ||||||
chr13:51964108 | AAC | A | 6 | a0003c0003t0005g0018a0005c0006t0004g0121a0005c0006t0004g0154others(3): Show | 7 | HG01256.hp1 HG01361.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1869+762_1869+763d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964108 | ||||||
chr13:51964129 | A | G | 1 | a0010c0035t0001g0212 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1869+743T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964129 | ||||||
chr13:51964199 | C | T | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1869+673G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964199 | ||||||
chr13:51964356 | C | A | 8 | a0003c0003t0004g0125a0003c0003t0004g0137a0003c0003t0004g0139others(5): Show | 8 | HG02135.hp2 HG02738.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1869+516G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964356 | ||||||
chr13:51964446 | C | T | 3 | a0003c0003t0006g0258a0003c0003t0006g0259a0003c0003t0006g0261 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1869+426G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964446 | ||||||
chr13:51964505 | G | A | 1 | a0002c0002t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1869+367C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964505 | ||||||
chr13:51964528 | C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(269): Show | 295 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.1869+344G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964528 | ||||||
chr13:51964753 | A | G | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+119T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 5/20 | chr13 | 51964753 | ||||||
chr13:51965390 | T | G | 72 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(69): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1708-357A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965390 | ||||||
chr13:51965479 | A | G | 3 | a0003c0003t0006g0258a0003c0003t0006g0259a0003c0003t0006g0261 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1708-446T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965479 | ||||||
chr13:51965486 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1708-453G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965486 | ||||||
chr13:51965563 | G | A | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1708-530C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965563 | ||||||
chr13:51965643 | C | T | 13 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(10): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1708-610G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965643 | ||||||
chr13:51965653 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1708-620C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965653 | ||||||
chr13:51965675 | A | G | 3 | a0002c0002t0002g0116a0002c0002t0002g0135a0002c0002t0002g0136 | 3 | HG00408.hp2 HG00423.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1708-642T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965675 | ||||||
chr13:51965708 | G | A | 1 | a0003c0003t0004g0137 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1708-675C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965708 | ||||||
chr13:51965708 | G | C | 13 | a0003c0003t0006g0013a0003c0003t0006g0164a0003c0003t0006g0165others(10): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1708-675C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965708 | ||||||
chr13:51965731 | G | A | 2 | a0003c0003t0005g0157a0017c0033t0005g0240 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1708-698C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965731 | ||||||
chr13:51965876 | C | T | 5 | a0003c0003t0005g0157a0003c0003t0009g0248a0003c0003t0009g0251others(2): Show | 5 | HG02717.hp2 HG02896.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1708-843G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51965876 | ||||||
chr13:51966270 | C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1708-1237G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966270 | ||||||
chr13:51966299 | C | T | 1 | a0002c0002t0007g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1708-1266G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966299 | ||||||
chr13:51966342 | C | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1708-1309G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966342 | ||||||
chr13:51966460 | G | A | 2 | a0003c0003t0005g0018a0003c0003t0005g0260 | 3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1708-1427C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966460 | ||||||
chr13:51966486 | T | G | 2 | a0003c0003t0009g0248a0003c0003t0009g0251 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1708-1453A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966486 | ||||||
chr13:51966496 | C | T | 3 | a0001c0001t0001g0203a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-1463G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966496 | ||||||
chr13:51966650 | C | T | 14 | a0002c0011t0010g0080a0002c0011t0010g0082a0002c0011t0018g0035others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1708-1617G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966650 | ||||||
chr13:51966733 | G | A | 85 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(82): Show | 94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1708-1700C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966733 | ||||||
chr13:51966867 | T | C | 2 | a0002c0002t0002g0108a0002c0002t0002g0109 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1707+1577A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966867 | ||||||
chr13:51966942 | T | C | 2 | a0002c0002t0002g0108a0002c0002t0002g0109 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1707+1502A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966942 | ||||||
chr13:51966954 | T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0019others(237): Show | 261 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1707+1490A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966954 | ||||||
chr13:51966994 | A | C | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1707+1450T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51966994 | ||||||
chr13:51967080 | T | C | 1 | a0005c0012t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1707+1364A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51967080 | ||||||
chr13:51967514 | C | T | 1 | a0003c0003t0005g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1707+930G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51967514 | ||||||
chr13:51967633 | A | G | 1 | a0002c0002t0002g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1707+811T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51967633 | ||||||
chr13:51967987 | C | T | 8 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0095others(5): Show | 8 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1707+457G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51967987 | ||||||
chr13:51968036 | C | A | 2 | a0007c0008t0003g0027a0007c0008t0003g0028 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1707+408G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51968036 | ||||||
chr13:51968078 | T | C | 4 | a0002c0002t0002g0006a0002c0002t0002g0088a0002c0002t0002g0091others(1): Show | 5 | HG01069.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1707+366A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51968078 | ||||||
chr13:51968248 | T | C | 1 | a0002c0011t0010g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1707+196A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51968248 | ||||||
chr13:51968346 | C | T | 2 | a0002c0002t0009g0010a0004c0004t0001g0160 | 3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1707+98G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51968346 | ||||||
chr13:51968387 | G | A | 4 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0003t0009g0248others(1): Show | 4 | HG03130.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+57C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51968387 | ||||||
chr13:51968435 | A | G | 4 | a0003c0003t0005g0275a0005c0012t0001g0176a0005c0012t0003g0128others(1): Show | 4 | HG01074.hp1 HG01891.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+9T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 4/20 | chr13 | 51968435 | ||||||
chr13:51968660 | T | G | 174 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0174others(171): Show | 188 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.1544-53A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968660 | ||||||
chr13:51968749 | T | C | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1544-142A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968749 | ||||||
chr13:51968863 | C | CT | 5 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0181others(2): Show | 6 | HG02055.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-257dupA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968863 | ||||||
chr13:51968863 | CT | C | 95 | a0001c0001t0001g0216a0001c0001t0003g0119a0002c0002t0002g0002others(92): Show | 104 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1544-257delA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968863 | ||||||
chr13:51968863 | CTTTTTTT | C | 6 | a0003c0003t0005g0157a0005c0006t0004g0009a0005c0006t0004g0121others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1544-263_1544-257d others(9): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968863 | ||||||
chr13:51968911 | G | A | 7 | a0003c0003t0006g0013a0003c0003t0006g0167a0003c0003t0006g0181others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544-304C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968911 | ||||||
chr13:51968920 | G | A | 2 | a0002c0002t0002g0032a0002c0002t0002g0092 | 2 | HG00438.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.1544-313C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51968920 | ||||||
chr13:51969105 | C | T | 2 | a0002c0002t0002g0048a0018c0017t0002g0036 | 2 | NA18978.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1544-498G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969105 | ||||||
chr13:51969136 | T | A | 7 | a0001c0001t0001g0277a0003c0003t0004g0037a0003c0003t0006g0278others(4): Show | 7 | HG01891.hp2 HG01978.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1544-529A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969136 | ||||||
chr13:51969137 | A | T | 21 | a0001c0001t0001g0171a0001c0001t0001g0194a0003c0003t0005g0018others(18): Show | 23 | HG00558.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1544-530T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969137 | ||||||
chr13:51969536 | T | G | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1544-929A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969536 | ||||||
chr13:51969571 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1543+921G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969571 | ||||||
chr13:51969623 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1543+869T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969623 | ||||||
chr13:51969811 | A | G | 3 | a0003c0003t0006g0164a0003c0003t0006g0165a0003c0003t0006g0166 | 3 | HG01891.hp1 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1543+681T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969811 | ||||||
chr13:51969875 | G | A | 1 | a0003c0003t0004g0137 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1543+617C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969875 | ||||||
chr13:51969944 | G | A | 17 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0013others(14): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1543+548C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51969944 | ||||||
chr13:51970025 | G | A | 2 | a0002c0002t0002g0114a0002c0002t0002g0115 | 2 | HG01261.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1543+467C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51970025 | ||||||
chr13:51970143 | G | T | 4 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0003t0009g0248others(1): Show | 4 | HG03130.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+349C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51970143 | ||||||
chr13:51970367 | T | C | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1543+125A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51970367 | ||||||
chr13:51970441 | C | T | 6 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+51G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 3/20 | chr13 | 51970441 | ||||||
chr13:51970841 | T | C | 6 | a0003c0003t0005g0274a0003c0003t0005g0275a0003c0015t0005g0273others(3): Show | 6 | HG01192.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286-92A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51970841 | ||||||
chr13:51970842 | T | G | 96 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(93): Show | 105 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1286-93A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51970842 | ||||||
chr13:51970902 | G | A | 1 | a0017c0033t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1286-153C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51970902 | ||||||
chr13:51971005 | A | G | 96 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(93): Show | 105 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1286-256T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971005 | ||||||
chr13:51971090 | T | C | 11 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0164others(8): Show | 12 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286-341A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971090 | ||||||
chr13:51971190 | T | C | 1 | a0003c0003t0004g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1286-441A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971190 | ||||||
chr13:51971245 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1286-496C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971245 | ||||||
chr13:51971281 | A | G | 4 | a0007c0008t0001g0266a0007c0008t0003g0027a0007c0008t0003g0028others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286-532T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971281 | ||||||
chr13:51971284 | T | C | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1286-535A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971284 | ||||||
chr13:51971309 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1286-560A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971309 | ||||||
chr13:51971359 | A | C | 96 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(93): Show | 105 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1286-610T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971359 | ||||||
chr13:51971602 | A | G | 6 | a0003c0003t0006g0164a0003c0003t0006g0165a0003c0003t0006g0166others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286-853T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971602 | ||||||
chr13:51971616 | T | C | 4 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0003t0009g0248others(1): Show | 4 | HG03130.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286-867A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971616 | ||||||
chr13:51971857 | G | A | 4 | a0001c0009t0001g0217a0001c0009t0001g0218a0001c0009t0001g0219others(1): Show | 4 | HG03017.hp1 HG03490.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286-1108C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971857 | ||||||
chr13:51971889 | C | T | 1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1286-1140G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971889 | ||||||
chr13:51971948 | G | A | 2 | a0003c0005t0004g0023a0003c0005t0004g0024 | 2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1286-1199C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51971948 | ||||||
chr13:51972028 | C | T | 5 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0258others(2): Show | 6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286-1279G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972028 | ||||||
chr13:51972201 | G | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(241): Show | 266 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1286-1452C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972201 | ||||||
chr13:51972247 | C | T | 14 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(11): Show | 15 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1286-1498G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972247 | ||||||
chr13:51972337 | G | A | 1 | a0008c0010t0006g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1286-1588C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972337 | ||||||
chr13:51972351 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1285+1584A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972351 | ||||||
chr13:51972411 | C | CTCAAT | 142 | a0001c0001t0001g0239a0001c0001t0001g0277a0001c0025t0003g0147others(139): Show | 152 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1285+1523_1285+152 others(9): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972411 | ||||||
chr13:51972474 | A | G | 2 | a0003c0003t0009g0251a0005c0006t0005g0158 | 2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1285+1461T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972474 | ||||||
chr13:51972492 | T | A | 3 | a0007c0008t0003g0027a0007c0008t0003g0028a0014c0024t0005g0169 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1285+1443A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972492 | ||||||
chr13:51972539 | C | T | 9 | a0001c0025t0003g0147a0005c0006t0004g0009a0005c0006t0004g0121others(6): Show | 10 | HG01074.hp1 HG01109.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285+1396G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972539 | ||||||
chr13:51972542 | T | C | 1 | a0002c0002t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1285+1393A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972542 | ||||||
chr13:51972682 | G | T | 2 | a0005c0006t0004g0121a0005c0006t0004g0154 | 2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1285+1253C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972682 | ||||||
chr13:51972738 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1285+1197C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972738 | ||||||
chr13:51972828 | C | T | 1 | a0003c0003t0016g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1285+1107G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51972828 | ||||||
chr13:51973021 | A | T | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(92): Show | 104 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1285+914T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973021 | ||||||
chr13:51973022 | T | A | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1285+913A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973022 | ||||||
chr13:51973122 | C | T | 2 | a0003c0003t0005g0275a0017c0033t0005g0240 | 2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1285+813G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973122 | ||||||
chr13:51973326 | C | T | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1285+609G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973326 | ||||||
chr13:51973488 | C | T | 1 | a0003c0003t0006g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1285+447G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973488 | ||||||
chr13:51973576 | G | A | 3 | a0005c0012t0001g0176a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1285+359C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973576 | ||||||
chr13:51973648 | C | T | 99 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(96): Show | 108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1285+287G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 2/20 | chr13 | 51973648 | ||||||
chr13:51975372 | GCTAA | G | 3 | a0003c0003t0006g0164a0003c0003t0006g0165a0003c0003t0006g0166 | 3 | HG01891.hp1 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.52-208_52-205delTT others(2): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51975372 | ||||||
chr13:51975474 | G | A | 1 | a0002c0002t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52-306C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51975474 | ||||||
chr13:51975577 | C | A | 1 | a0002c0002t0002g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.52-409G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51975577 | ||||||
chr13:51975806 | T | C | 2 | a0002c0002t0002g0053a0002c0002t0002g0055 | 2 | NA19000.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.52-638A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51975806 | ||||||
chr13:51976111 | C | A | 1 | a0008c0010t0006g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.52-943G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51976111 | ||||||
chr13:51976379 | A | G | 1 | a0002c0002t0002g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.52-1211T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51976379 | ||||||
chr13:51976410 | T | A | 1 | a0002c0002t0002g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.52-1242A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51976410 | ||||||
chr13:51976599 | G | A | 99 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(96): Show | 108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.52-1431C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51976599 | ||||||
chr13:51976687 | T | C | 2 | a0002c0002t0002g0053a0002c0002t0002g0055 | 2 | NA19000.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.52-1519A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51976687 | ||||||
chr13:51976704 | C | T | 1 | a0003c0003t0006g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.52-1536G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51976704 | ||||||
chr13:51977106 | T | G | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-1938A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977106 | ||||||
chr13:51977135 | C | A | 1 | a0005c0012t0003g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.52-1967G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977135 | ||||||
chr13:51977231 | A | AT | 262 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(259): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.52-2064dupA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977231 | ||||||
chr13:51977252 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52-2084C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977252 | ||||||
chr13:51977257 | T | C | 2 | a0007c0008t0003g0027a0007c0008t0003g0028 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.52-2089A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977257 | ||||||
chr13:51977260 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.52-2092A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977260 | ||||||
chr13:51977406 | A | G | 4 | a0006c0007t0003g0042a0006c0007t0003g0043a0006c0007t0003g0044others(1): Show | 4 | HG00423.hp2 HG00621.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2238T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977406 | ||||||
chr13:51977415 | G | A | 8 | a0001c0025t0003g0147a0005c0006t0004g0009a0005c0006t0004g0121others(5): Show | 9 | HG01074.hp1 HG01109.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-2247C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977415 | ||||||
chr13:51977583 | CT | C | 9 | a0002c0002t0007g0039a0002c0002t0007g0073a0002c0002t0007g0094others(6): Show | 9 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-2416delA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977583 | ||||||
chr13:51977658 | T | C | 8 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0105others(5): Show | 9 | HG02071.hp2 HG02129.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-2490A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977658 | ||||||
chr13:51977802 | G | C | 1 | a0002c0002t0020g0054 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.52-2634C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977802 | ||||||
chr13:51977807 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.52-2639G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51977807 | ||||||
chr13:51978085 | C | T | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(92): Show | 104 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.52-2917G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978085 | ||||||
chr13:51978092 | T | A | 5 | a0003c0003t0005g0274a0003c0003t0005g0275a0003c0015t0005g0273others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-2924A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978092 | ||||||
chr13:51978444 | C | T | 1 | a0001c0025t0003g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.52-3276G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978444 | ||||||
chr13:51978613 | CTAGT | C | 6 | a0001c0001t0001g0277a0002c0002t0002g0055a0003c0003t0006g0278others(3): Show | 6 | HG02258.hp1 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-3449_52-3446del others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978613 | ||||||
chr13:51978829 | A | G | 4 | a0003c0005t0004g0022a0003c0005t0004g0025a0003c0005t0012g0021others(1): Show | 4 | HG00544.hp2 NA19003.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-3661T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978829 | ||||||
chr13:51978962 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.52-3794G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978962 | ||||||
chr13:51978966 | C | T | 122 | a0001c0025t0003g0147a0002c0002t0002g0002a0002c0002t0002g0003others(119): Show | 133 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.52-3798G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51978966 | ||||||
chr13:51979073 | G | C | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-3905C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51979073 | ||||||
chr13:51979222 | G | T | 108 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0005others(105): Show | 118 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.52-4054C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51979222 | ||||||
chr13:51979505 | A | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0193others(2): Show | 5 | NA18945.hp1 NA18959.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-4337T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51979505 | ||||||
chr13:51979634 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.52-4466T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51979634 | ||||||
chr13:51980083 | T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG00673.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.52-4915A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980083 | ||||||
chr13:51980115 | T | G | 1 | a0002c0002t0002g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.52-4947A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980115 | ||||||
chr13:51980258 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.52-5090G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980258 | ||||||
chr13:51980539 | C | A | 1 | a0001c0001t0001g0192 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.52-5371G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980539 | ||||||
chr13:51980540 | A | C | 1 | a0001c0001t0001g0192 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.52-5372T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980540 | ||||||
chr13:51980772 | C | T | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.52-5604G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980772 | ||||||
chr13:51980846 | GAGGCAAA others(14): Show |
G | 1 | a0001c0009t0001g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.52-5699_52-5679del others(21): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980846 | ||||||
chr13:51980870 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-5702C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980870 | ||||||
chr13:51980885 | T | C | 138 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(135): Show | 148 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.52-5717A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980885 | ||||||
chr13:51980914 | T | A | 3 | a0005c0006t0005g0158a0005c0012t0003g0128a0005c0012t0003g0129 | 3 | HG01074.hp1 HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.52-5746A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980914 | ||||||
chr13:51980969 | G | A | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-5801C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980969 | ||||||
chr13:51980998 | A | T | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-5830T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51980998 | ||||||
chr13:51981034 | T | C | 2 | a0001c0031t0001g0201a0007c0008t0001g0214 | 2 | HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.52-5866A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981034 | ||||||
chr13:51981061 | G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0246 | 3 | HG02735.hp2 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.52-5893C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981061 | ||||||
chr13:51981152 | C | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(253): Show | 278 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.52-5984G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981152 | ||||||
chr13:51981260 | G | A | 3 | a0008c0010t0011g0151a0008c0010t0011g0152a0008c0010t0011g0153 | 3 | HG01243.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.52-6092C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981260 | ||||||
chr13:51981363 | C | G | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-6195G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981363 | ||||||
chr13:51981444 | G | A | 6 | a0003c0003t0006g0167a0003c0003t0006g0181a0003c0003t0006g0182others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-6276C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981444 | ||||||
chr13:51981629 | C | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-6461G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981629 | ||||||
chr13:51981666 | C | G | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-6498G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981666 | ||||||
chr13:51981878 | G | A | 18 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(15): Show | 19 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.52-6710C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51981878 | ||||||
chr13:51982005 | A | AT | 102 | a0001c0001t0001g0174a0001c0001t0001g0277a0001c0001t0003g0056others(99): Show | 111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.52-6838dupA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982005 | ||||||
chr13:51982005 | A | ATTT | 11 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(8): Show | 11 | HG00544.hp2 HG01099.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-6840_52-6838dup others(3): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982005 | ||||||
chr13:51982033 | T | A | 1 | a0008c0010t0006g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.52-6865A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982033 | ||||||
chr13:51982113 | T | A | 16 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(13): Show | 17 | HG00642.hp2 HG01099.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.52-6945A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982113 | ||||||
chr13:51982268 | T | C | 8 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-7100A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982268 | ||||||
chr13:51982304 | C | T | 2 | a0003c0003t0006g0258a0003c0003t0006g0259 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52-7136G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982304 | ||||||
chr13:51982519 | T | C | 2 | a0003c0005t0004g0026a0003c0005t0004g0029 | 2 | HG06807.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.52-7351A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982519 | ||||||
chr13:51982532 | C | T | 5 | a0002c0002t0002g0046a0003c0005t0012g0058a0004c0004t0003g0004others(2): Show | 6 | HG02071.hp1 NA18942.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-7364G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982532 | ||||||
chr13:51982702 | T | C | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-7534A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982702 | ||||||
chr13:51982726 | C | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.52-7558G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982726 | ||||||
chr13:51982845 | C | T | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-7677G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982845 | ||||||
chr13:51982867 | T | C | 149 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(146): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.52-7699A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982867 | ||||||
chr13:51982996 | A | G | 152 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(149): Show | 163 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.52-7828T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51982996 | ||||||
chr13:51983086 | G | A | 138 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(135): Show | 148 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.52-7918C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983086 | ||||||
chr13:51983094 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.52-7926T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983094 | ||||||
chr13:51983202 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.52-8034C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983202 | ||||||
chr13:51983224 | T | C | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-8056A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983224 | ||||||
chr13:51983226 | G | A | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-8058C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983226 | ||||||
chr13:51983282 | G | A | 26 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(23): Show | 27 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.52-8114C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983282 | ||||||
chr13:51983469 | G | C | 12 | a0002c0002t0002g0046a0002c0002t0002g0059a0003c0005t0012g0058others(9): Show | 13 | HG00423.hp2 HG00621.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.52-8301C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983469 | ||||||
chr13:51983662 | G | GC | 183 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0174others(180): Show | 196 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.52-8495_52-8494ins others(1): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983662 | ||||||
chr13:51983680 | A | G | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-8512T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983680 | ||||||
chr13:51983738 | G | A | 11 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(8): Show | 11 | HG00544.hp2 HG01099.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-8570C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983738 | ||||||
chr13:51983896 | G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.52-8728C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51983896 | ||||||
chr13:51984024 | C | T | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-8856G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984024 | ||||||
chr13:51984062 | G | A | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-8894C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984062 | ||||||
chr13:51984141 | C | A | 5 | a0003c0003t0006g0181a0003c0003t0006g0182a0003c0003t0006g0183others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-8973G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984141 | ||||||
chr13:51984142 | C | A | 5 | a0003c0003t0006g0181a0003c0003t0006g0182a0003c0003t0006g0183others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-8974G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984142 | ||||||
chr13:51984291 | C | T | 2 | a0002c0002t0009g0010a0004c0004t0001g0160 | 3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.52-9123G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984291 | ||||||
chr13:51984292 | G | A | 1 | a0002c0002t0002g0061 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.52-9124C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984292 | ||||||
chr13:51984318 | G | A | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-9150C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984318 | ||||||
chr13:51984413 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.52-9245A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984413 | ||||||
chr13:51984983 | T | C | 8 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(5): Show | 8 | HG00544.hp2 HG01099.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-9815A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51984983 | ||||||
chr13:51985007 | A | C | 1 | a0003c0003t0008g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.52-9839T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985007 | ||||||
chr13:51985123 | G | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0200a0003c0003t0008g0238 | 3 | HG00609.hp2 HG02165.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.52-9955C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985123 | ||||||
chr13:51985156 | C | T | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-9988G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985156 | ||||||
chr13:51985202 | G | A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-10034C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985202 | ||||||
chr13:51985237 | T | C | 1 | a0002c0002t0002g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52-10069A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985237 | ||||||
chr13:51985272 | T | C | 1 | a0001c0009t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.52-10104A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985272 | ||||||
chr13:51985681 | A | C | 1 | a0003c0003t0005g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.52-10513T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985681 | ||||||
chr13:51985767 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.52-10599A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985767 | ||||||
chr13:51985784 | C | T | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-10616G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985784 | ||||||
chr13:51985922 | T | C | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-10754A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985922 | ||||||
chr13:51985949 | C | A | 1 | a0004c0004t0003g0062 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52-10781G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985949 | ||||||
chr13:51985949 | C | T | 1 | a0003c0005t0012g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.52-10781G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51985949 | ||||||
chr13:51986083 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.52-10915A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986083 | ||||||
chr13:51986163 | G | A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-10995C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986163 | ||||||
chr13:51986531 | T | C | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-11363A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986531 | ||||||
chr13:51986544 | A | G | 10 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(7): Show | 10 | HG00544.hp2 HG01099.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-11376T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986544 | ||||||
chr13:51986709 | T | C | 26 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(23): Show | 27 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.52-11541A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986709 | ||||||
chr13:51986727 | C | T | 3 | a0003c0003t0006g0164a0003c0003t0006g0165a0003c0003t0006g0166 | 3 | HG01891.hp1 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.52-11559G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986727 | ||||||
chr13:51986781 | C | T | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-11613G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986781 | ||||||
chr13:51986807 | A | G | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-11639T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986807 | ||||||
chr13:51986822 | T | C | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.52-11654A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986822 | ||||||
chr13:51986995 | T | A | 1 | a0008c0010t0011g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52-11827A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51986995 | ||||||
chr13:51987237 | C | A | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-12069G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987237 | ||||||
chr13:51987314 | G | T | 1 | a0005c0012t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.52-12146C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987314 | ||||||
chr13:51987486 | C | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-12318G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987486 | ||||||
chr13:51987505 | T | C | 125 | a0001c0001t0003g0008a0001c0001t0003g0056a0001c0001t0003g0111others(122): Show | 134 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.52-12337A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987505 | ||||||
chr13:51987632 | C | T | 3 | a0003c0003t0005g0274a0003c0015t0005g0273a0003c0032t0005g0272 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.52-12464G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987632 | ||||||
chr13:51987633 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.52-12465C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987633 | ||||||
chr13:51987751 | T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0174others(14): Show | 19 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.52-12583A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987751 | ||||||
chr13:51987799 | GCAATGGG others(9): Show |
G | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.52-12647_52-12632d others(18): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987799 | ||||||
chr13:51987802 | A | T | 1 | a0008c0010t0006g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.52-12634T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987802 | ||||||
chr13:51987816 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.52-12648G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51987816 | ||||||
chr13:51988222 | AC | A | 3 | a0001c0001t0001g0237a0003c0003t0004g0137a0003c0015t0005g0268 | 3 | HG03471.hp2 NA19043.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.52-13055delG | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51988222 | ||||||
chr13:51988281 | T | C | 1 | a0003c0015t0005g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52-13113A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51988281 | ||||||
chr13:51988600 | C | T | 2 | a0003c0003t0006g0258a0003c0003t0006g0259 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52-13432G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51988600 | ||||||
chr13:51988922 | G | A | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-13754C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51988922 | ||||||
chr13:51988962 | G | A | 1 | a0002c0002t0002g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.52-13794C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51988962 | ||||||
chr13:51988969 | T | C | 1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.52-13801A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51988969 | ||||||
chr13:51989060 | T | A | 26 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(23): Show | 27 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.52-13892A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51989060 | ||||||
chr13:51989068 | G | T | 1 | a0003c0005t0004g0074 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.52-13900C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51989068 | ||||||
chr13:51989339 | A | G | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-14171T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51989339 | ||||||
chr13:51989645 | C | G | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-14477G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51989645 | ||||||
chr13:51989654 | A | G | 1 | a0002c0002t0002g0093 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.52-14486T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51989654 | ||||||
chr13:51989939 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.52-14771A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51989939 | ||||||
chr13:51990086 | T | C | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-14918A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990086 | ||||||
chr13:51990214 | G | A | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-15046C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990214 | ||||||
chr13:51990249 | A | G | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-15081T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990249 | ||||||
chr13:51990423 | G | A | 143 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(140): Show | 153 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.52-15255C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990423 | ||||||
chr13:51990424 | T | A | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.52-15256A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990424 | ||||||
chr13:51990443 | T | TTTAC | 40 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(37): Show | 44 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.52-15279_52-15276d others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990443 | ||||||
chr13:51990477 | G | C | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.52-15309C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990477 | ||||||
chr13:51990624 | C | G | 149 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(146): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.52-15456G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990624 | ||||||
chr13:51990751 | A | G | 5 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0258others(2): Show | 6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-15583T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990751 | ||||||
chr13:51990894 | C | T | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.52-15726G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51990894 | ||||||
chr13:51991007 | G | T | 1 | a0001c0031t0001g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.52-15839C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991007 | ||||||
chr13:51991032 | G | A | 3 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0261 | 4 | HG02717.hp1 HG03579.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-15864C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991032 | ||||||
chr13:51991088 | T | C | 5 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0258others(2): Show | 6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-15920A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991088 | ||||||
chr13:51991142 | C | G | 1 | a0003c0005t0012g0021 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.52-15974G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991142 | ||||||
chr13:51991214 | T | C | 1 | a0006c0007t0003g0045 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.52-16046A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991214 | ||||||
chr13:51991234 | G | A | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.52-16066C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991234 | ||||||
chr13:51991235 | C | G | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.52-16067G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991235 | ||||||
chr13:51991245 | C | G | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.52-16077G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991245 | ||||||
chr13:51991324 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.52-16156A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991324 | ||||||
chr13:51991541 | A | G | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.52-16373T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991541 | ||||||
chr13:51991639 | C | T | 1 | a0004c0004t0003g0030 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.52-16471G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991639 | ||||||
chr13:51991794 | C | T | 3 | a0003c0003t0006g0164a0003c0003t0006g0165a0003c0003t0006g0166 | 3 | HG01891.hp1 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.52-16626G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991794 | ||||||
chr13:51991795 | G | A | 125 | a0001c0001t0003g0008a0001c0001t0003g0056a0001c0001t0003g0111others(122): Show | 134 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.52-16627C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991795 | ||||||
chr13:51991798 | G | A | 5 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0105others(2): Show | 5 | NA18956.hp2 NA18959.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-16630C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991798 | ||||||
chr13:51991958 | C | T | 1 | a0005c0012t0003g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.52-16790G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991958 | ||||||
chr13:51991990 | T | G | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-16822A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51991990 | ||||||
chr13:51992121 | G | A | 1 | a0003c0015t0005g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52-16953C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992121 | ||||||
chr13:51992131 | T | TA | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG00673.hp2 HG02074.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.52-16964dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992131 | ||||||
chr13:51992131 | TA | T | 14 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(11): Show | 14 | HG00609.hp2 HG00642.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-16964delT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992131 | ||||||
chr13:51992265 | T | C | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-17097A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992265 | ||||||
chr13:51992441 | T | C | 2 | a0002c0002t0002g0114a0002c0002t0002g0115 | 2 | HG01261.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.52-17273A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992441 | ||||||
chr13:51992468 | A | T | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.52-17300T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992468 | ||||||
chr13:51992559 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.52-17391A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992559 | ||||||
chr13:51992634 | A | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0265 | 4 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-17466T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992634 | ||||||
chr13:51992675 | G | A | 1 | a0009c0016t0005g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.52-17507C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992675 | ||||||
chr13:51992787 | G | A | 19 | a0002c0002t0002g0006a0002c0002t0002g0038a0002c0002t0002g0068others(16): Show | 20 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.52-17619C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992787 | ||||||
chr13:51992802 | A | C | 11 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(8): Show | 11 | HG00544.hp2 HG01099.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-17634T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992802 | ||||||
chr13:51992886 | G | A | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-17718C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992886 | ||||||
chr13:51992979 | C | CA | 12 | a0001c0001t0001g0188a0001c0001t0001g0227a0002c0002t0002g0047others(9): Show | 14 | HG01981.hp2 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-17812dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992979 | ||||||
chr13:51992979 | C | CAA | 79 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(76): Show | 86 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.52-17813_52-17812d others(4): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992979 | ||||||
chr13:51992979 | C | CAAA | 21 | a0001c0025t0003g0147a0002c0002t0002g0063a0002c0002t0002g0064others(18): Show | 21 | HG00323.hp2 HG00438.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.52-17814_52-17812d others(5): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992979 | ||||||
chr13:51992979 | C | CAAAA | 16 | a0001c0001t0003g0008a0001c0001t0003g0126a0001c0001t0003g0143others(13): Show | 17 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.52-17815_52-17812d others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992979 | ||||||
chr13:51992979 | C | CAAAAA | 7 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0144others(4): Show | 7 | HG01099.hp2 HG01123.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.52-17816_52-17812d others(7): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992979 | ||||||
chr13:51992979 | CA | C | 18 | a0001c0001t0001g0170a0001c0001t0001g0186a0001c0001t0001g0194others(15): Show | 19 | HG00544.hp2 HG01099.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.52-17812delT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51992979 | ||||||
chr13:51993066 | G | A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52-17898C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993066 | ||||||
chr13:51993104 | T | G | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.52-17936A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993104 | ||||||
chr13:51993147 | C | T | 5 | a0002c0002t0002g0068a0002c0002t0002g0069a0002c0002t0002g0070others(2): Show | 5 | HG00642.hp1 HG00741.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-17979G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993147 | ||||||
chr13:51993213 | G | A | 1 | a0003c0003t0005g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.52-18045C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993213 | ||||||
chr13:51993233 | T | C | 2 | a0001c0001t0001g0012a0001c0028t0001g0161 | 3 | HG00733.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.51+18054A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993233 | ||||||
chr13:51993259 | T | C | 14 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(11): Show | 15 | HG01192.hp1 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+18028A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993259 | ||||||
chr13:51993374 | C | T | 2 | a0003c0003t0006g0164a0003c0003t0006g0165 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.51+17913G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993374 | ||||||
chr13:51993487 | C | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | NA18959.hp2 NA19056.hp2 NA19060.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+17800G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993487 | ||||||
chr13:51993582 | AAAAC | A | 8 | a0002c0002t0007g0039a0002c0002t0007g0094a0002c0002t0007g0095others(5): Show | 8 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+17701_51+17704d others(6): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993582 | ||||||
chr13:51993957 | C | A | 99 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(96): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.51+17330G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51993957 | ||||||
chr13:51994057 | A | G | 1 | a0003c0003t0006g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.51+17230T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994057 | ||||||
chr13:51994076 | C | T | 1 | a0005c0012t0003g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.51+17211G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994076 | ||||||
chr13:51994117 | C | T | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+17170G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994117 | ||||||
chr13:51994346 | A | C | 1 | a0001c0001t0001g0192 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.51+16941T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994346 | ||||||
chr13:51994366 | G | A | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16921C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994366 | ||||||
chr13:51994371 | C | G | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16916G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994371 | ||||||
chr13:51994372 | C | A | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16915G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994372 | ||||||
chr13:51994373 | A | T | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16914T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994373 | ||||||
chr13:51994374 | A | C | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16913T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994374 | ||||||
chr13:51994375 | A | G | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16912T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994375 | ||||||
chr13:51994378 | G | T | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16909C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994378 | ||||||
chr13:51994380 | C | T | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16907G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994380 | ||||||
chr13:51994381 | A | T | 1 | a0002c0002t0002g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.51+16906T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994381 | ||||||
chr13:51994700 | C | A | 3 | a0002c0002t0002g0100a0002c0002t0002g0102a0002c0019t0002g0101 | 3 | HG01192.hp2 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.51+16587G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994700 | ||||||
chr13:51994760 | G | C | 2 | a0003c0003t0013g0155a0003c0003t0013g0156 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.51+16527C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994760 | ||||||
chr13:51994903 | C | T | 5 | a0005c0006t0004g0009a0005c0006t0004g0121a0005c0006t0004g0123others(2): Show | 6 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+16384G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994903 | ||||||
chr13:51994939 | A | C | 5 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0258others(2): Show | 6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+16348T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994939 | ||||||
chr13:51994962 | C | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | NA19060.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.51+16325G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51994962 | ||||||
chr13:51995093 | T | G | 159 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(156): Show | 170 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.51+16194A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995093 | ||||||
chr13:51995185 | T | C | 1 | a0002c0002t0002g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.51+16102A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995185 | ||||||
chr13:51995221 | A | G | 14 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0005t0004g0022others(11): Show | 14 | HG00544.hp2 HG01099.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.51+16066T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995221 | ||||||
chr13:51995229 | C | G | 4 | a0006c0007t0003g0042a0006c0007t0003g0043a0006c0007t0003g0044others(1): Show | 4 | HG00423.hp2 HG00621.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+16058G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995229 | ||||||
chr13:51995315 | T | C | 10 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(7): Show | 10 | HG00544.hp2 HG01099.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.51+15972A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995315 | ||||||
chr13:51995369 | T | C | 1 | a0005c0006t0005g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51+15918A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995369 | ||||||
chr13:51995385 | T | C | 1 | a0003c0003t0004g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.51+15902A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995385 | ||||||
chr13:51995474 | G | A | 1 | a0003c0003t0008g0238 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.51+15813C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995474 | ||||||
chr13:51995827 | T | C | 184 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0174others(181): Show | 197 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.51+15460A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51995827 | ||||||
chr13:51996182 | T | C | 2 | a0002c0002t0002g0135a0002c0002t0002g0136 | 2 | HG00408.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.51+15105A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996182 | ||||||
chr13:51996259 | G | A | 40 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(37): Show | 44 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.51+15028C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996259 | ||||||
chr13:51996458 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.51+14829C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996458 | ||||||
chr13:51996562 | C | T | 1 | a0002c0002t0002g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51+14725G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996562 | ||||||
chr13:51996592 | G | A | 144 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(141): Show | 154 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.51+14695C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996592 | ||||||
chr13:51996755 | T | G | 1 | a0003c0003t0021g0146 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.51+14532A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996755 | ||||||
chr13:51996773 | T | G | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+14514A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996773 | ||||||
chr13:51996984 | G | A | 1 | a0003c0003t0006g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.51+14303C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51996984 | ||||||
chr13:51997003 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.51+14284C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997003 | ||||||
chr13:51997132 | T | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+14155A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997132 | ||||||
chr13:51997360 | C | G | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+13927G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997360 | ||||||
chr13:51997451 | C | T | 1 | a0003c0003t0006g0013 | 2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.51+13836G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997451 | ||||||
chr13:51997683 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51+13604C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997683 | ||||||
chr13:51997720 | G | C | 22 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119others(19): Show | 23 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.51+13567C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997720 | ||||||
chr13:51997952 | C | T | 1 | a0003c0005t0010g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.51+13335G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51997952 | ||||||
chr13:51998309 | C | G | 2 | a0001c0013t0001g0011a0001c0013t0001g0189 | 3 | HG03490.hp1 HG03492.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.51+12978G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51998309 | ||||||
chr13:51998465 | C | G | 145 | a0001c0001t0001g0277a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 154 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.51+12822G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51998465 | ||||||
chr13:51998790 | G | A | 5 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0105others(2): Show | 5 | NA18956.hp2 NA18959.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+12497C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51998790 | ||||||
chr13:51998916 | G | A | 1 | a0002c0002t0002g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.51+12371C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51998916 | ||||||
chr13:51998924 | C | T | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.51+12363G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51998924 | ||||||
chr13:51999286 | G | A | 95 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(92): Show | 102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.51+12001C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 51999286 | ||||||
chr13:52000401 | C | T | 5 | a0003c0003t0004g0130a0003c0003t0004g0131a0003c0003t0004g0132others(2): Show | 5 | HG00323.hp2 HG00733.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+10886G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52000401 | ||||||
chr13:52000778 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.51+10509A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52000778 | ||||||
chr13:52000844 | G | A | 1 | a0003c0015t0005g0273 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.51+10443C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52000844 | ||||||
chr13:52001004 | T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0256 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.51+10283A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001004 | ||||||
chr13:52001448 | T | C | 6 | a0001c0001t0003g0122a0005c0006t0004g0009a0005c0006t0004g0121others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+9839A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001448 | ||||||
chr13:52001567 | T | C | 1 | a0005c0006t0024g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.51+9720A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001567 | ||||||
chr13:52001673 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51+9614A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001673 | ||||||
chr13:52001741 | T | C | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+9546A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001741 | ||||||
chr13:52001796 | AT | A | 96 | a0001c0001t0001g0247a0001c0001t0003g0056a0001c0001t0003g0111others(93): Show | 103 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.51+9490delA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001796 | ||||||
chr13:52001826 | T | C | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+9461A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001826 | ||||||
chr13:52001876 | C | T | 6 | a0001c0001t0003g0122a0005c0006t0004g0009a0005c0006t0004g0121others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+9411G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001876 | ||||||
chr13:52001937 | C | T | 95 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(92): Show | 102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.51+9350G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52001937 | ||||||
chr13:52002170 | C | T | 2 | a0002c0002t0009g0010a0004c0004t0001g0160 | 3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.51+9117G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002170 | ||||||
chr13:52002194 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.51+9093A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002194 | ||||||
chr13:52002210 | G | A | 1 | a0001c0025t0003g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.51+9077C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002210 | ||||||
chr13:52002288 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.51+8999C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002288 | ||||||
chr13:52002362 | A | G | 122 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0003g0056others(119): Show | 131 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.51+8925T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002362 | ||||||
chr13:52002382 | T | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.51+8905A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002382 | ||||||
chr13:52002396 | T | TA | 8 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0003g0122others(5): Show | 9 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+8890dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002396 | ||||||
chr13:52002512 | A | G | 38 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(35): Show | 42 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.51+8775T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002512 | ||||||
chr13:52002603 | A | AAGGGGAA others(138): Show |
1 | a0003c0003t0009g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(145): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(164): Show |
2 | a0005c0012t0003g0128a0005c0012t0003g0129 | 2 | HG01074.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.51+8683_51+8684ins others(171): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(142): Show |
91 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(88): Show | 98 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.51+8683_51+8684ins others(149): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(138): Show |
1 | a0001c0001t0001g0252 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(145): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(131): Show |
1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(138): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(143): Show |
18 | a0001c0001t0003g0122a0003c0005t0004g0022a0003c0005t0004g0023others(15): Show | 19 | HG00544.hp2 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.51+8683_51+8684ins others(150): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(134): Show |
1 | a0014c0024t0005g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(141): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(138): Show |
151 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(148): Show | 166 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.51+8683_51+8684ins others(145): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(138): Show |
1 | a0002c0002t0008g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(145): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(143): Show |
4 | a0002c0002t0002g0038a0002c0002t0007g0039a0003c0003t0004g0037others(1): Show | 4 | HG01978.hp2 HG02280.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+8683_51+8684ins others(150): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(144): Show |
1 | a0003c0005t0010g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(151): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(139): Show |
4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01981.hp2 NA18956.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+8683_51+8684ins others(146): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(140): Show |
1 | a0003c0003t0016g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(147): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002603 | A | AAGGGGAA others(143): Show |
1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+8683_51+8684ins others(150): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002603 | ||||||
chr13:52002750 | T | A | 2 | a0002c0002t0002g0108a0002c0002t0002g0109 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.51+8537A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002750 | ||||||
chr13:52002973 | T | C | 1 | a0003c0005t0005g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.51+8314A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52002973 | ||||||
chr13:52003095 | C | T | 1 | a0002c0011t0018g0035 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.51+8192G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003095 | ||||||
chr13:52003241 | T | C | 1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+8046A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003241 | ||||||
chr13:52003446 | T | A | 1 | a0002c0002t0002g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51+7841A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003446 | ||||||
chr13:52003483 | A | G | 13 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(10): Show | 13 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+7804T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003483 | ||||||
chr13:52003489 | G | A | 2 | a0002c0002t0002g0007a0002c0002t0002g0033 | 3 | HG01257.hp2 HG01346.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.51+7798C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003489 | ||||||
chr13:52003499 | T | C | 95 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(92): Show | 102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.51+7788A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003499 | ||||||
chr13:52003626 | T | TA | 16 | a0001c0001t0003g0122a0005c0006t0004g0009a0005c0006t0004g0121others(13): Show | 17 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+7660dupT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003626 | ||||||
chr13:52003626 | T | TAA | 102 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(99): Show | 109 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.51+7659_51+7660dup others(2): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003626 | ||||||
chr13:52003713 | A | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0174others(14): Show | 19 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.51+7574T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003713 | ||||||
chr13:52003823 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.51+7464C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52003823 | ||||||
chr13:52004012 | C | T | 3 | a0001c0001t0001g0159a0002c0002t0009g0010a0004c0004t0001g0160 | 4 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7275G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004012 | ||||||
chr13:52004075 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.51+7212A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004075 | ||||||
chr13:52004095 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.51+7192A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004095 | ||||||
chr13:52004104 | T | A | 126 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0003g0056others(123): Show | 135 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.51+7183A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004104 | ||||||
chr13:52004144 | C | A | 2 | a0002c0002t0009g0010a0004c0004t0001g0160 | 3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.51+7143G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004144 | ||||||
chr13:52004144 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.51+7143G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004144 | ||||||
chr13:52004253 | C | T | 3 | a0003c0003t0005g0274a0003c0015t0005g0273a0003c0032t0005g0272 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.51+7034G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004253 | ||||||
chr13:52004294 | T | C | 1 | a0003c0034t0005g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.51+6993A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004294 | ||||||
chr13:52004477 | C | A | 95 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(92): Show | 102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.51+6810G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004477 | ||||||
chr13:52004751 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.51+6536A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004751 | ||||||
chr13:52004861 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.51+6426C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004861 | ||||||
chr13:52004956 | T | C | 1 | a0002c0002t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.51+6331A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52004956 | ||||||
chr13:52005056 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51+6231A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005056 | ||||||
chr13:52005295 | T | C | 2 | a0002c0002t0002g0114a0002c0002t0002g0115 | 2 | HG01261.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.51+5992A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005295 | ||||||
chr13:52005326 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.51+5961T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005326 | ||||||
chr13:52005444 | G | A | 1 | a0003c0003t0006g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.51+5843C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005444 | ||||||
chr13:52005489 | G | C | 1 | a0003c0003t0006g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.51+5798C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005489 | ||||||
chr13:52005623 | G | A | 1 | a0003c0003t0005g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.51+5664C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005623 | ||||||
chr13:52005703 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.51+5584G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005703 | ||||||
chr13:52005726 | C | T | 1 | a0001c0030t0001g0172 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.51+5561G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005726 | ||||||
chr13:52005941 | GT | G | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.51+5345delA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52005941 | ||||||
chr13:52006114 | G | A | 1 | a0002c0002t0002g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.51+5173C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006114 | ||||||
chr13:52006193 | T | C | 122 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0003g0056others(119): Show | 131 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.51+5094A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006193 | ||||||
chr13:52006427 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.51+4860T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006427 | ||||||
chr13:52006551 | A | T | 3 | a0001c0001t0001g0159a0002c0002t0009g0010a0004c0004t0001g0160 | 4 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+4736T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006551 | ||||||
chr13:52006558 | T | C | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+4729A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006558 | ||||||
chr13:52006723 | C | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+4564G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006723 | ||||||
chr13:52006770 | G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.51+4517C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52006770 | ||||||
chr13:52007029 | T | A | 1 | a0002c0002t0002g0117 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.51+4258A>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007029 | ||||||
chr13:52007112 | G | A | 1 | a0003c0005t0004g0025 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.51+4175C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007112 | ||||||
chr13:52007134 | AACTGTGG others(7): Show |
A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+4139_51+4152del others(14): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007134 | ||||||
chr13:52007232 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.51+4055A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007232 | ||||||
chr13:52007292 | G | A | 5 | a0003c0003t0005g0018a0003c0003t0005g0260a0003c0003t0006g0258others(2): Show | 6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+3995C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007292 | ||||||
chr13:52007339 | C | A | 1 | a0007c0008t0001g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+3948G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007339 | ||||||
chr13:52007481 | T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.51+3806A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007481 | ||||||
chr13:52007505 | G | A | 95 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(92): Show | 102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.51+3782C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007505 | ||||||
chr13:52007540 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.51+3747G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007540 | ||||||
chr13:52007604 | C | T | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.51+3683G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007604 | ||||||
chr13:52007747 | A | T | 1 | a0003c0003t0004g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.51+3540T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007747 | ||||||
chr13:52007848 | T | C | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+3439A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007848 | ||||||
chr13:52007916 | T | C | 2 | a0001c0001t0003g0149a0001c0001t0003g0150 | 2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.51+3371A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007916 | ||||||
chr13:52007949 | C | T | 95 | a0001c0001t0003g0056a0001c0001t0003g0111a0002c0002t0002g0002others(92): Show | 102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.51+3338G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52007949 | ||||||
chr13:52008042 | T | C | 1 | a0003c0005t0004g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.51+3245A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008042 | ||||||
chr13:52008073 | G | T | 6 | a0001c0001t0003g0122a0005c0006t0004g0009a0005c0006t0004g0121others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+3214C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008073 | ||||||
chr13:52008244 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.51+3043C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008244 | ||||||
chr13:52008246 | C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0265 | 4 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+3041G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008246 | ||||||
chr13:52008250 | G | T | 1 | a0014c0024t0005g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.51+3037C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008250 | ||||||
chr13:52008251 | A | T | 1 | a0014c0024t0005g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.51+3036T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008251 | ||||||
chr13:52008265 | G | A | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+3022C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008265 | ||||||
chr13:52008298 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51+2989G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008298 | ||||||
chr13:52008300 | A | G | 1 | a0003c0003t0006g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.51+2987T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008300 | ||||||
chr13:52008301 | C | T | 1 | a0005c0006t0004g0121 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.51+2986G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008301 | ||||||
chr13:52008413 | T | C | 2 | a0007c0008t0003g0027a0007c0008t0003g0028 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.51+2874A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008413 | ||||||
chr13:52008416 | T | C | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.51+2871A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008416 | ||||||
chr13:52008636 | G | A | 116 | a0001c0001t0003g0056a0001c0001t0003g0111a0001c0001t0003g0122others(113): Show | 124 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.51+2651C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008636 | ||||||
chr13:52008684 | T | C | 6 | a0001c0001t0003g0122a0005c0006t0004g0009a0005c0006t0004g0121others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2603A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008684 | ||||||
chr13:52008883 | C | T | 14 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(11): Show | 14 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.51+2404G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008883 | ||||||
chr13:52008883 | CT | C | 108 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0003g0056others(105): Show | 117 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.51+2403delA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008883 | ||||||
chr13:52008884 | T | C | 14 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(11): Show | 14 | HG00544.hp2 HG01099.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.51+2403A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52008884 | ||||||
chr13:52009027 | A | G | 6 | a0001c0001t0003g0122a0005c0006t0004g0009a0005c0006t0004g0121others(3): Show | 7 | HG01109.hp1 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2260T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009027 | ||||||
chr13:52009102 | C | T | 1 | a0005c0026t0004g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.51+2185G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009102 | ||||||
chr13:52009279 | G | A | 1 | a0003c0005t0004g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.51+2008C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009279 | ||||||
chr13:52009352 | T | G | 1 | a0003c0015t0005g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.51+1935A>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009352 | ||||||
chr13:52009522 | T | C | 2 | a0009c0016t0005g0269a0009c0016t0005g0270 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.51+1765A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009522 | ||||||
chr13:52009661 | C | T | 5 | a0003c0003t0006g0164a0003c0003t0006g0165a0003c0003t0006g0166others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+1626G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009661 | ||||||
chr13:52009805 | G | C | 3 | a0001c0001t0001g0159a0002c0002t0009g0010a0004c0004t0001g0160 | 4 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1482C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009805 | ||||||
chr13:52009871 | T | C | 1 | a0005c0006t0004g0154 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.51+1416A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009871 | ||||||
chr13:52009910 | G | A | 1 | a0003c0003t0006g0271 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51+1377C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009910 | ||||||
chr13:52009923 | G | C | 1 | a0003c0003t0006g0271 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51+1364C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009923 | ||||||
chr13:52009930 | A | G | 3 | a0001c0001t0003g0008a0001c0001t0003g0118a0001c0001t0003g0119 | 4 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1357T>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52009930 | ||||||
chr13:52010086 | G | T | 2 | a0002c0002t0002g0031a0004c0004t0003g0030 | 2 | HG00673.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.51+1201C>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010086 | ||||||
chr13:52010108 | C | T | 96 | a0001c0001t0001g0012a0001c0001t0003g0056a0001c0001t0003g0111others(93): Show | 104 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.51+1179G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010108 | ||||||
chr13:52010241 | G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0015others(274): Show | 300 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.51+1046C>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010241 | ||||||
chr13:52010573 | C | A | 1 | a0003c0003t0005g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.51+714G>T | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010573 | ||||||
chr13:52010586 | A | AT | 7 | a0001c0001t0001g0159a0001c0001t0001g0277a0002c0002t0009g0010others(4): Show | 8 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+700dupA | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010586 | ||||||
chr13:52010606 | T | C | 10 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(7): Show | 10 | HG00544.hp2 HG01099.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.51+681A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010606 | ||||||
chr13:52010642 | T | C | 156 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0277others(153): Show | 167 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.51+645A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010642 | ||||||
chr13:52010736 | T | C | 145 | a0001c0001t0001g0012a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.51+551A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010736 | ||||||
chr13:52010739 | A | T | 145 | a0001c0001t0001g0012a0001c0001t0003g0008a0001c0001t0003g0056others(142): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.51+548T>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010739 | ||||||
chr13:52010764 | A | C | 96 | a0001c0001t0001g0012a0001c0001t0003g0056a0001c0001t0003g0111others(93): Show | 104 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.51+523T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010764 | ||||||
chr13:52010892 | TA | T | 4 | a0001c0001t0001g0159a0002c0002t0009g0010a0004c0004t0001g0160others(1): Show | 5 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+394delT | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010892 | ||||||
chr13:52010924 | ATACCATA others(4): Show |
A | 1 | a0002c0002t0008g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.51+352_51+362delCA others(9): Show |
ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010924 | ||||||
chr13:52010936 | G | C | 1 | a0002c0002t0008g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.51+351C>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52010936 | ||||||
chr13:52011030 | A | C | 1 | a0001c0013t0001g0011 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.51+257T>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52011030 | ||||||
chr13:52011070 | T | C | 3 | a0001c0001t0001g0277a0003c0003t0006g0278a0003c0034t0005g0279 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.51+217A>G | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52011070 | ||||||
chr13:52011159 | C | G | 4 | a0001c0001t0001g0159a0002c0002t0009g0010a0004c0004t0001g0160others(1): Show | 5 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+128G>C | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52011159 | ||||||
chr13:52011177 | C | T | 10 | a0003c0005t0004g0022a0003c0005t0004g0023a0003c0005t0004g0024others(7): Show | 10 | HG00544.hp2 HG01099.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.51+110G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52011177 | ||||||
chr13:52011256 | C | T | 1 | a0003c0003t0005g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.51+31G>A | ATP7B | ENSG00000123191.17 | transcript | ENST00000242839.10 | protein_coding | 1/20 | chr13 | 52011256 |