geneid | 50488 |
---|---|
ensemblid | ENSG00000141503.17 |
hgncid | 17565 |
symbol | MINK1 |
name | misshapen like kinase 1 |
refseq_nuc | NM_153827.5 |
refseq_prot | NP_722549.2 |
ensembl_nuc | ENST00000355280.11 |
ensembl_prot | ENSP00000347427.6 |
mane_status | MANE Select |
chr | chr17 |
start | 4833340 |
end | 4898061 |
strand | + |
ver | v1.2 |
region | chr17:4833340-4898061 |
region5000 | chr17:4828340-4903061 |
regionname0 | MINK1_chr17_4833340_4898061 |
regionname5000 | MINK1_chr17_4828340_4903061 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1332 | 196 | 71 | 37 | 70 | 8 | 9 | 54 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002 | 1/0 | 1332 | 81 | 15 | 28 | 17 | 5 | 15 | 16 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003 | 0/0 | 1332 | 68 | 1 | 6 | 45 | 1 | 15 | 33 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0004 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0005 | 0/0 | 1332 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0006 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0007 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0008 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0009 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0010 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0011 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0012 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3999 | 147 | 48 | 31 | 54 | 6 | 8 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0002 | 1/0 | 3999 | 77 | 15 | 24 | 17 | 5 | 15 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0003 | 0/0 | 3999 | 63 | 1 | 6 | 40 | 1 | 15 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0004 | 0/1 | 3999 | 24 | 1 | 4 | 16 | 2 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0005 | 0/0 | 3999 | 17 | 16 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0006 | 0/0 | 3999 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0007 | 0/0 | 3999 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0008 | 0/0 | 3999 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0009 | 0/0 | 3999 | 2 | 0 | 1 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0010 | 0/0 | 3999 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0011 | 0/0 | 3999 | 2 | 2 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0012 | 0/0 | 3999 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0013 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0014 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0015 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0016 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0017 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0018 | 0/0 | 3999 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0019 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0020 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0021 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0022 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0023 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0024 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0025 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
c0026 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1022 | 50 | 4 | 19 | 9 | 5 | 13 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0002 | 0/0 | 1022 | 49 | 11 | 14 | 17 | 2 | 5 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0003 | 0/0 | 1022 | 39 | 1 | 2 | 23 | 1 | 12 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0004 | 0/0 | 1022 | 23 | 17 | 5 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0005 | 0/0 | 1022 | 21 | 6 | 9 | 6 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0006 | 0/0 | 1019 | 19 | 3 | 2 | 13 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0007 | 0/0 | 1022 | 15 | 1 | 4 | 6 | 3 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0008 | 0/0 | 1019 | 12 | 10 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0009 | 0/0 | 1022 | 12 | 10 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0010 | 0/0 | 1019 | 9 | 0 | 3 | 4 | 0 | 2 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0011 | 0/0 | 1022 | 8 | 0 | 0 | 7 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0012 | 0/0 | 1022 | 8 | 1 | 0 | 7 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0013 | 0/0 | 1022 | 7 | 0 | 0 | 7 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0014 | 0/0 | 1022 | 7 | 2 | 0 | 5 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0015 | 0/0 | 1022 | 7 | 0 | 4 | 0 | 0 | 3 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0016 | 0/0 | 1022 | 5 | 4 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0017 | 0/0 | 1022 | 5 | 0 | 0 | 5 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0018 | 0/0 | 1019 | 4 | 2 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0019 | 0/1 | 1022 | 4 | 0 | 2 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0020 | 0/0 | 1022 | 4 | 1 | 1 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0021 | 0/0 | 1022 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0022 | 0/0 | 1022 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0023 | 0/0 | 1022 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0024 | 0/0 | 1022 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0025 | 0/0 | 1019 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0026 | 0/0 | 1022 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0027 | 0/0 | 1019 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0028 | 0/0 | 1022 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0029 | 0/0 | 1022 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0030 | 0/0 | 1019 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0031 | 0/0 | 1022 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0032 | 0/0 | 1022 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0033 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0034 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0035 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0036 | 0/0 | 1022 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0037 | 0/0 | 1019 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0038 | 0/0 | 1022 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0039 | 0/0 | 1019 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0040 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0041 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0042 | 0/0 | 1019 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0043 | 0/0 | 1019 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0044 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0045 | 1/0 | 1019 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0046 | 0/0 | 1022 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0047 | 0/0 | 1022 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0048 | 0/0 | 1022 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0049 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0050 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0051 | 0/0 | 1022 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0052 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0053 | 0/0 | 1022 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0054 | 0/0 | 1022 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0055 | 0/0 | 1022 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
t0056 | 0/0 | 1022 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0336 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3999 | 147 | 48 | 31 | 54 | 6 | 8 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0004 | 0/1 | 3999 | 24 | 1 | 4 | 16 | 2 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005 | 0/0 | 3999 | 17 | 16 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0008 | 0/0 | 3999 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0011 | 0/0 | 3999 | 2 | 2 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0014 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0017 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0018 | 0/0 | 3999 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002 | 1/0 | 3999 | 77 | 15 | 24 | 17 | 5 | 15 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0010 | 0/0 | 3999 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0012 | 0/0 | 3999 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003 | 0/0 | 3999 | 63 | 1 | 6 | 40 | 1 | 15 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0007 | 0/0 | 3999 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0013 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0020 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0004c0006 | 0/0 | 3999 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0005c0009 | 0/0 | 3999 | 2 | 0 | 1 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0005c0023 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0006c0021 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0006c0025 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0007c0024 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0008c0015 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0009c0016 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0010c0019 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0011c0022 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0012c0026 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5020 | 42 | 6 | 14 | 16 | 2 | 4 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0003 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0004 | 0/0 | 5020 | 7 | 6 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0005 | 0/0 | 5020 | 20 | 5 | 9 | 6 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0007 | 0/0 | 5020 | 14 | 0 | 4 | 6 | 3 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0008 | 0/0 | 5017 | 4 | 2 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0009 | 0/0 | 5020 | 10 | 8 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0012 | 0/0 | 5020 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0013 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0014 | 0/0 | 5020 | 3 | 2 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0016 | 0/0 | 5020 | 4 | 4 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0017 | 0/0 | 5020 | 5 | 0 | 0 | 5 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0018 | 0/0 | 5017 | 4 | 2 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0020 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0021 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0023 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0024 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0025 | 0/0 | 5017 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0029 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0030 | 0/0 | 5017 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0031 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0032 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0043 | 0/0 | 5017 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0046 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0047 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0048 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0050 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0051 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0052 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0055 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0001t0056 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0004t0006 | 0/0 | 5017 | 16 | 1 | 2 | 12 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0004t0016 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0004t0019 | 0/1 | 5020 | 4 | 0 | 2 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0004t0027 | 0/0 | 5017 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0004t0042 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0002 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0006 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0008 | 0/0 | 5017 | 8 | 8 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0012 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0022 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0037 | 0/0 | 5017 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0049 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0005t0054 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0008t0002 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0011t0006 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0011t0041 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0014t0009 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0017t0002 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0001c0018t0004 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0001 | 0/0 | 5020 | 48 | 4 | 18 | 9 | 5 | 12 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0002 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0004 | 0/0 | 5020 | 13 | 10 | 3 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0014 | 0/0 | 5020 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0015 | 0/0 | 5020 | 5 | 0 | 2 | 0 | 0 | 3 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0020 | 0/0 | 5020 | 3 | 0 | 1 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0035 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0040 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0002t0045 | 1/0 | 5017 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0010t0015 | 0/0 | 5020 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0012t0001 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0002c0012t0004 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0003 | 0/0 | 5020 | 33 | 1 | 2 | 18 | 1 | 11 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0010 | 0/0 | 5017 | 9 | 0 | 3 | 4 | 0 | 2 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0011 | 0/0 | 5020 | 7 | 0 | 0 | 6 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0013 | 0/0 | 5020 | 6 | 0 | 0 | 6 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0026 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0028 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0033 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0034 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0036 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0038 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0003t0039 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0007t0003 | 0/0 | 5020 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0013t0003 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0003c0020t0011 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0004c0006t0012 | 0/0 | 5020 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0005c0009t0044 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0005c0009t0053 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0005c0023t0009 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0006c0021t0007 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0006c0025t0005 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0007c0024t0006 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0008c0015t0002 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0009c0016t0028 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0010c0019t0001 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0011c0022t0004 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
a0012c0026t0003 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | copy fasta | chr17 | 4828340 | 4903061 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0014g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0014g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0021g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0021g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0023g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0023g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0024g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0024g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0024g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0025g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0025g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0029g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0029g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0030g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0030g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0031g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0031g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0032g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0043g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0046g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0047g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0048g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0050g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0051g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0052g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0055g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0056g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0016g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0336 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0027g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0027g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0042g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0022g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0037g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0049g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0054g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0008t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0008t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0008t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0011t0006g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0011t0041g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0014t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0017t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0018t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0020g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0020g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0020g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0035g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0040g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0045g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0010t0015g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0010t0015g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0012t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0012t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0026g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0028g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0033g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0034g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0036g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0038g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0039g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0007t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0007t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0013t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0020t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0005c0009t0044g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0005c0009t0053g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0005c0023t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0006c0021t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0006c0025t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0007c0024t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0008c0015t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0009c0016t0028g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0010c0019t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0011c0022t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0012c0026t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0287 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0294 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0272 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0104 | EUR | FIN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00280 | hp2 | a0003 | c0003 | t0003 | g0007 | EUR | FIN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00423 | hp1 | a0003 | c0003 | t0011 | g0027 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00438 | hp1 | a0003 | c0003 | t0010 | g0014 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00438 | hp2 | a0001 | c0001 | t0012 | g0097 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00544 | hp2 | a0003 | c0003 | t0010 | g0065 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00558 | hp1 | a0001 | c0001 | t0008 | g0118 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00558 | hp2 | a0003 | c0003 | t0013 | g0077 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00609 | hp1 | a0001 | c0004 | t0006 | g0338 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00609 | hp2 | a0003 | c0003 | t0003 | g0035 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00621 | hp1 | a0001 | c0004 | t0006 | g0348 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00621 | hp2 | a0004 | c0006 | t0012 | g0117 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00639 | hp2 | a0003 | c0003 | t0010 | g0039 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0323 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00642 | hp2 | a0001 | c0005 | t0037 | g0058 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00673 | hp1 | a0001 | c0004 | t0006 | g0329 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00673 | hp2 | a0001 | c0001 | t0050 | g0131 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00733 | hp1 | a0002 | c0002 | t0004 | g0274 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0309 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00738 | hp2 | a0002 | c0012 | t0001 | g0153 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00741 | hp2 | a0002 | c0002 | t0015 | g0325 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0315 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01069 | hp2 | a0001 | c0004 | t0006 | g0344 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01074 | hp1 | a0001 | c0004 | t0006 | g0345 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01074 | hp2 | a0001 | c0001 | t0032 | g0191 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01099 | hp1 | a0002 | c0002 | t0020 | g0312 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01099 | hp2 | a0002 | c0010 | t0015 | g0301 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01106 | hp2 | a0002 | c0010 | t0015 | g0296 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0276 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01167 | hp1 | a0005 | c0009 | t0053 | g0204 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0219 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0317 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0310 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01192 | hp1 | a0001 | c0004 | t0019 | g0349 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01243 | hp1 | a0001 | c0001 | t0043 | g0161 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01243 | hp2 | a0001 | c0018 | t0004 | g0333 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01256 | hp1 | a0003 | c0003 | t0003 | g0044 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01256 | hp2 | a0002 | c0002 | t0004 | g0267 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01257 | hp2 | a0002 | c0002 | t0015 | g0269 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01258 | hp1 | a0002 | c0002 | t0004 | g0268 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01261 | hp2 | a0003 | c0003 | t0010 | g0066 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0084 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01346 | hp2 | a0003 | c0003 | t0010 | g0031 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0099 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01361 | hp2 | a0003 | c0003 | t0003 | g0037 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0106 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0105 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0300 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01517 | hp1 | a0001 | c0004 | t0019 | g0343 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0087 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01884 | hp2 | a0001 | c0005 | t0054 | g0206 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01891 | hp1 | a0001 | c0005 | t0008 | g0232 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01891 | hp2 | a0001 | c0001 | t0009 | g0209 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01928 | hp2 | a0001 | c0001 | t0007 | g0103 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0314 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0111 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02027 | hp2 | a0001 | c0001 | t0030 | g0098 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02055 | hp2 | a0001 | c0001 | t0023 | g0244 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02083 | hp1 | a0003 | c0003 | t0003 | g0009 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02083 | hp2 | a0001 | c0001 | t0008 | g0101 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02129 | hp1 | a0003 | c0003 | t0011 | g0043 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02129 | hp2 | a0001 | c0001 | t0029 | g0178 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02132 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02132 | hp2 | a0003 | c0003 | t0003 | g0049 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02135 | hp1 | a0003 | c0007 | t0003 | g0002 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0273 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02145 | hp2 | a0001 | c0005 | t0022 | g0151 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02148 | hp2 | a0001 | c0004 | t0019 | g0332 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02155 | hp1 | a0001 | c0001 | t0017 | g0113 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02155 | hp2 | a0003 | c0003 | t0003 | g0026 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02165 | hp1 | a0003 | c0003 | t0039 | g0078 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02165 | hp2 | a0003 | c0003 | t0013 | g0064 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0245 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02257 | hp2 | a0001 | c0001 | t0055 | g0198 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02258 | hp2 | a0011 | c0022 | t0004 | g0144 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02280 | hp2 | a0002 | c0002 | t0004 | g0142 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02451 | hp1 | a0001 | c0001 | t0016 | g0223 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02523 | hp2 | a0001 | c0001 | t0018 | g0128 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02572 | hp2 | a0001 | c0011 | t0041 | g0347 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02602 | hp2 | a0003 | c0003 | t0010 | g0013 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02615 | hp1 | a0001 | c0005 | t0008 | g0230 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02615 | hp2 | a0001 | c0008 | t0002 | g0158 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02622 | hp1 | a0001 | c0001 | t0021 | g0079 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02622 | hp2 | a0001 | c0005 | t0008 | g0235 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02630 | hp2 | a0001 | c0005 | t0006 | g0233 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0275 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0055 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0326 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02717 | hp1 | a0001 | c0008 | t0002 | g0157 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02717 | hp2 | a0001 | c0001 | t0046 | g0197 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02723 | hp1 | a0006 | c0021 | t0007 | g0220 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0102 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02735 | hp2 | a0003 | c0003 | t0003 | g0050 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0140 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02818 | hp1 | a0001 | c0001 | t0016 | g0224 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02886 | hp1 | a0001 | c0001 | t0024 | g0253 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02886 | hp2 | a0001 | c0005 | t0012 | g0152 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02895 | hp1 | a0001 | c0005 | t0008 | g0228 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02897 | hp1 | a0001 | c0005 | t0008 | g0229 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02922 | hp1 | a0001 | c0005 | t0008 | g0227 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02965 | hp1 | a0001 | c0001 | t0021 | g0080 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02965 | hp2 | a0001 | c0005 | t0022 | g0221 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0040 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03017 | hp2 | a0002 | c0002 | t0015 | g0295 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03041 | hp1 | a0001 | c0005 | t0049 | g0234 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03041 | hp2 | a0001 | c0001 | t0014 | g0195 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0286 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0207 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03130 | hp1 | a0001 | c0001 | t0021 | g0081 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0211 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03195 | hp2 | a0008 | c0015 | t0002 | g0196 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03209 | hp1 | a0001 | c0001 | t0016 | g0226 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03209 | hp2 | a0001 | c0005 | t0022 | g0149 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03239 | hp1 | a0001 | c0001 | t0047 | g0130 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0225 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03453 | hp2 | a0001 | c0011 | t0006 | g0334 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0208 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0320 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03491 | hp2 | a0003 | c0003 | t0003 | g0032 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0319 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03492 | hp2 | a0003 | c0003 | t0003 | g0047 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03516 | hp1 | a0001 | c0005 | t0008 | g0236 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03579 | hp1 | a0002 | c0002 | t0004 | g0240 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03579 | hp2 | a0002 | c0002 | t0040 | g0146 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0321 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0041 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0328 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03704 | hp2 | a0003 | c0003 | t0011 | g0061 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03710 | hp1 | a0001 | c0001 | t0048 | g0095 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0071 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0288 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03831 | hp2 | a0003 | c0003 | t0003 | g0038 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03834 | hp1 | a0002 | c0002 | t0015 | g0280 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03834 | hp2 | a0003 | c0003 | t0003 | g0045 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0298 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0255 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03942 | hp1 | a0001 | c0017 | t0002 | g0192 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03942 | hp2 | a0010 | c0019 | t0001 | g0260 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04184 | hp1 | a0002 | c0002 | t0015 | g0324 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04184 | hp2 | a0003 | c0003 | t0010 | g0028 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0046 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0285 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04204 | hp2 | a0003 | c0003 | t0036 | g0033 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18522 | hp1 | a0001 | c0001 | t0018 | g0279 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18522 | hp2 | a0002 | c0002 | t0004 | g0145 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0259 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18906 | hp2 | a0001 | c0001 | t0014 | g0251 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18940 | hp2 | a0003 | c0003 | t0011 | g0017 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18942 | hp1 | a0003 | c0003 | t0013 | g0054 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18943 | hp1 | a0001 | c0001 | t0007 | g0093 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18943 | hp2 | a0003 | c0003 | t0011 | g0067 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0052 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18944 | hp2 | a0001 | c0004 | t0006 | g0337 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18947 | hp1 | a0003 | c0003 | t0013 | g0042 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18947 | hp2 | a0001 | c0001 | t0013 | g0075 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18948 | hp2 | a0001 | c0001 | t0031 | g0088 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18949 | hp1 | a0001 | c0001 | t0012 | g0096 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18949 | hp2 | a0003 | c0007 | t0003 | g0002 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18950 | hp1 | a0002 | c0002 | t0014 | g0322 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18950 | hp2 | a0001 | c0001 | t0018 | g0172 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18951 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18951 | hp2 | a0001 | c0001 | t0029 | g0132 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18954 | hp1 | a0001 | c0004 | t0016 | g0352 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18954 | hp2 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18961 | hp2 | a0001 | c0001 | t0017 | g0091 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18962 | hp1 | a0003 | c0003 | t0003 | g0068 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18962 | hp2 | a0003 | c0013 | t0003 | g0056 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18964 | hp2 | a0003 | c0003 | t0003 | g0048 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18966 | hp1 | a0004 | c0006 | t0012 | g0100 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18966 | hp2 | a0003 | c0020 | t0011 | g0022 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18967 | hp1 | a0003 | c0003 | t0026 | g0082 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18968 | hp1 | a0001 | c0004 | t0006 | g0136 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18968 | hp2 | a0001 | c0004 | t0027 | g0074 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18969 | hp1 | a0004 | c0006 | t0012 | g0112 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18969 | hp2 | a0002 | c0002 | t0014 | g0292 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18970 | hp1 | a0001 | c0001 | t0025 | g0138 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18971 | hp1 | a0001 | c0001 | t0025 | g0133 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18973 | hp1 | a0004 | c0006 | t0012 | g0125 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18973 | hp2 | a0001 | c0004 | t0042 | g0346 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18975 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18975 | hp2 | a0001 | c0004 | t0006 | g0350 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18979 | hp1 | a0001 | c0004 | t0006 | g0135 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18979 | hp2 | a0003 | c0003 | t0003 | g0011 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18980 | hp1 | a0003 | c0003 | t0003 | g0073 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18980 | hp2 | a0001 | c0004 | t0006 | g0331 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18983 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18983 | hp2 | a0003 | c0007 | t0003 | g0060 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18988 | hp1 | a0001 | c0004 | t0006 | g0351 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18988 | hp2 | a0002 | c0002 | t0020 | g0291 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18989 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18990 | hp1 | a0005 | c0009 | t0044 | g0121 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18990 | hp2 | a0003 | c0003 | t0034 | g0024 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18994 | hp1 | a0012 | c0026 | t0003 | g0076 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18995 | hp1 | a0009 | c0016 | t0028 | g0015 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18995 | hp2 | a0001 | c0001 | t0030 | g0085 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18998 | hp1 | a0003 | c0003 | t0003 | g0034 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18999 | hp1 | a0003 | c0003 | t0003 | g0053 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18999 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19000 | hp1 | a0001 | c0001 | t0017 | g0124 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19000 | hp2 | a0003 | c0003 | t0033 | g0019 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19004 | hp1 | a0001 | c0001 | t0052 | g0134 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19005 | hp1 | a0001 | c0004 | t0027 | g0059 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19010 | hp1 | a0002 | c0002 | t0014 | g0318 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19010 | hp2 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19011 | hp1 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19012 | hp2 | a0002 | c0002 | t0035 | g0070 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19030 | hp1 | a0001 | c0014 | t0009 | g0216 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19030 | hp2 | a0005 | c0023 | t0009 | g0353 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19043 | hp1 | a0001 | c0001 | t0051 | g0217 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19043 | hp2 | a0001 | c0005 | t0008 | g0231 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0107 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19057 | hp2 | a0001 | c0004 | t0006 | g0339 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19063 | hp1 | a0003 | c0003 | t0011 | g0018 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19064 | hp1 | a0003 | c0003 | t0003 | g0036 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19065 | hp1 | a0003 | c0003 | t0013 | g0051 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19065 | hp2 | a0001 | c0001 | t0025 | g0139 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19066 | hp2 | a0002 | c0002 | t0014 | g0307 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19070 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19070 | hp2 | a0001 | c0001 | t0031 | g0120 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19074 | hp1 | a0003 | c0003 | t0010 | g0008 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19074 | hp2 | a0002 | c0002 | t0020 | g0299 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19077 | hp2 | a0003 | c0003 | t0010 | g0030 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0023 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0123 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19081 | hp2 | a0003 | c0003 | t0011 | g0020 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19084 | hp1 | a0003 | c0003 | t0013 | g0057 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19085 | hp1 | a0001 | c0004 | t0006 | g0340 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19085 | hp2 | a0003 | c0003 | t0028 | g0016 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19087 | hp1 | a0001 | c0004 | t0006 | g0335 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19090 | hp1 | a0007 | c0024 | t0006 | g0330 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19090 | hp2 | a0003 | c0003 | t0026 | g0072 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0063 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | ASW | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20129 | hp2 | a0001 | c0001 | t0023 | g0252 | AFR | ASW | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0261 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20805 | hp1 | a0001 | c0004 | t0006 | g0342 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20805 | hp2 | a0001 | c0001 | t0056 | g0256 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20905 | hp1 | a0003 | c0003 | t0003 | g0012 | SAS | GIH | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | GIH | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01123 | hp1 | a0003 | c0003 | t0038 | g0021 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01123 | hp2 | a0002 | c0012 | t0004 | g0188 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02109 | hp1 | a0003 | c0003 | t0003 | g0029 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02486 | hp1 | a0001 | c0001 | t0020 | g0148 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02559 | hp1 | a0002 | c0002 | t0004 | g0143 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02559 | hp2 | a0002 | c0002 | t0004 | g0266 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03471 | hp2 | a0001 | c0001 | t0024 | g0205 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG06807 | hp1 | a0001 | c0005 | t0002 | g0150 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20300 | hp1 | a0001 | c0008 | t0002 | g0156 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20300 | hp2 | a0001 | c0004 | t0006 | g0341 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA21309 | hp1 | a0006 | c0025 | t0005 | g0147 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA21309 | hp2 | a0002 | c0002 | t0004 | g0141 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0019 | g0336 | REF | REF | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0045 | g0239 | REF | REF | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4887670
|
A | ACAGCAGC others(8): Show |
1 | a0007 | 1 | NA19090.hp1 | disruptive_inframe_insertion | MODERATE | c.1124_1138dupTGCAGC others(9): Show |
p.Leu375_Gln379dup | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/32 | 1383/5017 | 1139/3999 | 380/1332 | INFO_REALIGN_3_PRIME | chr17 | 4887670 | |
chr17:4891691
|
G | A | 1 | a0004 | 4 | HG00621.hp2 NA18966.hp1 NA18969.hp1 others(1): Show |
missense_variant | MODERATE | c.1976G>A | p.Arg659His | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/32 | 2220/5017 | 1976/3999 | 659/1332 | chr17 | 4891691 | ||
chr17:4891716
|
G | T | 1 | a0011 | 1 | HG02258.hp2 | missense_variant&splice_region_variant | MODERATE | c.2001G>T | p.Lys667Asn | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/32 | 2245/5017 | 2001/3999 | 667/1332 | chr17 | 4891716 | ||
chr17:4892427
|
A | C | 1 | a0006 | 2 | HG02723.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2113A>C | p.Ile705Leu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 18/32 | 2357/5017 | 2113/3999 | 705/1332 | chr17 | 4892427 | ||
chr17:4892979
|
T | C | 9 | a0001a0003a0004others(6): Show | 277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
missense_variant&splice_region_variant | MODERATE | c.2312T>C | p.Val771Ala | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/32 | 2556/5017 | 2312/3999 | 771/1332 | chr17 | 4892979 | ||
chr17:4892991
|
C | T | 8 | a0001a0003a0004others(5): Show | 274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
missense_variant | MODERATE | c.2324C>T | p.Pro775Leu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/32 | 2568/5017 | 2324/3999 | 775/1332 | chr17 | 4892991 | ||
chr17:4893535
|
G | C | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.2502G>C | p.Glu834Asp | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/32 | 2746/5017 | 2502/3999 | 834/1332 | chr17 | 4893535 | ||
chr17:4894010
|
G | A | 3 | a0003a0009a0012 | 70 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
missense_variant | MODERATE | c.2587G>A | p.Val863Ile | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 22/32 | 2831/5017 | 2587/3999 | 863/1332 | chr17 | 4894010 | ||
chr17:4894532
|
C | A | 1 | a0009 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.2816C>A | p.Ser939Tyr | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/32 | 3060/5017 | 2816/3999 | 939/1332 | chr17 | 4894532 | ||
chr17:4894615
|
G | A | 1 | a0010 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2899G>A | p.Asp967Asn | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/32 | 3143/5017 | 2899/3999 | 967/1332 | chr17 | 4894615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4833589
|
C | T | 1 | a0001c0008 | 3 | HG02615.hp2 HG02717.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.6C>T | p.Gly2Gly | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/32 | 250/5017 | 6/3999 | 2/1332 | chr17 | 4833589 | ||
chr17:4884425
|
C | T | 1 | a0002c0012 | 2 | HG00738.hp2 HG01123.hp2 |
synonymous_variant | LOW | c.369C>T | p.Asn123Asn | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/32 | 613/5017 | 369/3999 | 123/1332 | chr17 | 4884425 | ||
chr17:4884983
|
G | A | 1 | a0003c0013 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.489G>A | p.Glu163Glu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 6/32 | 733/5017 | 489/3999 | 163/1332 | chr17 | 4884983 | ||
chr17:4887658
|
A | G | 2 | a0001c0005a0006c0025 | 18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.1098A>G | p.Ser366Ser | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/32 | 1342/5017 | 1098/3999 | 366/1332 | chr17 | 4887658 | ||
chr17:4889757
|
C | T | 4 | a0001c0004a0001c0011a0005c0023others(1): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
synonymous_variant | LOW | c.1341C>T | p.Arg447Arg | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/32 | 1585/5017 | 1341/3999 | 447/1332 | chr17 | 4889757 | ||
chr17:4891097
|
G | A | 1 | a0001c0014 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1713G>A | p.Pro571Pro | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/32 | 1957/5017 | 1713/3999 | 571/1332 | chr17 | 4891097 | ||
chr17:4892761
|
C | T | 1 | a0003c0020 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.2304C>T | p.Arg768Arg | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/32 | 2548/5017 | 2304/3999 | 768/1332 | chr17 | 4892761 | ||
chr17:4894066
|
C | T | 2 | a0003c0007a0012c0026 | 4 | HG02135.hp1 NA18949.hp2 NA18983.hp2 others(1): Show |
synonymous_variant | LOW | c.2643C>T | p.Tyr881Tyr | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 22/32 | 2887/5017 | 2643/3999 | 881/1332 | chr17 | 4894066 | ||
chr17:4894236
|
C | T | 1 | a0001c0011 | 2 | HG02572.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.2733C>T | p.Asp911Asp | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/32 | 2977/5017 | 2733/3999 | 911/1332 | chr17 | 4894236 | ||
chr17:4895435
|
G | A | 1 | a0001c0017 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.3171G>A | p.Arg1057Arg | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/32 | 3415/5017 | 3171/3999 | 1057/1332 | chr17 | 4895435 | ||
chr17:4896028
|
G | A | 1 | a0002c0010 | 2 | HG01099.hp2 HG01106.hp2 |
synonymous_variant | LOW | c.3390G>A | p.Leu1130Leu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 28/32 | 3634/5017 | 3390/3999 | 1130/1332 | chr17 | 4896028 | ||
chr17:4896521
|
C | T | 1 | a0001c0018 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.3708C>T | p.Tyr1236Tyr | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 30/32 | 3952/5017 | 3708/3999 | 1236/1332 | chr17 | 4896521 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4833398
|
G | C | 1 | a0001c0001t0032 | 1 | HG01074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-186G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/32 | 186 | chr17 | 4833398 | |||||
chr17:4833543
|
G | A | 22 | a0001c0001t0003a0001c0001t0013a0001c0001t0021others(19): Show | 79 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-41G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/32 | 41 | chr17 | 4833543 | |||||
chr17:4897288
|
C | T | 2 | a0001c0001t0056a0003c0003t0039 | 2 | HG02165.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 1 | chr17 | 4897288 | |||||
chr17:4897404
|
C | G | 2 | a0001c0001t0055a0001c0005t0054 | 2 | HG01884.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*117C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 117 | chr17 | 4897404 | |||||
chr17:4897424
|
G | A | 1 | a0002c0002t0040 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 137 | chr17 | 4897424 | |||||
chr17:4897495
|
G | C | 1 | a0003c0003t0033 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 208 | chr17 | 4897495 | |||||
chr17:4897723
|
A | G | 1 | a0005c0009t0053 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 436 | chr17 | 4897723 | |||||
chr17:4897806
|
A | C | 7 | a0001c0001t0009a0001c0001t0025a0001c0001t0050others(4): Show | 18 | HG00673.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*519A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 519 | chr17 | 4897806 | |||||
chr17:4897828
|
G | A | 1 | a0001c0011t0041 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 541 | chr17 | 4897828 | |||||
chr17:4897830
|
C | G | 27 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(24): Show | 93 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 543 | chr17 | 4897830 | |||||
chr17:4897833
|
C | T | 1 | a0001c0001t0046 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 546 | chr17 | 4897833 | |||||
chr17:4897860
|
C | T | 1 | a0001c0005t0049 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 573 | chr17 | 4897860 | |||||
chr17:4897868
|
C | A | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0016others(37): Show | 164 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*581C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 581 | chr17 | 4897868 | |||||
chr17:4897899
|
T | C | 39 | a0001c0001t0002a0001c0001t0003a0001c0001t0014others(36): Show | 155 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*612T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 612 | chr17 | 4897899 | |||||
chr17:4897978
|
T | TCTC | 69 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(66): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*693_*695dupTCC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 696 | INFO_REALIGN_3_PRIME | chr17 | 4897978 | ||||
chr17:4897991
|
C | T | 56 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(53): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 704 | chr17 | 4897991 | |||||
chr17:4897993
|
A | C | 18 | a0001c0001t0007a0001c0001t0021a0001c0001t0023others(15): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 706 | chr17 | 4897993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4833732
|
G | A | 1 | a0003c0003t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.57+92G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4833732 | ||||||
chr17:4833747
|
T | C | 128 | a0001c0001t0002g0129a0001c0001t0003g0062a0001c0001t0005g0001others(125): Show | 133 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.57+107T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4833747 | ||||||
chr17:4834151
|
G | T | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+511G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834151 | ||||||
chr17:4834176
|
G | A | 78 | a0001c0001t0003g0062a0001c0001t0013g0075a0001c0001t0021g0079others(75): Show | 79 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+536G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834176 | ||||||
chr17:4834195
|
T | C | 87 | a0001c0001t0002g0137a0001c0001t0003g0062a0001c0001t0013g0075others(84): Show | 88 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.57+555T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834195 | ||||||
chr17:4834342
|
TTC | T | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+706_57+707delCT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4834342 | |||||
chr17:4834396
|
A | G | 1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.57+756A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834396 | ||||||
chr17:4834422
|
G | A | 7 | a0002c0002t0004g0140a0002c0002t0004g0141a0002c0002t0004g0142others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+782G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834422 | ||||||
chr17:4834619
|
A | AT | 27 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(24): Show | 27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+982dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4834619 | |||||
chr17:4834810
|
G | A | 1 | a0001c0001t0008g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.57+1170G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834810 | ||||||
chr17:4834875
|
G | C | 1 | a0003c0003t0003g0007 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.57+1235G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834875 | ||||||
chr17:4835018
|
C | T | 1 | a0001c0001t0047g0130 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.57+1378C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835018 | ||||||
chr17:4835614
|
G | A | 50 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(47): Show | 54 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.57+1974G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835614 | ||||||
chr17:4835663
|
C | T | 45 | a0001c0001t0018g0286a0002c0002t0001g0005a0002c0002t0001g0285others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.57+2023C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835663 | ||||||
chr17:4835825
|
G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+2185G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835825 | ||||||
chr17:4835866
|
T | G | 151 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0154others(148): Show | 156 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.57+2226T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835866 | ||||||
chr17:4835925
|
A | T | 9 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(6): Show | 9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+2285A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835925 | ||||||
chr17:4836117
|
T | A | 10 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0225others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+2477T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836117 | ||||||
chr17:4836401
|
A | G | 1 | a0001c0001t0025g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.57+2761A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836401 | ||||||
chr17:4836795
|
T | A | 11 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0225others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+3155T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836795 | ||||||
chr17:4836900
|
G | A | 9 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(6): Show | 9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+3260G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836900 | ||||||
chr17:4836971
|
G | A | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+3331G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836971 | ||||||
chr17:4836978
|
G | A | 1 | a0003c0003t0010g0008 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.57+3338G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836978 | ||||||
chr17:4837017
|
T | TA | 9 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(6): Show | 9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+3387dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4837017 | |||||
chr17:4837249
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.57+3609A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837249 | ||||||
chr17:4837332
|
C | T | 2 | a0002c0002t0001g0283a0002c0002t0001g0284 | 2 | HG00735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.57+3692C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837332 | ||||||
chr17:4837452
|
G | T | 9 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(6): Show | 9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+3812G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837452 | ||||||
chr17:4837652
|
A | G | 1 | a0003c0003t0039g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.57+4012A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837652 | ||||||
chr17:4837713
|
C | G | 1 | a0001c0001t0025g0138 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.57+4073C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837713 | ||||||
chr17:4837745
|
A | G | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+4105A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837745 | ||||||
chr17:4837801
|
C | T | 2 | a0002c0002t0001g0328a0005c0023t0009g0353 | 2 | HG03688.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.57+4161C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837801 | ||||||
chr17:4838228
|
C | T | 3 | a0001c0001t0002g0137a0001c0004t0006g0135a0001c0004t0006g0136 | 3 | NA18939.hp1 NA18968.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.57+4588C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838228 | ||||||
chr17:4838359
|
A | G | 335 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.57+4719A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838359 | ||||||
chr17:4838423
|
A | G | 27 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(24): Show | 27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+4783A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838423 | ||||||
chr17:4838479
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.57+4839C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838479 | ||||||
chr17:4838498
|
G | A | 4 | a0001c0005t0002g0150a0001c0005t0012g0152a0001c0005t0022g0149others(1): Show | 4 | HG02145.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+4858G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838498 | ||||||
chr17:4838509
|
T | C | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+4869T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838509 | ||||||
chr17:4838622
|
G | A | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+4982G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838622 | ||||||
chr17:4838690
|
A | T | 1 | a0003c0003t0013g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.57+5050A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838690 | ||||||
chr17:4838817
|
A | G | 86 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0009g0276others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.57+5177A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838817 | ||||||
chr17:4838947
|
C | CT | 25 | a0001c0004t0006g0331a0001c0004t0006g0335a0001c0004t0006g0337others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.57+5321dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4838947 | |||||
chr17:4838966
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.57+5326C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838966 | ||||||
chr17:4838967
|
G | A | 1 | a0001c0001t0007g0084 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.57+5327G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838967 | ||||||
chr17:4838975
|
G | A | 1 | a0003c0003t0003g0009 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.57+5335G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838975 | ||||||
chr17:4838977
|
A | T | 1 | a0003c0003t0003g0009 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.57+5337A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838977 | ||||||
chr17:4839004
|
C | T | 1 | a0001c0001t0021g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.57+5364C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839004 | ||||||
chr17:4839006
|
C | T | 2 | a0001c0001t0021g0081a0002c0002t0001g0327 | 2 | HG00423.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.57+5366C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839006 | ||||||
chr17:4839012
|
T | C | 57 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(54): Show | 58 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.57+5372T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839012 | ||||||
chr17:4839036
|
C | T | 2 | a0001c0005t0022g0221a0006c0021t0007g0220 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+5396C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839036 | ||||||
chr17:4839037
|
A | G | 1 | a0002c0002t0001g0326 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57+5397A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839037 | ||||||
chr17:4839083
|
A | G | 50 | a0001c0001t0005g0001a0001c0001t0005g0086a0001c0001t0005g0089others(47): Show | 54 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.57+5443A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839083 | ||||||
chr17:4839084
|
T | C | 2 | a0002c0002t0001g0254a0002c0012t0001g0153 | 2 | HG00738.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.57+5444T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839084 | ||||||
chr17:4839093
|
G | A | 1 | a0002c0012t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.57+5453G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839093 | ||||||
chr17:4839155
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+5515G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839155 | ||||||
chr17:4839164
|
T | C | 4 | a0001c0001t0002g0155a0001c0008t0002g0156a0001c0008t0002g0157others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+5524T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839164 | ||||||
chr17:4839165
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.57+5525G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839165 | ||||||
chr17:4839189
|
C | T | 2 | a0001c0004t0006g0351a0001c0004t0016g0352 | 2 | NA18954.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.57+5549C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839189 | ||||||
chr17:4839195
|
A | G | 2 | a0001c0005t0006g0233a0001c0005t0008g0232 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.57+5555A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839195 | ||||||
chr17:4839235
|
G | A | 4 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0225others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+5595G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839235 | ||||||
chr17:4839338
|
T | A | 1 | a0001c0001t0030g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.57+5698T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839338 | ||||||
chr17:4839397
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.57+5757C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839397 | ||||||
chr17:4839649
|
A | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+6009A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839649 | ||||||
chr17:4839659
|
A | G | 1 | a0003c0003t0003g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.57+6019A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839659 | ||||||
chr17:4839680
|
A | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.57+6040A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839680 | ||||||
chr17:4839934
|
T | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+6294T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839934 | ||||||
chr17:4839935
|
ATTAATGT others(3): Show |
A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+6297_57+6306del others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839935 | |||||
chr17:4839939
|
A | ATATGTGT others(3): Show |
1 | a0001c0001t0025g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.57+6300_57+6301ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
A | ATG | 6 | a0001c0001t0005g0242a0001c0001t0005g0243a0001c0004t0006g0135others(3): Show | 6 | HG00741.hp2 HG01884.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+6344_57+6345dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
A | ATGTG | 3 | a0001c0001t0002g0137a0001c0001t0025g0138a0001c0001t0029g0132 | 3 | NA18939.hp1 NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.57+6342_57+6345dup others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0025g0133a0001c0001t0052g0134 | 2 | NA18971.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.57+6336_57+6345dup others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATG | A | 60 | a0001c0001t0002g0199a0001c0001t0002g0277a0001c0001t0009g0218others(57): Show | 61 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.57+6344_57+6345del others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTG | A | 17 | a0001c0001t0005g0210a0001c0001t0009g0208a0001c0001t0009g0209others(14): Show | 17 | HG01891.hp2 HG02523.hp2 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.57+6342_57+6345del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTG | A | 20 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(17): Show | 20 | HG00099.hp2 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+6340_57+6345del others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTGT others(1): Show |
A | 22 | a0001c0001t0002g0222a0001c0001t0007g0084a0001c0001t0007g0126others(19): Show | 22 | HG01167.hp1 HG01346.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.57+6338_57+6345del others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTGT others(3): Show |
A | 97 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0154others(94): Show | 102 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.57+6336_57+6345del others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0002g0160a0001c0001t0005g0086a0001c0001t0020g0148others(1): Show | 4 | HG02135.hp2 HG02273.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+6334_57+6345del others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0002g0159a0003c0003t0026g0072a0006c0025t0005g0147 | 3 | HG03491.hp1 NA19090.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.57+6332_57+6345del others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTGT others(13): Show |
A | 75 | a0001c0001t0003g0062a0001c0001t0021g0079a0001c0001t0021g0080others(72): Show | 76 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+6326_57+6345del others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4839939
|
ATGTGTGT others(17): Show |
A | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+6322_57+6345del others(24): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | |||||
chr17:4840040
|
A | T | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+6400A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840040 | ||||||
chr17:4840093
|
A | G | 1 | a0001c0004t0006g0350 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.57+6453A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840093 | ||||||
chr17:4840224
|
G | C | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+6584G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840224 | ||||||
chr17:4840299
|
A | G | 4 | a0002c0002t0035g0070a0003c0003t0003g0068a0003c0003t0003g0069others(1): Show | 4 | HG03710.hp2 NA18951.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+6659A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840299 | ||||||
chr17:4840477
|
G | T | 1 | a0002c0002t0001g0317 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.57+6837G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840477 | ||||||
chr17:4840507
|
G | GA | 29 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(26): Show | 29 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.57+6867_57+6868ins others(1): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840507 | ||||||
chr17:4840599
|
T | C | 2 | a0003c0003t0003g0068a0003c0003t0003g0069 | 2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.57+6959T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840599 | ||||||
chr17:4840834
|
A | G | 338 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(335): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.57+7194A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840834 | ||||||
chr17:4840963
|
T | C | 1 | a0002c0002t0001g0289 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.57+7323T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840963 | ||||||
chr17:4840963
|
T | G | 1 | a0001c0001t0014g0195 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.57+7323T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840963 | ||||||
chr17:4841009
|
C | T | 28 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+7369C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841009 | ||||||
chr17:4841093
|
C | G | 261 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.57+7453C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841093 | ||||||
chr17:4841093
|
C | T | 1 | a0003c0003t0011g0067 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.57+7453C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841093 | ||||||
chr17:4841102
|
C | T | 9 | a0001c0005t0008g0227a0001c0005t0008g0228a0001c0005t0008g0229others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+7462C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841102 | ||||||
chr17:4841103
|
G | A | 1 | a0003c0003t0010g0008 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.57+7463G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841103 | ||||||
chr17:4841128
|
A | C | 28 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+7488A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841128 | ||||||
chr17:4841365
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+7725G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841365 | ||||||
chr17:4841388
|
A | G | 3 | a0001c0001t0002g0277a0002c0002t0001g0281a0002c0002t0001g0288 | 3 | HG00738.hp1 HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.57+7748A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841388 | ||||||
chr17:4841522
|
C | T | 9 | a0001c0005t0008g0227a0001c0005t0008g0228a0001c0005t0008g0229others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+7882C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841522 | ||||||
chr17:4841526
|
C | G | 2 | a0001c0005t0022g0221a0006c0021t0007g0220 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+7886C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841526 | ||||||
chr17:4841528
|
T | C | 161 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.57+7888T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841528 | ||||||
chr17:4841531
|
G | A | 1 | a0003c0003t0003g0010 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.57+7891G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841531 | ||||||
chr17:4841942
|
C | T | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.57+8302C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841942 | ||||||
chr17:4841947
|
C | G | 10 | a0002c0002t0001g0005a0002c0002t0001g0309a0002c0002t0001g0310others(7): Show | 11 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+8307C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841947 | ||||||
chr17:4842076
|
T | C | 2 | a0001c0001t0014g0195a0001c0001t0043g0161 | 2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.57+8436T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842076 | ||||||
chr17:4842080
|
C | T | 7 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(4): Show | 7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+8440C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842080 | ||||||
chr17:4842164
|
T | C | 2 | a0001c0005t0012g0152a0001c0005t0022g0151 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.57+8524T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842164 | ||||||
chr17:4842179
|
A | G | 28 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+8539A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842179 | ||||||
chr17:4842202
|
C | T | 6 | a0001c0001t0046g0197a0001c0001t0055g0198a0001c0004t0006g0348others(3): Show | 6 | HG00621.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+8562C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842202 | ||||||
chr17:4842204
|
A | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+8564A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842204 | ||||||
chr17:4842210
|
C | T | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+8570C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842210 | ||||||
chr17:4842222
|
C | CA | 160 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0154others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.57+8597dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4842222 | |||||
chr17:4842222
|
C | CAA | 24 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(21): Show | 24 | HG00423.hp2 HG00735.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.57+8596_57+8597dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4842222 | |||||
chr17:4842309
|
C | T | 1 | a0001c0001t0009g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.57+8669C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842309 | ||||||
chr17:4842318
|
G | A | 1 | a0001c0001t0051g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+8678G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842318 | ||||||
chr17:4842321
|
G | C | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+8681G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842321 | ||||||
chr17:4842692
|
G | C | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+9052G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842692 | ||||||
chr17:4842905
|
C | A | 1 | a0005c0009t0053g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.57+9265C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842905 | ||||||
chr17:4842999
|
A | G | 28 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+9359A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842999 | ||||||
chr17:4843062
|
C | T | 1 | a0001c0001t0018g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57+9422C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843062 | ||||||
chr17:4843129
|
A | T | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+9489A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843129 | ||||||
chr17:4843146
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57+9506C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843146 | ||||||
chr17:4843186
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+9546G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843186 | ||||||
chr17:4843248
|
A | G | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+9608A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843248 | ||||||
chr17:4843275
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+9635G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843275 | ||||||
chr17:4843457
|
G | A | 78 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0009g0276others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.57+9817G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843457 | ||||||
chr17:4843463
|
A | G | 1 | a0002c0002t0001g0293 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.57+9823A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843463 | ||||||
chr17:4843473
|
G | A | 2 | a0001c0001t0007g0093a0001c0001t0014g0092 | 2 | NA18943.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.57+9833G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843473 | ||||||
chr17:4843488
|
GAAAGAA | G | 8 | a0001c0001t0002g0162a0001c0001t0002g0166a0001c0001t0002g0168others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+9864_57+9869del others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4843488 | |||||
chr17:4843600
|
T | A | 1 | a0001c0005t0049g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+9960T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843600 | ||||||
chr17:4843601
|
G | A | 1 | a0001c0005t0049g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+9961G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843601 | ||||||
chr17:4843602
|
C | T | 1 | a0001c0005t0049g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+9962C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843602 | ||||||
chr17:4843728
|
T | C | 28 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+10088T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843728 | ||||||
chr17:4843872
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+10232G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843872 | ||||||
chr17:4843885
|
C | G | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+10245C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843885 | ||||||
chr17:4843893
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+10253A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843893 | ||||||
chr17:4844048
|
G | A | 2 | a0001c0005t0022g0221a0006c0021t0007g0220 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+10408G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844048 | ||||||
chr17:4844334
|
G | A | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+10694G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844334 | ||||||
chr17:4844595
|
G | A | 1 | a0001c0001t0024g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.57+10955G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844595 | ||||||
chr17:4844841
|
G | T | 7 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(4): Show | 7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+11201G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844841 | ||||||
chr17:4844844
|
T | G | 75 | a0001c0001t0003g0062a0001c0004t0006g0135a0001c0004t0006g0136others(72): Show | 76 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+11204T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844844 | ||||||
chr17:4844875
|
C | G | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+11235C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844875 | ||||||
chr17:4845129
|
G | A | 1 | a0002c0002t0004g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.57+11489G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845129 | ||||||
chr17:4845155
|
T | G | 1 | a0002c0002t0001g0283 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.57+11515T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845155 | ||||||
chr17:4845287
|
G | C | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+11647G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845287 | ||||||
chr17:4845409
|
G | C | 1 | a0001c0001t0005g0094 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.57+11769G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845409 | ||||||
chr17:4845638
|
A | AT | 15 | a0001c0001t0005g0241a0001c0001t0017g0124a0001c0001t0025g0133others(12): Show | 15 | HG00438.hp1 HG00673.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.57+12013dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4845638 | |||||
chr17:4845676
|
C | T | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.57+12036C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845676 | ||||||
chr17:4845721
|
C | G | 1 | a0001c0004t0006g0348 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.57+12081C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845721 | ||||||
chr17:4845730
|
G | A | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+12090G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845730 | ||||||
chr17:4845773
|
T | C | 10 | a0001c0001t0002g0137a0001c0001t0021g0079a0001c0001t0021g0080others(7): Show | 10 | HG00673.hp2 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+12133T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845773 | ||||||
chr17:4845803
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+12163G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845803 | ||||||
chr17:4845887
|
C | T | 7 | a0001c0001t0002g0162a0001c0001t0002g0168a0001c0001t0002g0169others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+12247C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845887 | ||||||
chr17:4845893
|
T | C | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+12253T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845893 | ||||||
chr17:4845911
|
A | G | 170 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.57+12271A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845911 | ||||||
chr17:4845945
|
T | G | 4 | a0003c0003t0010g0008a0003c0003t0010g0065a0003c0003t0028g0016others(1): Show | 4 | HG00544.hp2 NA18995.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+12305T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845945 | ||||||
chr17:4845950
|
T | G | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+12310T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845950 | ||||||
chr17:4846000
|
C | T | 2 | a0001c0001t0007g0122a0001c0001t0007g0123 | 2 | NA18967.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.57+12360C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846000 | ||||||
chr17:4846239
|
G | A | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+12599G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846239 | ||||||
chr17:4846379
|
A | C | 1 | a0003c0003t0013g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.57+12739A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846379 | ||||||
chr17:4846535
|
T | C | 81 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(78): Show | 82 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.57+12895T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846535 | ||||||
chr17:4846558
|
CATCCTT | C | 75 | a0001c0001t0003g0062a0001c0004t0006g0135a0001c0004t0006g0136others(72): Show | 76 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+12920_57+12925d others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4846558 | |||||
chr17:4846610
|
G | A | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.57+12970G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846610 | ||||||
chr17:4846641
|
T | C | 81 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(78): Show | 82 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.57+13001T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846641 | ||||||
chr17:4846712
|
C | G | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+13072C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846712 | ||||||
chr17:4846728
|
C | T | 4 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(1): Show | 4 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+13088C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846728 | ||||||
chr17:4846794
|
C | G | 3 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204 | 3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+13154C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846794 | ||||||
chr17:4846926
|
G | A | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.57+13286G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846926 | ||||||
chr17:4847138
|
A | G | 7 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(4): Show | 7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+13498A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847138 | ||||||
chr17:4847230
|
G | GTTCA | 71 | a0001c0001t0002g0166a0001c0001t0002g0168a0001c0001t0002g0169others(68): Show | 72 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.57+13623_57+13626d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4847230 | |||||
chr17:4847230
|
G | GTTCATTC others(1): Show |
6 | a0001c0001t0003g0062a0001c0001t0021g0079a0001c0001t0021g0080others(3): Show | 6 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+13619_57+13626d others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4847230 | |||||
chr17:4847230
|
GTTCA | G | 28 | a0001c0001t0002g0278a0001c0001t0005g0210a0001c0001t0009g0208others(25): Show | 28 | HG01168.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+13623_57+13626d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4847230 | |||||
chr17:4847278
|
G | A | 74 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0018g0279others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.57+13638G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847278 | ||||||
chr17:4847588
|
G | A | 4 | a0002c0002t0001g0294a0002c0002t0001g0319a0002c0002t0001g0320others(1): Show | 4 | HG00140.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+13948G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847588 | ||||||
chr17:4847752
|
G | A | 1 | a0005c0009t0053g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.57+14112G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847752 | ||||||
chr17:4848180
|
A | G | 4 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081others(1): Show | 4 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+14540A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848180 | ||||||
chr17:4848225
|
A | G | 3 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204 | 3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+14585A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848225 | ||||||
chr17:4848523
|
G | A | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.57+14883G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848523 | ||||||
chr17:4848621
|
A | G | 5 | a0001c0004t0027g0059a0003c0003t0011g0061a0003c0007t0003g0002others(2): Show | 6 | HG02135.hp1 HG03704.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+14981A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848621 | ||||||
chr17:4848650
|
G | A | 74 | a0001c0001t0003g0062a0001c0004t0006g0135a0001c0004t0006g0136others(71): Show | 75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.57+15010G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848650 | ||||||
chr17:4848965
|
G | A | 78 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0016g0223others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.57+15325G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848965 | ||||||
chr17:4848999
|
CT | C | 7 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(4): Show | 7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+15360delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848999 | ||||||
chr17:4849058
|
A | ATGGCTGA others(11): Show |
1 | a0005c0009t0044g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.57+15421_57+15438d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4849058 | |||||
chr17:4849137
|
C | G | 78 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0016g0223others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.57+15497C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849137 | ||||||
chr17:4849170
|
A | G | 1 | a0002c0002t0004g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.57+15530A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849170 | ||||||
chr17:4849210
|
C | T | 4 | a0001c0005t0002g0150a0001c0005t0012g0152a0001c0005t0022g0149others(1): Show | 4 | HG02145.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+15570C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849210 | ||||||
chr17:4849323
|
C | T | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+15683C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849323 | ||||||
chr17:4849496
|
C | G | 1 | a0002c0002t0001g0308 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+15856C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849496 | ||||||
chr17:4849508
|
T | C | 7 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(4): Show | 7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+15868T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849508 | ||||||
chr17:4849540
|
GCTAACTC others(4): Show |
G | 3 | a0001c0001t0002g0194a0001c0001t0032g0191a0001c0017t0002g0192 | 3 | HG01074.hp2 HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.57+15903_57+15913d others(13): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4849540 | |||||
chr17:4849619
|
C | T | 1 | a0003c0003t0003g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.57+15979C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849619 | ||||||
chr17:4849665
|
T | C | 1 | a0003c0003t0011g0027 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.57+16025T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849665 | ||||||
chr17:4849675
|
G | A | 13 | a0001c0001t0005g0210a0001c0001t0009g0208a0001c0001t0009g0209others(10): Show | 13 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+16035G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849675 | ||||||
chr17:4849784
|
G | C | 1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.57+16144G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849784 | ||||||
chr17:4849895
|
C | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+16255C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849895 | ||||||
chr17:4849981
|
C | T | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+16341C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849981 | ||||||
chr17:4850015
|
T | A | 1 | a0003c0003t0010g0028 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+16375T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850015 | ||||||
chr17:4850188
|
C | T | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+16548C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850188 | ||||||
chr17:4850190
|
AGCAAT | A | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+16553_57+16557d others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4850190 | |||||
chr17:4850364
|
A | C | 1 | a0001c0001t0031g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.57+16724A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850364 | ||||||
chr17:4850439
|
A | G | 22 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(19): Show | 22 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+16799A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850439 | ||||||
chr17:4850519
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+16879G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850519 | ||||||
chr17:4850519
|
G | GC | 138 | a0001c0001t0002g0004a0001c0001t0002g0159a0001c0001t0002g0160others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.57+16887dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4850519 | |||||
chr17:4850528
|
G | A | 1 | a0001c0005t0022g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+16888G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850528 | ||||||
chr17:4851023
|
C | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+17383C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851023 | ||||||
chr17:4851345
|
A | C | 195 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.57+17705A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851345 | ||||||
chr17:4851417
|
T | G | 1 | a0001c0005t0008g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57+17777T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851417 | ||||||
chr17:4851499
|
C | T | 12 | a0001c0001t0005g0210a0001c0001t0009g0208a0001c0001t0009g0209others(9): Show | 12 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+17859C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851499 | ||||||
chr17:4851541
|
A | G | 1 | a0003c0003t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.57+17901A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851541 | ||||||
chr17:4851566
|
T | C | 1 | a0001c0001t0056g0256 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.57+17926T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851566 | ||||||
chr17:4851603
|
T | C | 31 | a0001c0001t0002g0137a0001c0001t0004g0246a0001c0001t0004g0247others(28): Show | 31 | HG00673.hp2 HG01167.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+17963T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851603 | ||||||
chr17:4851732
|
G | A | 159 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.57+18092G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851732 | ||||||
chr17:4851953
|
T | C | 1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.57+18313T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851953 | ||||||
chr17:4851999
|
C | CA | 21 | a0001c0001t0004g0247a0001c0001t0004g0248a0001c0001t0004g0249others(18): Show | 21 | HG00438.hp2 HG01358.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+18387dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4851999
|
C | CAAA | 6 | a0001c0001t0004g0246a0001c0005t0006g0233a0001c0005t0008g0235others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+18385_57+18387d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4851999
|
C | CAAAA | 9 | a0001c0001t0002g0278a0001c0005t0002g0150a0001c0005t0008g0227others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+18384_57+18387d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4851999
|
C | CAAAAAAA | 6 | a0001c0001t0009g0208a0001c0001t0009g0211a0001c0001t0009g0212others(3): Show | 6 | HG02258.hp1 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+18381_57+18387d others(9): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4851999
|
CA | C | 58 | a0001c0001t0003g0062a0001c0001t0005g0243a0001c0001t0007g0119others(55): Show | 59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.57+18387delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4851999
|
CAA | C | 15 | a0001c0001t0002g0155a0001c0001t0002g0171a0001c0001t0002g0173others(12): Show | 16 | HG00735.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+18386_57+18387d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4851999
|
CAAA | C | 150 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0159others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.57+18385_57+18387d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | |||||
chr17:4852023
|
A | C | 138 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.57+18383A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852023 | ||||||
chr17:4852082
|
G | A | 1 | a0001c0001t0009g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+18442G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852082 | ||||||
chr17:4852129
|
A | G | 109 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(106): Show | 110 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.57+18489A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852129 | ||||||
chr17:4852630
|
C | G | 1 | a0001c0001t0004g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+18990C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852630 | ||||||
chr17:4852754
|
G | A | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+19114G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852754 | ||||||
chr17:4852757
|
G | C | 352 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(349): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.57+19117G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852757 | ||||||
chr17:4852758
|
G | A | 352 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(349): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.57+19118G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852758 | ||||||
chr17:4852769
|
T | TGGGGGAG others(466): Show |
1 | a0001c0005t0002g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(475): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(450): Show |
1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(459): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(467): Show |
28 | a0001c0001t0002g0278a0001c0001t0009g0208a0001c0001t0009g0209others(25): Show | 28 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(476): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(612): Show |
5 | a0001c0004t0006g0344a0001c0004t0006g0345a0001c0004t0019g0332others(2): Show | 5 | HG01069.hp2 HG01074.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(621): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(503): Show |
1 | a0004c0006t0012g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(512): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(451): Show |
1 | a0001c0001t0002g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(460): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(555): Show |
1 | a0003c0003t0003g0036 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(553): Show |
1 | a0010c0019t0001g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(562): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(555): Show |
1 | a0001c0001t0025g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(538): Show |
8 | a0001c0001t0002g0137a0001c0001t0025g0138a0001c0001t0025g0139others(5): Show | 8 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(554): Show |
9 | a0001c0001t0020g0148a0002c0002t0001g0005a0002c0002t0001g0309others(6): Show | 10 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(563): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(535): Show |
2 | a0003c0003t0003g0037a0003c0003t0010g0066 | 2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(544): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(549): Show |
1 | a0001c0001t0004g0246 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(558): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(553): Show |
1 | a0001c0001t0007g0122 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(562): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(503): Show |
1 | a0001c0001t0008g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(512): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(521): Show |
44 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(41): Show | 48 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(457): Show |
1 | a0001c0001t0008g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(466): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(607): Show |
1 | a0002c0002t0004g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(616): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(538): Show |
17 | a0001c0001t0004g0248a0001c0001t0004g0249a0001c0001t0004g0250others(14): Show | 17 | HG01358.hp2 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(555): Show |
1 | a0001c0001t0004g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(534): Show |
2 | a0001c0005t0022g0221a0006c0021t0007g0220 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(543): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(537): Show |
62 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0024g0205others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(572): Show |
3 | a0001c0001t0016g0224a0001c0001t0016g0225a0001c0001t0016g0226 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(581): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(538): Show |
2 | a0002c0002t0001g0310a0002c0002t0001g0323 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(521): Show |
1 | a0003c0003t0003g0038 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(554): Show |
1 | a0003c0003t0003g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(563): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(521): Show |
2 | a0003c0003t0010g0031a0003c0003t0010g0039 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(538): Show |
64 | a0001c0001t0003g0062a0001c0001t0023g0244a0001c0001t0023g0245others(61): Show | 65 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(520): Show |
1 | a0003c0003t0003g0034 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(529): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(538): Show |
1 | a0003c0013t0003g0056 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(504): Show |
1 | a0001c0001t0007g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(513): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(555): Show |
1 | a0001c0001t0016g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(520): Show |
3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(529): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(521): Show |
2 | a0002c0002t0035g0070a0003c0003t0010g0008 | 2 | NA19012.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(537): Show |
1 | a0002c0002t0001g0272 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(642): Show |
1 | a0003c0003t0003g0035 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(651): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(572): Show |
2 | a0001c0001t0018g0279a0001c0001t0018g0286 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(581): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(448): Show |
7 | a0001c0001t0002g0163a0001c0001t0002g0170a0001c0001t0002g0171others(4): Show | 7 | NA18940.hp1 NA18950.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(457): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(451): Show |
1 | a0001c0001t0002g0177 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(460): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(452): Show |
42 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(39): Show | 43 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(461): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852769
|
T | TGGGGGAG others(522): Show |
1 | a0001c0001t0048g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(531): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | |||||
chr17:4852776
|
G | GTGTGGTT others(537): Show |
1 | a0002c0002t0001g0317 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852776 | |||||
chr17:4852785
|
A | G | 24 | a0001c0001t0007g0119a0001c0004t0006g0329a0001c0004t0006g0331others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19145A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852785 | ||||||
chr17:4852790
|
T | G | 24 | a0001c0001t0007g0119a0001c0004t0006g0329a0001c0004t0006g0331others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19150T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852790 | ||||||
chr17:4852798
|
G | GA | 4 | a0001c0001t0007g0119a0001c0008t0002g0156a0001c0008t0002g0157others(1): Show | 4 | HG02615.hp2 HG02717.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+19158_57+19159i others(3): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852798 | ||||||
chr17:4852799
|
T | A | 20 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.57+19159T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852799 | ||||||
chr17:4852802
|
G | GTGGGGGA others(537): Show |
1 | a0001c0001t0007g0119 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.57+19162_57+19163i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852802 | ||||||
chr17:4852802
|
G | GTGGGGGA others(468): Show |
3 | a0001c0008t0002g0156a0001c0008t0002g0157a0001c0008t0002g0158 | 3 | HG02615.hp2 HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.57+19162_57+19163i others(477): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852802 | ||||||
chr17:4852802
|
G | T | 20 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.57+19162G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852802 | ||||||
chr17:4852816
|
G | GTTGGTGG others(578): Show |
1 | a0001c0018t0004g0333 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.57+19178_57+19179i others(587): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | |||||
chr17:4852816
|
G | GTTGGTGG others(578): Show |
16 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(13): Show | 16 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+19178_57+19179i others(587): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | |||||
chr17:4852816
|
G | GTTGGTGG others(595): Show |
2 | a0001c0004t0006g0342a0001c0004t0019g0336 | 2 | NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.57+19178_57+19179i others(604): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | |||||
chr17:4852816
|
G | GTTGGTGG others(595): Show |
1 | a0001c0004t0042g0346 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.57+19178_57+19179i others(604): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | |||||
chr17:4852819
|
T | G | 25 | a0001c0001t0007g0119a0001c0001t0020g0148a0001c0004t0006g0329others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+19179T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852819 | ||||||
chr17:4852833
|
GTT | G | 7 | a0001c0001t0007g0087a0001c0001t0007g0099a0001c0001t0007g0102others(4): Show | 7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19194_57+19195d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852833 | ||||||
chr17:4852836
|
G | C | 7 | a0001c0001t0007g0087a0001c0001t0007g0099a0001c0001t0007g0102others(4): Show | 7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19196G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852836 | ||||||
chr17:4852836
|
G | T | 20 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.57+19196G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852836 | ||||||
chr17:4852837
|
G | C | 7 | a0001c0001t0007g0087a0001c0001t0007g0099a0001c0001t0007g0102others(4): Show | 7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19197G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852837 | ||||||
chr17:4852884
|
A | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+19244A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852884 | ||||||
chr17:4852887
|
T | G | 27 | a0001c0001t0046g0197a0001c0001t0055g0198a0001c0004t0006g0329others(24): Show | 27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+19247T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852887 | ||||||
chr17:4852901
|
G | A | 5 | a0001c0004t0006g0344a0001c0004t0006g0345a0001c0004t0019g0332others(2): Show | 5 | HG01069.hp2 HG01074.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+19261G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852901 | ||||||
chr17:4852904
|
G | GGTGGGGG others(10): Show |
20 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.57+19277_57+19278i others(19): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852904 | |||||
chr17:4852904
|
G | T | 5 | a0001c0004t0006g0344a0001c0004t0006g0345a0001c0004t0019g0332others(2): Show | 5 | HG01069.hp2 HG01074.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+19264G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852904 | ||||||
chr17:4853012
|
G | A | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.57+19372G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853012 | ||||||
chr17:4853076
|
A | ATGGGGGG others(11): Show |
1 | a0003c0003t0003g0055 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+19443_57+19460d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853076 | |||||
chr17:4853089
|
G | A | 1 | a0003c0003t0010g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.57+19449G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853089 | ||||||
chr17:4853123
|
T | TTGGGGGA others(10): Show |
3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+19483_57+19484i others(19): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853123 | ||||||
chr17:4853124
|
G | GGGAGTGT others(7): Show |
1 | a0001c0001t0005g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+19486_57+19487i others(16): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853124 | |||||
chr17:4853124
|
G | GGGGGGAG others(10): Show |
306 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(303): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.57+19517_57+19533d others(19): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853124 | |||||
chr17:4853124
|
G | T | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+19484G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853124 | ||||||
chr17:4853132
|
T | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+19492T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853132 | ||||||
chr17:4853173
|
G | GGTGGGGG others(28): Show |
24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19533_57+19534i others(37): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853173 | ||||||
chr17:4853174
|
A | G | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19534A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853174 | ||||||
chr17:4853174
|
A | T | 1 | a0001c0011t0041g0347 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+19534A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853174 | ||||||
chr17:4853205
|
TTGG | T | 4 | a0001c0004t0027g0059a0003c0007t0003g0002a0003c0007t0003g0060others(1): Show | 5 | HG02135.hp1 NA18949.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+19569_57+19571d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853205 | |||||
chr17:4853213
|
G | A | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19573G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853213 | ||||||
chr17:4853214
|
G | A | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19574G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853214 | ||||||
chr17:4853214
|
G | GGAGTGTG others(11): Show |
1 | a0001c0011t0041g0347 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+19588_57+19589i others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853214 | |||||
chr17:4853272
|
G | T | 1 | a0001c0005t0022g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+19632G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853272 | ||||||
chr17:4853300
|
GGAGTGTG others(11): Show |
G | 1 | a0001c0001t0002g0190 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.57+19677_57+19694d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853300 | |||||
chr17:4853352
|
A | AAGAGTGT others(8): Show |
1 | a0001c0001t0008g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.57+19713_57+19727d others(17): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853352 | |||||
chr17:4853368
|
GGAGTGTG others(11): Show |
G | 2 | a0003c0003t0003g0040a0003c0003t0003g0041 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.57+19741_57+19758d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853368 | |||||
chr17:4853423
|
T | C | 51 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.57+19783T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853423 | ||||||
chr17:4853500
|
G | C | 76 | a0001c0001t0003g0062a0001c0001t0023g0244a0001c0001t0023g0245others(73): Show | 77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.57+19860G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853500 | ||||||
chr17:4853620
|
T | G | 132 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.57+19980T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853620 | ||||||
chr17:4854228
|
C | G | 2 | a0002c0002t0001g0270a0002c0002t0001g0271 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.57+20588C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854228 | ||||||
chr17:4854303
|
T | C | 109 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(106): Show | 110 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.57+20663T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854303 | ||||||
chr17:4854434
|
G | C | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+20794G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854434 | ||||||
chr17:4854482
|
T | G | 84 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(81): Show | 85 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.57+20842T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854482 | ||||||
chr17:4854565
|
G | C | 3 | a0001c0001t0004g0248a0001c0001t0004g0249a0001c0001t0004g0250 | 3 | HG02486.hp2 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.57+20925G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854565 | ||||||
chr17:4854566
|
T | C | 71 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(68): Show | 72 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.57+20926T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854566 | ||||||
chr17:4854879
|
C | A | 339 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(336): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.57+21239C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854879 | ||||||
chr17:4854949
|
A | G | 84 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(81): Show | 85 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.57+21309A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854949 | ||||||
chr17:4855023
|
A | G | 1 | a0001c0018t0004g0333 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.57+21383A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855023 | ||||||
chr17:4855190
|
T | TAA | 72 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0056g0256others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.57+21563_57+21564d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855190 | |||||
chr17:4855190
|
TA | T | 28 | a0001c0001t0029g0132a0001c0004t0006g0329a0001c0004t0006g0331others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+21564delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855190 | |||||
chr17:4855226
|
C | G | 3 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204 | 3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+21586C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855226 | ||||||
chr17:4855235
|
C | T | 20 | a0001c0001t0056g0256a0002c0002t0001g0254a0002c0002t0001g0255others(17): Show | 20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+21595C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855235 | ||||||
chr17:4855314
|
G | A | 1 | a0001c0005t0008g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.57+21674G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855314 | ||||||
chr17:4855403
|
G | A | 1 | a0002c0002t0015g0280 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.57+21763G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855403 | ||||||
chr17:4855485
|
C | CA | 211 | a0001c0001t0002g0277a0001c0001t0003g0062a0001c0001t0004g0246others(208): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.57+21860dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855485 | |||||
chr17:4855485
|
C | CAA | 114 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(111): Show | 115 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.57+21859_57+21860d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855485 | |||||
chr17:4855485
|
C | CAAA | 8 | a0001c0001t0002g0155a0001c0001t0002g0170a0001c0001t0002g0173others(5): Show | 8 | HG00621.hp1 HG00741.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+21858_57+21860d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855485 | |||||
chr17:4855504
|
C | T | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+21864C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855504 | ||||||
chr17:4855505
|
G | A | 1 | a0001c0005t0054g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.57+21865G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855505 | ||||||
chr17:4855553
|
C | T | 83 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(80): Show | 84 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.57+21913C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855553 | ||||||
chr17:4855556
|
G | A | 2 | a0001c0005t0022g0221a0006c0021t0007g0220 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+21916G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855556 | ||||||
chr17:4855687
|
G | A | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+22047G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855687 | ||||||
chr17:4855726
|
C | T | 5 | a0001c0001t0007g0087a0001c0001t0007g0099a0001c0001t0007g0104others(2): Show | 5 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+22086C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855726 | ||||||
chr17:4855752
|
A | G | 3 | a0003c0003t0003g0007a0003c0003t0003g0036a0003c0003t0026g0082 | 3 | HG00280.hp2 NA18967.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.57+22112A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855752 | ||||||
chr17:4855769
|
C | CA | 9 | a0001c0001t0002g0129a0001c0001t0002g0190a0001c0001t0007g0107others(6): Show | 9 | HG00741.hp1 HG01993.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+22147dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855769 | |||||
chr17:4855769
|
C | CAA | 20 | a0001c0004t0006g0329a0001c0004t0006g0337a0001c0004t0006g0338others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.57+22146_57+22147d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855769 | |||||
chr17:4855784
|
A | G | 2 | a0002c0002t0001g0270a0002c0002t0001g0271 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.57+22144A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855784 | ||||||
chr17:4855785
|
A | G | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+22145A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855785 | ||||||
chr17:4856046
|
G | C | 1 | a0002c0002t0001g0264 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.58-22271G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856046 | ||||||
chr17:4856048
|
C | T | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-22269C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856048 | ||||||
chr17:4856429
|
C | T | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-21888C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856429 | ||||||
chr17:4856436
|
T | C | 1 | a0003c0003t0003g0034 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58-21881T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856436 | ||||||
chr17:4856491
|
C | T | 2 | a0002c0002t0001g0285a0002c0002t0001g0317 | 2 | HG01168.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.58-21826C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856491 | ||||||
chr17:4856510
|
G | A | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-21807G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856510 | ||||||
chr17:4856564
|
G | A | 2 | a0002c0002t0001g0283a0002c0002t0001g0284 | 2 | HG00735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.58-21753G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856564 | ||||||
chr17:4856657
|
C | G | 28 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(25): Show | 28 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.58-21660C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856657 | ||||||
chr17:4856736
|
C | G | 74 | a0001c0001t0003g0062a0001c0001t0007g0093a0001c0001t0014g0092others(71): Show | 75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.58-21581C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856736 | ||||||
chr17:4856837
|
G | C | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-21480G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856837 | ||||||
chr17:4856891
|
G | T | 1 | a0001c0001t0002g0194 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58-21426G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856891 | ||||||
chr17:4857115
|
C | T | 1 | a0001c0001t0018g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-21202C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857115 | ||||||
chr17:4857313
|
A | G | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-21004A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857313 | ||||||
chr17:4857422
|
T | C | 2 | a0001c0001t0008g0083a0001c0001t0008g0127 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.58-20895T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857422 | ||||||
chr17:4857458
|
G | GT | 152 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0160others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.58-20833dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | |||||
chr17:4857458
|
G | GTT | 41 | a0001c0001t0002g0277a0001c0001t0009g0208a0001c0001t0009g0209others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-20834_58-20833d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | |||||
chr17:4857458
|
G | GTTT | 5 | a0001c0001t0018g0286a0002c0002t0001g0005a0002c0002t0001g0310others(2): Show | 6 | HG00642.hp1 HG01175.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-20835_58-20833d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | |||||
chr17:4857458
|
GT | G | 9 | a0001c0005t0022g0221a0002c0002t0004g0140a0002c0002t0004g0141others(6): Show | 9 | HG00558.hp2 HG02165.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-20833delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | |||||
chr17:4857670
|
G | A | 1 | a0001c0001t0056g0256 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.58-20647G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857670 | ||||||
chr17:4857938
|
GAACTT | G | 31 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(28): Show | 31 | HG00642.hp2 HG01168.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.58-20371_58-20367d others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857938 | |||||
chr17:4858045
|
G | T | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-20272G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858045 | ||||||
chr17:4858100
|
T | C | 44 | a0001c0004t0027g0059a0002c0002t0035g0070a0003c0003t0003g0006others(41): Show | 45 | HG00280.hp2 HG00423.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.58-20217T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858100 | ||||||
chr17:4858180
|
A | G | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-20137A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858180 | ||||||
chr17:4858296
|
G | C | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-20021G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858296 | ||||||
chr17:4858467
|
A | T | 139 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.58-19850A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858467 | ||||||
chr17:4858479
|
A | AT | 12 | a0001c0001t0002g0129a0001c0001t0005g0114a0001c0001t0017g0124others(9): Show | 12 | HG02293.hp2 HG02523.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-19823dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4858479 | |||||
chr17:4858479
|
A | T | 1 | a0002c0002t0001g0272 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.58-19838A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858479 | ||||||
chr17:4858479
|
AT | A | 50 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(47): Show | 50 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-19823delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4858479 | |||||
chr17:4858617
|
C | T | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-19700C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858617 | ||||||
chr17:4858665
|
T | C | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-19652T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858665 | ||||||
chr17:4858740
|
A | C | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-19577A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858740 | ||||||
chr17:4858827
|
G | A | 1 | a0002c0002t0001g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58-19490G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858827 | ||||||
chr17:4858963
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.58-19354G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858963 | ||||||
chr17:4858974
|
C | G | 1 | a0002c0002t0001g0289 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58-19343C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858974 | ||||||
chr17:4858995
|
AC | A | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-19319delC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4858995 | |||||
chr17:4859077
|
C | T | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-19240C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859077 | ||||||
chr17:4859586
|
G | A | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-18731G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859586 | ||||||
chr17:4859769
|
CAA | C | 11 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-18547_58-18546d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859769 | ||||||
chr17:4859788
|
C | CA | 78 | a0001c0001t0004g0246a0001c0001t0004g0249a0001c0001t0004g0250others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.58-18502dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
C | CAA | 21 | a0001c0001t0002g0277a0001c0001t0004g0247a0001c0001t0004g0248others(18): Show | 21 | HG00642.hp2 HG00673.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.58-18503_58-18502d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
C | CAAA | 8 | a0001c0001t0002g0137a0001c0001t0004g0282a0001c0001t0029g0132others(5): Show | 8 | HG00673.hp1 HG03139.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-18504_58-18502d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
C | CAAAA | 9 | a0001c0004t0006g0331a0001c0004t0006g0335a0001c0004t0006g0341others(6): Show | 9 | HG01074.hp1 NA18954.hp1 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-18505_58-18502d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
C | CAAAAA | 9 | a0001c0004t0006g0337a0001c0004t0006g0338a0001c0004t0006g0340others(6): Show | 9 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-18506_58-18502d others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
CA | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0160others(56): Show | 60 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.58-18502delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
CAAAAAAA others(1): Show |
C | 69 | a0001c0001t0003g0062a0001c0004t0027g0059a0002c0002t0035g0070others(66): Show | 70 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.58-18509_58-18502d others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859788
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0009g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58-18514_58-18502d others(15): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | |||||
chr17:4859863
|
TA | T | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-18444delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859863 | |||||
chr17:4859903
|
T | C | 1 | a0001c0001t0018g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-18414T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859903 | ||||||
chr17:4859911
|
C | T | 1 | a0001c0001t0007g0106 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.58-18406C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859911 | ||||||
chr17:4860031
|
T | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-18286T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860031 | ||||||
chr17:4860256
|
T | C | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-18061T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860256 | ||||||
chr17:4860312
|
A | G | 1 | a0001c0005t0054g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58-18005A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860312 | ||||||
chr17:4860484
|
TAATC | T | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-17830_58-17827d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4860484 | |||||
chr17:4860732
|
T | C | 2 | a0003c0003t0028g0016a0009c0016t0028g0015 | 2 | NA18995.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.58-17585T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860732 | ||||||
chr17:4860946
|
G | A | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-17371G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860946 | ||||||
chr17:4861064
|
C | T | 135 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.58-17253C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861064 | ||||||
chr17:4861257
|
C | T | 1 | a0002c0002t0001g0315 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.58-17060C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861257 | ||||||
chr17:4861395
|
G | A | 1 | a0001c0001t0029g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.58-16922G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861395 | ||||||
chr17:4861694
|
T | G | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-16623T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861694 | ||||||
chr17:4861748
|
G | A | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-16569G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861748 | ||||||
chr17:4861807
|
A | G | 1 | a0001c0005t0008g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.58-16510A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861807 | ||||||
chr17:4861950
|
T | C | 1 | a0001c0001t0005g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.58-16367T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861950 | ||||||
chr17:4862168
|
C | G | 28 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(25): Show | 28 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.58-16149C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862168 | ||||||
chr17:4862425
|
C | T | 11 | a0001c0005t0006g0233a0001c0005t0008g0227a0001c0005t0008g0228others(8): Show | 11 | HG00642.hp2 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-15892C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862425 | ||||||
chr17:4862465
|
G | A | 1 | a0010c0019t0001g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.58-15852G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862465 | ||||||
chr17:4862470
|
C | T | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-15847C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862470 | ||||||
chr17:4862506
|
C | T | 193 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.58-15811C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862506 | ||||||
chr17:4862569
|
G | A | 51 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-15748G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862569 | ||||||
chr17:4862608
|
T | C | 193 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.58-15709T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862608 | ||||||
chr17:4862611
|
G | A | 51 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-15706G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862611 | ||||||
chr17:4862653
|
CA | C | 59 | a0001c0001t0002g0186a0001c0001t0007g0107a0001c0001t0009g0208others(56): Show | 59 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.58-15651delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4862653 | |||||
chr17:4862759
|
G | A | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-15558G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862759 | ||||||
chr17:4862791
|
T | C | 206 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.58-15526T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862791 | ||||||
chr17:4862849
|
C | T | 54 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(51): Show | 54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-15468C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862849 | ||||||
chr17:4862881
|
A | C | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-15436A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862881 | ||||||
chr17:4862986
|
A | G | 193 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.58-15331A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862986 | ||||||
chr17:4863160
|
A | G | 202 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.58-15157A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863160 | ||||||
chr17:4863245
|
T | C | 43 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(40): Show | 43 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.58-15072T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863245 | ||||||
chr17:4863304
|
C | G | 16 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(13): Show | 16 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-15013C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863304 | ||||||
chr17:4863334
|
C | T | 5 | a0002c0002t0001g0302a0002c0002t0001g0305a0002c0002t0001g0327others(2): Show | 5 | HG00423.hp2 NA18988.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-14983C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863334 | ||||||
chr17:4863509
|
G | C | 72 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0056g0256others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.58-14808G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863509 | ||||||
chr17:4863598
|
C | T | 75 | a0001c0001t0002g0159a0001c0001t0002g0199a0001c0001t0002g0222others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.58-14719C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863598 | ||||||
chr17:4863642
|
T | C | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-14675T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863642 | ||||||
chr17:4863652
|
A | G | 1 | a0001c0001t0017g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.58-14665A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863652 | ||||||
chr17:4863780
|
C | CATT | 157 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.58-14515_58-14513d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4863780 | |||||
chr17:4863780
|
C | CATTATT | 5 | a0001c0001t0016g0225a0001c0001t0046g0197a0001c0001t0055g0198others(2): Show | 5 | HG01069.hp1 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-14518_58-14513d others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4863780 | |||||
chr17:4864212
|
C | T | 1 | a0002c0002t0001g0315 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.58-14105C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864212 | ||||||
chr17:4864213
|
G | A | 4 | a0001c0001t0020g0148a0001c0001t0024g0205a0001c0001t0024g0207others(1): Show | 4 | HG01167.hp1 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-14104G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864213 | ||||||
chr17:4864292
|
G | C | 55 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(52): Show | 55 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-14025G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864292 | ||||||
chr17:4864501
|
G | A | 1 | a0002c0002t0015g0325 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58-13816G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864501 | ||||||
chr17:4864514
|
T | C | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-13803T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864514 | ||||||
chr17:4864652
|
G | A | 3 | a0002c0002t0001g0257a0002c0002t0001g0264a0002c0002t0001g0272 | 3 | HG00140.hp2 HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.58-13665G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864652 | ||||||
chr17:4864680
|
G | A | 1 | a0001c0005t0054g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58-13637G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864680 | ||||||
chr17:4864680
|
G | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.58-13637G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864680 | ||||||
chr17:4864778
|
C | T | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-13539C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864778 | ||||||
chr17:4864913
|
C | G | 1 | a0003c0003t0039g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.58-13404C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864913 | ||||||
chr17:4865001
|
C | T | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58-13316C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865001 | ||||||
chr17:4865071
|
C | G | 1 | a0002c0002t0001g0293 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.58-13246C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865071 | ||||||
chr17:4865082
|
ATTTTTAT others(7): Show |
A | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-13223_58-13210d others(16): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865082 | |||||
chr17:4865202
|
G | A | 2 | a0002c0002t0001g0303a0002c0002t0001g0306 | 2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.58-13115G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865202 | ||||||
chr17:4865272
|
AAC | A | 55 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(52): Show | 55 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-13039_58-13038d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865272 | |||||
chr17:4865300
|
G | C | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-13017G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865300 | ||||||
chr17:4865436
|
A | AAAAT | 11 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(8): Show | 11 | HG00673.hp2 HG03710.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-12858_58-12855d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865436 | |||||
chr17:4865472
|
G | A | 2 | a0002c0002t0001g0303a0002c0002t0001g0306 | 2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.58-12845G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865472 | ||||||
chr17:4865548
|
C | A | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-12769C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865548 | ||||||
chr17:4865551
|
C | G | 2 | a0002c0002t0004g0267a0002c0002t0004g0268 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.58-12766C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865551 | ||||||
chr17:4865674
|
G | T | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-12643G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865674 | ||||||
chr17:4865719
|
C | CA | 27 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(24): Show | 27 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.58-12578dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | |||||
chr17:4865719
|
CA | C | 212 | a0001c0001t0002g0129a0001c0001t0002g0137a0001c0001t0002g0277others(209): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.58-12578delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | |||||
chr17:4865719
|
CAA | C | 33 | a0001c0001t0002g0162a0001c0001t0002g0176a0001c0001t0013g0075others(30): Show | 33 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.58-12579_58-12578d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | |||||
chr17:4865719
|
CAAA | C | 51 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(48): Show | 52 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.58-12580_58-12578d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | |||||
chr17:4865835
|
C | T | 2 | a0001c0001t0007g0122a0001c0001t0007g0123 | 2 | NA18967.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.58-12482C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865835 | ||||||
chr17:4865879
|
AGT | A | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-12436_58-12435d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865879 | |||||
chr17:4865942
|
G | A | 5 | a0001c0005t0002g0150a0001c0005t0012g0152a0001c0005t0022g0149others(2): Show | 5 | HG02145.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-12375G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865942 | ||||||
chr17:4866123
|
C | T | 39 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0159others(36): Show | 40 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.58-12194C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866123 | ||||||
chr17:4866268
|
C | G | 1 | a0001c0004t0006g0351 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.58-12049C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866268 | ||||||
chr17:4866471
|
TA | T | 9 | a0001c0001t0008g0083a0001c0001t0030g0085a0001c0001t0030g0098others(6): Show | 9 | HG01069.hp1 HG01081.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-11831delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866471 | |||||
chr17:4866515
|
G | A | 4 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0187others(1): Show | 4 | HG00741.hp1 HG01070.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-11802G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866515 | ||||||
chr17:4866527
|
T | C | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58-11790T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866527 | ||||||
chr17:4866609
|
C | CA | 18 | a0001c0001t0005g0110a0001c0001t0012g0096a0001c0001t0012g0097others(15): Show | 18 | HG00438.hp2 HG00673.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.58-11691dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866609 | |||||
chr17:4866609
|
CA | C | 60 | a0001c0001t0002g0176a0001c0001t0009g0208a0001c0001t0009g0209others(57): Show | 60 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.58-11691delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866609 | |||||
chr17:4866609
|
CAA | C | 132 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.58-11692_58-11691d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866609 | |||||
chr17:4866659
|
C | T | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-11658C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866659 | ||||||
chr17:4866796
|
G | A | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-11521G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866796 | ||||||
chr17:4866799
|
C | T | 51 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-11518C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866799 | ||||||
chr17:4866849
|
G | A | 3 | a0001c0008t0002g0156a0001c0008t0002g0157a0001c0008t0002g0158 | 3 | HG02615.hp2 HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.58-11468G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866849 | ||||||
chr17:4866859
|
G | T | 1 | a0001c0004t0027g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.58-11458G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866859 | ||||||
chr17:4866902
|
T | C | 45 | a0001c0001t0002g0277a0002c0002t0001g0005a0002c0002t0001g0281others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.58-11415T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866902 | ||||||
chr17:4866929
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.58-11388C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866929 | ||||||
chr17:4867074
|
A | AAAT | 27 | a0001c0001t0002g0137a0001c0001t0004g0247a0001c0001t0004g0248others(24): Show | 28 | HG00438.hp2 HG00621.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.58-11213_58-11211d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAAT | 52 | a0001c0001t0003g0062a0001c0001t0018g0279a0001c0001t0018g0286others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-11216_58-11211d others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(2): Show |
58 | a0001c0001t0002g0202a0001c0001t0050g0131a0001c0004t0006g0331others(55): Show | 58 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.58-11219_58-11211d others(11): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(5): Show |
56 | a0001c0001t0002g0277a0001c0001t0016g0223a0001c0001t0016g0224others(53): Show | 57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.58-11222_58-11211d others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(8): Show |
26 | a0001c0001t0002g0166a0001c0001t0002g0168a0001c0001t0002g0169others(23): Show | 26 | HG00140.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.58-11225_58-11211d others(17): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(11): Show |
38 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(35): Show | 39 | HG00544.hp2 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.58-11228_58-11211d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(14): Show |
19 | a0001c0001t0002g0160a0001c0001t0002g0165a0001c0001t0002g0175others(16): Show | 19 | HG00099.hp1 HG01074.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-11231_58-11211d others(23): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(17): Show |
5 | a0001c0001t0002g0173a0001c0001t0002g0184a0001c0001t0005g0210others(2): Show | 5 | HG01928.hp1 HG02004.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-11234_58-11211d others(26): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | AAATAATA others(20): Show |
3 | a0001c0001t0002g0159a0001c0001t0002g0185a0001c0001t0002g0186 | 3 | HG00639.hp1 HG02273.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.58-11237_58-11211d others(29): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | |||||
chr17:4867074
|
A | ATAAT | 3 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204 | 3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-11243_58-11242i others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867074 | ||||||
chr17:4867104
|
T | TAATAATA others(11): Show |
3 | a0001c0001t0009g0214a0001c0001t0009g0219a0001c0014t0009g0216 | 3 | HG01168.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.58-11211_58-11210i others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867104 | |||||
chr17:4867104
|
T | TAATAATA others(14): Show |
2 | a0001c0001t0002g0200a0001c0001t0009g0213 | 2 | HG01175.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.58-11211_58-11210i others(23): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867104 | |||||
chr17:4867104
|
T | TAATAATA others(17): Show |
1 | a0001c0001t0051g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-11211_58-11210i others(26): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867104 | |||||
chr17:4867105
|
A | AATAATAA others(13): Show |
1 | a0001c0001t0002g0193 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.58-11211_58-11210i others(22): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867105 | |||||
chr17:4867138
|
G | GTT | 7 | a0001c0001t0005g0237a0001c0001t0005g0242a0001c0005t0008g0227others(4): Show | 7 | HG00642.hp2 HG01358.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-11153_58-11152d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | |||||
chr17:4867138
|
G | GTTT | 13 | a0001c0001t0009g0211a0001c0001t0009g0212a0001c0001t0009g0213others(10): Show | 13 | HG01168.hp1 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-11154_58-11152d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | |||||
chr17:4867138
|
G | GTTTT | 10 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0215others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-11155_58-11152d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | |||||
chr17:4867138
|
GTT | G | 81 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0159others(78): Show | 82 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.58-11153_58-11152d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | |||||
chr17:4867138
|
GTTT | G | 216 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0163others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.58-11154_58-11152d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | |||||
chr17:4867138
|
GTTTT | G | 8 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(5): Show | 8 | HG00673.hp2 HG01993.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-11155_58-11152d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | |||||
chr17:4867147
|
T | G | 1 | a0001c0001t0002g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.58-11170T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867147 | ||||||
chr17:4867148
|
T | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-11169T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867148 | ||||||
chr17:4867153
|
T | G | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-11164T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867153 | ||||||
chr17:4867154
|
T | G | 49 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(46): Show | 53 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.58-11163T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867154 | ||||||
chr17:4867158
|
T | G | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-11159T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867158 | ||||||
chr17:4867388
|
A | G | 1 | a0001c0001t0005g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58-10929A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867388 | ||||||
chr17:4867750
|
G | A | 1 | a0003c0003t0010g0065 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.58-10567G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867750 | ||||||
chr17:4867768
|
C | T | 74 | a0001c0001t0003g0062a0001c0004t0006g0135a0001c0004t0006g0136others(71): Show | 75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.58-10549C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867768 | ||||||
chr17:4867829
|
G | T | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-10488G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867829 | ||||||
chr17:4867890
|
A | G | 1 | a0001c0004t0006g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.58-10427A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867890 | ||||||
chr17:4867971
|
CT | C | 8 | a0001c0001t0002g0159a0001c0001t0020g0148a0001c0001t0024g0205others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-10331delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867971 | |||||
chr17:4867971
|
CTT | C | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-10332_58-10331d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867971 | |||||
chr17:4868125
|
C | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.58-10192C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868125 | ||||||
chr17:4868133
|
C | T | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-10184C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868133 | ||||||
chr17:4868180
|
T | C | 1 | a0003c0003t0011g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.58-10137T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868180 | ||||||
chr17:4868204
|
T | C | 1 | a0001c0001t0007g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.58-10113T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868204 | ||||||
chr17:4868252
|
C | T | 2 | a0001c0001t0047g0130a0001c0001t0048g0095 | 2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.58-10065C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868252 | ||||||
chr17:4868256
|
C | T | 34 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(31): Show | 34 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.58-10061C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868256 | ||||||
chr17:4868391
|
C | T | 11 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-9926C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868391 | ||||||
chr17:4868431
|
T | C | 1 | a0002c0002t0001g0308 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-9886T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868431 | ||||||
chr17:4868444
|
C | T | 1 | a0003c0003t0010g0028 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.58-9873C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868444 | ||||||
chr17:4868488
|
A | G | 3 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204 | 3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-9829A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868488 | ||||||
chr17:4868549
|
A | G | 1 | a0001c0001t0051g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-9768A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868549 | ||||||
chr17:4868585
|
C | G | 2 | a0001c0001t0009g0219a0001c0014t0009g0216 | 2 | HG01168.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.58-9732C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868585 | ||||||
chr17:4868798
|
C | T | 3 | a0002c0002t0001g0294a0002c0002t0001g0319a0002c0002t0001g0320 | 3 | HG00140.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58-9519C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868798 | ||||||
chr17:4868816
|
G | A | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-9501G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868816 | ||||||
chr17:4868952
|
C | G | 1 | a0001c0001t0008g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.58-9365C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868952 | ||||||
chr17:4869033
|
C | T | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-9284C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869033 | ||||||
chr17:4869084
|
C | T | 1 | a0002c0002t0001g0109 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.58-9233C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869084 | ||||||
chr17:4869115
|
G | A | 28 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(25): Show | 28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.58-9202G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869115 | ||||||
chr17:4869219
|
C | T | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-9098C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869219 | ||||||
chr17:4869242
|
ATTATTAT others(4): Show |
A | 20 | a0001c0004t0006g0331a0001c0004t0006g0335a0001c0004t0006g0337others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-9069_58-9059del others(11): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869242 | |||||
chr17:4869242
|
ATTATTAT others(8): Show |
A | 4 | a0001c0004t0019g0332a0001c0004t0019g0336a0001c0004t0019g0343others(1): Show | 4 | HG01243.hp2 HG01517.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9069_58-9055del others(15): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869242 | |||||
chr17:4869245
|
A | ATTAT | 23 | a0001c0001t0005g0094a0001c0001t0005g0115a0001c0001t0007g0099others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.58-9029_58-9026dup others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | |||||
chr17:4869245
|
ATTAT | A | 30 | a0001c0001t0002g0137a0001c0001t0004g0246a0001c0001t0004g0282others(27): Show | 30 | HG00673.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.58-9029_58-9026del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | |||||
chr17:4869245
|
ATTATTTA others(1): Show |
A | 14 | a0001c0001t0009g0213a0001c0001t0009g0214a0001c0001t0009g0219others(11): Show | 14 | HG01168.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.58-9033_58-9026del others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | |||||
chr17:4869245
|
ATTATTTA others(5): Show |
A | 7 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(4): Show | 7 | HG02055.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-9037_58-9026del others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | |||||
chr17:4869245
|
ATTATTTA others(13): Show |
A | 135 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.58-9045_58-9026del others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | |||||
chr17:4869333
|
A | G | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58-8984A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869333 | ||||||
chr17:4869345
|
C | T | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-8972C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869345 | ||||||
chr17:4869397
|
C | A | 1 | a0001c0001t0002g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.58-8920C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869397 | ||||||
chr17:4869405
|
T | C | 1 | a0001c0001t0018g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-8912T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869405 | ||||||
chr17:4869466
|
G | A | 55 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(52): Show | 55 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-8851G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869466 | ||||||
chr17:4869467
|
G | A | 55 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(52): Show | 55 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-8850G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869467 | ||||||
chr17:4869502
|
C | T | 1 | a0001c0005t0008g0229 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.58-8815C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869502 | ||||||
chr17:4869513
|
GTGATCCT others(251): Show |
G | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58-8803_58-8546del | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869513 | ||||||
chr17:4869626
|
C | T | 1 | a0001c0004t0006g0136 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.58-8691C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869626 | ||||||
chr17:4869749
|
C | CT | 10 | a0001c0001t0009g0276a0001c0004t0019g0332a0001c0004t0019g0336others(7): Show | 10 | HG00140.hp1 HG01109.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-8557dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869749 | |||||
chr17:4869749
|
C | CTT | 20 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.58-8558_58-8557dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869749 | |||||
chr17:4869749
|
C | T | 1 | a0001c0004t0006g0339 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.58-8568C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869749 | ||||||
chr17:4869749
|
CT | C | 8 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(5): Show | 8 | HG00140.hp2 HG00673.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-8557delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869749 | |||||
chr17:4869821
|
G | GTTTA | 5 | a0001c0001t0007g0093a0001c0001t0014g0092a0001c0004t0006g0339others(2): Show | 5 | NA18943.hp1 NA18973.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-8468_58-8465dup others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | |||||
chr17:4869821
|
G | GTTTATTT others(1): Show |
21 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(18): Show | 21 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.58-8472_58-8465dup others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | |||||
chr17:4869821
|
G | GTTTATTT others(5): Show |
2 | a0001c0004t0006g0344a0001c0004t0006g0345 | 2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.58-8476_58-8465dup others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | |||||
chr17:4869821
|
GTTTA | G | 164 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(161): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.58-8468_58-8465del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | |||||
chr17:4869825
|
A | G | 1 | a0003c0003t0011g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.58-8492A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869825 | ||||||
chr17:4869837
|
A | G | 1 | a0001c0001t0005g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58-8480A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869837 | ||||||
chr17:4869914
|
C | CT | 11 | a0001c0005t0006g0233a0001c0005t0008g0227a0001c0005t0008g0228others(8): Show | 11 | HG00642.hp2 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-8393dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869914 | |||||
chr17:4869946
|
GC | G | 352 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(349): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.58-8367delC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869946 | |||||
chr17:4869991
|
C | T | 1 | a0002c0002t0015g0295 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.58-8326C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869991 | ||||||
chr17:4870134
|
G | A | 36 | a0001c0001t0002g0137a0001c0001t0009g0208a0001c0001t0009g0209others(33): Show | 36 | HG00642.hp2 HG00673.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.58-8183G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870134 | ||||||
chr17:4870207
|
C | T | 1 | a0005c0009t0053g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-8110C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870207 | ||||||
chr17:4870213
|
A | AT | 11 | a0001c0001t0002g0129a0001c0001t0004g0246a0001c0001t0004g0247others(8): Show | 11 | HG01358.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-8083dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4870213 | |||||
chr17:4870213
|
AT | A | 28 | a0001c0001t0002g0183a0001c0001t0002g0193a0001c0001t0021g0079others(25): Show | 28 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.58-8083delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4870213 | |||||
chr17:4870213
|
ATT | A | 31 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(28): Show | 31 | HG00642.hp2 HG01069.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.58-8084_58-8083del others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4870213 | |||||
chr17:4870277
|
G | A | 1 | a0003c0003t0003g0034 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58-8040G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870277 | ||||||
chr17:4870296
|
T | C | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58-8021T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870296 | ||||||
chr17:4870526
|
C | T | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58-7791C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870526 | ||||||
chr17:4870695
|
C | T | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-7622C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870695 | ||||||
chr17:4870789
|
C | T | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-7528C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870789 | ||||||
chr17:4870794
|
C | T | 1 | a0001c0004t0027g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.58-7523C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870794 | ||||||
chr17:4871046
|
G | A | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-7271G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871046 | ||||||
chr17:4871181
|
A | AT | 14 | a0001c0001t0002g0137a0001c0001t0002g0165a0001c0001t0002g0176others(11): Show | 14 | HG01243.hp2 HG01261.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-7114dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4871181 | |||||
chr17:4871181
|
A | ATT | 20 | a0001c0001t0018g0286a0001c0004t0006g0331a0001c0004t0006g0335others(17): Show | 20 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-7115_58-7114dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4871181 | |||||
chr17:4871181
|
AT | A | 86 | a0001c0001t0002g0183a0001c0001t0002g0187a0001c0001t0003g0062others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.58-7114delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4871181 | |||||
chr17:4871373
|
G | A | 1 | a0002c0002t0004g0274 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.58-6944G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871373 | ||||||
chr17:4871465
|
G | A | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-6852G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871465 | ||||||
chr17:4871492
|
A | G | 4 | a0004c0006t0012g0100a0004c0006t0012g0112a0004c0006t0012g0117others(1): Show | 4 | HG00621.hp2 NA18966.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-6825A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871492 | ||||||
chr17:4871519
|
C | G | 1 | a0002c0002t0001g0287 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.58-6798C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871519 | ||||||
chr17:4871685
|
T | C | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58-6632T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871685 | ||||||
chr17:4871947
|
T | C | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-6370T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871947 | ||||||
chr17:4872054
|
G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-6263G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872054 | ||||||
chr17:4872140
|
G | A | 1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-6177G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872140 | ||||||
chr17:4872329
|
T | TA | 15 | a0001c0001t0002g0160a0001c0001t0012g0096a0001c0001t0024g0205others(12): Show | 15 | HG01167.hp1 HG01517.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.58-5971dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4872329 | |||||
chr17:4872330
|
A | T | 1 | a0001c0001t0007g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.58-5987A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872330 | ||||||
chr17:4872456
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.58-5861G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872456 | ||||||
chr17:4872539
|
G | A | 5 | a0001c0001t0020g0148a0001c0001t0024g0205a0001c0001t0024g0207others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-5778G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872539 | ||||||
chr17:4872588
|
T | G | 1 | a0001c0001t0009g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-5729T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872588 | ||||||
chr17:4872838
|
G | A | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-5479G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872838 | ||||||
chr17:4872986
|
G | A | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.58-5331G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872986 | ||||||
chr17:4873109
|
C | A | 1 | a0003c0003t0039g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.58-5208C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873109 | ||||||
chr17:4873272
|
C | CACAATAG others(73): Show |
1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-4824_58-4745dup others(80): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873272 | |||||
chr17:4873272
|
CACAATAG others(73): Show |
C | 1 | a0002c0002t0015g0280 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.58-4824_58-4745del others(80): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873272 | |||||
chr17:4873317
|
A | G | 2 | a0003c0003t0003g0010a0003c0013t0003g0056 | 2 | NA18962.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.58-5000A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873317 | ||||||
chr17:4873395
|
A | G | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4922A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873395 | ||||||
chr17:4873423
|
G | A | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4894G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873423 | ||||||
chr17:4873433
|
A | G | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4884A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873433 | ||||||
chr17:4873475
|
A | G | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4842A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873475 | ||||||
chr17:4873584
|
C | T | 138 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.58-4733C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873584 | ||||||
chr17:4873617
|
C | CT | 81 | a0001c0001t0002g0177a0001c0001t0002g0183a0001c0001t0002g0187others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.58-4681dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | |||||
chr17:4873617
|
C | CTT | 49 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(46): Show | 50 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-4682_58-4681dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | |||||
chr17:4873617
|
C | CTTT | 6 | a0001c0001t0002g0164a0001c0001t0004g0181a0001c0001t0016g0223others(3): Show | 6 | HG01361.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-4683_58-4681dup others(3): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | |||||
chr17:4873617
|
CT | C | 29 | a0001c0001t0005g0114a0001c0001t0009g0208a0001c0001t0009g0209others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4681delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | |||||
chr17:4873637
|
G | A | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4680G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873637 | ||||||
chr17:4873679
|
C | T | 1 | a0001c0001t0008g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58-4638C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873679 | ||||||
chr17:4873912
|
G | T | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-4405G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873912 | ||||||
chr17:4873974
|
G | A | 2 | a0001c0004t0006g0341a0001c0004t0027g0074 | 2 | NA18968.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.58-4343G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873974 | ||||||
chr17:4874192
|
GTGAGCTC others(35): Show |
G | 1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-4122_58-4081del others(42): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4874192 | |||||
chr17:4874339
|
T | C | 55 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(52): Show | 55 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-3978T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874339 | ||||||
chr17:4874378
|
G | A | 5 | a0001c0005t0008g0227a0001c0005t0008g0228a0001c0005t0008g0229others(2): Show | 5 | HG00642.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-3939G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874378 | ||||||
chr17:4874499
|
A | G | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-3818A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874499 | ||||||
chr17:4874532
|
G | C | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-3785G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874532 | ||||||
chr17:4874809
|
A | G | 2 | a0001c0005t0006g0233a0001c0005t0008g0232 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.58-3508A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874809 | ||||||
chr17:4874894
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-3423G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874894 | ||||||
chr17:4874981
|
G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-3336G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874981 | ||||||
chr17:4875002
|
G | A | 1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-3315G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875002 | ||||||
chr17:4875020
|
T | C | 1 | a0001c0005t0054g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58-3297T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875020 | ||||||
chr17:4875192
|
G | A | 133 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.58-3125G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875192 | ||||||
chr17:4875323
|
G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-2994G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875323 | ||||||
chr17:4875348
|
G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-2969G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875348 | ||||||
chr17:4875355
|
A | G | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-2962A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875355 | ||||||
chr17:4875378
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.58-2939G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875378 | ||||||
chr17:4875713
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-2604G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875713 | ||||||
chr17:4875727
|
G | T | 1 | a0001c0005t0008g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.58-2590G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875727 | ||||||
chr17:4875796
|
G | GT | 9 | a0001c0001t0002g0137a0001c0001t0025g0133a0001c0001t0025g0138others(6): Show | 9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-2513dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4875796 | |||||
chr17:4875810
|
C | T | 1 | a0001c0008t0002g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.58-2507C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875810 | ||||||
chr17:4875814
|
G | A | 74 | a0001c0001t0002g0277a0001c0001t0009g0276a0001c0001t0018g0279others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.58-2503G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875814 | ||||||
chr17:4875835
|
G | A | 3 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204 | 3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-2482G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875835 | ||||||
chr17:4875928
|
T | C | 1 | a0002c0002t0004g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.58-2389T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875928 | ||||||
chr17:4876016
|
C | T | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58-2301C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876016 | ||||||
chr17:4876058
|
G | A | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-2259G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876058 | ||||||
chr17:4876098
|
A | ATTTTTTT others(29): Show |
1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-2209_58-2208ins others(36): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4876098 | |||||
chr17:4876202
|
C | G | 29 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(26): Show | 29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-2115C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876202 | ||||||
chr17:4876350
|
G | GT | 23 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(20): Show | 23 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.58-1967_58-1966ins others(1): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876350 | ||||||
chr17:4876435
|
A | T | 1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-1882A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876435 | ||||||
chr17:4876436
|
T | G | 1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-1881T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876436 | ||||||
chr17:4876438
|
G | A | 1 | a0001c0001t0029g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-1879G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876438 | ||||||
chr17:4876580
|
C | T | 51 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-1737C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876580 | ||||||
chr17:4876770
|
A | T | 17 | a0001c0001t0018g0286a0001c0005t0002g0150a0001c0005t0008g0227others(14): Show | 17 | HG00642.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.58-1547A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876770 | ||||||
chr17:4876799
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-1518G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876799 | ||||||
chr17:4877332
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58-985T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877332 | ||||||
chr17:4877414
|
G | A | 6 | a0001c0001t0002g0163a0001c0001t0002g0170a0001c0001t0002g0171others(3): Show | 6 | NA18940.hp1 NA18950.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-903G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877414 | ||||||
chr17:4877500
|
G | A | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-817G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877500 | ||||||
chr17:4877728
|
A | T | 139 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.58-589A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877728 | ||||||
chr17:4877809
|
C | CT | 36 | a0001c0001t0002g0173a0001c0001t0002g0202a0001c0001t0005g0210others(33): Show | 36 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.58-489dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4877809 | |||||
chr17:4877809
|
CT | C | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-489delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4877809 | |||||
chr17:4877896
|
T | C | 2 | a0001c0001t0025g0133a0001c0001t0025g0138 | 2 | NA18970.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.58-421T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877896 | ||||||
chr17:4878012
|
G | A | 1 | a0003c0003t0011g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-305G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878012 | ||||||
chr17:4878046
|
G | A | 1 | a0005c0009t0053g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-271G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878046 | ||||||
chr17:4878071
|
A | G | 74 | a0001c0001t0009g0276a0001c0001t0018g0279a0001c0001t0018g0286others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.58-246A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878071 | ||||||
chr17:4878099
|
C | T | 4 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0225others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-218C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878099 | ||||||
chr17:4878194
|
C | T | 3 | a0001c0001t0005g0116a0001c0001t0013g0075a0001c0001t0031g0088 | 3 | NA18947.hp2 NA18948.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.58-123C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878194 | ||||||
chr17:4878255
|
C | G | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58-62C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878255 | ||||||
chr17:4878497
|
A | G | 1 | a0001c0001t0013g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.123+115A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878497 | ||||||
chr17:4878595
|
G | A | 138 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.123+213G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878595 | ||||||
chr17:4878672
|
G | C | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123+290G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878672 | ||||||
chr17:4878941
|
G | T | 1 | a0003c0003t0038g0021 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.123+559G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878941 | ||||||
chr17:4878998
|
AAGGTGGC others(162): Show |
A | 1 | a0003c0003t0003g0036 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.123+636_123+804del | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4878998 | |||||
chr17:4879018
|
C | CACACTTG others(330): Show |
1 | a0001c0001t0005g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123+871_123+872ins others(337): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4879018 | |||||
chr17:4879032
|
GGGAGCCG others(106): Show |
G | 3 | a0003c0003t0003g0011a0003c0003t0003g0026a0003c0003t0003g0073 | 3 | HG02155.hp2 NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.123+692_123+804del | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4879032 | |||||
chr17:4879200
|
T | TGGGAGCC others(49): Show |
44 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(41): Show | 44 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.123+860_123+861ins others(56): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4879200 | |||||
chr17:4879264
|
G | A | 1 | a0001c0001t0025g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.123+882G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879264 | ||||||
chr17:4879629
|
C | T | 71 | a0001c0001t0003g0062a0001c0004t0027g0059a0003c0003t0003g0006others(68): Show | 72 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.123+1247C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879629 | ||||||
chr17:4879642
|
C | G | 51 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(48): Show | 55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.123+1260C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879642 | ||||||
chr17:4879702
|
G | A | 138 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.124-1282G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879702 | ||||||
chr17:4879764
|
G | A | 1 | a0003c0003t0011g0027 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.124-1220G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879764 | ||||||
chr17:4880043
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.124-941G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880043 | ||||||
chr17:4880045
|
C | G | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.124-939C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880045 | ||||||
chr17:4880280
|
G | A | 1 | a0001c0001t0032g0191 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124-704G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880280 | ||||||
chr17:4880300
|
C | CT | 20 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(17): Show | 20 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-669dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4880300 | |||||
chr17:4880349
|
G | A | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-635G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880349 | ||||||
chr17:4880540
|
G | A | 1 | a0001c0004t0016g0352 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124-444G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880540 | ||||||
chr17:4880582
|
C | T | 1 | a0001c0001t0025g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.124-402C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880582 | ||||||
chr17:4880628
|
G | A | 1 | a0001c0018t0004g0333 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-356G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880628 | ||||||
chr17:4880720
|
A | G | 1 | a0012c0026t0003g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.124-264A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880720 | ||||||
chr17:4880757
|
G | A | 1 | a0005c0009t0053g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.124-227G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880757 | ||||||
chr17:4880789
|
A | G | 11 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-195A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880789 | ||||||
chr17:4880882
|
A | C | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-102A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880882 | ||||||
chr17:4880886
|
C | T | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-98C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880886 | ||||||
chr17:4880899
|
C | CA | 12 | a0001c0004t0006g0136a0002c0002t0001g0255a0002c0002t0001g0258others(9): Show | 12 | HG00733.hp1 HG01256.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-75dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4880899 | |||||
chr17:4880954
|
A | C | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-30A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880954 | ||||||
chr17:4881078
|
G | T | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.180+38G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 3/31 | chr17 | 4881078 | ||||||
chr17:4881279
|
G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.306+22G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881279 | ||||||
chr17:4881431
|
G | A | 44 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(41): Show | 45 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.306+174G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881431 | ||||||
chr17:4881538
|
G | A | 1 | a0002c0002t0001g0109 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.306+281G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881538 | ||||||
chr17:4881548
|
TAATA | T | 6 | a0002c0002t0002g0304a0002c0002t0014g0292a0002c0002t0014g0307others(3): Show | 6 | NA18950.hp1 NA18969.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+300_306+303del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4881548 | |||||
chr17:4881664
|
A | C | 1 | a0002c0002t0001g0315 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.306+407A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881664 | ||||||
chr17:4881684
|
C | T | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.306+427C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881684 | ||||||
chr17:4881993
|
T | C | 1 | a0002c0002t0001g0289 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.306+736T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881993 | ||||||
chr17:4882136
|
C | G | 1 | a0001c0001t0002g0200 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.306+879C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882136 | ||||||
chr17:4882285
|
A | G | 1 | a0001c0001t0004g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.306+1028A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882285 | ||||||
chr17:4882523
|
A | G | 2 | a0002c0002t0001g0262a0002c0002t0001g0263 | 2 | HG01106.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.306+1266A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882523 | ||||||
chr17:4882530
|
T | C | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.306+1273T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882530 | ||||||
chr17:4882540
|
A | C | 2 | a0001c0005t0006g0233a0001c0005t0008g0232 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.306+1283A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882540 | ||||||
chr17:4882552
|
T | A | 188 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.306+1295T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882552 | ||||||
chr17:4882664
|
G | A | 44 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(41): Show | 44 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.306+1407G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882664 | ||||||
chr17:4882746
|
G | C | 1 | a0003c0003t0026g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.306+1489G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882746 | ||||||
chr17:4882879
|
G | A | 10 | a0002c0002t0001g0005a0002c0002t0001g0309a0002c0002t0001g0310others(7): Show | 11 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1484G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882879 | ||||||
chr17:4882950
|
G | A | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.307-1413G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882950 | ||||||
chr17:4883061
|
C | T | 1 | a0001c0004t0027g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.307-1302C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883061 | ||||||
chr17:4883120
|
C | CA | 8 | a0001c0001t0024g0207a0001c0004t0016g0352a0002c0002t0014g0322others(5): Show | 8 | HG03098.hp2 NA18950.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1228dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883120 | |||||
chr17:4883209
|
C | CT | 32 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(29): Show | 32 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.307-1141dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883209 | |||||
chr17:4883209
|
CT | C | 9 | a0001c0001t0002g0200a0001c0001t0004g0246a0001c0001t0004g0247others(6): Show | 9 | HG01175.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1141delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883209 | |||||
chr17:4883315
|
C | G | 1 | a0001c0001t0021g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.307-1048C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883315 | ||||||
chr17:4883329
|
T | C | 1 | a0001c0001t0004g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.307-1034T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883329 | ||||||
chr17:4883358
|
C | T | 1 | a0001c0005t0008g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.307-1005C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883358 | ||||||
chr17:4883394
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.307-969T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883394 | ||||||
chr17:4883411
|
A | G | 2 | a0001c0001t0002g0199a0001c0001t0002g0222 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.307-952A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883411 | ||||||
chr17:4883418
|
A | C | 1 | a0002c0002t0001g0314 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.307-945A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883418 | ||||||
chr17:4883428
|
A | T | 1 | a0001c0001t0029g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-935A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883428 | ||||||
chr17:4883429
|
T | C | 1 | a0001c0001t0029g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-934T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883429 | ||||||
chr17:4883443
|
A | G | 24 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(21): Show | 24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.307-920A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883443 | ||||||
chr17:4883451
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.307-912G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883451 | ||||||
chr17:4883472
|
A | G | 48 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(45): Show | 52 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.307-891A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883472 | ||||||
chr17:4883486
|
G | A | 1 | a0001c0001t0007g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.307-877G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883486 | ||||||
chr17:4883625
|
G | A | 1 | a0001c0018t0004g0333 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-738G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883625 | ||||||
chr17:4883636
|
G | A | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.307-727G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883636 | ||||||
chr17:4883688
|
C | T | 1 | a0002c0002t0001g0302 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.307-675C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883688 | ||||||
chr17:4883698
|
C | CT | 23 | a0001c0001t0002g0171a0001c0001t0002g0189a0001c0001t0004g0181others(20): Show | 23 | HG00642.hp1 HG00738.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.307-644dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883698 | |||||
chr17:4883698
|
CT | C | 48 | a0001c0001t0007g0107a0001c0004t0006g0329a0001c0004t0006g0331others(45): Show | 48 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.307-644delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883698 | |||||
chr17:4883720
|
A | G | 1 | a0003c0007t0003g0060 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.307-643A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883720 | ||||||
chr17:4883738
|
C | A | 1 | a0002c0002t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.307-625C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883738 | ||||||
chr17:4883789
|
C | T | 6 | a0002c0002t0004g0140a0002c0002t0004g0142a0002c0002t0004g0143others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-574C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883789 | ||||||
chr17:4883827
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.307-536C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883827 | ||||||
chr17:4883858
|
C | T | 1 | a0001c0001t0005g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.307-505C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883858 | ||||||
chr17:4883966
|
G | A | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.307-397G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883966 | ||||||
chr17:4883977
|
C | G | 18 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(15): Show | 18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-386C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883977 | ||||||
chr17:4884028
|
C | CT | 14 | a0001c0001t0002g0171a0001c0001t0004g0181a0001c0001t0009g0208others(11): Show | 14 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.307-317dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4884028 | |||||
chr17:4884028
|
CT | C | 47 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(44): Show | 47 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.307-317delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4884028 | |||||
chr17:4884051
|
C | T | 5 | a0002c0002t0001g0302a0002c0002t0001g0305a0002c0002t0001g0327others(2): Show | 5 | HG00423.hp2 NA18988.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-312C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884051 | ||||||
chr17:4884077
|
G | A | 141 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.307-286G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884077 | ||||||
chr17:4884103
|
G | T | 2 | a0002c0002t0001g0310a0002c0002t0001g0323 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.307-260G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884103 | ||||||
chr17:4884131
|
T | C | 18 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(15): Show | 18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-232T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884131 | ||||||
chr17:4884174
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-189C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884174 | ||||||
chr17:4884230
|
G | T | 1 | a0002c0002t0001g0289 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.307-133G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884230 | ||||||
chr17:4884486
|
C | A | 1 | a0002c0002t0001g0254 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.417+13C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/31 | chr17 | 4884486 | ||||||
chr17:4884509
|
G | A | 25 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.417+36G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/31 | chr17 | 4884509 | ||||||
chr17:4884519
|
C | T | 1 | a0002c0002t0001g0315 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.417+46C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/31 | chr17 | 4884519 | ||||||
chr17:4885028
|
C | T | 1 | a0002c0002t0015g0295 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.508+26C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 6/31 | chr17 | 4885028 | ||||||
chr17:4885320
|
C | T | 1 | a0003c0003t0003g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.509-163C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 6/31 | chr17 | 4885320 | ||||||
chr17:4885589
|
C | CCCTGATG others(117): Show |
1 | a0012c0026t0003g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.639+36_639+37insGA others(122): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr17 | 4885589 | |||||
chr17:4885676
|
G | A | 7 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+63G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 7/31 | chr17 | 4885676 | ||||||
chr17:4886117
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.695-3C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 8/31 | chr17 | 4886117 | ||||||
chr17:4886406
|
C | G | 16 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(13): Show | 16 | HG00673.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-45C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 9/31 | chr17 | 4886406 | ||||||
chr17:4886666
|
C | T | 26 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(23): Show | 26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.949+40C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886666 | ||||||
chr17:4886933
|
C | G | 1 | a0003c0003t0010g0065 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.950-177C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886933 | ||||||
chr17:4886936
|
T | TC | 44 | a0001c0004t0006g0329a0001c0004t0006g0331a0001c0004t0006g0335others(41): Show | 44 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.950-172dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr17 | 4886936 | |||||
chr17:4886961
|
C | T | 7 | a0002c0002t0004g0259a0002c0002t0004g0266a0002c0002t0004g0267others(4): Show | 7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.950-149C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886961 | ||||||
chr17:4886962
|
C | T | 1 | a0002c0002t0001g0297 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.950-148C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886962 | ||||||
chr17:4887506
|
G | GC | 73 | a0001c0001t0002g0199a0001c0001t0002g0222a0001c0001t0003g0062others(70): Show | 74 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1020-73dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr17 | 4887506 | |||||
chr17:4887822
|
G | A | 1 | a0003c0003t0003g0071 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1230+32G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4887822 | ||||||
chr17:4887823
|
C | T | 18 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(15): Show | 18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1230+33C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4887823 | ||||||
chr17:4888061
|
C | T | 77 | a0001c0001t0002g0199a0001c0001t0002g0222a0001c0001t0003g0062others(74): Show | 78 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1230+271C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888061 | ||||||
chr17:4888110
|
G | A | 1 | a0002c0002t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1230+320G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888110 | ||||||
chr17:4888124
|
G | T | 1 | a0001c0001t0007g0103 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1230+334G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888124 | ||||||
chr17:4888237
|
C | T | 1 | a0001c0017t0002g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1230+447C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888237 | ||||||
chr17:4888270
|
A | C | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+480A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888270 | ||||||
chr17:4888400
|
G | A | 73 | a0001c0001t0009g0276a0001c0001t0056g0256a0002c0002t0001g0005others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1230+610G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888400 | ||||||
chr17:4888413
|
G | A | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+623G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888413 | ||||||
chr17:4888440
|
A | G | 1 | a0001c0001t0051g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1230+650A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888440 | ||||||
chr17:4888664
|
C | T | 1 | a0003c0003t0003g0050 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1230+874C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888664 | ||||||
chr17:4888690
|
C | CT | 46 | a0001c0001t0004g0181a0001c0004t0006g0329a0001c0004t0006g0331others(43): Show | 46 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1230+920dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | |||||
chr17:4888690
|
CT | C | 185 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0154others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1230+920delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | |||||
chr17:4888690
|
CTT | C | 16 | a0001c0001t0002g0182a0001c0001t0004g0246a0001c0001t0004g0247others(13): Show | 16 | HG01993.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1230+919_1230+920d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | |||||
chr17:4888690
|
CTTT | C | 13 | a0001c0005t0006g0233a0001c0005t0008g0227a0001c0005t0008g0228others(10): Show | 13 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+918_1230+920d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | |||||
chr17:4888710
|
T | C | 18 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(15): Show | 18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1230+920T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888710 | ||||||
chr17:4888772
|
C | T | 5 | a0001c0001t0046g0197a0001c0001t0055g0198a0001c0008t0002g0156others(2): Show | 5 | HG02257.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-875C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888772 | ||||||
chr17:4888774
|
C | A | 132 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1231-873C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888774 | ||||||
chr17:4888786
|
C | T | 1 | a0002c0002t0001g0264 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1231-861C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888786 | ||||||
chr17:4888927
|
C | T | 1 | a0003c0003t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1231-720C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888927 | ||||||
chr17:4888972
|
T | C | 22 | a0001c0001t0002g0137a0001c0001t0009g0208a0001c0001t0009g0209others(19): Show | 22 | HG00673.hp2 HG01167.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1231-675T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888972 | ||||||
chr17:4889074
|
C | A | 1 | a0003c0003t0003g0034 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1231-573C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889074 | ||||||
chr17:4889112
|
T | G | 1 | a0001c0001t0002g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1231-535T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889112 | ||||||
chr17:4889115
|
G | T | 1 | a0003c0003t0011g0027 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1231-532G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889115 | ||||||
chr17:4889239
|
G | A | 1 | a0001c0001t0046g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1231-408G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889239 | ||||||
chr17:4889283
|
G | A | 2 | a0003c0003t0003g0032a0003c0003t0003g0047 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1231-364G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889283 | ||||||
chr17:4889337
|
C | T | 1 | a0001c0001t0005g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1231-310C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889337 | ||||||
chr17:4889376
|
T | C | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1231-271T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889376 | ||||||
chr17:4889524
|
G | A | 4 | a0001c0001t0024g0205a0001c0001t0024g0207a0005c0009t0053g0204others(1): Show | 4 | HG01167.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-123G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889524 | ||||||
chr17:4889546
|
C | G | 4 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0225others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-101C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889546 | ||||||
chr17:4889590
|
G | A | 18 | a0001c0001t0004g0247a0001c0005t0002g0150a0001c0005t0006g0233others(15): Show | 18 | HG00642.hp2 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-57G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889590 | ||||||
chr17:4889611
|
G | A | 5 | a0001c0001t0025g0133a0001c0001t0025g0138a0001c0001t0025g0139others(2): Show | 5 | HG00673.hp2 NA18970.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-36G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889611 | ||||||
chr17:4889803
|
C | T | 4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+40C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4889803 | ||||||
chr17:4889964
|
C | T | 1 | a0001c0001t0055g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1347+201C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4889964 | ||||||
chr17:4890072
|
T | C | 76 | a0001c0001t0002g0199a0001c0001t0002g0222a0001c0001t0003g0062others(73): Show | 77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1347+309T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4890072 | ||||||
chr17:4890354
|
T | G | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1348-163T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4890354 | ||||||
chr17:4890848
|
A | G | 3 | a0002c0002t0001g0255a0002c0002t0001g0258a0002c0002t0015g0269 | 3 | HG01257.hp2 HG01952.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1567-103A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 14/31 | chr17 | 4890848 | ||||||
chr17:4891195
|
C | CGT | 3 | a0002c0002t0001g0254a0002c0002t0001g0265a0002c0002t0001g0321 | 3 | HG01167.hp2 HG03669.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1740+72_1740+73ins others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891195 | |||||
chr17:4891196
|
G | A | 1 | a0003c0003t0003g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1740+72G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891196 | ||||||
chr17:4891197
|
C | T | 130 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1740+73C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891197 | ||||||
chr17:4891198
|
G | A | 91 | a0001c0001t0002g0199a0001c0001t0002g0222a0001c0001t0003g0062others(88): Show | 92 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1740+74G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891198 | ||||||
chr17:4891198
|
G | GCACGCAC others(5): Show |
1 | a0003c0003t0003g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1740+75_1740+76ins others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891198 | |||||
chr17:4891200
|
G | A | 5 | a0002c0002t0001g0254a0002c0002t0001g0265a0002c0002t0001g0321others(2): Show | 5 | HG01167.hp2 HG02258.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+76G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891200 | ||||||
chr17:4891200
|
G | GCA | 3 | a0001c0001t0004g0248a0001c0001t0004g0249a0001c0001t0004g0250 | 3 | HG02486.hp2 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1740+100_1740+101d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCACA | 66 | a0001c0001t0002g0129a0001c0001t0002g0137a0001c0001t0005g0001others(63): Show | 70 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1740+98_1740+101du others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCACACA | 6 | a0001c0001t0005g0116a0001c0001t0007g0122a0001c0001t0025g0139others(3): Show | 6 | HG00673.hp2 HG02155.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1740+96_1740+101du others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCACACAC others(1): Show |
4 | a0001c0001t0023g0244a0001c0001t0023g0245a0001c0001t0023g0252others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1740+94_1740+101du others(9): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCACACAC others(3): Show |
63 | a0001c0001t0002g0199a0001c0001t0002g0222a0001c0001t0003g0062others(60): Show | 64 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1740+92_1740+101du others(11): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCACACAC others(5): Show |
3 | a0001c0018t0004g0333a0003c0003t0013g0057a0012c0026t0003g0076 | 3 | HG01243.hp2 NA18994.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1740+90_1740+101du others(13): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCGCACAC others(1): Show |
3 | a0001c0005t0002g0150a0001c0005t0022g0221a0006c0025t0005g0147 | 3 | HG02965.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCGCACAC others(3): Show |
33 | a0001c0004t0006g0135a0001c0004t0006g0136a0001c0004t0006g0329others(30): Show | 33 | HG00609.hp1 HG00673.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCGCACAC others(5): Show |
4 | a0001c0004t0042g0346a0001c0005t0008g0228a0001c0005t0008g0229others(1): Show | 4 | HG02895.hp1 HG02897.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCGCACAC others(7): Show |
2 | a0001c0005t0008g0227a0001c0005t0037g0058 | 2 | HG00642.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCGCGCAC others(3): Show |
3 | a0001c0004t0006g0339a0001c0004t0006g0348a0003c0003t0003g0063 | 3 | HG00621.hp1 NA19057.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GCGCGCAC others(5): Show |
1 | a0003c0003t0003g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1740+77_1740+78ins others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
G | GTACACAC others(3): Show |
1 | a0003c0003t0003g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1740+76_1740+77ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891200 | ||||||
chr17:4891200
|
GCA | G | 3 | a0001c0001t0021g0079a0001c0001t0021g0080a0001c0001t0021g0081 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1740+100_1740+101d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891200
|
GCACACA | G | 48 | a0001c0004t0019g0349a0002c0002t0001g0005a0002c0002t0001g0281others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1740+96_1740+101de others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | |||||
chr17:4891202
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1740+78A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891202 | ||||||
chr17:4891206
|
A | G | 2 | a0001c0005t0012g0152a0001c0005t0022g0151 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1740+82A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891206 | ||||||
chr17:4891208
|
A | G | 2 | a0002c0002t0001g0290a0002c0002t0001g0300 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1740+84A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891208 | ||||||
chr17:4891235
|
C | T | 2 | a0001c0011t0006g0334a0001c0011t0041g0347 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1740+111C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891235 | ||||||
chr17:4891361
|
G | A | 1 | a0001c0001t0023g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1741-95G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891361 | ||||||
chr17:4891426
|
C | T | 1 | a0001c0001t0016g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1741-30C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891426 | ||||||
chr17:4891822
|
C | T | 1 | a0001c0004t0006g0340 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2001+106C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891822 | ||||||
chr17:4891894
|
C | T | 2 | a0001c0001t0004g0246a0001c0001t0004g0247 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2001+178C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891894 | ||||||
chr17:4891911
|
G | A | 2 | a0002c0002t0001g0303a0002c0002t0001g0306 | 2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2001+195G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891911 | ||||||
chr17:4891926
|
C | T | 1 | a0001c0001t0051g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2001+210C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891926 | ||||||
chr17:4892012
|
C | T | 124 | a0001c0001t0002g0154a0001c0001t0002g0159a0001c0001t0002g0160others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.2002-137C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892012 | ||||||
chr17:4892094
|
T | C | 1 | a0002c0002t0015g0295 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2002-55T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892094 | ||||||
chr17:4892102
|
G | A | 1 | a0002c0002t0001g0289 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2002-47G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892102 | ||||||
chr17:4892123
|
C | T | 1 | a0001c0001t0005g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2002-26C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892123 | ||||||
chr17:4892324
|
TG | T | 156 | a0001c0001t0002g0154a0001c0001t0002g0160a0001c0001t0002g0162others(153): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2088-73delG | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 4892324 | |||||
chr17:4892325
|
G | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0159others(104): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2088-77G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | chr17 | 4892325 | ||||||
chr17:4892329
|
G | T | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2088-73G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | chr17 | 4892329 | ||||||
chr17:4892330
|
T | G | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2088-72T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | chr17 | 4892330 | ||||||
chr17:4892359
|
G | GC | 11 | a0001c0001t0002g0137a0001c0001t0002g0177a0001c0011t0041g0347others(8): Show | 11 | HG01952.hp1 HG01981.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2088-36dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 4892359 | |||||
chr17:4892907
|
G | C | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2312-72G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/31 | chr17 | 4892907 | ||||||
chr17:4892908
|
G | T | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2312-71G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/31 | chr17 | 4892908 | ||||||
chr17:4892976
|
C | T | 47 | a0001c0001t0002g0129a0001c0001t0005g0001a0001c0001t0005g0086others(44): Show | 51 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(48): Show |
splice_region_variant&intron_variant | LOW | c.2312-3C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/31 | chr17 | 4892976 | ||||||
chr17:4893139
|
A | G | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2400+72A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893139 | ||||||
chr17:4893146
|
G | C | 74 | a0001c0001t0003g0062a0001c0001t0007g0126a0001c0001t0023g0244others(71): Show | 75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2400+79G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893146 | ||||||
chr17:4893165
|
G | A | 1 | a0001c0001t0007g0119 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2400+98G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893165 | ||||||
chr17:4893203
|
T | A | 1 | a0001c0005t0054g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2400+136T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893203 | ||||||
chr17:4893215
|
TTCCTAAC others(5): Show |
T | 23 | a0001c0001t0005g0167a0001c0001t0020g0148a0001c0004t0019g0349others(20): Show | 23 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.2400+174_2401-182d others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr17 | 4893215 | |||||
chr17:4893226
|
T | G | 90 | a0001c0001t0002g0137a0001c0001t0003g0062a0001c0001t0007g0126others(87): Show | 91 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2400+159T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893226 | ||||||
chr17:4893251
|
C | T | 5 | a0001c0001t0005g0237a0001c0001t0005g0238a0001c0001t0005g0241others(2): Show | 5 | HG01358.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401-183C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893251 | ||||||
chr17:4893361
|
T | C | 117 | a0001c0001t0002g0004a0001c0001t0002g0137a0001c0001t0002g0154others(114): Show | 118 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.2401-73T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893361 | ||||||
chr17:4893365
|
C | T | 7 | a0001c0001t0007g0087a0001c0001t0007g0099a0001c0001t0007g0102others(4): Show | 7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2401-69C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893365 | ||||||
chr17:4893618
|
C | A | 1 | a0001c0001t0052g0134 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2564+21C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893618 | ||||||
chr17:4893620
|
C | T | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2564+23C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893620 | ||||||
chr17:4893621
|
T | C | 1 | a0011c0022t0004g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2564+24T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893621 | ||||||
chr17:4893776
|
C | A | 18 | a0001c0005t0002g0150a0001c0005t0006g0233a0001c0005t0008g0227others(15): Show | 18 | HG00642.hp2 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2564+179C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893776 | ||||||
chr17:4894137
|
C | T | 12 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(9): Show | 12 | HG01109.hp1 HG01168.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2671-37C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 22/31 | chr17 | 4894137 | ||||||
chr17:4894322
|
C | T | 1 | a0001c0004t0006g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2808+11C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894322 | ||||||
chr17:4894323
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2808+12G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894323 | ||||||
chr17:4894338
|
G | A | 2 | a0001c0001t0024g0205a0001c0001t0024g0207 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2808+27G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894338 | ||||||
chr17:4894423
|
C | T | 79 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(76): Show | 80 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.2809-102C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894423 | ||||||
chr17:4894639
|
G | A | 1 | a0001c0004t0006g0348 | 1 | HG00621.hp1 | splice_region_variant&intron_variant | LOW | c.2917+6G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/31 | chr17 | 4894639 | ||||||
chr17:4894673
|
C | T | 9 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2917+40C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/31 | chr17 | 4894673 | ||||||
chr17:4894956
|
G | A | 1 | a0002c0002t0004g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2918-119G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/31 | chr17 | 4894956 | ||||||
chr17:4895279
|
G | A | 1 | a0003c0003t0026g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3085+37G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 25/31 | chr17 | 4895279 | ||||||
chr17:4895567
|
G | A | 17 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(14): Show | 17 | HG00673.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.3229+74G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/31 | chr17 | 4895567 | ||||||
chr17:4895607
|
C | G | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3230-91C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/31 | chr17 | 4895607 | ||||||
chr17:4895647
|
C | T | 1 | a0001c0001t0009g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3230-51C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/31 | chr17 | 4895647 | ||||||
chr17:4895941
|
C | T | 54 | a0001c0001t0002g0004a0001c0001t0002g0154a0001c0001t0002g0155others(51): Show | 55 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.3365-62C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 27/31 | chr17 | 4895941 | ||||||
chr17:4896353
|
C | T | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3615+11C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 29/31 | chr17 | 4896353 | ||||||
chr17:4896398
|
C | T | 1 | a0002c0002t0001g0288 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3616-31C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 29/31 | chr17 | 4896398 | ||||||
chr17:4896602
|
C | T | 69 | a0001c0001t0003g0062a0002c0002t0020g0291a0002c0002t0020g0299others(66): Show | 70 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.3775+14C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 30/31 | chr17 | 4896602 | ||||||
chr17:4896871
|
CCTGGGCA others(5): Show |
C | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3915+64_3915+75del others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 4896871 | |||||
chr17:4896885
|
T | G | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3915+72T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896885 | ||||||
chr17:4896885
|
T | TG | 34 | a0001c0001t0005g0237a0001c0001t0005g0238a0001c0001t0005g0241others(31): Show | 34 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.3915+76dupG | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 4896885 | |||||
chr17:4896903
|
G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3915+90G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896903 | ||||||
chr17:4896938
|
A | G | 320 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(317): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3915+125A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896938 | ||||||
chr17:4896942
|
G | A | 1 | a0001c0018t0004g0333 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3915+129G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896942 | ||||||
chr17:4896995
|
C | T | 207 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(204): Show | 213 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.3915+182C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896995 | ||||||
chr17:4897009
|
G | A | 169 | a0001c0001t0002g0004a0001c0001t0002g0129a0001c0001t0002g0137others(166): Show | 171 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.3916-195G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4897009 | ||||||
chr17:4897064
|
A | T | 2 | a0003c0003t0003g0009a0003c0003t0033g0019 | 2 | HG02083.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3916-140A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4897064 | ||||||
chr17:4897112
|
T | C | 12 | a0001c0001t0009g0208a0001c0001t0009g0209a0001c0001t0009g0211others(9): Show | 12 | HG01109.hp1 HG01168.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.3916-92T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4897112 | ||||||
chr17:4897129
|
CCCTTCTT others(1): Show |
C | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0018g0286others(1): Show | 4 | HG01175.hp2 HG03098.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916-72_3916-65del others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 4897129 |