geneid | 9130 |
---|---|
ensemblid | ENSG00000071859.15 |
hgncid | 18786 |
symbol | FAM50A |
name | family with sequence similarity 50 member A |
refseq_nuc | NM_004699.4 |
refseq_prot | NP_004690.1 |
ensembl_nuc | ENST00000393600.8 |
ensembl_prot | ENSP00000377225.3 |
mane_status | MANE Select |
chr | chrX |
start | 154444141 |
end | 154450654 |
strand | + |
ver | v1.2 |
region | chrX:154444141-154450654 |
region5000 | chrX:154439141-154455654 |
regionname0 | FAM50A_chrX_154444141_154450654 |
regionname5000 | FAM50A_chrX_154439141_154455654 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 339 | 272 | 74 | 60 | 100 | 7 | 29 | 71 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0002 | 0/0 | 140 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0003 | 0/0 | 172 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0004 | 0/0 | 98 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1020 | 272 | 74 | 60 | 100 | 7 | 29 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
c0002 | 0/0 | 1019 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
c0003 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
c0004 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 318 | 220 | 53 | 41 | 93 | 6 | 25 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0002 | 0/0 | 318 | 29 | 4 | 15 | 5 | 1 | 4 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0003 | 0/0 | 331 | 14 | 14 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0004 | 0/0 | 309 | 2 | 0 | 2 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0005 | 0/0 | 299 | 2 | 1 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0006 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0007 | 0/0 | 319 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0008 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0009 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0010 | 0/0 | 317 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0011 | 0/0 | 315 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0012 | 0/0 | 327 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
t0013 | 0/0 | 296 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 144 | 12 | 32 | 73 | 5 | 21 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0002 | 0/0 | 17 | 0 | 12 | 3 | 0 | 2 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0003 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0004 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0005 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0006 | 0/0 | 7 | 2 | 5 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0007 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0008 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1020 | 272 | 74 | 60 | 100 | 7 | 29 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0002c0003 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0003c0004 | 0/0 | 1022 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0004c0002 | 0/0 | 1019 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1337 | 219 | 53 | 41 | 92 | 6 | 25 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0002 | 0/0 | 1337 | 29 | 4 | 15 | 5 | 1 | 4 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0003 | 0/0 | 1350 | 14 | 14 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0004 | 0/0 | 1328 | 2 | 0 | 2 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0005 | 0/0 | 1318 | 2 | 1 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0007 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0008 | 0/0 | 1343 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0010 | 0/0 | 1336 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0011 | 0/0 | 1334 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0012 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0001c0001t0013 | 0/0 | 1315 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0002c0003t0001 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0003c0004t0009 | 0/0 | 1342 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
a0004c0002t0006 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | copy fasta | chrX | 154439141 | 154455654 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 142 | 12 | 32 | 71 | 5 | 21 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0004 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0007 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0008 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0002 | 0/0 | 14 | 0 | 10 | 2 | 0 | 2 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0006 | 0/0 | 6 | 2 | 4 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0003g0003 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0010g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0001c0001t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0002c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0003c0004t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
a0004c0002t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | GBR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01346 | hp1 | a0001 | c0001 | t0010 | g0002 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02145 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02257 | hp2 | a0001 | c0001 | t0013 | g0012 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18965 | hp1 | a0003 | c0004 | t0009 | g0049 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19006 | hp1 | a0004 | c0002 | t0006 | g0046 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19079 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19083 | hp1 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19085 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | USA | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | FAM50A_chrX_154439141_154455654 | FAM50A | chrX | 154439141 | 154455654 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154445899
|
AG | A | 1 | a0004 | 1 | NA19006.hp1 | frameshift_variant | HIGH | c.286delG | p.Glu96fs | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/13 | 381/1337 | 286/1020 | 96/339 | INFO_REALIGN_3_PRIME | chrX | 154445899 | |
chrX:154446506
|
G | GA | 1 | a0002 | 1 | NA19083.hp1 | frameshift_variant | HIGH | c.388_389insA | p.Gly130fs | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/13 | 484/1337 | 389/1020 | 130/339 | chrX | 154446506 | ||
chrX:154446509
|
G | C | 1 | a0002 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.391G>C | p.Gly131Arg | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/13 | 486/1337 | 391/1020 | 131/339 | chrX | 154446509 | ||
chrX:154448551
|
A | AG | 1 | a0003 | 1 | NA18965.hp1 | frameshift_variant | HIGH | c.511dupG | p.Asp171fs | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 5/13 | 607/1337 | 512/1020 | 171/339 | INFO_REALIGN_3_PRIME | chrX | 154448551 | |
chrX:154450054
|
T | TG | 1 | a0003 | 1 | NA18965.hp1 | frameshift_variant | HIGH | c.856dupG | p.Asp286fs | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 11/13 | 952/1337 | 857/1020 | 286/339 | INFO_REALIGN_3_PRIME | chrX | 154450054 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154446508
|
A | G | 1 | a0002c0003 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.390A>G | p.Gly130Gly | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/13 | 485/1337 | 390/1020 | 130/339 | chrX | 154446508 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154444160
|
A | AC | 1 | a0004c0002t0006 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 73 | INFO_REALIGN_3_PRIME | chrX | 154444160 | ||||
chrX:154444162
|
C | CGCCGCT | 1 | a0001c0001t0008 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60_-55dupCCGCTG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 54 | INFO_REALIGN_3_PRIME | chrX | 154444162 | ||||
chrX:154444174
|
T | C | 1 | a0001c0001t0007 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 62 | chrX | 154444174 | |||||
chrX:154444178
|
G | GC | 1 | a0001c0001t0007 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-57dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 56 | INFO_REALIGN_3_PRIME | chrX | 154444178 | ||||
chrX:154444180
|
T | C | 1 | a0001c0001t0007 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 56 | chrX | 154444180 | |||||
chrX:154444182
|
T | C | 1 | a0001c0001t0007 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 54 | chrX | 154444182 | |||||
chrX:154444186
|
T | C | 6 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(3): Show | 35 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-50T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 50 | chrX | 154444186 | |||||
chrX:154444188
|
T | C | 1 | a0001c0001t0007 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 48 | chrX | 154444188 | |||||
chrX:154444188
|
TCGC | T | 1 | a0001c0001t0011 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34_-32delGCC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 32 | INFO_REALIGN_3_PRIME | chrX | 154444188 | ||||
chrX:154444188
|
TCGCCGCC others(12): Show |
T | 1 | a0001c0001t0005 | 2 | HG01361.hp2 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-31_-13delCGCCGCCG others(11): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 13 | INFO_REALIGN_3_PRIME | chrX | 154444188 | ||||
chrX:154444188
|
TCGCCGCC others(15): Show |
T | 1 | a0001c0001t0013 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31_-10delCGCCGCCG others(14): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 10 | INFO_REALIGN_3_PRIME | chrX | 154444188 | ||||
chrX:154444190
|
G | GCCGCCGC others(6): Show |
1 | a0001c0001t0003 | 14 | HG02055.hp1 HG02258.hp1 HG02723.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-31_-19dupCGCCGCCG others(5): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 18 | INFO_REALIGN_3_PRIME | chrX | 154444190 | ||||
chrX:154444202
|
GC | G | 1 | a0001c0001t0010 | 1 | HG01346.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31delC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 31 | INFO_REALIGN_3_PRIME | chrX | 154444202 | ||||
chrX:154444203
|
C | CCCGCCGC others(2): Show |
1 | a0001c0001t0012 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-13_-5dupCGCCGCCGC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 4 | INFO_REALIGN_3_PRIME | chrX | 154444203 | ||||
chrX:154444203
|
CCCGCCGC others(2): Show |
C | 1 | a0001c0001t0004 | 2 | HG01123.hp2 HG01346.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13_-5delCGCCGCCGC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/13 | 5 | INFO_REALIGN_3_PRIME | chrX | 154444203 | ||||
chrX:154450450
|
C | CG | 2 | a0003c0004t0009a0004c0002t0006 | 2 | NA18965.hp1 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 13/13 | 21 | INFO_REALIGN_3_PRIME | chrX | 154450450 | ||||
chrX:154450478
|
T | TG | 1 | a0003c0004t0009 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 13/13 | 48 | INFO_REALIGN_3_PRIME | chrX | 154450478 | ||||
chrX:154450557
|
G | GC | 1 | a0003c0004t0009 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*126dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 13/13 | 127 | INFO_REALIGN_3_PRIME | chrX | 154450557 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:154444391
|
C | CT | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.111+45_111+46insT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154444391 | ||||||
chrX:154444396
|
G | GC | 1 | a0001c0001t0001g0019 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.111+54dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 154444396 | |||||
chrX:154444449
|
G | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.111+103G>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154444449 | ||||||
chrX:154444495
|
GCA | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 59 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.111+154_111+155del others(2): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 154444495 | |||||
chrX:154444635
|
G | GGGAC | 22 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(19): Show | 46 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.111+292_111+295dup others(4): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 154444635 | |||||
chrX:154444684
|
GCCCCTCG others(22): Show |
G | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.111+370_111+398del others(29): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 154444684 | |||||
chrX:154444838
|
CCT | C | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.111+493_111+494del others(2): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154444838 | ||||||
chrX:154445422
|
C | T | 1 | a0001c0001t0003g0003 | 12 | HG02055.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-211C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154445422 | ||||||
chrX:154445609
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.112-24C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154445609 | ||||||
chrX:154445611
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.112-22T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154445611 | ||||||
chrX:154445626
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 11 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.112-7C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 1/12 | chrX | 154445626 | ||||||
chrX:154445766
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 17 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.197-46G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 2/12 | chrX | 154445766 | ||||||
chrX:154445776
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.197-36C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 2/12 | chrX | 154445776 | ||||||
chrX:154445799
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197-13C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 2/12 | chrX | 154445799 | ||||||
chrX:154445960
|
TC | T | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.296+52delC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 154445960 | |||||
chrX:154445991
|
T | G | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.296+80T>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | chrX | 154445991 | ||||||
chrX:154446064
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 17 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.296+153T>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | chrX | 154446064 | ||||||
chrX:154446068
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0044 | 5 | HG01243.hp1 HG01891.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.296+157C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | chrX | 154446068 | ||||||
chrX:154446072
|
T | G | 1 | a0001c0001t0002g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.296+161T>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | chrX | 154446072 | ||||||
chrX:154446131
|
T | TG | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.296+223dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 154446131 | |||||
chrX:154446152
|
G | GT | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.296+242dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 154446152 | |||||
chrX:154446167
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.297-248G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | chrX | 154446167 | ||||||
chrX:154446291
|
T | TG | 1 | a0001c0001t0001g0042 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.297-120dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 154446291 | |||||
chrX:154446316
|
GC | G | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.297-95delC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 154446316 | |||||
chrX:154446351
|
GGAAGGGG others(7): Show |
G | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.297-63_297-50delGA others(12): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 3/12 | chrX | 154446351 | ||||||
chrX:154446583
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442+27dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154446583 | |||||
chrX:154446681
|
C | CA | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442+122dupA | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154446681 | |||||
chrX:154446699
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.442+139G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154446699 | ||||||
chrX:154446705
|
G | GGAA | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.442+148_442+150dup others(3): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154446705 | |||||
chrX:154446733
|
TG | T | 1 | a0004c0002t0006g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.442+176delG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154446733 | |||||
chrX:154446809
|
CG | C | 1 | a0001c0001t0001g0016 | 2 | HG00673.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.442+250delG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154446809 | ||||||
chrX:154446823
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 17 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.442+263A>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154446823 | ||||||
chrX:154446883
|
C | CG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+324dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154446883 | |||||
chrX:154446885
|
A | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 77 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.442+325A>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154446885 | ||||||
chrX:154447037
|
T | TC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+480dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447037 | |||||
chrX:154447102
|
CT | C | 1 | a0002c0003t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.442+544delT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447102 | |||||
chrX:154447104
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.442+544T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447104 | ||||||
chrX:154447105
|
G | C | 1 | a0002c0003t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.442+545G>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447105 | ||||||
chrX:154447114
|
C | CG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+557dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447114 | |||||
chrX:154447204
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442+644C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447204 | ||||||
chrX:154447205
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 11 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+645G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447205 | ||||||
chrX:154447209
|
A | AG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+650dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447209 | |||||
chrX:154447214
|
G | GT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+655dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447214 | |||||
chrX:154447248
|
C | CA | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442+692dupA | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447248 | |||||
chrX:154447278
|
G | GT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+719dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447278 | |||||
chrX:154447340
|
A | AG | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442+783dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447340 | |||||
chrX:154447373
|
T | TG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+815dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447373 | |||||
chrX:154447407
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.442+847A>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447407 | ||||||
chrX:154447407
|
AG | A | 1 | a0002c0003t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.442+851delG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447407 | |||||
chrX:154447443
|
A | AT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+883_442+884ins others(1): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447443 | ||||||
chrX:154447483
|
T | TA | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.442+927dupA | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447483 | |||||
chrX:154447535
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.443-949C>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447535 | ||||||
chrX:154447595
|
TG | T | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-888delG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447595 | ||||||
chrX:154447626
|
G | GT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-853dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447626 | |||||
chrX:154447647
|
G | GT | 2 | a0002c0003t0001g0027a0003c0004t0009g0049 | 2 | NA18965.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.443-832dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447647 | |||||
chrX:154447664
|
TC | T | 1 | a0002c0003t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.443-817delC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447664 | |||||
chrX:154447676
|
AG | A | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-806delG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447676 | |||||
chrX:154447719
|
A | ACATCAC | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-764_443-763ins others(6): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447719 | |||||
chrX:154447721
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-763C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447721 | ||||||
chrX:154447739
|
C | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 17 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.443-745C>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447739 | ||||||
chrX:154447740
|
C | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 17 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.443-744C>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447740 | ||||||
chrX:154447771
|
T | TA | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-712dupA | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447771 | |||||
chrX:154447874
|
T | TG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-605dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447874 | |||||
chrX:154447904
|
T | TC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-579dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447904 | |||||
chrX:154447952
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.443-532C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154447952 | ||||||
chrX:154447962
|
G | GT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-519dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447962 | |||||
chrX:154447966
|
A | AG | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-513dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447966 | |||||
chrX:154447984
|
AC | A | 1 | a0001c0001t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.443-496delC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154447984 | |||||
chrX:154448039
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-445T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154448039 | ||||||
chrX:154448039
|
T | TC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-444dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448039 | |||||
chrX:154448040
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-444C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154448040 | ||||||
chrX:154448067
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 19 | HG00642.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.443-417T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154448067 | ||||||
chrX:154448068
|
C | CT | 2 | a0001c0001t0001g0015a0001c0001t0005g0015 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.443-413dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448068 | |||||
chrX:154448072
|
C | CT | 8 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0050others(5): Show | 14 | HG00642.hp1 HG01081.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.443-398dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTT | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.443-399_443-398dup others(2): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.443-407_443-398dup others(10): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0004 | 11 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.443-408_443-398dup others(11): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0020 | 4 | HG01934.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-409_443-398dup others(12): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.443-410_443-398dup others(13): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0012a0001c0001t0013g0012 | 3 | HG02257.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.443-398_443-397ins others(16): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0013a0001c0001t0002g0054 | 4 | HG01168.hp1 HG01891.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-398_443-397ins others(17): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(11): Show |
8 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0002g0002others(5): Show | 25 | HG00438.hp2 HG00735.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.443-398_443-397ins others(18): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(12): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0002g0006others(3): Show | 14 | HG01346.hp2 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.443-398_443-397ins others(19): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-398_443-397ins others(20): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0002g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.443-398_443-397ins others(21): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.443-398_443-397ins others(22): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448072
|
CT | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0003g0003others(1): Show | 19 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.443-398delT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448072 | |||||
chrX:154448146
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-337dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448146 | |||||
chrX:154448149
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-331dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448149 | |||||
chrX:154448158
|
T | TCA | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-325_443-324ins others(2): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448158 | |||||
chrX:154448205
|
A | AT | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-279_443-278ins others(1): Show |
FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154448205 | ||||||
chrX:154448206
|
C | CT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-277dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448206 | |||||
chrX:154448213
|
T | TG | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-270dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448213 | |||||
chrX:154448215
|
C | T | 1 | a0001c0001t0001g0011 | 3 | HG00544.hp1 HG02040.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.443-269C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154448215 | ||||||
chrX:154448219
|
A | AC | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-263dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448219 | |||||
chrX:154448224
|
A | AC | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-257dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448224 | |||||
chrX:154448233
|
A | AT | 2 | a0001c0001t0001g0026a0003c0004t0009g0049 | 2 | NA18955.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.443-244dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448233 | |||||
chrX:154448253
|
A | AG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-230dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448253 | |||||
chrX:154448258
|
A | AG | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-224dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448258 | |||||
chrX:154448301
|
CA | C | 1 | a0001c0001t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-181delA | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448301 | |||||
chrX:154448310
|
C | CT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-172dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448310 | |||||
chrX:154448407
|
T | TG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.443-72dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 154448407 | |||||
chrX:154448453
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.443-31T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 4/12 | chrX | 154448453 | ||||||
chrX:154448629
|
A | AG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.520-59dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 154448629 | |||||
chrX:154448632
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.520-58C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 5/12 | chrX | 154448632 | ||||||
chrX:154448656
|
T | TG | 1 | a0001c0001t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.520-31dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 154448656 | |||||
chrX:154448818
|
T | TC | 1 | a0001c0001t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.586+63dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 154448818 | |||||
chrX:154448874
|
AG | A | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.587-17delG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 154448874 | |||||
chrX:154448876
|
G | GC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.587-16dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 154448876 | |||||
chrX:154448880
|
C | CT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.587-12dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 154448880 | |||||
chrX:154449103
|
G | GC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.649-115dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 154449103 | |||||
chrX:154449305
|
G | GT | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.725+9dupT | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 154449305 | |||||
chrX:154449325
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.725+28G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | chrX | 154449325 | ||||||
chrX:154449352
|
T | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(33): Show | 82 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.725+55T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | chrX | 154449352 | ||||||
chrX:154449429
|
A | AG | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.725+137dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 154449429 | |||||
chrX:154449430
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0020others(2): Show | 17 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.725+133G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | chrX | 154449430 | ||||||
chrX:154449448
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.725+151C>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | chrX | 154449448 | ||||||
chrX:154449530
|
T | TC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.726-149dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 154449530 | |||||
chrX:154449548
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 73 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.726-133A>G | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | chrX | 154449548 | ||||||
chrX:154449599
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.726-82G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 8/12 | chrX | 154449599 | ||||||
chrX:154449815
|
A | AG | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.781-66dupG | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 154449815 | |||||
chrX:154449945
|
A | AC | 1 | a0003c0004t0009g0049 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.829+17dupC | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 154449945 | |||||
chrX:154450186
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.901-23C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 11/12 | chrX | 154450186 | ||||||
chrX:154450195
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.901-14T>C | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 11/12 | chrX | 154450195 | ||||||
chrX:154450358
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 71 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1011+39C>T | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 12/12 | chrX | 154450358 | ||||||
chrX:154450384
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0038 | 2 | NA18940.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1012-40G>A | FAM50A | ENSG00000071859.15 | transcript | ENST00000393600.8 | protein_coding | 12/12 | chrX | 154450384 |