Item | Value |
---|---|
geneid | 441027 |
ensemblid | ENSG00000249242.8 |
hgncid | 37263 |
symbol | TMEM150C |
name | transmembrane protein 150C |
refseq_nuc | NM_001080506.3 |
refseq_prot | NP_001073975.1 |
ensembl_nuc | ENST00000449862.7 |
ensembl_prot | ENSP00000403438.2 |
mane_status | MANE Select |
chr | chr4 |
start | 82483176 |
end | 82561988 |
strand | - |
ver | v1.2 |
region | chr4:82483176-82561988 |
region5000 | chr4:82478176-82566988 |
regionname0 | TMEM150C_chr4_82483176_82561988 |
regionname5000 | TMEM150C_chr4_82478176_82566988 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 249 | 254 | 87 | 43 | 76 | 14 | 32 | 52 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0002 | 0/0 | 249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0003 | 0/0 | 249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 750 | 253 | 87 | 43 | 76 | 14 | 31 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
c0002 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
c0003 | 0/0 | 750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
c0004 | 0/0 | 750 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2429 | 67 | 5 | 14 | 33 | 2 | 12 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0002 | 0/0 | 2435 | 33 | 1 | 4 | 17 | 3 | 8 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0003 | 0/0 | 2430 | 31 | 11 | 6 | 11 | 0 | 3 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0004 | 0/0 | 2429 | 18 | 5 | 7 | 3 | 0 | 3 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0005 | 0/0 | 2433 | 12 | 12 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0006 | 0/0 | 2425 | 10 | 10 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0007 | 0/0 | 2432 | 9 | 7 | 0 | 0 | 2 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0008 | 0/0 | 2435 | 8 | 0 | 5 | 0 | 3 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0009 | 0/0 | 2430 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0010 | 0/0 | 2429 | 5 | 0 | 0 | 4 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0011 | 0/0 | 2431 | 5 | 1 | 2 | 0 | 2 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0012 | 0/0 | 2435 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0013 | 0/0 | 2434 | 4 | 0 | 1 | 0 | 1 | 2 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0014 | 0/0 | 2430 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0015 | 0/0 | 2428 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0016 | 0/0 | 2429 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0017 | 0/0 | 2436 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0018 | 0/1 | 2435 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0019 | 0/0 | 2425 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0020 | 0/0 | 2431 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0021 | 0/0 | 2429 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0022 | 0/0 | 2429 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0023 | 0/0 | 2429 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0024 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0025 | 0/0 | 2435 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0026 | 0/0 | 2434 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0027 | 0/0 | 2436 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0028 | 0/0 | 2435 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0029 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0030 | 0/0 | 2436 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0031 | 0/0 | 2436 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0032 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0033 | 0/0 | 2434 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0034 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0035 | 0/0 | 2431 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0036 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0037 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0038 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0039 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0040 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
t0041 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 750 | 253 | 87 | 43 | 76 | 14 | 31 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0004 | 0/0 | 750 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0002c0002 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0003c0003 | 0/0 | 750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3178 | 66 | 5 | 14 | 33 | 2 | 11 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0002 | 0/0 | 3184 | 33 | 1 | 4 | 17 | 3 | 8 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0003 | 0/0 | 3179 | 30 | 11 | 5 | 11 | 0 | 3 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0004 | 0/0 | 3178 | 18 | 5 | 7 | 3 | 0 | 3 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0005 | 0/0 | 3182 | 12 | 12 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0006 | 0/0 | 3174 | 10 | 10 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0007 | 0/0 | 3181 | 9 | 7 | 0 | 0 | 2 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0008 | 0/0 | 3184 | 8 | 0 | 5 | 0 | 3 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0009 | 0/0 | 3179 | 8 | 8 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0010 | 0/0 | 3178 | 5 | 0 | 0 | 4 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0011 | 0/0 | 3180 | 5 | 1 | 2 | 0 | 2 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0012 | 0/0 | 3184 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0013 | 0/0 | 3183 | 4 | 0 | 1 | 0 | 1 | 2 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0014 | 0/0 | 3179 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0015 | 0/0 | 3177 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0016 | 0/0 | 3178 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0017 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0018 | 0/1 | 3184 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0019 | 0/0 | 3174 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0020 | 0/0 | 3180 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0021 | 0/0 | 3178 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0022 | 0/0 | 3178 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0023 | 0/0 | 3178 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0024 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0025 | 0/0 | 3184 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0026 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0027 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0028 | 0/0 | 3184 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0029 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0030 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0031 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0032 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0033 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0034 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0035 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0037 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0038 | 0/0 | 3179 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0039 | 0/0 | 3178 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0040 | 0/0 | 3178 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0001t0041 | 0/0 | 3178 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0001c0004t0001 | 0/0 | 3178 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0002c0002t0036 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
a0003c0003t0003 | 0/0 | 3179 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | copy fasta | chr4 | 82478176 | 82566988 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0010g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0011g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0011g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0012g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0013g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0013g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0013g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0014g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0015g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0016g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0016g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0016g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0017g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0018g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0018g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0019g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0020g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0020g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0021g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0021g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0022g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0022g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0023g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0023g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0024g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0025g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0026g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0027g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0028g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0029g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0030g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0031g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0032g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0033g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0034g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0035g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0037g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0038g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0039g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0040g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0001t0041g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0002c0002t0036g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
a0003c0003t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0162 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0141 | EUR | GBR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00280 | hp2 | a0001 | c0001 | t0018 | g0048 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00323 | hp1 | a0001 | c0001 | t0013 | g0229 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0142 | EUR | FIN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00642 | hp2 | a0001 | c0001 | t0039 | g0015 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00673 | hp2 | a0001 | c0001 | t0010 | g0009 | EAS | CHS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00735 | hp1 | a0001 | c0001 | t0013 | g0242 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00735 | hp2 | a0001 | c0001 | t0022 | g0197 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01071 | hp1 | a0003 | c0003 | t0003 | g0191 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0218 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01167 | hp1 | a0001 | c0001 | t0011 | g0068 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0110 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0107 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01243 | hp2 | a0001 | c0001 | t0033 | g0171 | AMR | PUR | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01257 | hp1 | a0001 | c0001 | t0008 | g0216 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0223 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0222 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01515 | hp2 | a0001 | c0001 | t0011 | g0067 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0220 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01516 | hp2 | a0001 | c0001 | t0011 | g0056 | EUR | IBS | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01884 | hp1 | a0001 | c0001 | t0014 | g0032 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PEL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02056 | hp1 | a0001 | c0001 | t0010 | g0010 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02074 | hp1 | a0001 | c0001 | t0010 | g0201 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | CDX | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0031 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0099 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0170 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0029 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02717 | hp1 | a0001 | c0001 | t0019 | g0095 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0190 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02818 | hp1 | a0001 | c0001 | t0034 | g0167 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0147 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02886 | hp2 | a0001 | c0001 | t0025 | g0007 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02895 | hp1 | a0001 | c0001 | t0014 | g0026 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02895 | hp2 | a0001 | c0001 | t0031 | g0028 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02922 | hp1 | a0001 | c0001 | t0023 | g0089 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02970 | hp2 | a0001 | c0001 | t0030 | g0097 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02976 | hp1 | a0001 | c0001 | t0032 | g0033 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03041 | hp1 | a0001 | c0001 | t0019 | g0248 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03130 | hp1 | a0001 | c0001 | t0021 | g0078 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03130 | hp2 | a0001 | c0001 | t0015 | g0146 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0104 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0091 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03195 | hp1 | a0001 | c0001 | t0041 | g0038 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03195 | hp2 | a0001 | c0001 | t0017 | g0145 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0085 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03209 | hp2 | a0001 | c0001 | t0021 | g0149 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03453 | hp2 | a0002 | c0002 | t0036 | g0023 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0054 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ESN | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0098 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | GWD | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03688 | hp2 | a0001 | c0001 | t0020 | g0122 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03704 | hp1 | a0001 | c0001 | t0028 | g0224 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0196 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03710 | hp2 | a0001 | c0001 | t0027 | g0151 | SAS | PJL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0055 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0150 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG04204 | hp1 | a0001 | c0001 | t0013 | g0169 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0053 | SAS | STU | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0096 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18612 | hp2 | a0001 | c0001 | t0038 | g0243 | EAS | CHB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18906 | hp2 | a0001 | c0001 | t0014 | g0024 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18944 | hp1 | a0001 | c0001 | t0020 | g0247 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18956 | hp1 | a0001 | c0001 | t0010 | g0254 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18967 | hp2 | a0001 | c0001 | t0016 | g0158 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19000 | hp1 | a0001 | c0001 | t0016 | g0168 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19003 | hp1 | a0001 | c0001 | t0029 | g0049 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19011 | hp1 | a0001 | c0001 | t0024 | g0239 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19043 | hp1 | a0001 | c0001 | t0035 | g0154 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19043 | hp2 | a0001 | c0001 | t0026 | g0203 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19066 | hp1 | a0001 | c0001 | t0040 | g0125 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19068 | hp1 | a0001 | c0001 | t0016 | g0227 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | YRI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | TSI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | GIH | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01123 | hp1 | a0001 | c0001 | t0022 | g0183 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG01123 | hp2 | a0001 | c0001 | t0008 | g0219 | AMR | CLM | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02486 | hp1 | a0001 | c0001 | t0037 | g0080 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ACB | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | MSL | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA20300 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | USA | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | LWK | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0018 | g0047 | REF | REF | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0164 | REF | REF | TMEM150C_chr4_82478176_82566988 | TMEM150C | chr4 | 82478176 | 82566988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82485587
|
G | A | 1 | a0003 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.674C>T | p.Ser225Phe | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 767/3178 | 674/750 | 225/249 | chr4 | 82485587 | ||
chr4:82485624
|
C | T | 1 | a0002 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.637G>A | p.Val213Met | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 730/3178 | 637/750 | 213/249 | chr4 | 82485624 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82490173
|
G | A | 1 | a0001c0004 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.429C>T | p.Thr143Thr | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/8 | 522/3178 | 429/750 | 143/249 | chr4 | 82490173 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82483214
|
A | G | 1 | a0001c0001t0010 | 5 | HG00673.hp2 HG02056.hp1 HG02074.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2297T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2297 | chr4 | 82483214 | |||||
chr4:82483233
|
G | C | 2 | a0001c0001t0004a0001c0001t0037 | 19 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2278C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2278 | chr4 | 82483233 | |||||
chr4:82483237
|
G | C | 1 | a0001c0001t0022 | 2 | HG00735.hp2 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2274C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2274 | chr4 | 82483237 | |||||
chr4:82483388
|
G | T | 1 | a0001c0001t0025 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 2123 | chr4 | 82483388 | |||||
chr4:82483613
|
T | C | 4 | a0001c0001t0006a0001c0001t0007a0001c0001t0019others(1): Show | 22 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1898A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1898 | chr4 | 82483613 | |||||
chr4:82483788
|
C | CT | 6 | a0001c0001t0009a0001c0001t0023a0001c0001t0024others(3): Show | 14 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1722dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1722 | chr4 | 82483788 | |||||
chr4:82483789
|
TTTTTTTC | T | 2 | a0001c0001t0006a0001c0001t0019 | 12 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1715_*1721delGAAA others(3): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1715 | chr4 | 82483789 | |||||
chr4:82483795
|
TC | T | 6 | a0001c0001t0004a0001c0001t0013a0001c0001t0026others(3): Show | 26 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1715delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1715 | chr4 | 82483795 | |||||
chr4:82483796
|
C | T | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(24): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1715G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1715 | chr4 | 82483796 | |||||
chr4:82483798
|
T | TTC | 1 | a0001c0001t0011 | 5 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1712_*1713insGA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1712 | chr4 | 82483798 | |||||
chr4:82483972
|
A | G | 6 | a0001c0001t0003a0001c0001t0014a0001c0001t0016others(3): Show | 40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1539T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1539 | chr4 | 82483972 | |||||
chr4:82484079
|
C | T | 2 | a0001c0001t0014a0001c0001t0039 | 5 | HG00642.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1432G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1432 | chr4 | 82484079 | |||||
chr4:82484084
|
C | T | 3 | a0001c0001t0012a0001c0001t0025a0001c0001t0026 | 6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1427G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1427 | chr4 | 82484084 | |||||
chr4:82484230
|
T | C | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*1281A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1281 | chr4 | 82484230 | |||||
chr4:82484237
|
A | G | 1 | a0001c0001t0024 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1274T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1274 | chr4 | 82484237 | |||||
chr4:82484411
|
C | CA | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | 82 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1099dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1099 | chr4 | 82484411 | |||||
chr4:82484411
|
CA | C | 2 | a0001c0001t0015a0001c0001t0023 | 5 | HG01167.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1099delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 1099 | chr4 | 82484411 | |||||
chr4:82484805
|
T | A | 2 | a0001c0001t0004a0001c0001t0038 | 19 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 706 | chr4 | 82484805 | |||||
chr4:82485011
|
G | A | 1 | a0001c0001t0006 | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*500C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 500 | chr4 | 82485011 | |||||
chr4:82485041
|
G | A | 1 | a0001c0001t0037 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 470 | chr4 | 82485041 | |||||
chr4:82485052
|
T | C | 6 | a0001c0001t0009a0001c0001t0011a0001c0001t0023others(3): Show | 18 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 459 | chr4 | 82485052 | |||||
chr4:82485058
|
A | G | 1 | a0001c0001t0018 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*453T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 453 | chr4 | 82485058 | |||||
chr4:82485064
|
A | T | 1 | a0001c0001t0037 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 447 | chr4 | 82485064 | |||||
chr4:82485143
|
C | T | 1 | a0001c0001t0017 | 2 | HG02886.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 368 | chr4 | 82485143 | |||||
chr4:82485247
|
C | T | 6 | a0001c0001t0006a0001c0001t0007a0001c0001t0017others(3): Show | 25 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 264 | chr4 | 82485247 | |||||
chr4:82485334
|
T | C | 1 | a0001c0001t0008 | 8 | HG00099.hp2 HG01071.hp2 HG01123.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 177 | chr4 | 82485334 | |||||
chr4:82485367
|
A | G | 3 | a0001c0001t0004a0001c0001t0037a0001c0001t0038 | 20 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*144T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 144 | chr4 | 82485367 | |||||
chr4:82485396
|
A | ATG | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0019others(4): Show | 26 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*113_*114dupCA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 114 | chr4 | 82485396 | |||||
chr4:82485396
|
A | ATGTG | 3 | a0001c0001t0005a0001c0001t0032a0001c0001t0033 | 14 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*111_*114dupCACA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 114 | chr4 | 82485396 | |||||
chr4:82485396
|
A | ATGTGTG | 14 | a0001c0001t0002a0001c0001t0008a0001c0001t0012others(11): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*114dupCACACA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 8/8 | 114 | chr4 | 82485396 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82485944
|
T | G | 2 | a0001c0001t0021g0078a0001c0001t0021g0149 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.542-225A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82485944 | ||||||
chr4:82486002
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.542-283A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486002 | ||||||
chr4:82486014
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.542-295A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486014 | ||||||
chr4:82486232
|
G | A | 40 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0034others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.542-513C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486232 | ||||||
chr4:82486257
|
T | A | 2 | a0001c0001t0017g0145a0001c0001t0017g0147 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.542-538A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486257 | ||||||
chr4:82486335
|
T | TA | 64 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0058others(61): Show | 64 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.542-617dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | ||||||
chr4:82486335
|
T | TAA | 7 | a0001c0001t0001g0035a0001c0001t0001g0165a0001c0001t0003g0004others(4): Show | 7 | HG00642.hp2 HG02165.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-618_542-617dup others(2): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | ||||||
chr4:82486335
|
T | TAAAAA | 8 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0104others(5): Show | 8 | HG01167.hp1 HG01515.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.542-621_542-617dup others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | ||||||
chr4:82486335
|
TA | T | 15 | a0001c0001t0001g0061a0001c0001t0001g0111a0001c0001t0001g0244others(12): Show | 15 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.542-617delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | ||||||
chr4:82486335
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0021 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.542-631_542-617del others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486335 | ||||||
chr4:82486403
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.542-684C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486403 | ||||||
chr4:82486488
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG00738.hp2 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-769G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486488 | ||||||
chr4:82486555
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.542-836G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486555 | ||||||
chr4:82486569
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0088others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-850C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486569 | ||||||
chr4:82486691
|
A | G | 40 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0034others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.542-972T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486691 | ||||||
chr4:82486889
|
C | A | 1 | a0001c0001t0023g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.542-1170G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82486889 | ||||||
chr4:82487129
|
A | G | 2 | a0001c0001t0013g0169a0001c0001t0013g0242 | 2 | HG00735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.542-1410T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487129 | ||||||
chr4:82487173
|
A | G | 175 | a0001c0001t0002g0013a0001c0001t0002g0020a0001c0001t0002g0021others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.542-1454T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487173 | ||||||
chr4:82487224
|
G | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0131 | 2 | NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.542-1505C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487224 | ||||||
chr4:82487241
|
TAG | T | 12 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0039others(9): Show | 12 | HG00642.hp2 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-1524_542-1523d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487241 | ||||||
chr4:82487265
|
A | G | 1 | a0001c0001t0034g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.542-1546T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487265 | ||||||
chr4:82487284
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.542-1565T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487284 | ||||||
chr4:82487305
|
C | T | 65 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0034others(62): Show | 65 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.542-1586G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487305 | ||||||
chr4:82487805
|
A | C | 1 | a0001c0001t0003g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.542-2086T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487805 | ||||||
chr4:82487815
|
C | A | 65 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0034others(62): Show | 65 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.542-2096G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487815 | ||||||
chr4:82487819
|
C | A | 2 | a0001c0001t0007g0141a0001c0001t0007g0142 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.542-2100G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487819 | ||||||
chr4:82487836
|
G | A | 1 | a0001c0001t0028g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.542-2117C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82487836 | ||||||
chr4:82488027
|
T | C | 5 | a0001c0001t0012g0001a0001c0001t0012g0096a0001c0001t0012g0098others(2): Show | 6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+2034A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488027 | ||||||
chr4:82488051
|
T | C | 22 | a0001c0001t0006g0005a0001c0001t0006g0025a0001c0001t0006g0081others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.541+2010A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488051 | ||||||
chr4:82488178
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.541+1883T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488178 | ||||||
chr4:82488315
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208 | 3 | NA18944.hp2 NA18995.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.541+1746C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488315 | ||||||
chr4:82488354
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.541+1707C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488354 | ||||||
chr4:82488392
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(117): Show | 121 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.541+1669T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488392 | ||||||
chr4:82488499
|
T | C | 7 | a0001c0001t0005g0036a0001c0001t0005g0085a0001c0001t0005g0102others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+1562A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488499 | ||||||
chr4:82488954
|
G | A | 3 | a0001c0001t0003g0133a0001c0001t0003g0139a0001c0001t0003g0176 | 3 | HG00609.hp1 HG01943.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.541+1107C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82488954 | ||||||
chr4:82489037
|
G | A | 52 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0041others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.541+1024C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489037 | ||||||
chr4:82489062
|
A | AT | 45 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(42): Show | 45 | HG00738.hp2 HG01106.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.541+998dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489062 | ||||||
chr4:82489062
|
A | ATT | 9 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0050others(6): Show | 9 | HG00544.hp2 HG02486.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.541+997_541+998dup others(2): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489062 | ||||||
chr4:82489325
|
G | A | 12 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.541+736C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489325 | ||||||
chr4:82489411
|
ACCT | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(4): Show | 7 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+647_541+649del others(3): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489411 | ||||||
chr4:82489469
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.541+592G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489469 | ||||||
chr4:82489597
|
T | C | 1 | a0001c0001t0037g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.541+464A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489597 | ||||||
chr4:82489611
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(4): Show | 7 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+450A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489611 | ||||||
chr4:82489715
|
A | C | 17 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0086others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.541+346T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489715 | ||||||
chr4:82489893
|
T | C | 24 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(21): Show | 24 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.541+168A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82489893 | ||||||
chr4:82490044
|
T | C | 46 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0234others(43): Show | 46 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.541+17A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82490044 | ||||||
chr4:82490048
|
G | A | 43 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(40): Show | 44 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.541+13C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 7/7 | chr4 | 82490048 | ||||||
chr4:82490309
|
AT | A | 3 | a0001c0001t0011g0056a0001c0001t0011g0067a0001c0001t0011g0068 | 3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.364-72delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490309 | ||||||
chr4:82490311
|
A | C | 3 | a0001c0001t0011g0056a0001c0001t0011g0067a0001c0001t0011g0068 | 3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.364-73T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490311 | ||||||
chr4:82490482
|
A | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.364-244T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490482 | ||||||
chr4:82490508
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG00738.hp2 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-270A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490508 | ||||||
chr4:82490593
|
T | G | 20 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(17): Show | 20 | HG00544.hp2 HG01106.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-355A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490593 | ||||||
chr4:82490754
|
G | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.364-516C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490754 | ||||||
chr4:82490798
|
G | A | 1 | a0001c0001t0035g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.364-560C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490798 | ||||||
chr4:82490838
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.364-600C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490838 | ||||||
chr4:82490934
|
G | A | 4 | a0001c0001t0021g0078a0001c0001t0021g0149a0001c0001t0035g0154others(1): Show | 4 | HG02486.hp1 HG03130.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-696C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82490934 | ||||||
chr4:82491049
|
C | T | 2 | a0001c0001t0009g0213a0001c0001t0031g0028 | 2 | HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.364-811G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491049 | ||||||
chr4:82491209
|
C | T | 17 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0086others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-971G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491209 | ||||||
chr4:82491237
|
G | A | 2 | a0001c0001t0005g0036a0001c0001t0005g0204 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.364-999C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491237 | ||||||
chr4:82491446
|
G | A | 1 | a0001c0001t0007g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.364-1208C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491446 | ||||||
chr4:82491595
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-1357C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491595 | ||||||
chr4:82491702
|
A | G | 24 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0086others(21): Show | 25 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-1464T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491702 | ||||||
chr4:82491895
|
G | T | 47 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(44): Show | 48 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.364-1657C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491895 | ||||||
chr4:82491924
|
T | A | 1 | a0001c0001t0003g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364-1686A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491924 | ||||||
chr4:82491936
|
GT | G | 78 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(75): Show | 79 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.364-1699delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491936 | ||||||
chr4:82491949
|
G | T | 24 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(21): Show | 24 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-1711C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491949 | ||||||
chr4:82491991
|
GTGCAGTG others(19): Show |
G | 4 | a0001c0001t0005g0006a0001c0001t0005g0022a0001c0001t0005g0030others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1779_364-1754d others(28): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82491991 | ||||||
chr4:82492047
|
TG | T | 17 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0086others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-1810delC | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492047 | ||||||
chr4:82492117
|
TTTG | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(131): Show | 135 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.364-1882_364-1880d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492117 | ||||||
chr4:82492120
|
G | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 12 | HG00735.hp2 HG00738.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-1882C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492120 | ||||||
chr4:82492152
|
A | C | 1 | a0001c0001t0002g0198 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.364-1914T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492152 | ||||||
chr4:82492238
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.364-2000G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492238 | ||||||
chr4:82492344
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(4): Show | 7 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2106A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492344 | ||||||
chr4:82492391
|
G | A | 1 | a0001c0001t0004g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.364-2153C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492391 | ||||||
chr4:82492448
|
A | AT | 57 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(54): Show | 58 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.364-2211dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492448 | ||||||
chr4:82492792
|
C | CA | 19 | a0001c0001t0001g0003a0001c0001t0001g0159a0001c0001t0001g0165others(16): Show | 19 | HG01243.hp2 HG01261.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-2555dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492792 | ||||||
chr4:82492792
|
C | CAA | 5 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0050others(2): Show | 5 | HG02165.hp1 HG03098.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-2556_364-2555d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492792 | ||||||
chr4:82492805
|
AAAAAAC | A | 10 | a0001c0001t0005g0102a0001c0001t0006g0005a0001c0001t0006g0025others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-2573_364-2568d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492805 | ||||||
chr4:82492806
|
AAAAAC | A | 14 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.364-2573_364-2569d others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492806 | ||||||
chr4:82492809
|
AAC | A | 12 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(9): Show | 12 | HG01168.hp2 HG01192.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-2573_364-2572d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492809 | ||||||
chr4:82492810
|
AC | A | 5 | a0001c0001t0004g0196a0001c0001t0004g0209a0001c0001t0004g0237others(2): Show | 5 | HG00544.hp2 HG01515.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-2573delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492810 | ||||||
chr4:82492811
|
C | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(83): Show | 87 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.364-2573G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492811 | ||||||
chr4:82492858
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364-2620C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492858 | ||||||
chr4:82492864
|
G | GTA | 40 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0043others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.364-2628_364-2627d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATA | 20 | a0001c0001t0001g0060a0001c0001t0001g0120a0001c0001t0001g0124others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-2630_364-2627d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATA | 15 | a0001c0001t0001g0188a0001c0001t0002g0226a0001c0001t0003g0062others(12): Show | 15 | HG00673.hp1 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-2632_364-2627d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(1): Show |
13 | a0001c0001t0002g0127a0001c0001t0003g0040a0001c0001t0003g0108others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-2634_364-2627d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(3): Show |
7 | a0001c0001t0001g0182a0001c0001t0003g0034a0001c0001t0003g0140others(4): Show | 7 | HG00423.hp2 HG01884.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2636_364-2627d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(5): Show |
12 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0002g0128others(9): Show | 12 | HG01891.hp1 HG01981.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-2638_364-2627d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(7): Show |
4 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0235others(1): Show | 4 | HG01106.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-2640_364-2627d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0058a0001c0001t0003g0215a0001c0001t0003g0241 | 3 | HG01109.hp1 HG02027.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.364-2642_364-2627d others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0003g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364-2644_364-2627d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.364-2627_364-2626i others(32): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTGTATA | 3 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0144 | 3 | NA18961.hp1 NA18969.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.364-2627_364-2626i others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0035g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.364-2627_364-2626i others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTGTATAT others(5): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0123 | 3 | HG02165.hp1 NA18972.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.364-2627_364-2626i others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0017 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-2627_364-2626i others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTA | G | 17 | a0001c0001t0002g0069a0001c0001t0002g0118a0001c0001t0004g0016others(14): Show | 17 | HG01071.hp1 HG01261.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-2628_364-2627d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTATA | G | 15 | a0001c0001t0007g0142a0001c0001t0009g0086a0001c0001t0009g0087others(12): Show | 15 | HG00323.hp2 HG01167.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-2630_364-2627d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTATATA | G | 7 | a0001c0001t0002g0065a0001c0001t0005g0085a0001c0001t0005g0148others(4): Show | 7 | HG00140.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2632_364-2627d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTATATAT others(1): Show |
G | 20 | a0001c0001t0002g0013a0001c0001t0002g0236a0001c0001t0003g0039others(17): Show | 21 | HG00544.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.364-2634_364-2627d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTATATAT others(3): Show |
G | 3 | a0001c0001t0007g0103a0001c0001t0017g0145a0001c0001t0017g0147 | 3 | HG02886.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-2636_364-2627d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0020g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.364-2638_364-2627d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492864
|
GTATATAT others(7): Show |
G | 3 | a0001c0001t0001g0121a0001c0001t0004g0132a0001c0001t0004g0233 | 3 | HG01106.hp1 HG01975.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.364-2640_364-2627d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492864 | ||||||
chr4:82492866
|
A | G | 10 | a0001c0001t0004g0126a0001c0001t0004g0190a0001c0001t0004g0193others(7): Show | 10 | HG00544.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-2628T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492866 | ||||||
chr4:82492868
|
A | G | 21 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(18): Show | 21 | HG00544.hp2 HG01168.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.364-2630T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492868 | ||||||
chr4:82492870
|
A | G | 25 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(22): Show | 25 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-2632T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492870 | ||||||
chr4:82492872
|
A | G | 13 | a0001c0001t0009g0086a0001c0001t0009g0087a0001c0001t0009g0170others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-2634T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492872 | ||||||
chr4:82492874
|
A | G | 6 | a0001c0001t0012g0001a0001c0001t0012g0096a0001c0001t0012g0098others(3): Show | 7 | HG02886.hp2 HG02970.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2636T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492874 | ||||||
chr4:82492880
|
A | G | 2 | a0001c0001t0004g0132a0001c0001t0004g0233 | 2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.364-2642T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492880 | ||||||
chr4:82492882
|
A | G | 2 | a0001c0001t0004g0132a0001c0001t0004g0233 | 2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.364-2644T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492882 | ||||||
chr4:82492896
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0039g0015 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.364-2659_364-2658i others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492896 | ||||||
chr4:82492898
|
A | G | 7 | a0001c0001t0005g0085a0001c0001t0005g0148a0001c0001t0005g0172others(4): Show | 7 | HG02145.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-2660T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82492898 | ||||||
chr4:82493249
|
T | G | 2 | a0001c0001t0017g0145a0001c0001t0017g0147 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.363+2819A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493249 | ||||||
chr4:82493266
|
CAT | C | 3 | a0001c0001t0011g0056a0001c0001t0011g0067a0001c0001t0011g0068 | 3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.363+2800_363+2801d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493266 | ||||||
chr4:82493293
|
G | A | 1 | a0001c0001t0023g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+2775C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493293 | ||||||
chr4:82493342
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.363+2726T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493342 | ||||||
chr4:82493417
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.363+2651C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493417 | ||||||
chr4:82493512
|
T | C | 1 | a0001c0001t0033g0171 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.363+2556A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493512 | ||||||
chr4:82493667
|
A | C | 14 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+2401T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82493667 | ||||||
chr4:82494388
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(2): Show | 5 | HG02165.hp1 HG03098.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1680C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494388 | ||||||
chr4:82494662
|
C | A | 1 | a0001c0001t0003g0179 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.363+1406G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494662 | ||||||
chr4:82494696
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.363+1372T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494696 | ||||||
chr4:82494783
|
A | AT | 67 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0117others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.363+1284dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | ||||||
chr4:82494783
|
A | ATT | 70 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0002g0013others(67): Show | 70 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+1283_363+1284d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | ||||||
chr4:82494783
|
A | ATTT | 10 | a0001c0001t0001g0017a0001c0001t0001g0234a0001c0001t0003g0034others(7): Show | 10 | HG00609.hp1 HG00639.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+1282_363+1284d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | ||||||
chr4:82494783
|
ATTTTTT | A | 20 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0086others(17): Show | 21 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+1279_363+1284d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494783 | ||||||
chr4:82494954
|
T | A | 46 | a0001c0001t0001g0017a0001c0001t0002g0118a0001c0001t0004g0112others(43): Show | 47 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.363+1114A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494954 | ||||||
chr4:82494974
|
C | T | 1 | a0001c0001t0034g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.363+1094G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82494974 | ||||||
chr4:82495106
|
G | C | 5 | a0001c0001t0012g0001a0001c0001t0012g0096a0001c0001t0012g0098others(2): Show | 6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+962C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495106 | ||||||
chr4:82495145
|
A | G | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.363+923T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495145 | ||||||
chr4:82495201
|
G | A | 1 | a0001c0001t0011g0056 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.363+867C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495201 | ||||||
chr4:82495214
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.363+854C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495214 | ||||||
chr4:82495397
|
C | T | 8 | a0001c0001t0002g0118a0001c0001t0004g0126a0001c0001t0004g0190others(5): Show | 8 | HG01168.hp2 HG01192.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+671G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495397 | ||||||
chr4:82495605
|
T | C | 2 | a0001c0001t0022g0183a0001c0001t0022g0197 | 2 | HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.363+463A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495605 | ||||||
chr4:82495636
|
T | A | 1 | a0001c0001t0007g0037 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+432A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495636 | ||||||
chr4:82495872
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.363+196C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 6/7 | chr4 | 82495872 | ||||||
chr4:82496324
|
C | T | 2 | a0001c0001t0005g0036a0001c0001t0005g0204 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.236-129G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496324 | ||||||
chr4:82496396
|
A | G | 1 | a0001c0001t0004g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.236-201T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496396 | ||||||
chr4:82496635
|
C | A | 2 | a0001c0001t0003g0140a0001c0001t0016g0227 | 2 | HG00423.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.236-440G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496635 | ||||||
chr4:82496680
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.236-485T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496680 | ||||||
chr4:82496829
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0253 | 2 | NA18948.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.236-634C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82496829 | ||||||
chr4:82497045
|
T | G | 26 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.236-850A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497045 | ||||||
chr4:82497100
|
G | A | 1 | a0003c0003t0003g0191 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.236-905C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497100 | ||||||
chr4:82497306
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.236-1111G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497306 | ||||||
chr4:82497357
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.236-1162C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497357 | ||||||
chr4:82497360
|
C | T | 13 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0003g0004others(10): Show | 13 | HG00642.hp2 HG01109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-1165G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497360 | ||||||
chr4:82497432
|
A | C | 5 | a0001c0001t0006g0081a0001c0001t0006g0090a0001c0001t0006g0214others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-1237T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497432 | ||||||
chr4:82497512
|
T | C | 2 | a0001c0001t0005g0085a0001c0001t0005g0172 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.236-1317A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497512 | ||||||
chr4:82497588
|
T | C | 3 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0033g0171 | 3 | HG01243.hp2 HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.236-1393A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497588 | ||||||
chr4:82497648
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.236-1453T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497648 | ||||||
chr4:82497777
|
A | G | 51 | a0001c0001t0002g0118a0001c0001t0004g0016a0001c0001t0004g0112others(48): Show | 52 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.236-1582T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497777 | ||||||
chr4:82497887
|
G | A | 50 | a0001c0001t0001g0017a0001c0001t0002g0118a0001c0001t0003g0200others(47): Show | 51 | HG00544.hp2 HG01167.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.236-1692C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82497887 | ||||||
chr4:82498018
|
AT | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0035others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.236-1824delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82498018 | ||||||
chr4:82498384
|
G | A | 44 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0234others(41): Show | 44 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.236-2189C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82498384 | ||||||
chr4:82498759
|
G | T | 2 | a0001c0001t0009g0087a0001c0001t0009g0170 | 2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.236-2564C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82498759 | ||||||
chr4:82499028
|
G | C | 4 | a0001c0001t0005g0036a0001c0001t0005g0085a0001c0001t0005g0172others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-2833C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499028 | ||||||
chr4:82499248
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.236-3053G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499248 | ||||||
chr4:82499375
|
G | A | 1 | a0001c0001t0004g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236-3180C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499375 | ||||||
chr4:82499391
|
G | A | 25 | a0001c0001t0005g0148a0001c0001t0005g0173a0001c0001t0009g0018others(22): Show | 26 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-3196C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499391 | ||||||
chr4:82499424
|
AAAG | A | 4 | a0001c0001t0004g0114a0001c0001t0017g0145a0001c0001t0017g0147others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-3232_236-3230d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499424 | ||||||
chr4:82499487
|
C | T | 4 | a0001c0001t0004g0114a0001c0001t0017g0145a0001c0001t0017g0147others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+3240G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499487 | ||||||
chr4:82499488
|
G | A | 2 | a0001c0001t0021g0149a0001c0001t0037g0080 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.235+3239C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499488 | ||||||
chr4:82499503
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.235+3224G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499503 | ||||||
chr4:82499616
|
G | A | 5 | a0001c0001t0012g0001a0001c0001t0012g0096a0001c0001t0012g0098others(2): Show | 6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3111C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499616 | ||||||
chr4:82499685
|
T | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0088others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+3042A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499685 | ||||||
chr4:82499713
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.235+3014G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499713 | ||||||
chr4:82499719
|
C | CA | 61 | a0001c0001t0001g0044a0001c0001t0001g0123a0001c0001t0001g0124others(58): Show | 61 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.235+3007dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | ||||||
chr4:82499719
|
C | CAA | 38 | a0001c0001t0001g0017a0001c0001t0001g0165a0001c0001t0002g0118others(35): Show | 38 | HG00544.hp2 HG01106.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.235+3006_235+3007d others(4): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | ||||||
chr4:82499719
|
C | CAAA | 24 | a0001c0001t0003g0200a0001c0001t0004g0113a0001c0001t0004g0190others(21): Show | 25 | HG00140.hp2 HG00323.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.235+3005_235+3007d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | ||||||
chr4:82499719
|
C | CAAAA | 10 | a0001c0001t0002g0065a0001c0001t0002g0236a0001c0001t0005g0036others(7): Show | 10 | HG00544.hp1 HG01167.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+3004_235+3007d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | ||||||
chr4:82499719
|
C | CAAAAA | 10 | a0001c0001t0002g0013a0001c0001t0009g0018a0001c0001t0009g0029others(7): Show | 10 | HG01515.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+3003_235+3007d others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | ||||||
chr4:82499719
|
C | CAAAAAA | 6 | a0001c0001t0005g0173a0001c0001t0009g0088a0001c0001t0009g0104others(3): Show | 6 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3002_235+3007d others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499719 | ||||||
chr4:82499862
|
G | A | 4 | a0001c0001t0005g0036a0001c0001t0005g0085a0001c0001t0005g0172others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+2865C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499862 | ||||||
chr4:82499984
|
G | A | 3 | a0001c0001t0007g0027a0001c0001t0007g0103a0001c0001t0030g0097 | 3 | HG01884.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.235+2743C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82499984 | ||||||
chr4:82500011
|
A | T | 3 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0033g0171 | 3 | HG01243.hp2 HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.235+2716T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500011 | ||||||
chr4:82500066
|
A | C | 1 | a0001c0001t0003g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.235+2661T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500066 | ||||||
chr4:82500082
|
T | C | 1 | a0001c0001t0017g0147 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.235+2645A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500082 | ||||||
chr4:82500127
|
A | G | 1 | a0001c0001t0003g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.235+2600T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500127 | ||||||
chr4:82500287
|
G | T | 26 | a0001c0001t0001g0234a0001c0001t0003g0040a0001c0001t0003g0051others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+2440C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500287 | ||||||
chr4:82500583
|
G | A | 54 | a0001c0001t0001g0017a0001c0001t0002g0118a0001c0001t0003g0200others(51): Show | 55 | HG00544.hp2 HG01167.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.235+2144C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500583 | ||||||
chr4:82500743
|
T | C | 26 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+1984A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500743 | ||||||
chr4:82500991
|
C | T | 3 | a0001c0001t0004g0016a0001c0001t0004g0112a0001c0001t0004g0113 | 3 | HG02723.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.235+1736G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82500991 | ||||||
chr4:82501096
|
TAAATGCA others(5): Show |
T | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235+1619_235+1630d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501096 | ||||||
chr4:82501145
|
G | A | 2 | a0001c0001t0011g0067a0001c0001t0011g0068 | 2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.235+1582C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501145 | ||||||
chr4:82501475
|
C | A | 12 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+1252G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501475 | ||||||
chr4:82501861
|
A | AAT | 6 | a0001c0001t0012g0001a0001c0001t0012g0096a0001c0001t0012g0098others(3): Show | 7 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+864_235+865dup others(2): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82501861 | ||||||
chr4:82502070
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235+657A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502070 | ||||||
chr4:82502262
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.235+465T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502262 | ||||||
chr4:82502447
|
T | C | 19 | a0001c0001t0005g0148a0001c0001t0005g0173a0001c0001t0009g0018others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.235+280A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502447 | ||||||
chr4:82502584
|
A | G | 15 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0034others(12): Show | 15 | HG00642.hp2 HG01109.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+143T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502584 | ||||||
chr4:82502691
|
C | T | 26 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+36G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502691 | ||||||
chr4:82502707
|
G | A | 2 | a0001c0001t0005g0079a0001c0001t0005g0202 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235+20C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 5/7 | chr4 | 82502707 | ||||||
chr4:82502936
|
T | TA | 19 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 19 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.135-10dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 3/7 | chr4 | 82502936 | ||||||
chr4:82503049
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.134+10A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 3/7 | chr4 | 82503049 | ||||||
chr4:82503195
|
C | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.81-83G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503195 | ||||||
chr4:82503283
|
A | G | 1 | a0001c0001t0005g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.81-171T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503283 | ||||||
chr4:82503285
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0002g0118a0001c0001t0003g0200others(22): Show | 25 | HG00544.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.81-173A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503285 | ||||||
chr4:82503420
|
G | A | 4 | a0001c0001t0005g0036a0001c0001t0005g0085a0001c0001t0005g0172others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-308C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503420 | ||||||
chr4:82503577
|
G | A | 2 | a0001c0001t0012g0001a0001c0001t0026g0203 | 3 | NA18906.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.81-465C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503577 | ||||||
chr4:82503597
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0029a0001c0001t0009g0088others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-485A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503597 | ||||||
chr4:82503633
|
G | A | 1 | a0001c0001t0006g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-521C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503633 | ||||||
chr4:82503653
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.81-541T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503653 | ||||||
chr4:82503723
|
G | A | 5 | a0001c0001t0012g0001a0001c0001t0012g0096a0001c0001t0012g0098others(2): Show | 6 | HG02886.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-611C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503723 | ||||||
chr4:82503755
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-643G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503755 | ||||||
chr4:82503897
|
A | G | 4 | a0001c0001t0005g0036a0001c0001t0005g0085a0001c0001t0005g0172others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+681T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503897 | ||||||
chr4:82503973
|
C | T | 26 | a0001c0001t0001g0234a0001c0001t0003g0040a0001c0001t0003g0051others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+605G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82503973 | ||||||
chr4:82504106
|
T | C | 1 | a0001c0001t0001g0002 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.80+472A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504106 | ||||||
chr4:82504213
|
T | C | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.80+365A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504213 | ||||||
chr4:82504214
|
T | G | 2 | a0001c0001t0005g0036a0001c0001t0005g0204 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80+364A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504214 | ||||||
chr4:82504550
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.80+28A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 2/7 | chr4 | 82504550 | ||||||
chr4:82504826
|
C | A | 1 | a0001c0001t0037g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-10-159G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82504826 | ||||||
chr4:82504826
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0071others(11): Show | 14 | HG00673.hp2 HG01109.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-159G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82504826 | ||||||
chr4:82505108
|
A | G | 41 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0234others(38): Show | 41 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-10-441T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505108 | ||||||
chr4:82505128
|
G | C | 1 | a0001c0001t0034g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-461C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505128 | ||||||
chr4:82505219
|
A | T | 3 | a0001c0001t0001g0017a0001c0001t0003g0200a0001c0001t0021g0149 | 3 | HG02622.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-10-552T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505219 | ||||||
chr4:82505872
|
T | C | 3 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0033g0171 | 3 | HG01243.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-10-1205A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505872 | ||||||
chr4:82505955
|
A | G | 2 | a0001c0001t0005g0148a0001c0001t0005g0173 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-10-1288T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82505955 | ||||||
chr4:82506023
|
G | A | 1 | a0001c0001t0034g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-1356C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506023 | ||||||
chr4:82506084
|
T | G | 1 | a0001c0001t0003g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10-1417A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506084 | ||||||
chr4:82506311
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-10-1644A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506311 | ||||||
chr4:82506320
|
A | G | 4 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0019g0095others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1653T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506320 | ||||||
chr4:82506423
|
C | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0050others(3): Show | 6 | HG02165.hp1 NA18961.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1756G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506423 | ||||||
chr4:82506612
|
T | C | 19 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(16): Show | 19 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-1945A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506612 | ||||||
chr4:82506614
|
C | T | 4 | a0001c0001t0003g0133a0001c0001t0003g0139a0001c0001t0003g0176others(1): Show | 4 | HG00609.hp1 HG01106.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1947G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506614 | ||||||
chr4:82506817
|
C | T | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-2150G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506817 | ||||||
chr4:82506868
|
C | T | 1 | a0001c0001t0035g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10-2201G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506868 | ||||||
chr4:82506905
|
A | G | 2 | a0001c0001t0007g0014a0001c0001t0007g0077 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-2238T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506905 | ||||||
chr4:82506954
|
G | A | 1 | a0001c0001t0004g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10-2287C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506954 | ||||||
chr4:82506976
|
T | A | 3 | a0001c0001t0011g0056a0001c0001t0011g0067a0001c0001t0011g0068 | 3 | HG01167.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-10-2309A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82506976 | ||||||
chr4:82507030
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-10-2363T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507030 | ||||||
chr4:82507066
|
T | G | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-2399A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507066 | ||||||
chr4:82507270
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(111): Show | 115 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-10-2603A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507270 | ||||||
chr4:82507325
|
A | G | 4 | a0001c0001t0011g0107a0001c0001t0014g0024a0001c0001t0014g0026others(1): Show | 4 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-2658T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507325 | ||||||
chr4:82507346
|
G | T | 1 | a0001c0001t0023g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10-2679C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507346 | ||||||
chr4:82507362
|
G | T | 1 | a0001c0001t0002g0021 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10-2695C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507362 | ||||||
chr4:82507364
|
G | A | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0005g0204 | 3 | HG02258.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-10-2697C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507364 | ||||||
chr4:82507444
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(150): Show | 154 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-10-2777A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507444 | ||||||
chr4:82507570
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(111): Show | 115 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-10-2903T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507570 | ||||||
chr4:82507719
|
CTCTCTCT others(19): Show |
C | 6 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3078_-10-3053d others(28): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507719 | ||||||
chr4:82507719
|
CTCTCTCT others(21): Show |
C | 6 | a0001c0001t0005g0148a0001c0001t0005g0173a0001c0001t0011g0056others(3): Show | 6 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3080_-10-3053d others(30): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507719 | ||||||
chr4:82507719
|
CTCTCTCT others(22): Show |
C | 1 | a0001c0001t0009g0087 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-10-3081_-10-3053d others(31): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507719 | ||||||
chr4:82507723
|
CTCTCTTT others(3): Show |
C | 2 | a0001c0001t0007g0141a0001c0001t0007g0142 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-10-3066_-10-3057d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(4): Show |
C | 6 | a0001c0001t0002g0013a0001c0001t0002g0065a0001c0001t0002g0236others(3): Show | 6 | HG00544.hp1 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-3067_-10-3057d others(13): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(5): Show |
C | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-10-3068_-10-3057d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(7): Show |
C | 3 | a0001c0001t0003g0062a0001c0001t0023g0089a0001c0001t0023g0091 | 3 | HG02922.hp1 HG03139.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-10-3070_-10-3057d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(11): Show |
C | 2 | a0001c0001t0004g0150a0001c0001t0005g0030 | 2 | HG02572.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-10-3074_-10-3057d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(12): Show |
C | 19 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0064others(16): Show | 19 | HG00544.hp2 HG00738.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-3075_-10-3057d others(21): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(13): Show |
C | 74 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0052others(71): Show | 75 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-10-3076_-10-3057d others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(14): Show |
C | 5 | a0001c0001t0001g0002a0001c0001t0001g0177a0001c0001t0001g0228others(2): Show | 5 | HG02615.hp2 HG03041.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3077_-10-3057d others(23): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507723
|
CTCTCTTT others(19): Show |
C | 1 | a0001c0001t0004g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-10-3082_-10-3057d others(28): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507723 | ||||||
chr4:82507725
|
CTCTTTTT others(4): Show |
C | 3 | a0001c0001t0003g0140a0001c0001t0005g0172a0001c0001t0016g0227 | 3 | HG00423.hp2 HG03098.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-10-3069_-10-3059d others(13): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507725 | ||||||
chr4:82507725
|
CTCTTTTT others(5): Show |
C | 1 | a0001c0001t0009g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-10-3070_-10-3059d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507725 | ||||||
chr4:82507725
|
CTCTTTTT others(11): Show |
C | 2 | a0001c0001t0003g0004a0001c0001t0005g0102 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-10-3076_-10-3059d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507725 | ||||||
chr4:82507727
|
C | CT | 10 | a0001c0001t0001g0072a0001c0001t0001g0181a0001c0001t0001g0184others(7): Show | 10 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-3061dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0198a0001c0001t0008g0162 | 2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-10-3070_-10-3061d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0157others(2): Show | 5 | HG00735.hp1 HG01257.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3071_-10-3061d others(13): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0069a0001c0001t0002g0073 | 2 | HG00099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-10-3072_-10-3061d others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0071a0001c0001t0002g0046a0001c0001t0008g0221 | 3 | HG01256.hp1 HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-10-3073_-10-3061d others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0070a0001c0001t0002g0076a0001c0001t0002g0225 | 3 | HG02027.hp2 NA18990.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-10-3074_-10-3061d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0002g0195a0001c0001t0008g0222 | 2 | HG01515.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-10-3077_-10-3061d others(19): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0008g0219a0001c0001t0008g0220a0001c0001t0008g0223 | 3 | HG01123.hp2 HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-10-3078_-10-3061d others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-3060G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CT | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0060others(12): Show | 15 | HG00140.hp1 HG01167.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-3061delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0002g0152a0001c0001t0002g0212a0001c0001t0003g0051others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3068_-10-3061d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0001g0050a0001c0001t0001g0123a0001c0001t0001g0165others(16): Show | 19 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-3069_-10-3061d others(11): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10-3070_-10-3061d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0253a0001c0001t0002g0127a0001c0001t0002g0128others(2): Show | 5 | HG00438.hp2 HG00673.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-3073_-10-3061d others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0156a0001c0001t0018g0047a0001c0001t0021g0078 | 3 | HG01993.hp1 HG03130.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-10-3074_-10-3061d others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507727
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0002g0116a0001c0001t0002g0131a0001c0001t0002g0155 | 3 | HG01975.hp2 NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-10-3075_-10-3061d others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507727 | ||||||
chr4:82507729
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-10-3062A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507729 | ||||||
chr4:82507737
|
T | C | 1 | a0001c0001t0006g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-3070A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507737 | ||||||
chr4:82507744
|
T | C | 2 | a0001c0001t0002g0116a0001c0001t0002g0131 | 2 | NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-10-3077A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507744 | ||||||
chr4:82507789
|
C | A | 2 | a0001c0001t0007g0141a0001c0001t0007g0142 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-10-3122G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507789 | ||||||
chr4:82507921
|
TATTTTTT others(46): Show |
T | 1 | a0001c0001t0010g0254 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-10-3307_-10-3255d others(55): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507921 | ||||||
chr4:82507950
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10-3283C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507950 | ||||||
chr4:82507972
|
T | C | 1 | a0001c0004t0001g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-10-3305A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82507972 | ||||||
chr4:82508005
|
C | CTGCCCAG others(44): Show |
1 | a0001c0001t0010g0254 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-10-3339_-10-3338i others(53): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508005 | ||||||
chr4:82508320
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(86): Show | 90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-3653G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508320 | ||||||
chr4:82508434
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0003g0200a0001c0001t0035g0154 | 3 | HG02622.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-3767G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508434 | ||||||
chr4:82508470
|
C | CT | 7 | a0001c0001t0005g0148a0001c0001t0005g0173a0001c0001t0009g0087others(4): Show | 7 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3804dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508470 | ||||||
chr4:82508504
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10-3837G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508504 | ||||||
chr4:82508700
|
A | T | 2 | a0001c0001t0023g0089a0001c0001t0023g0091 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-10-4033T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508700 | ||||||
chr4:82508853
|
C | T | 5 | a0001c0001t0007g0103a0001c0001t0011g0107a0001c0001t0014g0024others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-4186G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508853 | ||||||
chr4:82508869
|
T | C | 20 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(17): Show | 20 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-4202A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82508869 | ||||||
chr4:82509044
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-10-4377G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509044 | ||||||
chr4:82509137
|
T | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0052others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10-4470A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509137 | ||||||
chr4:82509359
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | NA18944.hp2 NA18995.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-4692G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509359 | ||||||
chr4:82509430
|
A | G | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0005g0204 | 3 | HG02258.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-10-4763T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509430 | ||||||
chr4:82509513
|
C | T | 1 | a0001c0001t0009g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-4846G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509513 | ||||||
chr4:82509550
|
C | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(86): Show | 90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-4883G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509550 | ||||||
chr4:82509607
|
C | A | 2 | a0001c0001t0003g0140a0001c0001t0016g0227 | 2 | HG00423.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-10-4940G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509607 | ||||||
chr4:82509613
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(86): Show | 90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-4946A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509613 | ||||||
chr4:82509884
|
G | C | 5 | a0001c0001t0007g0103a0001c0001t0011g0107a0001c0001t0014g0024others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-5217C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509884 | ||||||
chr4:82509895
|
G | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(86): Show | 90 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10-5228C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509895 | ||||||
chr4:82509905
|
G | A | 2 | a0001c0001t0004g0126a0001c0001t0004g0251 | 2 | HG01192.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-10-5238C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509905 | ||||||
chr4:82509960
|
C | G | 1 | a0001c0001t0002g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-10-5293G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82509960 | ||||||
chr4:82510150
|
G | A | 26 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0003g0039others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-10-5483C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510150 | ||||||
chr4:82510193
|
C | T | 2 | a0001c0001t0005g0172a0001c0001t0009g0029 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10-5526G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510193 | ||||||
chr4:82510204
|
G | A | 1 | a0001c0001t0015g0110 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-10-5537C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510204 | ||||||
chr4:82510205
|
G | C | 6 | a0001c0001t0006g0005a0001c0001t0009g0088a0001c0001t0015g0146others(3): Show | 6 | HG02886.hp1 HG02896.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5538C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510205 | ||||||
chr4:82510339
|
G | C | 6 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5672C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510339 | ||||||
chr4:82510637
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(150): Show | 154 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-10-5970A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510637 | ||||||
chr4:82510798
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10-6131C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510798 | ||||||
chr4:82510806
|
C | T | 1 | a0001c0001t0009g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-6139G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82510806 | ||||||
chr4:82511125
|
G | A | 5 | a0001c0001t0007g0103a0001c0001t0011g0107a0001c0001t0014g0024others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-6458C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511125 | ||||||
chr4:82511472
|
A | AT | 10 | a0001c0001t0002g0020a0001c0001t0002g0118a0001c0001t0003g0004others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-6806dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTT | 9 | a0001c0001t0001g0017a0001c0001t0003g0140a0001c0001t0003g0174others(6): Show | 9 | HG00423.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-6808_-10-6806d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTTT | 20 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0003g0039others(17): Show | 20 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-6809_-10-6806d others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTTTT | 16 | a0001c0001t0003g0176a0001c0001t0003g0230a0001c0001t0005g0148others(13): Show | 16 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-6810_-10-6806d others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTTTTTT | 57 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0052others(54): Show | 58 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-6812_-10-6806d others(9): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTTTTTT others(1): Show |
19 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0178others(16): Show | 19 | HG00140.hp2 HG00544.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-6813_-10-6806d others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTTTTTT others(2): Show |
20 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00544.hp2 HG00738.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-6814_-10-6806d others(11): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511472
|
A | ATTTTTTT others(3): Show |
8 | a0001c0001t0004g0115a0001c0001t0004g0150a0001c0001t0004g0193others(5): Show | 8 | HG01168.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-6815_-10-6806d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511472 | ||||||
chr4:82511819
|
A | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-7152T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511819 | ||||||
chr4:82511845
|
A | C | 13 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-7178T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511845 | ||||||
chr4:82511994
|
C | T | 7 | a0001c0001t0002g0065a0001c0001t0002g0236a0001c0001t0007g0094others(4): Show | 7 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-7327G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82511994 | ||||||
chr4:82512079
|
A | G | 1 | a0001c0001t0008g0216 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-10-7412T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512079 | ||||||
chr4:82512253
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(79): Show | 83 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-10-7586G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512253 | ||||||
chr4:82512254
|
G | A | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-7587C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512254 | ||||||
chr4:82512273
|
AC | A | 7 | a0001c0001t0005g0148a0001c0001t0005g0173a0001c0001t0009g0087others(4): Show | 7 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-7607delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512273 | ||||||
chr4:82512309
|
G | A | 2 | a0001c0001t0010g0009a0001c0001t0010g0055 | 2 | HG00673.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-10-7642C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512309 | ||||||
chr4:82512581
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0003g0200a0001c0001t0035g0154 | 3 | HG02622.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-7914G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512581 | ||||||
chr4:82512760
|
C | A | 13 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-8093G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512760 | ||||||
chr4:82512796
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10-8129A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512796 | ||||||
chr4:82512932
|
G | A | 1 | a0001c0001t0010g0254 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-10-8265C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82512932 | ||||||
chr4:82513034
|
G | C | 42 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0002g0065others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.-10-8367C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513034 | ||||||
chr4:82513075
|
C | T | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-8408G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513075 | ||||||
chr4:82513136
|
C | T | 13 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(10): Show | 13 | HG01167.hp1 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-8469G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513136 | ||||||
chr4:82513168
|
G | C | 35 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0003g0004others(32): Show | 35 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10-8501C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513168 | ||||||
chr4:82513248
|
C | T | 2 | a0001c0001t0005g0172a0001c0001t0009g0029 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10-8581G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513248 | ||||||
chr4:82513249
|
A | C | 5 | a0001c0001t0007g0103a0001c0001t0011g0107a0001c0001t0014g0024others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-8582T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513249 | ||||||
chr4:82513402
|
G | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(151): Show | 155 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.-10-8735C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513402 | ||||||
chr4:82513458
|
A | C | 1 | a0001c0001t0010g0010 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-10-8791T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513458 | ||||||
chr4:82513494
|
A | T | 4 | a0001c0001t0003g0019a0001c0001t0005g0022a0001c0001t0006g0105others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-8827T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513494 | ||||||
chr4:82513559
|
T | C | 1 | a0001c0001t0041g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-8892A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513559 | ||||||
chr4:82513608
|
T | C | 36 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(33): Show | 36 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-10-8941A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513608 | ||||||
chr4:82513834
|
G | C | 1 | a0001c0001t0009g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-9167C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82513834 | ||||||
chr4:82514220
|
G | A | 33 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-10-9553C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514220 | ||||||
chr4:82514363
|
T | C | 2 | a0001c0001t0002g0063a0001c0001t0013g0054 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-10-9696A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514363 | ||||||
chr4:82514437
|
C | T | 1 | a0001c0001t0009g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-9770G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514437 | ||||||
chr4:82514457
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-9790G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514457 | ||||||
chr4:82514471
|
C | A | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-9804G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514471 | ||||||
chr4:82514607
|
C | T | 5 | a0001c0001t0007g0103a0001c0001t0011g0107a0001c0001t0014g0024others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-9940G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514607 | ||||||
chr4:82514738
|
T | C | 7 | a0001c0001t0005g0148a0001c0001t0005g0173a0001c0001t0009g0087others(4): Show | 7 | HG01167.hp1 HG01515.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-10071A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514738 | ||||||
chr4:82514796
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-10129G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514796 | ||||||
chr4:82514797
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-10130C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514797 | ||||||
chr4:82514842
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-10175A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514842 | ||||||
chr4:82514853
|
G | T | 39 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.-10-10186C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82514853 | ||||||
chr4:82515133
|
CT | C | 6 | a0001c0001t0004g0016a0001c0001t0006g0081a0001c0001t0006g0090others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-10467delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515133 | ||||||
chr4:82515267
|
T | C | 38 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-10600A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515267 | ||||||
chr4:82515298
|
G | A | 1 | a0001c0001t0015g0110 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-10-10631C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515298 | ||||||
chr4:82515459
|
C | T | 38 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-10792G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515459 | ||||||
chr4:82515504
|
C | T | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-10837G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515504 | ||||||
chr4:82515524
|
G | T | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-10-10857C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515524 | ||||||
chr4:82515554
|
T | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-10887A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515554 | ||||||
chr4:82515594
|
G | T | 38 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-10927C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515594 | ||||||
chr4:82515607
|
C | T | 34 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-10940G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515607 | ||||||
chr4:82515610
|
G | A | 34 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-10943C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515610 | ||||||
chr4:82515637
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0050others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.-10-10970A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515637 | ||||||
chr4:82515652
|
G | A | 1 | a0001c0001t0004g0255 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-10-10985C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515652 | ||||||
chr4:82515715
|
C | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0043others(84): Show | 88 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-10-11048G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515715 | ||||||
chr4:82515736
|
CA | C | 40 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10-11070delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515736 | ||||||
chr4:82515847
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-11180C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515847 | ||||||
chr4:82515876
|
G | A | 1 | a0001c0001t0005g0202 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-11209C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82515876 | ||||||
chr4:82516030
|
A | G | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-11363T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516030 | ||||||
chr4:82516031
|
C | T | 5 | a0001c0001t0007g0103a0001c0001t0011g0107a0001c0001t0014g0024others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-11364G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516031 | ||||||
chr4:82516286
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-11619C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516286 | ||||||
chr4:82516614
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10-11947A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516614 | ||||||
chr4:82516825
|
G | A | 32 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10-12158C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516825 | ||||||
chr4:82516856
|
T | C | 29 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0165others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.-10-12189A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516856 | ||||||
chr4:82516895
|
A | G | 1 | a0001c0001t0007g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10-12228T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516895 | ||||||
chr4:82516959
|
C | T | 5 | a0001c0001t0004g0190a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG01168.hp2 HG01496.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-12292G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82516959 | ||||||
chr4:82517277
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-10-12610T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517277 | ||||||
chr4:82517492
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0001g0129others(17): Show | 20 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-12825A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517492 | ||||||
chr4:82517496
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0003g0174a0001c0001t0003g0175others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-12829A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517496 | ||||||
chr4:82517623
|
T | A | 7 | a0001c0001t0004g0016a0001c0001t0006g0081a0001c0001t0006g0090others(4): Show | 7 | HG02572.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-12956A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517623 | ||||||
chr4:82517890
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-10-13223C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82517890 | ||||||
chr4:82518007
|
A | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0050others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-10-13340T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518007 | ||||||
chr4:82518008
|
A | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0050others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-10-13341T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518008 | ||||||
chr4:82518086
|
C | T | 1 | a0001c0001t0007g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10-13419G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518086 | ||||||
chr4:82518090
|
C | T | 1 | a0001c0001t0008g0218 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-10-13423G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518090 | ||||||
chr4:82518132
|
A | G | 3 | a0001c0001t0005g0172a0001c0001t0007g0014a0001c0001t0009g0029 | 3 | HG02647.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-13465T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518132 | ||||||
chr4:82518171
|
G | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0003g0215others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-13504C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518171 | ||||||
chr4:82518190
|
C | A | 2 | a0001c0001t0006g0025a0001c0001t0007g0027 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-10-13523G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518190 | ||||||
chr4:82518241
|
G | A | 1 | a0001c0001t0004g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10-13574C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518241 | ||||||
chr4:82518303
|
G | A | 3 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0033g0171 | 3 | HG01243.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-10-13636C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518303 | ||||||
chr4:82518393
|
C | T | 1 | a0001c0001t0003g0230 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-10-13726G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518393 | ||||||
chr4:82518422
|
C | G | 25 | a0001c0001t0001g0130a0001c0001t0001g0163a0001c0001t0001g0184others(22): Show | 25 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-13755G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518422 | ||||||
chr4:82518812
|
G | A | 1 | a0001c0001t0013g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-14145C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82518812 | ||||||
chr4:82519095
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-10-14428A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519095 | ||||||
chr4:82519302
|
G | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0166a0001c0001t0002g0020others(8): Show | 11 | HG02055.hp1 HG02486.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-14635C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519302 | ||||||
chr4:82519392
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-10-14725C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519392 | ||||||
chr4:82519398
|
C | G | 1 | a0001c0001t0005g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-14731G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519398 | ||||||
chr4:82519410
|
TTTTC | T | 15 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0002g0020others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-14747_-10-1474 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519410 | ||||||
chr4:82519422
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10-14755G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519422 | ||||||
chr4:82519429
|
T | A | 142 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-10-14762A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519429 | ||||||
chr4:82519574
|
G | A | 3 | a0001c0001t0003g0215a0001c0001t0003g0241a0001c0001t0019g0248 | 3 | HG01109.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-10-14907C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519574 | ||||||
chr4:82519818
|
A | T | 1 | a0001c0001t0014g0026 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-10-15151T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519818 | ||||||
chr4:82519877
|
T | A | 1 | a0001c0001t0005g0202 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-15210A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82519877 | ||||||
chr4:82520422
|
T | G | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-15755A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82520422 | ||||||
chr4:82520491
|
T | C | 2 | a0001c0001t0005g0148a0001c0001t0009g0029 | 2 | HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-10-15824A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82520491 | ||||||
chr4:82520714
|
G | T | 204 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(201): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-10-16047C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82520714 | ||||||
chr4:82521007
|
C | T | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-16340G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521007 | ||||||
chr4:82521140
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-16473T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521140 | ||||||
chr4:82521264
|
G | A | 2 | a0001c0001t0003g0175a0001c0001t0033g0171 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-10-16597C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521264 | ||||||
chr4:82521438
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-10-16771C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521438 | ||||||
chr4:82521479
|
G | A | 163 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-10-16812C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521479 | ||||||
chr4:82521538
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00738.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-10-16871G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521538 | ||||||
chr4:82521754
|
C | T | 4 | a0001c0001t0005g0202a0001c0001t0005g0204a0001c0001t0007g0103others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-17087G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521754 | ||||||
chr4:82521755
|
G | A | 45 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0165others(42): Show | 46 | HG00140.hp2 HG00323.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.-10-17088C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521755 | ||||||
chr4:82521884
|
G | T | 1 | a0001c0001t0003g0040 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-10-17217C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521884 | ||||||
chr4:82521901
|
G | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01167.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10-17234C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82521901 | ||||||
chr4:82522166
|
C | G | 1 | a0001c0001t0003g0230 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-10-17499G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522166 | ||||||
chr4:82522169
|
C | T | 1 | a0001c0001t0007g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-10-17502G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522169 | ||||||
chr4:82522196
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0007g0141a0001c0001t0007g0142 | 3 | HG00140.hp2 HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-10-17529G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522196 | ||||||
chr4:82522355
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-17688G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522355 | ||||||
chr4:82522771
|
G | A | 1 | a0001c0001t0005g0202 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-18104C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82522771 | ||||||
chr4:82523032
|
A | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-18365T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523032 | ||||||
chr4:82523100
|
T | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-10-18433A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523100 | ||||||
chr4:82523204
|
C | T | 2 | a0001c0001t0005g0006a0001c0001t0006g0005 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-10-18537G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523204 | ||||||
chr4:82523210
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00738.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-10-18543G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523210 | ||||||
chr4:82523338
|
C | CATGTTTG others(10): Show |
1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-18672_-10-1867 others(21): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523338 | ||||||
chr4:82523339
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-18672A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523339 | ||||||
chr4:82523340
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-18673G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523340 | ||||||
chr4:82523449
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0253 | 2 | NA18948.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-10-18782C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523449 | ||||||
chr4:82523531
|
G | C | 12 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0005g0204others(9): Show | 12 | HG00642.hp2 HG01243.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-18864C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523531 | ||||||
chr4:82523697
|
CT | C | 28 | a0001c0001t0001g0064a0001c0001t0001g0165a0001c0001t0001g0166others(25): Show | 28 | HG00642.hp2 HG01168.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-10-19031delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523697 | ||||||
chr4:82523711
|
T | A | 26 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0003g0004others(23): Show | 26 | HG00642.hp2 HG01243.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-10-19044A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523711 | ||||||
chr4:82523829
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-10-19162G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82523829 | ||||||
chr4:82524102
|
C | CA | 66 | a0001c0001t0001g0044a0001c0001t0001g0111a0001c0001t0001g0117others(63): Show | 66 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-10-19436dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524102 | ||||||
chr4:82524102
|
C | CAA | 28 | a0001c0001t0001g0017a0001c0001t0001g0124a0001c0001t0001g0143others(25): Show | 29 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.-10-19437_-10-1943 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524102 | ||||||
chr4:82524203
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10-19536C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524203 | ||||||
chr4:82524430
|
C | A | 2 | a0001c0001t0005g0204a0001c0001t0009g0087 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-10-19763G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524430 | ||||||
chr4:82524513
|
C | A | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-19846G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524513 | ||||||
chr4:82524516
|
T | C | 6 | a0001c0001t0001g0228a0001c0001t0002g0231a0001c0001t0003g0230others(3): Show | 6 | HG00323.hp1 HG00609.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-19849A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524516 | ||||||
chr4:82524534
|
T | C | 1 | a0002c0002t0036g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10-19867A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524534 | ||||||
chr4:82524746
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0031g0028 | 2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-10-20079G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524746 | ||||||
chr4:82524751
|
T | C | 7 | a0001c0001t0008g0216a0001c0001t0008g0218a0001c0001t0008g0219others(4): Show | 7 | HG01071.hp2 HG01123.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-20084A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82524751 | ||||||
chr4:82525106
|
A | G | 2 | a0001c0001t0002g0198a0001c0001t0028g0224 | 2 | HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-10-20439T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525106 | ||||||
chr4:82525142
|
C | T | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-20475G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525142 | ||||||
chr4:82525247
|
G | C | 4 | a0001c0001t0003g0004a0001c0001t0005g0204a0001c0001t0009g0087others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-20580C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525247 | ||||||
chr4:82525297
|
T | C | 1 | a0001c0004t0001g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-10-20630A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525297 | ||||||
chr4:82525352
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(121): Show | 125 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-10-20685G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525352 | ||||||
chr4:82525802
|
G | A | 48 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0001g0165others(45): Show | 49 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-10-21135C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525802 | ||||||
chr4:82525814
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(8): Show | 11 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-21147C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525814 | ||||||
chr4:82525919
|
T | A | 2 | a0001c0001t0001g0058a0001c0001t0003g0059 | 2 | HG02027.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-10-21252A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525919 | ||||||
chr4:82525966
|
A | C | 3 | a0001c0001t0003g0215a0001c0001t0006g0214a0001c0001t0025g0007 | 3 | HG01109.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-10-21299T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525966 | ||||||
chr4:82525971
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0002g0073 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.-10-21304G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525971 | ||||||
chr4:82525983
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-10-21316G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82525983 | ||||||
chr4:82526308
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-21641A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526308 | ||||||
chr4:82526379
|
A | G | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-21712T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526379 | ||||||
chr4:82526488
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(65): Show | 69 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.-10-21821G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526488 | ||||||
chr4:82526584
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10-21917G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526584 | ||||||
chr4:82526675
|
A | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-22008T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526675 | ||||||
chr4:82526680
|
C | A | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10-22013G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526680 | ||||||
chr4:82526788
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(134): Show | 138 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-10-22121G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526788 | ||||||
chr4:82526890
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-10-22223C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526890 | ||||||
chr4:82526910
|
T | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-22243A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82526910 | ||||||
chr4:82527019
|
C | CT | 18 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0187others(15): Show | 18 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.-10-22353dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | ||||||
chr4:82527019
|
C | CTT | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(5): Show | 8 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-22354_-10-2235 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | ||||||
chr4:82527019
|
CT | C | 71 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(68): Show | 72 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-10-22353delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | ||||||
chr4:82527019
|
CTT | C | 8 | a0001c0001t0003g0034a0001c0001t0004g0016a0001c0001t0005g0030others(5): Show | 8 | HG01515.hp1 HG01884.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-22354_-10-2235 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | ||||||
chr4:82527019
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-10-22364_-10-2235 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527019 | ||||||
chr4:82527102
|
G | A | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-22435C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527102 | ||||||
chr4:82527165
|
T | C | 1 | a0001c0001t0038g0243 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-10-22498A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527165 | ||||||
chr4:82527187
|
T | C | 7 | a0001c0001t0003g0034a0001c0001t0004g0016a0001c0001t0005g0030others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-22520A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527187 | ||||||
chr4:82527196
|
G | A | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-22529C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527196 | ||||||
chr4:82527210
|
C | T | 59 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(56): Show | 59 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-22543G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527210 | ||||||
chr4:82527210
|
CAA | C | 5 | a0001c0001t0003g0004a0001c0001t0004g0016a0001c0001t0005g0102others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-22545_-10-2254 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527210 | ||||||
chr4:82527227
|
C | T | 1 | a0001c0001t0005g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-10-22560G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527227 | ||||||
chr4:82527228
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-10-22561C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527228 | ||||||
chr4:82527324
|
T | A | 3 | a0001c0001t0003g0004a0001c0001t0005g0204a0001c0001t0009g0087 | 3 | HG02258.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-10-22657A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527324 | ||||||
chr4:82527354
|
A | G | 105 | a0001c0001t0001g0017a0001c0001t0001g0111a0001c0001t0001g0117others(102): Show | 106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-10-22687T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527354 | ||||||
chr4:82527386
|
C | T | 1 | a0001c0001t0020g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-10-22719G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527386 | ||||||
chr4:82527540
|
G | A | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-22873C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527540 | ||||||
chr4:82527611
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(99): Show | 103 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-10-22944T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527611 | ||||||
chr4:82527623
|
T | C | 2 | a0001c0001t0004g0193a0001c0001t0004g0194 | 2 | HG01168.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-10-22956A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527623 | ||||||
chr4:82527640
|
C | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | NA18944.hp2 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-22973G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527640 | ||||||
chr4:82527643
|
T | C | 34 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0019others(31): Show | 35 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10-22976A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527643 | ||||||
chr4:82527752
|
T | A | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23085A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527752 | ||||||
chr4:82527757
|
T | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-23090A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527757 | ||||||
chr4:82527833
|
A | G | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23166T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527833 | ||||||
chr4:82527836
|
C | A | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23169G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527836 | ||||||
chr4:82527954
|
A | AAGGAGAG others(16): Show |
15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23288_-10-2328 others(27): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82527954 | ||||||
chr4:82528034
|
T | C | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-23367A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528034 | ||||||
chr4:82528084
|
T | C | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23417A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528084 | ||||||
chr4:82528238
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-10-23571T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528238 | ||||||
chr4:82528239
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-10-23572C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528239 | ||||||
chr4:82528294
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-10-23627G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528294 | ||||||
chr4:82528334
|
G | A | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23667C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528334 | ||||||
chr4:82528488
|
G | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-23821C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528488 | ||||||
chr4:82528570
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(7): Show | 10 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-23903A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528570 | ||||||
chr4:82528601
|
G | A | 14 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(11): Show | 14 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-23934C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528601 | ||||||
chr4:82528601
|
G | T | 2 | a0001c0001t0002g0046a0001c0001t0018g0047 | 2 | NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-10-23934C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528601 | ||||||
chr4:82528605
|
C | CT | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23939dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528605 | ||||||
chr4:82528605
|
C | CTT | 16 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(13): Show | 16 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-23940_-10-2393 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528605 | ||||||
chr4:82528638
|
A | G | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-23971T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528638 | ||||||
chr4:82528780
|
A | G | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-24113T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528780 | ||||||
chr4:82528894
|
C | T | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-24227G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82528894 | ||||||
chr4:82529055
|
AC | A | 14 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(11): Show | 14 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-24389delG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529055 | ||||||
chr4:82529065
|
T | G | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-24398A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529065 | ||||||
chr4:82529099
|
G | A | 13 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(10): Show | 13 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10-24432C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529099 | ||||||
chr4:82529224
|
T | G | 15 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(12): Show | 15 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10-24557A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529224 | ||||||
chr4:82529297
|
CT | C | 18 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(15): Show | 18 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-24631delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529297 | ||||||
chr4:82529363
|
A | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-24696T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529363 | ||||||
chr4:82529435
|
T | C | 18 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(15): Show | 18 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-24768A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529435 | ||||||
chr4:82529619
|
G | C | 1 | a0001c0001t0007g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-10-24952C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529619 | ||||||
chr4:82529918
|
A | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10-25251T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529918 | ||||||
chr4:82529975
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(7): Show | 10 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-25308C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82529975 | ||||||
chr4:82530084
|
A | ATCTC | 4 | a0001c0001t0003g0004a0001c0001t0005g0204a0001c0001t0009g0087others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-25421_-10-2541 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530084 | ||||||
chr4:82530084
|
ATCTC | A | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25421_-10-2541 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530084 | ||||||
chr4:82530104
|
C | A | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25437G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530104 | ||||||
chr4:82530105
|
T | G | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25438A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530105 | ||||||
chr4:82530198
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-10-25531T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530198 | ||||||
chr4:82530417
|
T | C | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25750A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530417 | ||||||
chr4:82530513
|
C | T | 3 | a0001c0001t0004g0016a0001c0001t0005g0006a0001c0001t0006g0005 | 3 | HG02818.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-10-25846G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530513 | ||||||
chr4:82530630
|
A | T | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-25963T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530630 | ||||||
chr4:82530735
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(131): Show | 135 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-10-26068T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530735 | ||||||
chr4:82530832
|
T | C | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26165A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530832 | ||||||
chr4:82530861
|
C | A | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26194G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530861 | ||||||
chr4:82530862
|
G | A | 4 | a0001c0001t0003g0004a0001c0001t0005g0204a0001c0001t0009g0087others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-26195C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530862 | ||||||
chr4:82530944
|
C | A | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26277G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530944 | ||||||
chr4:82530994
|
C | T | 2 | a0001c0001t0005g0204a0001c0001t0009g0087 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-10-26327G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82530994 | ||||||
chr4:82531115
|
T | C | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-26448A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531115 | ||||||
chr4:82531219
|
C | T | 63 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(60): Show | 63 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-10-26552G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531219 | ||||||
chr4:82531230
|
G | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-10-26563C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531230 | ||||||
chr4:82531311
|
A | T | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-10-26644T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531311 | ||||||
chr4:82531417
|
G | A | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-10-26750C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531417 | ||||||
chr4:82531616
|
G | A | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26949C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531616 | ||||||
chr4:82531626
|
A | G | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-26959T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531626 | ||||||
chr4:82531703
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-10-27036G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531703 | ||||||
chr4:82531704
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-10-27037C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531704 | ||||||
chr4:82531754
|
C | CA | 42 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(39): Show | 42 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-10-27088dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | ||||||
chr4:82531754
|
C | CAA | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0195others(2): Show | 5 | HG01361.hp1 HG02280.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-27089_-10-2708 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | ||||||
chr4:82531754
|
CA | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0117others(55): Show | 58 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-10-27088delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | ||||||
chr4:82531754
|
CAA | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0084others(27): Show | 30 | HG01168.hp1 HG01257.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.-10-27089_-10-2708 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | ||||||
chr4:82531754
|
CAAAAAAA others(5): Show |
C | 23 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(20): Show | 24 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10-27099_-10-2708 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531754 | ||||||
chr4:82531839
|
G | A | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-27172C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531839 | ||||||
chr4:82531902
|
G | A | 4 | a0001c0001t0003g0004a0001c0001t0005g0204a0001c0001t0009g0087others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27235C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531902 | ||||||
chr4:82531920
|
T | C | 23 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(20): Show | 24 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10-27253A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531920 | ||||||
chr4:82531996
|
T | C | 16 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0025others(13): Show | 16 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-27329A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82531996 | ||||||
chr4:82532593
|
T | C | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-27926A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532593 | ||||||
chr4:82532606
|
G | A | 52 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(49): Show | 52 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10-27939C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532606 | ||||||
chr4:82532608
|
G | A | 4 | a0001c0001t0004g0016a0001c0001t0004g0112a0001c0001t0004g0113others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27941C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532608 | ||||||
chr4:82532885
|
C | A | 1 | a0001c0001t0002g0065 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-10-28218G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532885 | ||||||
chr4:82532885
|
C | T | 14 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10-28218G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532885 | ||||||
chr4:82532886
|
G | A | 1 | a0001c0001t0031g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-10-28219C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532886 | ||||||
chr4:82532889
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10-28222G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532889 | ||||||
chr4:82532964
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0007g0141a0001c0001t0007g0142 | 3 | HG00140.hp2 HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-10-28297C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82532964 | ||||||
chr4:82533020
|
G | A | 50 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(47): Show | 50 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-28353C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533020 | ||||||
chr4:82533176
|
TTATAAC | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(105): Show | 108 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-10-28515_-10-2851 others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533176 | ||||||
chr4:82533216
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0198others(1): Show | 4 | HG01168.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-28549C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533216 | ||||||
chr4:82533232
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(10): Show | 13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-28565G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533232 | ||||||
chr4:82533261
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-10-28594G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533261 | ||||||
chr4:82533306
|
CTT | C | 4 | a0001c0001t0005g0036a0001c0001t0007g0037a0001c0001t0012g0001others(1): Show | 5 | HG03486.hp1 NA18906.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+28598_-11+2859 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533306 | ||||||
chr4:82533369
|
A | G | 17 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0005g0079others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+28537T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533369 | ||||||
chr4:82533491
|
A | C | 1 | a0001c0001t0002g0250 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-11+28415T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533491 | ||||||
chr4:82533641
|
C | T | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+28265G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533641 | ||||||
chr4:82533824
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0009g0104 | 2 | HG02602.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-11+28082G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533824 | ||||||
chr4:82533953
|
C | T | 53 | a0001c0001t0001g0060a0001c0001t0001g0111a0001c0001t0001g0117others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-11+27953G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533953 | ||||||
chr4:82533970
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11+27936C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82533970 | ||||||
chr4:82534115
|
C | CCA | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(134): Show | 138 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11+27789_-11+2779 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534115 | ||||||
chr4:82534178
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(10): Show | 13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+27728G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534178 | ||||||
chr4:82534207
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0003g0059 | 2 | HG02027.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-11+27699C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534207 | ||||||
chr4:82534244
|
T | C | 1 | a0002c0002t0036g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+27662A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534244 | ||||||
chr4:82534390
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-11+27516T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534390 | ||||||
chr4:82534671
|
T | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(10): Show | 13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+27235A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534671 | ||||||
chr4:82534743
|
T | C | 1 | a0001c0001t0007g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+27163A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534743 | ||||||
chr4:82534834
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+27072C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534834 | ||||||
chr4:82534979
|
G | T | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+26927C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82534979 | ||||||
chr4:82535230
|
G | C | 3 | a0001c0001t0005g0148a0001c0001t0005g0202a0001c0001t0009g0029 | 3 | HG02145.hp1 HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-11+26676C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535230 | ||||||
chr4:82535541
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(10): Show | 13 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+26365C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535541 | ||||||
chr4:82535733
|
T | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(67): Show | 70 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11+26173A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535733 | ||||||
chr4:82535742
|
T | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(67): Show | 70 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11+26164A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82535742 | ||||||
chr4:82536013
|
C | T | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+25893G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536013 | ||||||
chr4:82536050
|
C | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(104): Show | 107 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-11+25856G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536050 | ||||||
chr4:82536066
|
T | C | 4 | a0001c0001t0006g0093a0001c0001t0007g0094a0001c0001t0007g0103others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+25840A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536066 | ||||||
chr4:82536095
|
T | G | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+25811A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536095 | ||||||
chr4:82536356
|
C | CA | 34 | a0001c0001t0001g0057a0001c0001t0001g0153a0001c0001t0001g0180others(31): Show | 34 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+25549dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536356 | ||||||
chr4:82536356
|
CA | C | 50 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(47): Show | 50 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11+25549delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536356 | ||||||
chr4:82536356
|
CAAAAAAA others(6): Show |
C | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(54): Show | 58 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+25537_-11+2554 others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536356 | ||||||
chr4:82536395
|
G | A | 2 | a0001c0001t0002g0198a0001c0001t0028g0224 | 2 | HG01168.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-11+25511C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536395 | ||||||
chr4:82536419
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(118): Show | 122 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-11+25487G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536419 | ||||||
chr4:82536734
|
G | T | 1 | a0001c0001t0041g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11+25172C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536734 | ||||||
chr4:82536865
|
A | G | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+25041T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536865 | ||||||
chr4:82536877
|
C | T | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+25029G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536877 | ||||||
chr4:82536967
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | NA18944.hp2 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+24939G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82536967 | ||||||
chr4:82537019
|
C | T | 1 | a0001c0001t0006g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+24887G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537019 | ||||||
chr4:82537143
|
G | A | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+24763C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537143 | ||||||
chr4:82537175
|
T | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 6 | HG01123.hp1 HG01361.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+24731A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537175 | ||||||
chr4:82537192
|
A | G | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+24714T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537192 | ||||||
chr4:82537280
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(48): Show | 52 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11+24626G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537280 | ||||||
chr4:82537415
|
A | G | 13 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0005g0204others(10): Show | 13 | HG00642.hp2 HG01243.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+24491T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537415 | ||||||
chr4:82537468
|
G | T | 1 | a0001c0001t0023g0089 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+24438C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537468 | ||||||
chr4:82537477
|
T | A | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+24429A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537477 | ||||||
chr4:82537514
|
C | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(114): Show | 118 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-11+24392G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537514 | ||||||
chr4:82537782
|
A | G | 1 | a0001c0001t0016g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-11+24124T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537782 | ||||||
chr4:82537942
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+23964A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537942 | ||||||
chr4:82537978
|
C | A | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+23928G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82537978 | ||||||
chr4:82538000
|
GA | G | 7 | a0001c0001t0001g0017a0001c0001t0007g0014a0001c0001t0011g0099others(4): Show | 7 | HG02451.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+23905delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538000 | ||||||
chr4:82538099
|
C | G | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0009g0086 | 3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+23807G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538099 | ||||||
chr4:82538100
|
C | T | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+23806G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538100 | ||||||
chr4:82538344
|
C | T | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+23562G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538344 | ||||||
chr4:82538357
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+23549G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538357 | ||||||
chr4:82538507
|
T | C | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+23399A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538507 | ||||||
chr4:82538529
|
TAA | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+23375_-11+2337 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538529 | ||||||
chr4:82538603
|
G | A | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+23303C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538603 | ||||||
chr4:82538665
|
A | G | 1 | a0001c0001t0025g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11+23241T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538665 | ||||||
chr4:82538673
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0007g0141a0001c0001t0007g0142 | 3 | HG00140.hp2 HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-11+23233C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538673 | ||||||
chr4:82538686
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0182 | 2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-11+23220G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538686 | ||||||
chr4:82538863
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(7): Show | 10 | HG01168.hp1 HG01433.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+23043G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538863 | ||||||
chr4:82538869
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11+23037A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538869 | ||||||
chr4:82538882
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(49): Show | 53 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11+23024C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538882 | ||||||
chr4:82538935
|
G | C | 2 | a0001c0001t0001g0234a0001c0001t0003g0066 | 2 | HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-11+22971C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82538935 | ||||||
chr4:82539357
|
AATT | A | 2 | a0001c0001t0007g0077a0001c0001t0031g0028 | 2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+22546_-11+2254 others(7): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539357 | ||||||
chr4:82539385
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0003g0059 | 2 | HG02027.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-11+22521C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539385 | ||||||
chr4:82539414
|
G | A | 2 | a0001c0001t0005g0204a0001c0001t0009g0087 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-11+22492C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539414 | ||||||
chr4:82539432
|
T | A | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+22474A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539432 | ||||||
chr4:82539459
|
C | CTTTTT | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(49): Show | 53 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11+22442_-11+2244 others(9): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539459 | ||||||
chr4:82539459
|
C | CTTTTTT | 67 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(64): Show | 67 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-11+22441_-11+2244 others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539459 | ||||||
chr4:82539539
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11+22367C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539539 | ||||||
chr4:82539546
|
G | A | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+22360C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539546 | ||||||
chr4:82539625
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11+22281A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539625 | ||||||
chr4:82539970
|
T | C | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0009g0086 | 3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+21936A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82539970 | ||||||
chr4:82540114
|
C | CT | 52 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11+21791dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
C | CTT | 5 | a0001c0001t0001g0074a0001c0001t0001g0178a0001c0001t0001g0238others(2): Show | 5 | HG02074.hp2 NA18967.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+21790_-11+2179 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0003g0200others(4): Show | 7 | HG00140.hp2 HG00323.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+21782_-11+2179 others(14): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(4): Show |
C | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(17): Show | 21 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11+21781_-11+2179 others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(5): Show |
C | 23 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0003g0108others(20): Show | 23 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-11+21780_-11+2179 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0004g0113a0001c0001t0005g0202a0001c0001t0009g0018others(1): Show | 4 | HG00642.hp2 HG02622.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+21779_-11+2179 others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(7): Show |
C | 56 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(53): Show | 56 | HG00438.hp2 HG00673.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.-11+21778_-11+2179 others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(8): Show |
C | 11 | a0001c0001t0001g0111a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 11 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+21777_-11+2179 others(19): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(9): Show |
C | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0211others(8): Show | 11 | HG01256.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+21776_-11+2179 others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0004g0115a0001c0001t0011g0067a0001c0001t0011g0068 | 3 | HG01167.hp1 HG01515.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-11+21774_-11+2179 others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+21771_-11+2179 others(25): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540114
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0003g0175 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+21770_-11+2179 others(26): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540114 | ||||||
chr4:82540129
|
T | C | 3 | a0001c0001t0005g0006a0001c0001t0006g0005a0001c0001t0015g0110 | 3 | HG01167.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+21777A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540129 | ||||||
chr4:82540130
|
T | C | 2 | a0001c0001t0009g0018a0001c0001t0039g0015 | 2 | HG00642.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-11+21776A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540130 | ||||||
chr4:82540131
|
T | C | 51 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0121others(48): Show | 51 | HG00438.hp2 HG00673.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11+21775A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540131 | ||||||
chr4:82540132
|
T | C | 9 | a0001c0001t0001g0111a0001c0001t0001g0137a0001c0001t0001g0138others(6): Show | 9 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+21774A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540132 | ||||||
chr4:82540133
|
T | C | 2 | a0001c0001t0007g0027a0001c0001t0014g0026 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-11+21773A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540133 | ||||||
chr4:82540468
|
G | T | 1 | a0001c0001t0031g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+21438C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540468 | ||||||
chr4:82540515
|
TTATTAA | T | 2 | a0001c0001t0007g0077a0001c0001t0031g0028 | 2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+21385_-11+2139 others(10): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540515 | ||||||
chr4:82540658
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11+21248T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82540658 | ||||||
chr4:82541238
|
T | A | 1 | a0001c0001t0002g0195 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-11+20668A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541238 | ||||||
chr4:82541292
|
T | G | 7 | a0001c0001t0004g0016a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 7 | HG02258.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+20614A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541292 | ||||||
chr4:82541606
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(130): Show | 134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+20300C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541606 | ||||||
chr4:82541782
|
T | C | 51 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(48): Show | 51 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11+20124A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541782 | ||||||
chr4:82541891
|
C | A | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+20015G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541891 | ||||||
chr4:82541979
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+19927T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82541979 | ||||||
chr4:82542024
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+19882C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542024 | ||||||
chr4:82542164
|
A | C | 1 | a0001c0001t0002g0157 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-11+19742T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542164 | ||||||
chr4:82542428
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+19478C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542428 | ||||||
chr4:82542728
|
G | C | 1 | a0001c0001t0002g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-11+19178C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542728 | ||||||
chr4:82542865
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+19041G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542865 | ||||||
chr4:82542896
|
G | A | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+19010C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542896 | ||||||
chr4:82542931
|
A | T | 1 | a0001c0001t0006g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11+18975T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82542931 | ||||||
chr4:82543069
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+18837A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82543069 | ||||||
chr4:82543517
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-11+18389T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82543517 | ||||||
chr4:82543660
|
A | C | 1 | a0001c0001t0041g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11+18246T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82543660 | ||||||
chr4:82544023
|
G | A | 19 | a0001c0001t0003g0019a0001c0001t0003g0034a0001c0001t0004g0114others(16): Show | 19 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-11+17883C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544023 | ||||||
chr4:82544049
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+17857G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544049 | ||||||
chr4:82544161
|
C | T | 3 | a0001c0001t0006g0105a0001c0001t0006g0106a0001c0001t0009g0104 | 3 | HG01891.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-11+17745G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544161 | ||||||
chr4:82544252
|
C | T | 3 | a0001c0001t0003g0215a0001c0001t0006g0214a0001c0001t0025g0007 | 3 | HG01109.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-11+17654G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544252 | ||||||
chr4:82544257
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0002g0069 | 3 | HG01256.hp1 HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-11+17649C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544257 | ||||||
chr4:82544309
|
G | A | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+17597C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544309 | ||||||
chr4:82544345
|
G | A | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+17561C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544345 | ||||||
chr4:82544409
|
C | A | 1 | a0001c0001t0019g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11+17497G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544409 | ||||||
chr4:82544473
|
A | G | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0009g0086 | 3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+17433T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544473 | ||||||
chr4:82544569
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+17337T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544569 | ||||||
chr4:82544569
|
AG | A | 3 | a0001c0001t0005g0204a0001c0001t0009g0087a0001c0001t0021g0149 | 3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+17336delC | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544569 | ||||||
chr4:82544580
|
A | C | 1 | a0001c0001t0003g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-11+17326T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544580 | ||||||
chr4:82544610
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(130): Show | 134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+17296A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544610 | ||||||
chr4:82544711
|
A | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(130): Show | 134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+17195T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544711 | ||||||
chr4:82544775
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0020a0001c0001t0003g0108 | 2 | HG02922.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(15): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | ||||||
chr4:82544775
|
C | CAAAAAAA others(5): Show |
29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(26): Show | 30 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(16): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | ||||||
chr4:82544775
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0143a0001c0001t0003g0004a0001c0001t0004g0114others(2): Show | 5 | HG02602.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(17): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | ||||||
chr4:82544775
|
C | CAAAAAAA others(7): Show |
13 | a0001c0001t0003g0019a0001c0001t0003g0200a0001c0001t0004g0016others(10): Show | 13 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(18): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | ||||||
chr4:82544775
|
C | CAAAAAAA others(8): Show |
7 | a0001c0001t0004g0112a0001c0001t0004g0113a0001c0001t0006g0025others(4): Show | 7 | HG01884.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(19): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | ||||||
chr4:82544775
|
C | CAAAAAAA others(9): Show |
6 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+17130_-11+1713 others(20): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544775 | ||||||
chr4:82544827
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+17079T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82544827 | ||||||
chr4:82545405
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(29): Show | 33 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11+16501C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545405 | ||||||
chr4:82545434
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-11+16472T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545434 | ||||||
chr4:82545439
|
A | G | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-11+16467T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545439 | ||||||
chr4:82545586
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+16320T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545586 | ||||||
chr4:82545889
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+16017G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545889 | ||||||
chr4:82545932
|
CA | C | 100 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(97): Show | 100 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-11+15973delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82545932 | ||||||
chr4:82546050
|
A | G | 4 | a0001c0001t0004g0016a0001c0001t0004g0112a0001c0001t0004g0113others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+15856T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546050 | ||||||
chr4:82546255
|
T | G | 30 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0034others(27): Show | 30 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11+15651A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546255 | ||||||
chr4:82546594
|
C | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0200a0001c0001t0006g0025others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+15312G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546594 | ||||||
chr4:82546610
|
C | T | 50 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(47): Show | 50 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-11+15296G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546610 | ||||||
chr4:82546656
|
G | A | 1 | a0001c0001t0041g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11+15250C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546656 | ||||||
chr4:82546783
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+15123G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546783 | ||||||
chr4:82546797
|
A | T | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+15109T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82546797 | ||||||
chr4:82547285
|
G | GA | 8 | a0001c0001t0001g0017a0001c0001t0003g0039a0001c0001t0007g0014others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+14620dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547285 | ||||||
chr4:82547285
|
GA | G | 17 | a0001c0001t0003g0019a0001c0001t0003g0034a0001c0001t0005g0030others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+14620delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547285 | ||||||
chr4:82547326
|
T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(129): Show | 133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+14580A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547326 | ||||||
chr4:82547363
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-11+14543G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547363 | ||||||
chr4:82547462
|
G | A | 1 | a0001c0001t0004g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-11+14444C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547462 | ||||||
chr4:82547592
|
T | TA | 13 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+14313dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547592 | ||||||
chr4:82547718
|
G | T | 3 | a0001c0001t0005g0006a0001c0001t0006g0005a0001c0001t0015g0110 | 3 | HG01167.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+14188C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82547718 | ||||||
chr4:82548000
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+13906G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548000 | ||||||
chr4:82548125
|
T | C | 1 | a0001c0001t0009g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11+13781A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548125 | ||||||
chr4:82548451
|
G | T | 3 | a0001c0001t0005g0006a0001c0001t0006g0005a0001c0001t0015g0110 | 3 | HG01167.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+13455C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548451 | ||||||
chr4:82548471
|
G | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+13435C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548471 | ||||||
chr4:82548478
|
G | A | 9 | a0001c0001t0003g0004a0001c0001t0003g0200a0001c0001t0004g0016others(6): Show | 9 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+13428C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548478 | ||||||
chr4:82548515
|
T | C | 2 | a0001c0001t0004g0016a0001c0001t0005g0102 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-11+13391A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548515 | ||||||
chr4:82548723
|
T | G | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0005g0172others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+13183A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548723 | ||||||
chr4:82548771
|
T | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0039others(16): Show | 20 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+13135A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548771 | ||||||
chr4:82548842
|
G | C | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+13064C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82548842 | ||||||
chr4:82549141
|
AAT | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(129): Show | 133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+12763_-11+1276 others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549141 | ||||||
chr4:82549227
|
A | C | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+12679T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549227 | ||||||
chr4:82549305
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(129): Show | 133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+12601C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549305 | ||||||
chr4:82549469
|
G | T | 73 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(70): Show | 73 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11+12437C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549469 | ||||||
chr4:82549542
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-11+12364G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549542 | ||||||
chr4:82549568
|
C | T | 1 | a0001c0001t0035g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11+12338G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549568 | ||||||
chr4:82549645
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-11+12261A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549645 | ||||||
chr4:82549745
|
G | A | 3 | a0001c0001t0015g0146a0001c0001t0017g0145a0001c0001t0017g0147 | 3 | HG02886.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+12161C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549745 | ||||||
chr4:82549788
|
G | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(129): Show | 133 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-11+12118C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549788 | ||||||
chr4:82549840
|
G | T | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+12066C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549840 | ||||||
chr4:82549931
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG00639.hp2 HG00738.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+11975G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82549931 | ||||||
chr4:82550157
|
G | A | 1 | a0001c0001t0007g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-11+11749C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550157 | ||||||
chr4:82550444
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(246): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-11+11462T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550444 | ||||||
chr4:82550488
|
T | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(30): Show | 34 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+11418A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550488 | ||||||
chr4:82550489
|
T | G | 3 | a0001c0001t0006g0105a0001c0001t0006g0106a0001c0001t0009g0104 | 3 | HG01891.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-11+11417A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550489 | ||||||
chr4:82550507
|
A | G | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0009g0086 | 3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+11399T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550507 | ||||||
chr4:82550664
|
C | A | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+11242G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550664 | ||||||
chr4:82550664
|
C | T | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+11242G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550664 | ||||||
chr4:82550799
|
AAAAG | A | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+11103_-11+1110 others(8): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550799 | ||||||
chr4:82550967
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+10939C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82550967 | ||||||
chr4:82551098
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+10808C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551098 | ||||||
chr4:82551268
|
T | C | 4 | a0001c0001t0004g0016a0001c0001t0004g0112a0001c0001t0004g0113others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+10638A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551268 | ||||||
chr4:82551328
|
T | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0143a0001c0001t0003g0004others(17): Show | 21 | HG00140.hp2 HG00323.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11+10578A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551328 | ||||||
chr4:82551375
|
T | C | 1 | a0001c0001t0031g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+10531A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551375 | ||||||
chr4:82551589
|
A | G | 3 | a0001c0001t0005g0204a0001c0001t0009g0087a0001c0001t0021g0149 | 3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+10317T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551589 | ||||||
chr4:82551686
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+10220A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551686 | ||||||
chr4:82551693
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(30): Show | 34 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+10213G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551693 | ||||||
chr4:82551702
|
T | G | 1 | a0001c0001t0007g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-11+10204A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551702 | ||||||
chr4:82551761
|
T | G | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+10145A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551761 | ||||||
chr4:82551804
|
C | T | 1 | a0001c0001t0004g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11+10102G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551804 | ||||||
chr4:82551914
|
C | T | 1 | a0001c0001t0005g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11+9992G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82551914 | ||||||
chr4:82552603
|
T | C | 20 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0004g0114others(17): Show | 20 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11+9303A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82552603 | ||||||
chr4:82552778
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+9128G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82552778 | ||||||
chr4:82552909
|
G | T | 10 | a0001c0001t0001g0189a0001c0001t0002g0195a0001c0001t0003g0192others(7): Show | 10 | HG01071.hp1 HG01109.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+8997C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82552909 | ||||||
chr4:82553108
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-11+8798A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82553108 | ||||||
chr4:82553384
|
A | G | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0198others(1): Show | 4 | HG01168.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+8522T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82553384 | ||||||
chr4:82553943
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(130): Show | 134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+7963T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82553943 | ||||||
chr4:82554159
|
A | T | 46 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(43): Show | 46 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-11+7747T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554159 | ||||||
chr4:82554490
|
T | C | 3 | a0001c0001t0005g0204a0001c0001t0009g0087a0001c0001t0021g0149 | 3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+7416A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554490 | ||||||
chr4:82554578
|
A | G | 1 | a0001c0001t0012g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-11+7328T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554578 | ||||||
chr4:82554635
|
A | G | 3 | a0001c0001t0003g0215a0001c0001t0006g0214a0001c0001t0025g0007 | 3 | HG01109.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-11+7271T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554635 | ||||||
chr4:82554657
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(130): Show | 134 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+7249T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554657 | ||||||
chr4:82554948
|
T | TC | 3 | a0001c0001t0004g0112a0001c0001t0004g0113a0001c0001t0005g0102 | 3 | HG02723.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+6957dupG | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554948 | ||||||
chr4:82554970
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-11+6936T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82554970 | ||||||
chr4:82555199
|
T | C | 3 | a0001c0001t0005g0204a0001c0001t0009g0087a0001c0001t0021g0149 | 3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+6707A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555199 | ||||||
chr4:82555231
|
C | T | 1 | a0001c0001t0004g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11+6675G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555231 | ||||||
chr4:82555375
|
T | C | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+6531A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555375 | ||||||
chr4:82555411
|
A | T | 1 | a0001c0001t0009g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-11+6495T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555411 | ||||||
chr4:82555865
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+6041G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555865 | ||||||
chr4:82555878
|
A | G | 56 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(53): Show | 56 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-11+6028T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555878 | ||||||
chr4:82555969
|
T | A | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+5937A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82555969 | ||||||
chr4:82556028
|
G | A | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+5878C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556028 | ||||||
chr4:82556069
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-11+5837C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556069 | ||||||
chr4:82556071
|
G | T | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+5835C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556071 | ||||||
chr4:82556087
|
T | G | 1 | a0001c0001t0007g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11+5819A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556087 | ||||||
chr4:82556109
|
G | A | 7 | a0001c0001t0008g0216a0001c0001t0008g0218a0001c0001t0008g0219others(4): Show | 7 | HG01071.hp2 HG01123.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+5797C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556109 | ||||||
chr4:82556214
|
G | C | 1 | a0001c0001t0019g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-11+5692C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556214 | ||||||
chr4:82556463
|
A | T | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+5443T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556463 | ||||||
chr4:82556495
|
T | A | 14 | a0001c0001t0003g0019a0001c0001t0004g0114a0001c0001t0005g0079others(11): Show | 14 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+5411A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556495 | ||||||
chr4:82556541
|
T | C | 3 | a0001c0001t0005g0204a0001c0001t0009g0087a0001c0001t0021g0149 | 3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+5365A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556541 | ||||||
chr4:82556569
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | NA18944.hp2 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5337G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556569 | ||||||
chr4:82556859
|
C | T | 3 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0009g0086 | 3 | HG03209.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+5047G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556859 | ||||||
chr4:82556932
|
T | C | 1 | a0001c0001t0021g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+4974A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556932 | ||||||
chr4:82556998
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0002g0195a0001c0001t0003g0174others(13): Show | 16 | HG01071.hp1 HG01109.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+4908G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82556998 | ||||||
chr4:82557235
|
A | G | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+4671T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557235 | ||||||
chr4:82557238
|
C | T | 1 | a0001c0001t0003g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11+4668G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557238 | ||||||
chr4:82557477
|
C | T | 2 | a0001c0001t0003g0004a0001c0001t0004g0016 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-11+4429G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557477 | ||||||
chr4:82557531
|
G | A | 94 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(91): Show | 94 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-11+4375C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557531 | ||||||
chr4:82557589
|
C | A | 1 | a0001c0001t0031g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+4317G>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557589 | ||||||
chr4:82557734
|
C | CT | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(22): Show | 25 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11+4171dupA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557734 | ||||||
chr4:82557734
|
CT | C | 91 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(88): Show | 91 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-11+4171delA | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557734 | ||||||
chr4:82557734
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+4162_-11+4171d others(12): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557734 | ||||||
chr4:82557756
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-11+4150A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557756 | ||||||
chr4:82557808
|
A | G | 19 | a0001c0001t0003g0019a0001c0001t0003g0034a0001c0001t0004g0114others(16): Show | 19 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-11+4098T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557808 | ||||||
chr4:82557918
|
A | G | 3 | a0001c0001t0005g0204a0001c0001t0009g0087a0001c0001t0021g0149 | 3 | HG02258.hp1 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11+3988T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82557918 | ||||||
chr4:82558267
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-11+3639A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558267 | ||||||
chr4:82558289
|
C | T | 16 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0004g0016others(13): Show | 16 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11+3617G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558289 | ||||||
chr4:82558353
|
T | C | 2 | a0001c0001t0003g0004a0001c0001t0004g0016 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-11+3553A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558353 | ||||||
chr4:82558393
|
T | G | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+3513A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558393 | ||||||
chr4:82558637
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-11+3269A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558637 | ||||||
chr4:82558765
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(23): Show | 27 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11+3141C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558765 | ||||||
chr4:82558889
|
A | AAAG | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(127): Show | 131 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-11+3014_-11+3016d others(5): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558889 | ||||||
chr4:82558971
|
A | G | 5 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0007g0077others(2): Show | 5 | HG01884.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2935T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82558971 | ||||||
chr4:82559010
|
A | ACCCCTAA others(13): Show |
1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+2895_-11+2896i others(22): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559010 | ||||||
chr4:82559040
|
C | T | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0003g0040 | 3 | NA18980.hp1 NA19011.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-11+2866G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559040 | ||||||
chr4:82559053
|
T | C | 8 | a0001c0001t0004g0114a0001c0001t0005g0085a0001c0001t0006g0025others(5): Show | 8 | HG01884.hp2 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+2853A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559053 | ||||||
chr4:82559115
|
A | G | 11 | a0001c0001t0003g0019a0001c0001t0005g0079a0001c0001t0006g0081others(8): Show | 11 | HG00642.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+2791T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559115 | ||||||
chr4:82559206
|
T | C | 8 | a0001c0001t0001g0189a0001c0001t0002g0195a0001c0001t0003g0192others(5): Show | 8 | HG01071.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+2700A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559206 | ||||||
chr4:82559216
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11+2690G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559216 | ||||||
chr4:82559286
|
T | C | 2 | a0001c0001t0005g0148a0001c0001t0009g0029 | 2 | HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-11+2620A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559286 | ||||||
chr4:82559302
|
T | G | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+2604A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559302 | ||||||
chr4:82559316
|
G | A | 17 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0022others(14): Show | 17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11+2590C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559316 | ||||||
chr4:82559390
|
C | CA | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(31): Show | 35 | HG01168.hp1 HG01433.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+2515dupT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559390 | ||||||
chr4:82559487
|
G | A | 1 | a0001c0001t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+2419C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559487 | ||||||
chr4:82559658
|
T | G | 5 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0007g0077others(2): Show | 5 | HG01884.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2248A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559658 | ||||||
chr4:82559678
|
A | G | 1 | a0001c0001t0005g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+2228T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559678 | ||||||
chr4:82559691
|
T | C | 2 | a0001c0001t0003g0215a0001c0001t0006g0214 | 2 | HG01109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-11+2215A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559691 | ||||||
chr4:82559812
|
G | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(31): Show | 35 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.-11+2094C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559812 | ||||||
chr4:82559831
|
A | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2075T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559831 | ||||||
chr4:82559832
|
A | C | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2074T>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559832 | ||||||
chr4:82559833
|
T | A | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2073A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559833 | ||||||
chr4:82559834
|
G | C | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2072C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559834 | ||||||
chr4:82559836
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2070G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559836 | ||||||
chr4:82559838
|
A | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2068T>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559838 | ||||||
chr4:82559839
|
G | C | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2067C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559839 | ||||||
chr4:82559841
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2065A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559841 | ||||||
chr4:82559843
|
G | A | 45 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0120others(42): Show | 45 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-11+2063C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559843 | ||||||
chr4:82559844
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2062G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559844 | ||||||
chr4:82559845
|
A | G | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2061T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559845 | ||||||
chr4:82559846
|
G | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+2060C>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559846 | ||||||
chr4:82559869
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+2037G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559869 | ||||||
chr4:82559892
|
T | C | 2 | a0001c0001t0007g0077a0001c0001t0031g0028 | 2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+2014A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559892 | ||||||
chr4:82559955
|
C | G | 54 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0180others(51): Show | 54 | HG00438.hp1 HG00558.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-11+1951G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82559955 | ||||||
chr4:82560002
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(72): Show | 76 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-11+1904A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560002 | ||||||
chr4:82560078
|
T | G | 3 | a0001c0001t0015g0146a0001c0001t0017g0145a0001c0001t0017g0147 | 3 | HG02886.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+1828A>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560078 | ||||||
chr4:82560117
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+1789G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560117 | ||||||
chr4:82560119
|
CA | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(92): Show | 96 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-11+1786delT | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560119 | ||||||
chr4:82560352
|
T | C | 14 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0004g0016others(11): Show | 14 | HG00642.hp2 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+1554A>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560352 | ||||||
chr4:82560427
|
C | T | 5 | a0001c0001t0003g0034a0001c0001t0005g0030a0001c0001t0014g0031others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1479G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560427 | ||||||
chr4:82560471
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(79): Show | 83 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-11+1435G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560471 | ||||||
chr4:82560479
|
C | T | 1 | a0001c0001t0004g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-11+1427G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560479 | ||||||
chr4:82560571
|
A | G | 3 | a0001c0001t0006g0025a0001c0001t0007g0027a0001c0001t0014g0026 | 3 | HG01884.hp2 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+1335T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560571 | ||||||
chr4:82560675
|
A | G | 5 | a0001c0001t0004g0112a0001c0001t0004g0113a0001c0001t0004g0114others(2): Show | 5 | HG02723.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1231T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560675 | ||||||
chr4:82560871
|
A | G | 3 | a0001c0001t0007g0014a0001c0001t0014g0024a0001c0001t0039g0015 | 3 | HG00642.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11+1035T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82560871 | ||||||
chr4:82561127
|
TTAAAATG others(41): Show |
T | 1 | a0001c0001t0014g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-11+731_-11+778del others(48): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561127 | ||||||
chr4:82561157
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+749A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561157 | ||||||
chr4:82561162
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+744A>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561162 | ||||||
chr4:82561218
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+688G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561218 | ||||||
chr4:82561279
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-11+627C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561279 | ||||||
chr4:82561430
|
C | G | 31 | a0001c0001t0001g0017a0001c0001t0003g0019a0001c0001t0003g0215others(28): Show | 31 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11+476G>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561430 | ||||||
chr4:82561441
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11+465C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561441 | ||||||
chr4:82561446
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+460T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561446 | ||||||
chr4:82561460
|
C | T | 4 | a0001c0001t0005g0022a0001c0001t0007g0109a0001c0001t0015g0110others(1): Show | 4 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+446G>A | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561460 | ||||||
chr4:82561529
|
G | A | 1 | a0001c0001t0022g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11+377C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561529 | ||||||
chr4:82561546
|
A | ACGGGGC | 9 | a0001c0001t0001g0017a0001c0001t0002g0020a0001c0001t0002g0021others(6): Show | 9 | HG00642.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+354_-11+359dup others(6): Show |
TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561546 | ||||||
chr4:82561548
|
G | A | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0238others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+358C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561548 | ||||||
chr4:82561594
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-11+312C>T | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561594 | ||||||
chr4:82561641
|
G | C | 151 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0043others(148): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.-11+265C>G | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561641 | ||||||
chr4:82561838
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-11+68T>C | TMEM150C | ENSG00000249242.8 | transcript | ENST00000449862.7 | protein_coding | 1/7 | chr4 | 82561838 |