| geneid | 23505 |
|---|---|
| ensemblid | ENSG00000075568.17 |
| hgncid | 30366 |
| symbol | TMEM131 |
| name | transmembrane protein 131 |
| refseq_nuc | NM_015348.2 |
| refseq_prot | NP_056163.1 |
| ensembl_nuc | ENST00000186436.10 |
| ensembl_prot | ENSP00000186436.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 97756336 |
| end | 97995948 |
| strand | - |
| ver | v1.2 |
| region | chr2:97756336-97995948 |
| region5000 | chr2:97751336-98000948 |
| regionname0 | TMEM131_chr2_97756336_97995948 |
| regionname5000 | TMEM131_chr2_97751336_98000948 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1883 | 206 | 80 | 36 | 69 | 8 | 11 | 53 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0002 | 0/0 | 1883 | 30 | 1 | 15 | 1 | 5 | 8 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0003 | 0/0 | 1883 | 26 | 0 | 0 | 25 | 0 | 1 | 21 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0004 | 0/0 | 1883 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0005 | 0/0 | 1883 | 6 | 1 | 4 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0006 | 0/0 | 1883 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0007 | 0/0 | 1883 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0008 | 0/0 | 1883 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0009 | 0/0 | 1883 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0010 | 0/0 | 1883 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0011 | 0/0 | 1883 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0012 | 0/0 | 1883 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0013 | 0/0 | 1883 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0014 | 0/0 | 1883 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0015 | 0/0 | 1883 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 5652 | 108 | 55 | 17 | 26 | 8 | 2 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0002 | 1/1 | 5652 | 71 | 5 | 14 | 43 | 0 | 7 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0003 | 0/0 | 5652 | 27 | 1 | 12 | 1 | 5 | 8 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0004 | 0/0 | 5652 | 26 | 0 | 0 | 25 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0005 | 0/0 | 5652 | 10 | 8 | 2 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0006 | 0/0 | 5652 | 6 | 1 | 4 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0007 | 0/0 | 5652 | 6 | 5 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0008 | 0/0 | 5652 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0009 | 0/0 | 5652 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0010 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0011 | 0/0 | 5652 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0012 | 0/0 | 5652 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0013 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0014 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0015 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0016 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0017 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0018 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0019 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0020 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0021 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0022 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0023 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0024 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0025 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0026 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0027 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| c0028 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1050 | 80 | 8 | 17 | 42 | 0 | 11 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0002 | 0/0 | 1050 | 53 | 25 | 0 | 27 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0003 | 0/0 | 1050 | 50 | 18 | 12 | 13 | 7 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0004 | 0/0 | 1050 | 42 | 5 | 16 | 7 | 5 | 9 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0005 | 0/0 | 1050 | 37 | 23 | 11 | 0 | 2 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0006 | 0/0 | 1050 | 12 | 12 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0007 | 0/0 | 1051 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0008 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0009 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0010 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| t0011 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5652 | 108 | 55 | 17 | 26 | 8 | 2 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0002 | 1/1 | 5652 | 71 | 5 | 14 | 43 | 0 | 7 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0005 | 0/0 | 5652 | 10 | 8 | 2 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0007 | 0/0 | 5652 | 6 | 5 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0010 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0011 | 0/0 | 5652 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0012 | 0/0 | 5652 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0022 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0023 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0024 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0026 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0027 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0002c0003 | 0/0 | 5652 | 27 | 1 | 12 | 1 | 5 | 8 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0002c0009 | 0/0 | 5652 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0003c0004 | 0/0 | 5652 | 26 | 0 | 0 | 25 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0004c0008 | 0/0 | 5652 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0004c0014 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0005c0006 | 0/0 | 5652 | 6 | 1 | 4 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0006c0021 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0007c0019 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0008c0020 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0009c0025 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0010c0018 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0011c0017 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0012c0016 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0013c0028 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0014c0015 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0015c0013 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6701 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0002 | 0/0 | 6701 | 20 | 18 | 0 | 2 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0003 | 0/0 | 6701 | 40 | 11 | 11 | 11 | 7 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0004 | 0/0 | 6701 | 10 | 4 | 0 | 6 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0005 | 0/0 | 6701 | 18 | 11 | 5 | 0 | 1 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0006 | 0/0 | 6701 | 11 | 11 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0007 | 0/0 | 6702 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0001t0008 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0002t0001 | 1/1 | 6701 | 69 | 5 | 14 | 41 | 0 | 7 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0002t0009 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0002t0010 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0005t0005 | 0/0 | 6701 | 10 | 8 | 2 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0007t0003 | 0/0 | 6701 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0007t0011 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0010t0005 | 0/0 | 6701 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0011t0001 | 0/0 | 6701 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0012t0001 | 0/0 | 6701 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0022t0003 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0023t0003 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0024t0001 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0026t0001 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0001c0027t0001 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0002c0003t0004 | 0/0 | 6701 | 27 | 1 | 12 | 1 | 5 | 8 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0002c0009t0004 | 0/0 | 6701 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0003c0004t0002 | 0/0 | 6701 | 26 | 0 | 0 | 25 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0004c0008t0002 | 0/0 | 6701 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0004c0014t0002 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0005c0006t0005 | 0/0 | 6701 | 6 | 1 | 4 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0006c0021t0006 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0007c0019t0004 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0008c0020t0004 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0009c0025t0001 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0010c0018t0003 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0011c0017t0003 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0012c0016t0003 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0013c0028t0001 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0014c0015t0002 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| a0015c0013t0005 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | copy fasta | chr2 | 97751336 | 98000948 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0002t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0005t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0007t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0007t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0007t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0007t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0007t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0010t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0010t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0011t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0011t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0012t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0012t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0022t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0023t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0024t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0026t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0001c0027t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0009t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0009t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0002c0009t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0003c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0004c0008t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0004c0008t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0004c0008t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0004c0008t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0004c0008t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0004c0014t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0005c0006t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0005c0006t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0005c0006t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0005c0006t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0005c0006t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0005c0006t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0006c0021t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0007c0019t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0008c0020t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0009c0025t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0010c0018t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0011c0017t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0012c0016t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0013c0028t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0014c0015t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| a0015c0013t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0050 | EUR | GBR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0025 | EUR | GBR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00280 | hp1 | a0002 | c0003 | t0004 | g0173 | EUR | FIN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0057 | EUR | FIN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | CHS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | CHS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | CHS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00544 | hp2 | a0003 | c0004 | t0002 | g0110 | EAS | CHS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | CHS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00597 | hp2 | a0003 | c0004 | t0002 | g0104 | EAS | CHS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00642 | hp1 | a0001 | c0005 | t0005 | g0134 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00642 | hp2 | a0002 | c0003 | t0004 | g0189 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG00733 | hp2 | a0002 | c0003 | t0004 | g0176 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01069 | hp2 | a0002 | c0003 | t0004 | g0175 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01070 | hp2 | a0002 | c0003 | t0004 | g0194 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01168 | hp1 | a0002 | c0009 | t0004 | g0182 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01169 | hp1 | a0002 | c0009 | t0004 | g0187 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01175 | hp2 | a0005 | c0006 | t0005 | g0142 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01192 | hp1 | a0002 | c0003 | t0004 | g0198 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01243 | hp1 | a0001 | c0005 | t0005 | g0144 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01255 | hp1 | a0002 | c0003 | t0004 | g0172 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01257 | hp1 | a0005 | c0006 | t0005 | g0136 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01258 | hp1 | a0005 | c0006 | t0005 | g0137 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01261 | hp2 | a0001 | c0007 | t0003 | g0037 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01496 | hp2 | a0002 | c0003 | t0004 | g0179 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01515 | hp1 | a0005 | c0006 | t0005 | g0131 | EUR | IBS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0047 | EUR | IBS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0052 | EUR | IBS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01516 | hp2 | a0002 | c0003 | t0004 | g0180 | EUR | IBS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01517 | hp1 | a0002 | c0003 | t0004 | g0181 | EUR | IBS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0048 | EUR | IBS | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01934 | hp1 | a0001 | c0011 | t0001 | g0229 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01943 | hp1 | a0008 | c0020 | t0004 | g0170 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01975 | hp1 | a0002 | c0003 | t0004 | g0186 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01978 | hp2 | a0002 | c0003 | t0004 | g0184 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01981 | hp1 | a0001 | c0011 | t0001 | g0248 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01993 | hp1 | a0002 | c0003 | t0004 | g0185 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02004 | hp1 | a0002 | c0003 | t0004 | g0183 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02129 | hp2 | a0003 | c0004 | t0002 | g0101 | EAS | KHV | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02257 | hp1 | a0001 | c0010 | t0005 | g0080 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02280 | hp1 | a0001 | c0023 | t0003 | g0061 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02293 | hp1 | a0002 | c0003 | t0004 | g0197 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02572 | hp2 | a0001 | c0005 | t0005 | g0140 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02602 | hp2 | a0003 | c0004 | t0002 | g0114 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02622 | hp1 | a0001 | c0005 | t0005 | g0135 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02622 | hp2 | a0001 | c0010 | t0005 | g0079 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02630 | hp1 | a0001 | c0005 | t0005 | g0141 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02735 | hp1 | a0001 | c0012 | t0001 | g0233 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02735 | hp2 | a0002 | c0003 | t0004 | g0177 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02818 | hp1 | a0001 | c0007 | t0003 | g0035 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02818 | hp2 | a0004 | c0008 | t0002 | g0094 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02886 | hp2 | a0001 | c0005 | t0005 | g0139 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02896 | hp1 | a0004 | c0008 | t0002 | g0093 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02896 | hp2 | a0001 | c0026 | t0001 | g0266 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02897 | hp2 | a0004 | c0008 | t0002 | g0091 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02922 | hp2 | a0001 | c0005 | t0005 | g0130 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02970 | hp2 | a0001 | c0022 | t0003 | g0123 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03041 | hp2 | a0001 | c0007 | t0003 | g0034 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03098 | hp1 | a0001 | c0007 | t0003 | g0036 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03130 | hp1 | a0004 | c0008 | t0002 | g0095 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03195 | hp1 | a0001 | c0005 | t0005 | g0133 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03209 | hp2 | a0001 | c0007 | t0011 | g0284 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03239 | hp1 | a0002 | c0003 | t0004 | g0190 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03453 | hp1 | a0006 | c0021 | t0006 | g0164 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03490 | hp2 | a0002 | c0003 | t0004 | g0192 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03492 | hp1 | a0001 | c0012 | t0001 | g0235 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03492 | hp2 | a0002 | c0003 | t0004 | g0191 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03540 | hp2 | a0012 | c0016 | t0003 | g0039 | AFR | GWD | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03654 | hp1 | a0002 | c0003 | t0004 | g0195 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0230 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03669 | hp1 | a0007 | c0019 | t0004 | g0196 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03710 | hp1 | a0002 | c0003 | t0004 | g0201 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | BEB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | BEB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0261 | SAS | STU | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG04228 | hp2 | a0002 | c0003 | t0004 | g0178 | SAS | STU | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | YRI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | YRI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | CHB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18612 | hp2 | a0003 | c0004 | t0002 | g0111 | EAS | CHB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | YRI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | YRI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0118 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18941 | hp2 | a0003 | c0004 | t0002 | g0099 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18942 | hp2 | a0003 | c0004 | t0002 | g0097 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18951 | hp1 | a0010 | c0018 | t0003 | g0063 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18951 | hp2 | a0003 | c0004 | t0002 | g0106 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18952 | hp2 | a0003 | c0004 | t0002 | g0108 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18954 | hp2 | a0002 | c0003 | t0004 | g0199 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18956 | hp1 | a0003 | c0004 | t0002 | g0116 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18957 | hp1 | a0003 | c0004 | t0002 | g0098 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18974 | hp2 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18977 | hp2 | a0003 | c0004 | t0002 | g0105 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18982 | hp2 | a0003 | c0004 | t0002 | g0113 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18991 | hp2 | a0003 | c0004 | t0002 | g0120 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18993 | hp1 | a0003 | c0004 | t0002 | g0117 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18995 | hp2 | a0003 | c0004 | t0002 | g0119 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18998 | hp1 | a0013 | c0028 | t0001 | g0246 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA18998 | hp2 | a0003 | c0004 | t0002 | g0103 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19002 | hp1 | a0003 | c0004 | t0002 | g0100 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19003 | hp1 | a0001 | c0002 | t0010 | g0243 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19011 | hp2 | a0003 | c0004 | t0002 | g0109 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19030 | hp1 | a0001 | c0005 | t0005 | g0132 | AFR | LWK | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19030 | hp2 | a0015 | c0013 | t0005 | g0001 | AFR | LWK | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19043 | hp1 | a0001 | c0027 | t0001 | g0265 | AFR | LWK | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19043 | hp2 | a0004 | c0014 | t0002 | g0090 | AFR | LWK | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19054 | hp1 | a0003 | c0004 | t0002 | g0102 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19058 | hp1 | a0003 | c0004 | t0002 | g0115 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19060 | hp1 | a0003 | c0004 | t0002 | g0146 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19065 | hp1 | a0003 | c0004 | t0002 | g0096 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19066 | hp2 | a0003 | c0004 | t0002 | g0112 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19072 | hp2 | a0011 | c0017 | t0003 | g0065 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19083 | hp2 | a0003 | c0004 | t0002 | g0107 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19084 | hp2 | a0001 | c0002 | t0009 | g0262 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19240 | hp1 | a0001 | c0024 | t0001 | g0263 | AFR | YRI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | YRI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ASW | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | ASW | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | TSI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20752 | hp2 | a0002 | c0003 | t0004 | g0174 | EUR | TSI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | TSI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20805 | hp2 | a0002 | c0003 | t0004 | g0171 | EUR | TSI | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20905 | hp1 | a0002 | c0003 | t0004 | g0200 | SAS | GIH | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20905 | hp2 | a0009 | c0025 | t0001 | g0249 | SAS | GIH | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01123 | hp1 | a0005 | c0006 | t0005 | g0143 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG01123 | hp2 | a0002 | c0009 | t0004 | g0188 | AMR | CLM | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02486 | hp1 | a0014 | c0015 | t0002 | g0129 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG02486 | hp2 | a0002 | c0003 | t0004 | g0193 | AFR | ACB | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03471 | hp1 | a0004 | c0008 | t0002 | g0092 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG03471 | hp2 | a0001 | c0005 | t0005 | g0145 | AFR | MSL | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | USA | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | USA | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | USA | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA20300 | hp2 | a0001 | c0007 | t0003 | g0038 | AFR | USA | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | LWK | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| NA21309 | hp2 | a0005 | c0006 | t0005 | g0138 | AFR | LWK | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0236 | REF | REF | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0283 | REF | REF | TMEM131_chr2_97751336_98000948 | TMEM131 | chr2 | 97751336 | 98000948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97757200
|
C | A | 1 | a0010 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.5551G>T | p.Asp1851Tyr | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 5837/6701 | 5551/5652 | 1851/1883 | chr2 | 97757200 | ||
| chr2:97757379
|
A | T | 1 | a0005 | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
missense_variant | MODERATE | c.5372T>A | p.Val1791Asp | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 5658/6701 | 5372/5652 | 1791/1883 | chr2 | 97757379 | ||
| chr2:97757380
|
C | T | 1 | a0009 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.5371G>A | p.Val1791Ile | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 5657/6701 | 5371/5652 | 1791/1883 | chr2 | 97757380 | ||
| chr2:97759678
|
A | T | 1 | a0011 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.5180T>A | p.Phe1727Tyr | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 39/41 | 5466/6701 | 5180/5652 | 1727/1883 | chr2 | 97759678 | ||
| chr2:97760895
|
G | A | 1 | a0007 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.4909C>T | p.Pro1637Ser | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 37/41 | 5195/6701 | 4909/5652 | 1637/1883 | chr2 | 97760895 | ||
| chr2:97766487
|
T | G | 1 | a0012 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.4564A>C | p.Lys1522Gln | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 34/41 | 4850/6701 | 4564/5652 | 1522/1883 | chr2 | 97766487 | ||
| chr2:97766528
|
G | C | 1 | a0013 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.4523C>G | p.Pro1508Arg | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 34/41 | 4809/6701 | 4523/5652 | 1508/1883 | chr2 | 97766528 | ||
| chr2:97775986
|
G | A | 1 | a0008 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.4177C>T | p.Pro1393Ser | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/41 | 4463/6701 | 4177/5652 | 1393/1883 | chr2 | 97775986 | ||
| chr2:97792455
|
C | T | 1 | a0003 | 26 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(23): Show |
missense_variant | MODERATE | c.4075G>A | p.Asp1359Asn | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/41 | 4361/6701 | 4075/5652 | 1359/1883 | chr2 | 97792455 | ||
| chr2:97792583
|
G | A | 4 | a0002a0004a0007others(1): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(35): Show |
missense_variant | MODERATE | c.3947C>T | p.Pro1316Leu | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/41 | 4233/6701 | 3947/5652 | 1316/1883 | chr2 | 97792583 | ||
| chr2:97792730
|
G | A | 1 | a0006 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3800C>T | p.Ser1267Leu | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/41 | 4086/6701 | 3800/5652 | 1267/1883 | chr2 | 97792730 | ||
| chr2:97792935
|
C | T | 1 | a0014 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.3595G>A | p.Ala1199Thr | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/41 | 3881/6701 | 3595/5652 | 1199/1883 | chr2 | 97792935 | ||
| chr2:97927482
|
C | T | 1 | a0004 | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.193G>A | p.Val65Ile | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/41 | 479/6701 | 193/5652 | 65/1883 | chr2 | 97927482 | ||
| chr2:97995542
|
C | T | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.121G>A | p.Gly41Ser | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/41 | 407/6701 | 121/5652 | 41/1883 | chr2 | 97995542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97757330
|
G | A | 1 | a0001c0026 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.5421C>T | p.Ser1807Ser | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 5707/6701 | 5421/5652 | 1807/1883 | chr2 | 97757330 | ||
| chr2:97759022
|
C | T | 1 | a0001c0012 | 2 | HG02735.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.5238G>A | p.Ser1746Ser | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/41 | 5524/6701 | 5238/5652 | 1746/1883 | chr2 | 97759022 | ||
| chr2:97759746
|
C | T | 1 | a0002c0009 | 3 | HG01123.hp2 HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.5112G>A | p.Ser1704Ser | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 39/41 | 5398/6701 | 5112/5652 | 1704/1883 | chr2 | 97759746 | ||
| chr2:97766154
|
T | C | 1 | a0001c0027 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.4683A>G | p.Pro1561Pro | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/41 | 4969/6701 | 4683/5652 | 1561/1883 | chr2 | 97766154 | ||
| chr2:97766211
|
C | T | 1 | a0004c0014 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4626G>A | p.Pro1542Pro | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/41 | 4912/6701 | 4626/5652 | 1542/1883 | chr2 | 97766211 | ||
| chr2:97766488
|
C | T | 1 | a0012c0016 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.4563G>A | p.Gln1521Gln | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 34/41 | 4849/6701 | 4563/5652 | 1521/1883 | chr2 | 97766488 | ||
| chr2:97775855
|
C | T | 1 | a0001c0024 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.4308G>A | p.Pro1436Pro | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/41 | 4594/6701 | 4308/5652 | 1436/1883 | chr2 | 97775855 | ||
| chr2:97797415
|
T | G | 1 | a0001c0007 | 6 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.2820A>C | p.Val940Val | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 26/41 | 3106/6701 | 2820/5652 | 940/1883 | chr2 | 97797415 | ||
| chr2:97811170
|
C | T | 3 | a0001c0005a0005c0006a0015c0013 | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
synonymous_variant | LOW | c.1926G>A | p.Glu642Glu | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/41 | 2212/6701 | 1926/5652 | 642/1883 | chr2 | 97811170 | ||
| chr2:97812427
|
T | C | 1 | a0001c0022 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1857A>G | p.Gln619Gln | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 17/41 | 2143/6701 | 1857/5652 | 619/1883 | chr2 | 97812427 | ||
| chr2:97814100
|
T | C | 1 | a0001c0010 | 2 | HG02257.hp1 HG02622.hp2 |
synonymous_variant | LOW | c.1488A>G | p.Glu496Glu | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/41 | 1774/6701 | 1488/5652 | 496/1883 | chr2 | 97814100 | ||
| chr2:97888099
|
A | G | 1 | a0001c0011 | 2 | HG01934.hp1 HG01981.hp1 |
synonymous_variant | LOW | c.312T>C | p.Asn104Asn | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/41 | 598/6701 | 312/5652 | 104/1883 | chr2 | 97888099 | ||
| chr2:97908696
|
G | A | 1 | a0001c0023 | 1 | HG02280.hp1 | splice_region_variant&synonymous_variant | LOW | c.252C>T | p.Thr84Thr | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/41 | 538/6701 | 252/5652 | 84/1883 | chr2 | 97908696 | ||
| chr2:97995531
|
G | T | 20 | a0001c0001a0001c0005a0001c0007others(17): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
synonymous_variant | LOW | c.132C>A | p.Gly44Gly | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/41 | 418/6701 | 132/5652 | 44/1883 | chr2 | 97995531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97756367
|
C | A | 1 | a0001c0002t0009 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 732 | chr2 | 97756367 | |||||
| chr2:97756517
|
A | G | 9 | a0001c0001t0003a0001c0001t0008a0001c0007t0003others(6): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*582T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 582 | chr2 | 97756517 | |||||
| chr2:97756543
|
C | T | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(17): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*556G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 556 | chr2 | 97756543 | |||||
| chr2:97756661
|
G | A | 1 | a0001c0002t0010 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 438 | chr2 | 97756661 | |||||
| chr2:97756852
|
C | CT | 1 | a0001c0001t0007 | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*246dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 41/41 | 246 | chr2 | 97756852 | |||||
| chr2:97995797
|
T | C | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(5): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-135A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/41 | 135 | chr2 | 97995797 | |||||
| chr2:97995803
|
A | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
5_prime_UTR_variant | MODIFIER | c.-141T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/41 | 141 | chr2 | 97995803 | |||||
| chr2:97995901
|
G | C | 1 | a0001c0007t0011 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-239C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/41 | 239 | chr2 | 97995901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97757387
|
C | T | 10 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(7): Show | 10 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.5368-4G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757387 | ||||||
| chr2:97757390
|
C | G | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.5368-7G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757390 | ||||||
| chr2:97757402
|
C | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.5368-19G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757402 | ||||||
| chr2:97757445
|
G | C | 5 | a0002c0003t0004g0200a0002c0003t0004g0201a0002c0009t0004g0182others(2): Show | 5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.5368-62C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757445 | ||||||
| chr2:97757479
|
C | T | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5368-96G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757479 | ||||||
| chr2:97757540
|
T | G | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.5368-157A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757540 | ||||||
| chr2:97757764
|
G | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.5368-381C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757764 | ||||||
| chr2:97757783
|
C | G | 2 | a0003c0004t0002g0119a0003c0004t0002g0120 | 2 | NA18991.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.5368-400G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757783 | ||||||
| chr2:97757857
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5368-474C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757857 | ||||||
| chr2:97757934
|
C | T | 72 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.5368-551G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757934 | ||||||
| chr2:97757942
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.5368-559G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97757942 | ||||||
| chr2:97758049
|
A | G | 87 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.5368-666T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758049 | ||||||
| chr2:97758104
|
C | T | 42 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(39): Show | 42 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.5368-721G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758104 | ||||||
| chr2:97758111
|
T | G | 1 | a0001c0002t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5368-728A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758111 | ||||||
| chr2:97758131
|
C | CA | 13 | a0001c0001t0003g0062a0001c0001t0003g0067a0001c0002t0001g0206others(10): Show | 13 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.5368-749dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758131 | ||||||
| chr2:97758481
|
C | T | 2 | a0001c0002t0001g0247a0001c0002t0001g0259 | 2 | NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.5367+412G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758481 | ||||||
| chr2:97758496
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.5367+397A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758496 | ||||||
| chr2:97758518
|
T | C | 1 | a0006c0021t0006g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5367+375A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758518 | ||||||
| chr2:97758710
|
A | C | 1 | a0001c0010t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5367+183T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758710 | ||||||
| chr2:97758793
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.5367+100A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 40/40 | chr2 | 97758793 | ||||||
| chr2:97759259
|
A | G | 103 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.5207-206T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 39/40 | chr2 | 97759259 | ||||||
| chr2:97759338
|
C | G | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5207-285G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 39/40 | chr2 | 97759338 | ||||||
| chr2:97759450
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.5206+202C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 39/40 | chr2 | 97759450 | ||||||
| chr2:97759488
|
G | T | 1 | a0011c0017t0003g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.5206+164C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 39/40 | chr2 | 97759488 | ||||||
| chr2:97759877
|
G | C | 11 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(8): Show | 11 | HG00642.hp1 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.5109-128C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97759877 | ||||||
| chr2:97759924
|
C | A | 1 | a0001c0001t0007g0018 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5109-175G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97759924 | ||||||
| chr2:97760005
|
A | AT | 37 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(34): Show | 37 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.5109-257dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97760005 | ||||||
| chr2:97760127
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.5109-378T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97760127 | ||||||
| chr2:97760526
|
TA | T | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.5108+66delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97760526 | ||||||
| chr2:97760543
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.5108+50C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97760543 | ||||||
| chr2:97760571
|
G | A | 12 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(9): Show | 12 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.5108+22C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 38/40 | chr2 | 97760571 | ||||||
| chr2:97760940
|
T | G | 2 | a0001c0005t0005g0135a0001c0005t0005g0139 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4890-26A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97760940 | ||||||
| chr2:97761003
|
T | C | 1 | a0001c0002t0001g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4890-89A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761003 | ||||||
| chr2:97761049
|
A | T | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 101 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.4890-135T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761049 | ||||||
| chr2:97761181
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4890-267G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761181 | ||||||
| chr2:97761202
|
G | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.4890-288C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761202 | ||||||
| chr2:97761294
|
C | A | 1 | a0011c0017t0003g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4890-380G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761294 | ||||||
| chr2:97761727
|
A | G | 2 | a0001c0002t0001g0205a0001c0002t0001g0206 | 2 | HG01978.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.4889+308T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761727 | ||||||
| chr2:97761853
|
G | C | 1 | a0001c0001t0003g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4889+182C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761853 | ||||||
| chr2:97761862
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4889+173T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 36/40 | chr2 | 97761862 | ||||||
| chr2:97762248
|
C | T | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4724-48G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97762248 | ||||||
| chr2:97762319
|
C | T | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4724-119G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97762319 | ||||||
| chr2:97762689
|
G | A | 3 | a0001c0002t0001g0277a0001c0002t0001g0281a0001c0002t0001g0282 | 3 | HG02129.hp1 NA18612.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4724-489C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97762689 | ||||||
| chr2:97762804
|
C | T | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 101 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.4724-604G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97762804 | ||||||
| chr2:97763129
|
G | C | 198 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.4724-929C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763129 | ||||||
| chr2:97763129
|
G | T | 6 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0068others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4724-929C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763129 | ||||||
| chr2:97763144
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4724-944C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763144 | ||||||
| chr2:97763198
|
TCA | T | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.4724-1000_4724-999 others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763198 | ||||||
| chr2:97763252
|
G | C | 2 | a0002c0003t0004g0179a0002c0003t0004g0193 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.4724-1052C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763252 | ||||||
| chr2:97763350
|
G | A | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 101 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.4724-1150C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763350 | ||||||
| chr2:97763443
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4724-1243G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763443 | ||||||
| chr2:97763550
|
T | C | 1 | a0001c0001t0005g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4724-1350A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763550 | ||||||
| chr2:97763589
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4724-1389G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763589 | ||||||
| chr2:97763605
|
G | A | 2 | a0001c0001t0003g0045a0001c0001t0003g0046 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.4724-1405C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763605 | ||||||
| chr2:97763625
|
G | C | 2 | a0001c0001t0003g0045a0001c0001t0003g0046 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.4724-1425C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763625 | ||||||
| chr2:97763925
|
G | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4724-1725C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763925 | ||||||
| chr2:97763931
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.4724-1731A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763931 | ||||||
| chr2:97763984
|
T | A | 1 | a0002c0003t0004g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4724-1784A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97763984 | ||||||
| chr2:97764064
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4724-1864G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764064 | ||||||
| chr2:97764218
|
T | C | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.4723+1896A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764218 | ||||||
| chr2:97764305
|
G | A | 1 | a0002c0003t0004g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4723+1809C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764305 | ||||||
| chr2:97764323
|
G | A | 3 | a0002c0003t0004g0190a0002c0003t0004g0191a0002c0003t0004g0192 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4723+1791C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764323 | ||||||
| chr2:97764383
|
C | CTGGGTTT others(19): Show |
1 | a0001c0002t0001g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4723+1705_4723+173 others(30): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764383 | ||||||
| chr2:97764480
|
C | A | 1 | a0011c0017t0003g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4723+1634G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764480 | ||||||
| chr2:97764483
|
G | T | 1 | a0011c0017t0003g0065 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4723+1631C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764483 | ||||||
| chr2:97764490
|
G | A | 9 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(6): Show | 9 | HG00642.hp1 HG01243.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4723+1624C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764490 | ||||||
| chr2:97764639
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.4723+1475G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764639 | ||||||
| chr2:97764987
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4723+1127G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97764987 | ||||||
| chr2:97765532
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4723+582G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97765532 | ||||||
| chr2:97765614
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4723+500T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97765614 | ||||||
| chr2:97765854
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4723+260G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97765854 | ||||||
| chr2:97766031
|
C | A | 1 | a0001c0007t0003g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4723+83G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 35/40 | chr2 | 97766031 | ||||||
| chr2:97766423
|
G | A | 33 | a0001c0001t0003g0053a0002c0003t0004g0171a0002c0003t0004g0172others(30): Show | 33 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.4573+55C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 34/40 | chr2 | 97766423 | ||||||
| chr2:97767094
|
T | G | 2 | a0001c0002t0001g0242a0001c0002t0001g0254 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.4449-492A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97767094 | ||||||
| chr2:97767175
|
G | A | 9 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(6): Show | 9 | HG00642.hp1 HG01243.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4449-573C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97767175 | ||||||
| chr2:97767430
|
G | C | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.4449-828C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97767430 | ||||||
| chr2:97767558
|
C | G | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4449-956G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97767558 | ||||||
| chr2:97767787
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4449-1185C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97767787 | ||||||
| chr2:97767828
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4449-1226C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97767828 | ||||||
| chr2:97768065
|
ATTTTC | A | 120 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(117): Show | 120 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.4449-1468_4449-146 others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768065 | ||||||
| chr2:97768173
|
T | C | 77 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.4449-1571A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768173 | ||||||
| chr2:97768181
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4449-1579T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768181 | ||||||
| chr2:97768404
|
G | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.4449-1802C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768404 | ||||||
| chr2:97768453
|
T | C | 1 | a0001c0011t0001g0248 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4449-1851A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768453 | ||||||
| chr2:97768461
|
TAAG | T | 8 | a0002c0003t0004g0176a0002c0003t0004g0177a0002c0003t0004g0180others(5): Show | 8 | HG00733.hp2 HG01070.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.4449-1862_4449-186 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768461 | ||||||
| chr2:97768674
|
T | A | 1 | a0001c0005t0005g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4449-2072A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768674 | ||||||
| chr2:97768675
|
C | T | 1 | a0001c0005t0005g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4449-2073G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768675 | ||||||
| chr2:97768716
|
G | C | 1 | a0002c0003t0004g0184 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4449-2114C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768716 | ||||||
| chr2:97768836
|
C | T | 2 | a0001c0001t0005g0081a0001c0001t0005g0082 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4449-2234G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768836 | ||||||
| chr2:97768844
|
GCCTCCCA others(389): Show |
G | 33 | a0001c0002t0001g0205a0001c0002t0001g0207a0001c0002t0001g0210others(30): Show | 33 | HG00544.hp1 HG01257.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.4449-2638_4449-224 others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97768844 | ||||||
| chr2:97769110
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4449-2508C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97769110 | ||||||
| chr2:97769304
|
T | A | 77 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.4449-2702A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97769304 | ||||||
| chr2:97769439
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4449-2837G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97769439 | ||||||
| chr2:97769493
|
C | G | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4448+2804G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97769493 | ||||||
| chr2:97769544
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4448+2753A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97769544 | ||||||
| chr2:97769658
|
G | A | 1 | a0002c0003t0004g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4448+2639C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97769658 | ||||||
| chr2:97770233
|
T | C | 85 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.4448+2064A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97770233 | ||||||
| chr2:97770268
|
T | C | 56 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(53): Show | 56 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.4448+2029A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97770268 | ||||||
| chr2:97770305
|
C | G | 1 | a0001c0001t0003g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4448+1992G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97770305 | ||||||
| chr2:97770473
|
C | G | 283 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4448+1824G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97770473 | ||||||
| chr2:97770715
|
G | A | 76 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.4448+1582C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97770715 | ||||||
| chr2:97770799
|
C | A | 1 | a0003c0004t0002g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4448+1498G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97770799 | ||||||
| chr2:97771222
|
G | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4448+1075C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97771222 | ||||||
| chr2:97771452
|
C | G | 2 | a0001c0002t0001g0251a0001c0002t0001g0257 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.4448+845G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97771452 | ||||||
| chr2:97771611
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4448+686C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 33/40 | chr2 | 97771611 | ||||||
| chr2:97772576
|
C | A | 2 | a0002c0003t0004g0200a0002c0003t0004g0201 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4321-152G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97772576 | ||||||
| chr2:97772623
|
C | T | 70 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.4321-199G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97772623 | ||||||
| chr2:97772632
|
A | G | 3 | a0005c0006t0005g0136a0005c0006t0005g0137a0005c0006t0005g0138 | 3 | HG01257.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4321-208T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97772632 | ||||||
| chr2:97772862
|
A | C | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4321-438T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97772862 | ||||||
| chr2:97772910
|
A | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.4321-486T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97772910 | ||||||
| chr2:97772920
|
G | A | 3 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019 | 3 | NA18965.hp1 NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.4321-496C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97772920 | ||||||
| chr2:97773467
|
G | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4321-1043C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97773467 | ||||||
| chr2:97773654
|
G | GT | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 102 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.4321-1231dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97773654 | ||||||
| chr2:97773696
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4321-1272C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97773696 | ||||||
| chr2:97773709
|
C | T | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4321-1285G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97773709 | ||||||
| chr2:97773994
|
G | C | 1 | a0001c0005t0005g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4321-1570C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97773994 | ||||||
| chr2:97774150
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4320+1693T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774150 | ||||||
| chr2:97774329
|
A | G | 1 | a0001c0010t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4320+1514T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774329 | ||||||
| chr2:97774463
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4320+1380A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774463 | ||||||
| chr2:97774567
|
G | A | 1 | a0001c0001t0004g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4320+1276C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774567 | ||||||
| chr2:97774636
|
C | G | 1 | a0001c0001t0004g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4320+1207G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774636 | ||||||
| chr2:97774654
|
G | A | 48 | a0001c0001t0002g0012a0001c0001t0003g0032a0001c0001t0003g0033others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.4320+1189C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774654 | ||||||
| chr2:97774742
|
G | C | 17 | a0001c0001t0002g0014a0001c0001t0005g0086a0001c0002t0001g0242others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4320+1101C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774742 | ||||||
| chr2:97774809
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4320+1034G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774809 | ||||||
| chr2:97774878
|
T | C | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.4320+965A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774878 | ||||||
| chr2:97774892
|
C | T | 197 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.4320+951G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774892 | ||||||
| chr2:97774898
|
C | T | 19 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(16): Show | 19 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.4320+945G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774898 | ||||||
| chr2:97774951
|
C | A | 192 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(189): Show | 192 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.4320+892G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97774951 | ||||||
| chr2:97775109
|
A | C | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4320+734T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97775109 | ||||||
| chr2:97775255
|
C | G | 1 | a0001c0001t0003g0049 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4320+588G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97775255 | ||||||
| chr2:97775424
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.4320+419C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97775424 | ||||||
| chr2:97775660
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4320+183A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97775660 | ||||||
| chr2:97775784
|
T | C | 1 | a0002c0003t0004g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4320+59A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97775784 | ||||||
| chr2:97775839
|
G | A | 18 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.4320+4C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 32/40 | chr2 | 97775839 | ||||||
| chr2:97776337
|
G | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.4145-319C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97776337 | ||||||
| chr2:97776447
|
CT | C | 28 | a0001c0001t0002g0121a0001c0001t0007g0017a0003c0004t0002g0096others(25): Show | 28 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.4145-430delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97776447 | ||||||
| chr2:97776768
|
C | T | 50 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(47): Show | 50 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.4145-750G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97776768 | ||||||
| chr2:97776769
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4145-751C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97776769 | ||||||
| chr2:97776779
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4145-761G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97776779 | ||||||
| chr2:97777014
|
G | A | 1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4145-996C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777014 | ||||||
| chr2:97777121
|
CT | C | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.4145-1104delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777121 | ||||||
| chr2:97777214
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4145-1196C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777214 | ||||||
| chr2:97777337
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4145-1319C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777337 | ||||||
| chr2:97777431
|
C | T | 32 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.4145-1413G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777431 | ||||||
| chr2:97777497
|
A | T | 1 | a0003c0004t0002g0097 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4145-1479T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777497 | ||||||
| chr2:97777523
|
T | C | 1 | a0003c0004t0002g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4145-1505A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777523 | ||||||
| chr2:97777715
|
T | C | 2 | a0001c0001t0003g0066a0001c0001t0003g0067 | 2 | NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.4145-1697A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777715 | ||||||
| chr2:97777748
|
A | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.4145-1730T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777748 | ||||||
| chr2:97777840
|
G | GCCAAA | 22 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0004g0153others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.4145-1827_4145-182 others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97777840 | ||||||
| chr2:97778050
|
A | G | 1 | a0001c0001t0006g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4145-2032T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97778050 | ||||||
| chr2:97778174
|
G | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4145-2156C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97778174 | ||||||
| chr2:97778550
|
C | CA | 8 | a0001c0001t0001g0203a0001c0001t0002g0015a0001c0001t0002g0016others(5): Show | 8 | HG02027.hp2 HG02071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.4145-2533dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97778550 | ||||||
| chr2:97778608
|
A | G | 1 | a0001c0002t0001g0279 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4145-2590T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97778608 | ||||||
| chr2:97778971
|
GTGTGGAT others(9): Show |
G | 2 | a0001c0002t0001g0279a0001c0002t0001g0280 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4145-2969_4145-295 others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97778971 | ||||||
| chr2:97779190
|
A | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.4145-3172T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97779190 | ||||||
| chr2:97779454
|
G | A | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4145-3436C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97779454 | ||||||
| chr2:97779570
|
C | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.4145-3552G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97779570 | ||||||
| chr2:97779856
|
A | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(19): Show | 22 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.4145-3838T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97779856 | ||||||
| chr2:97780035
|
AAAACAAA others(8): Show |
A | 1 | a0001c0001t0003g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4145-4032_4145-401 others(19): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780035 | ||||||
| chr2:97780058
|
C | A | 8 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0125others(5): Show | 8 | HG01346.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.4145-4040G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780058 | ||||||
| chr2:97780058
|
C | CA | 17 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0005g0030others(14): Show | 17 | HG00597.hp1 HG01070.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.4145-4041dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780058 | ||||||
| chr2:97780631
|
C | T | 9 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(6): Show | 9 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.4145-4613G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780631 | ||||||
| chr2:97780681
|
A | C | 1 | a0001c0002t0001g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4145-4663T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780681 | ||||||
| chr2:97780838
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.4145-4820G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780838 | ||||||
| chr2:97780867
|
G | A | 30 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(27): Show | 30 | HG00597.hp1 HG01884.hp2 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.4145-4849C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780867 | ||||||
| chr2:97780868
|
G | GAAGT | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.4145-4854_4145-485 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780868 | ||||||
| chr2:97780930
|
G | C | 5 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(2): Show | 5 | HG02027.hp2 HG02071.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.4145-4912C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780930 | ||||||
| chr2:97780961
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4145-4943G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97780961 | ||||||
| chr2:97781313
|
T | C | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4145-5295A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781313 | ||||||
| chr2:97781347
|
C | A | 1 | a0001c0001t0002g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4145-5329G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781347 | ||||||
| chr2:97781348
|
C | G | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.4145-5330G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781348 | ||||||
| chr2:97781437
|
T | C | 1 | a0001c0002t0001g0206 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4145-5419A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781437 | ||||||
| chr2:97781597
|
A | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.4145-5579T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781597 | ||||||
| chr2:97781751
|
G | C | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.4145-5733C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781751 | ||||||
| chr2:97781900
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4145-5882T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781900 | ||||||
| chr2:97781946
|
C | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.4145-5928G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781946 | ||||||
| chr2:97781960
|
G | A | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4145-5942C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97781960 | ||||||
| chr2:97782161
|
C | T | 2 | a0001c0002t0001g0247a0001c0002t0001g0259 | 2 | NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4145-6143G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782161 | ||||||
| chr2:97782462
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4145-6444A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782462 | ||||||
| chr2:97782485
|
A | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4145-6467T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782485 | ||||||
| chr2:97782628
|
C | T | 1 | a0002c0003t0004g0194 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4145-6610G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782628 | ||||||
| chr2:97782862
|
T | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.4145-6844A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782862 | ||||||
| chr2:97782953
|
A | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4145-6935T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782953 | ||||||
| chr2:97782967
|
TA | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4145-6950delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97782967 | ||||||
| chr2:97783339
|
A | G | 3 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149 | 3 | NA19001.hp1 NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.4145-7321T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97783339 | ||||||
| chr2:97783360
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4145-7342C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97783360 | ||||||
| chr2:97783722
|
T | C | 2 | a0001c0002t0001g0247a0001c0002t0001g0259 | 2 | NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4145-7704A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97783722 | ||||||
| chr2:97783738
|
G | A | 3 | a0002c0009t0004g0182a0002c0009t0004g0187a0002c0009t0004g0188 | 3 | HG01123.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4145-7720C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97783738 | ||||||
| chr2:97783835
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4145-7817T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97783835 | ||||||
| chr2:97783847
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4145-7829A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97783847 | ||||||
| chr2:97784043
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4145-8025C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784043 | ||||||
| chr2:97784405
|
T | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4144+7981A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784405 | ||||||
| chr2:97784643
|
C | CG | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4144+7742dupC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784643 | ||||||
| chr2:97784650
|
G | A | 1 | a0001c0002t0001g0241 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4144+7736C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784650 | ||||||
| chr2:97784692
|
TA | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4144+7693delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784692 | ||||||
| chr2:97784801
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4144+7585A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784801 | ||||||
| chr2:97784923
|
A | G | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.4144+7463T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97784923 | ||||||
| chr2:97785078
|
T | A | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4144+7308A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785078 | ||||||
| chr2:97785135
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0013 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4144+7251G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785135 | ||||||
| chr2:97785294
|
G | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4144+7092C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785294 | ||||||
| chr2:97785396
|
T | C | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.4144+6990A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785396 | ||||||
| chr2:97785622
|
T | C | 1 | a0001c0002t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4144+6764A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785622 | ||||||
| chr2:97785635
|
T | G | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4144+6751A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785635 | ||||||
| chr2:97785804
|
G | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.4144+6582C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785804 | ||||||
| chr2:97785817
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4144+6569A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785817 | ||||||
| chr2:97785823
|
T | C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4144+6563A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785823 | ||||||
| chr2:97785887
|
AC | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.4144+6498delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97785887 | ||||||
| chr2:97786290
|
T | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.4144+6096A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97786290 | ||||||
| chr2:97786309
|
G | C | 32 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.4144+6077C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97786309 | ||||||
| chr2:97786487
|
C | G | 1 | a0004c0008t0002g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4144+5899G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97786487 | ||||||
| chr2:97786615
|
A | G | 1 | a0002c0003t0004g0184 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4144+5771T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97786615 | ||||||
| chr2:97786617
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4144+5769C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97786617 | ||||||
| chr2:97786954
|
T | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4144+5432A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97786954 | ||||||
| chr2:97787046
|
G | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.4144+5340C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97787046 | ||||||
| chr2:97787220
|
C | T | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.4144+5166G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97787220 | ||||||
| chr2:97787616
|
G | T | 5 | a0001c0001t0003g0062a0001c0001t0003g0124a0001c0022t0003g0123others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4144+4770C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97787616 | ||||||
| chr2:97787923
|
A | G | 7 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(4): Show | 7 | HG02074.hp1 HG02083.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.4144+4463T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97787923 | ||||||
| chr2:97787944
|
C | T | 1 | a0005c0006t0005g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4144+4442G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97787944 | ||||||
| chr2:97788506
|
C | G | 1 | a0001c0001t0006g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4144+3880G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97788506 | ||||||
| chr2:97788571
|
T | C | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.4144+3815A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97788571 | ||||||
| chr2:97788705
|
C | G | 3 | a0003c0004t0002g0099a0003c0004t0002g0106a0003c0004t0002g0107 | 3 | NA18941.hp2 NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.4144+3681G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97788705 | ||||||
| chr2:97788923
|
C | T | 1 | a0002c0003t0004g0197 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4144+3463G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97788923 | ||||||
| chr2:97788948
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.4144+3438A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97788948 | ||||||
| chr2:97788951
|
A | G | 3 | a0001c0002t0001g0247a0001c0002t0001g0259a0013c0028t0001g0246 | 3 | NA18998.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4144+3435T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97788951 | ||||||
| chr2:97789212
|
C | G | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.4144+3174G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789212 | ||||||
| chr2:97789212
|
C | T | 1 | a0001c0012t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4144+3174G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789212 | ||||||
| chr2:97789232
|
C | T | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.4144+3154G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789232 | ||||||
| chr2:97789405
|
T | C | 1 | a0001c0002t0001g0206 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4144+2981A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789405 | ||||||
| chr2:97789425
|
T | C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4144+2961A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789425 | ||||||
| chr2:97789466
|
A | G | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.4144+2920T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789466 | ||||||
| chr2:97789548
|
G | A | 1 | a0005c0006t0005g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4144+2838C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789548 | ||||||
| chr2:97789866
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4144+2520G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97789866 | ||||||
| chr2:97790120
|
T | G | 1 | a0001c0010t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4144+2266A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97790120 | ||||||
| chr2:97790269
|
ACTGT | A | 5 | a0002c0003t0004g0183a0002c0003t0004g0184a0002c0003t0004g0185others(2): Show | 5 | HG00642.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.4144+2113_4144+211 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97790269 | ||||||
| chr2:97790705
|
T | C | 24 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(21): Show | 24 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.4144+1681A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97790705 | ||||||
| chr2:97790887
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.4144+1499G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97790887 | ||||||
| chr2:97791204
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.4144+1182G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97791204 | ||||||
| chr2:97791586
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.4144+800G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97791586 | ||||||
| chr2:97791599
|
C | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.4144+787G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97791599 | ||||||
| chr2:97791637
|
A | C | 1 | a0001c0002t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4144+749T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97791637 | ||||||
| chr2:97791822
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4144+564C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97791822 | ||||||
| chr2:97791925
|
A | G | 1 | a0013c0028t0001g0246 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.4144+461T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97791925 | ||||||
| chr2:97792263
|
A | T | 1 | a0001c0001t0005g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4144+123T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97792263 | ||||||
| chr2:97792373
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4144+13C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97792373 | ||||||
| chr2:97792380
|
G | A | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.4144+6C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 31/40 | chr2 | 97792380 | ||||||
| chr2:97793102
|
T | C | 89 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(86): Show | 89 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.3546-118A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 30/40 | chr2 | 97793102 | ||||||
| chr2:97793992
|
T | A | 7 | a0001c0002t0001g0237a0001c0002t0001g0238a0001c0002t0001g0239others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3387-439A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97793992 | ||||||
| chr2:97793993
|
C | CA | 31 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.3387-441dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97793993 | ||||||
| chr2:97793993
|
C | CAA | 18 | a0001c0001t0003g0046a0001c0001t0003g0048a0001c0001t0003g0051others(15): Show | 18 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3387-442_3387-441d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97793993 | ||||||
| chr2:97793993
|
CA | C | 134 | a0001c0001t0002g0016a0001c0001t0002g0121a0001c0001t0002g0125others(131): Show | 134 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.3387-441delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97793993 | ||||||
| chr2:97793993
|
CAA | C | 22 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0014others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3387-442_3387-441d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97793993 | ||||||
| chr2:97793993
|
CAAA | C | 12 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(9): Show | 12 | HG01346.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3387-443_3387-441d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97793993 | ||||||
| chr2:97794008
|
A | C | 1 | a0001c0001t0004g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3387-455T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794008 | ||||||
| chr2:97794015
|
AC | A | 14 | a0001c0001t0005g0024a0001c0001t0005g0026a0001c0001t0005g0029others(11): Show | 14 | HG01099.hp1 HG01257.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.3387-463delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794015 | ||||||
| chr2:97794016
|
C | A | 65 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.3387-463G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794016 | ||||||
| chr2:97794035
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3387-482A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794035 | ||||||
| chr2:97794225
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.3387-672C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794225 | ||||||
| chr2:97794306
|
G | T | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3386+624C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794306 | ||||||
| chr2:97794600
|
C | T | 1 | a0001c0002t0001g0210 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3386+330G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 29/40 | chr2 | 97794600 | ||||||
| chr2:97795208
|
A | T | 1 | a0001c0002t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3201-93T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795208 | ||||||
| chr2:97795236
|
T | C | 1 | a0001c0001t0005g0083 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3201-121A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795236 | ||||||
| chr2:97795426
|
C | T | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.3201-311G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795426 | ||||||
| chr2:97795451
|
T | C | 1 | a0001c0002t0001g0258 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3201-336A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795451 | ||||||
| chr2:97795576
|
G | A | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.3201-461C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795576 | ||||||
| chr2:97795599
|
G | T | 1 | a0001c0023t0003g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3201-484C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795599 | ||||||
| chr2:97795819
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.3200+399G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97795819 | ||||||
| chr2:97796099
|
G | GA | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3200+118dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97796099 | ||||||
| chr2:97796158
|
T | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3200+60A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 28/40 | chr2 | 97796158 | ||||||
| chr2:97796600
|
G | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.3014-196C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 27/40 | chr2 | 97796600 | ||||||
| chr2:97796757
|
A | T | 8 | a0001c0001t0003g0060a0001c0001t0003g0088a0001c0007t0003g0034others(5): Show | 8 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.3013+87T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 27/40 | chr2 | 97796757 | ||||||
| chr2:97797065
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2871-79A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 26/40 | chr2 | 97797065 | ||||||
| chr2:97797244
|
T | C | 1 | a0002c0003t0004g0194 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2870+121A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 26/40 | chr2 | 97797244 | ||||||
| chr2:97797318
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2870+47G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 26/40 | chr2 | 97797318 | ||||||
| chr2:97797552
|
T | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2719-36A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97797552 | ||||||
| chr2:97797908
|
G | T | 1 | a0001c0001t0002g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2719-392C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97797908 | ||||||
| chr2:97797954
|
G | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2719-438C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97797954 | ||||||
| chr2:97798083
|
T | C | 1 | a0001c0001t0003g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2719-567A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798083 | ||||||
| chr2:97798090
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2719-574G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798090 | ||||||
| chr2:97798220
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2719-704C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798220 | ||||||
| chr2:97798278
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2719-762C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798278 | ||||||
| chr2:97798333
|
C | T | 1 | a0001c0002t0001g0211 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2719-817G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798333 | ||||||
| chr2:97798841
|
T | C | 9 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2719-1325A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798841 | ||||||
| chr2:97798859
|
T | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2719-1343A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798859 | ||||||
| chr2:97798866
|
C | A | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2719-1350G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798866 | ||||||
| chr2:97798879
|
T | G | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2719-1363A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798879 | ||||||
| chr2:97798992
|
T | C | 2 | a0001c0001t0003g0062a0001c0023t0003g0061 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2719-1476A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97798992 | ||||||
| chr2:97799112
|
C | T | 1 | a0002c0003t0004g0186 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2719-1596G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799112 | ||||||
| chr2:97799120
|
GTTAT | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2719-1608_2719-160 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799120 | ||||||
| chr2:97799271
|
T | TA | 13 | a0003c0004t0002g0108a0003c0004t0002g0109a0003c0004t0002g0110others(10): Show | 13 | HG00544.hp2 HG02602.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.2719-1756dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799271 | ||||||
| chr2:97799444
|
C | T | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2719-1928G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799444 | ||||||
| chr2:97799654
|
G | A | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2719-2138C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799654 | ||||||
| chr2:97799667
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2719-2151G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799667 | ||||||
| chr2:97799669
|
A | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2719-2153T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799669 | ||||||
| chr2:97799691
|
T | C | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.2719-2175A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97799691 | ||||||
| chr2:97800007
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2718+1888A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800007 | ||||||
| chr2:97800311
|
C | T | 1 | a0001c0002t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2718+1584G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800311 | ||||||
| chr2:97800385
|
C | A | 29 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(26): Show | 29 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.2718+1510G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800385 | ||||||
| chr2:97800387
|
T | G | 29 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(26): Show | 29 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.2718+1508A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800387 | ||||||
| chr2:97800488
|
G | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2718+1407C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800488 | ||||||
| chr2:97800595
|
C | CAA | 8 | a0002c0003t0004g0176a0002c0003t0004g0177a0002c0003t0004g0180others(5): Show | 8 | HG00733.hp2 HG01070.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2718+1298_2718+129 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800595 | ||||||
| chr2:97800595
|
C | CAAAAAAA others(1): Show |
83 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2718+1292_2718+129 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800595 | ||||||
| chr2:97800595
|
C | CAAAAAAA others(2): Show |
87 | a0001c0001t0002g0007a0001c0001t0002g0015a0001c0001t0002g0016others(84): Show | 87 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2718+1291_2718+129 others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800595 | ||||||
| chr2:97800595
|
C | CAAAAAAA others(3): Show |
20 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0005g0023others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2718+1290_2718+129 others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800595 | ||||||
| chr2:97800595
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0005g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2718+1289_2718+129 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800595 | ||||||
| chr2:97800626
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2718+1269G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800626 | ||||||
| chr2:97800681
|
C | T | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2718+1214G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800681 | ||||||
| chr2:97800723
|
C | T | 6 | a0001c0007t0003g0034a0001c0007t0003g0035a0001c0007t0003g0036others(3): Show | 6 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2718+1172G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800723 | ||||||
| chr2:97800735
|
T | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2718+1160A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800735 | ||||||
| chr2:97800741
|
A | G | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2718+1154T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800741 | ||||||
| chr2:97800879
|
A | G | 1 | a0001c0002t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2718+1016T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800879 | ||||||
| chr2:97800921
|
T | C | 1 | a0001c0001t0003g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2718+974A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800921 | ||||||
| chr2:97800959
|
G | GA | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2718+935dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97800959 | ||||||
| chr2:97801000
|
C | T | 1 | a0001c0002t0001g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2718+895G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97801000 | ||||||
| chr2:97801363
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2718+532T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97801363 | ||||||
| chr2:97801649
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2718+246G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97801649 | ||||||
| chr2:97801769
|
G | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2718+126C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 25/40 | chr2 | 97801769 | ||||||
| chr2:97802088
|
C | T | 1 | a0005c0006t0005g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2652-127G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 24/40 | chr2 | 97802088 | ||||||
| chr2:97802215
|
T | C | 1 | a0001c0002t0001g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2651+213A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 24/40 | chr2 | 97802215 | ||||||
| chr2:97802233
|
T | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2651+195A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 24/40 | chr2 | 97802233 | ||||||
| chr2:97802349
|
CA | C | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2651+78delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 24/40 | chr2 | 97802349 | ||||||
| chr2:97802413
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2651+15G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 24/40 | chr2 | 97802413 | ||||||
| chr2:97803028
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2403-238A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803028 | ||||||
| chr2:97803029
|
G | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2403-239C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803029 | ||||||
| chr2:97803071
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2403-281C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803071 | ||||||
| chr2:97803185
|
A | G | 2 | a0001c0010t0005g0079a0001c0010t0005g0080 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2403-395T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803185 | ||||||
| chr2:97803263
|
T | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2403-473A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803263 | ||||||
| chr2:97803362
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2403-572G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803362 | ||||||
| chr2:97803517
|
C | T | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2403-727G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803517 | ||||||
| chr2:97803564
|
C | G | 3 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070 | 3 | HG01884.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2403-774G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803564 | ||||||
| chr2:97803615
|
A | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2403-825T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803615 | ||||||
| chr2:97803679
|
G | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2403-889C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803679 | ||||||
| chr2:97803968
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2402+1120A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97803968 | ||||||
| chr2:97804043
|
TAAAC | T | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.2402+1041_2402+104 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804043 | ||||||
| chr2:97804292
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2402+796A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804292 | ||||||
| chr2:97804406
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2402+682A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804406 | ||||||
| chr2:97804595
|
C | T | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2402+493G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804595 | ||||||
| chr2:97804621
|
C | CA | 37 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(34): Show | 37 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2402+466dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804621 | ||||||
| chr2:97804621
|
CA | C | 42 | a0001c0001t0003g0062a0001c0001t0005g0084a0001c0001t0005g0085others(39): Show | 42 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.2402+466delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804621 | ||||||
| chr2:97804742
|
A | C | 2 | a0001c0002t0001g0258a0001c0002t0001g0260 | 2 | HG00423.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2402+346T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804742 | ||||||
| chr2:97804780
|
T | C | 1 | a0001c0001t0006g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2402+308A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804780 | ||||||
| chr2:97804789
|
A | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2402+299T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804789 | ||||||
| chr2:97804901
|
A | G | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.2402+187T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 22/40 | chr2 | 97804901 | ||||||
| chr2:97805276
|
G | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2285-71C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 21/40 | chr2 | 97805276 | ||||||
| chr2:97805307
|
G | T | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.2284+69C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 21/40 | chr2 | 97805307 | ||||||
| chr2:97805520
|
A | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2208+31T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 20/40 | chr2 | 97805520 | ||||||
| chr2:97805539
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2208+12T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 20/40 | chr2 | 97805539 | ||||||
| chr2:97805833
|
T | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2056-130A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97805833 | ||||||
| chr2:97806049
|
G | A | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.2056-346C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806049 | ||||||
| chr2:97806186
|
T | G | 1 | a0001c0007t0003g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2056-483A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806186 | ||||||
| chr2:97806263
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2056-560T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806263 | ||||||
| chr2:97806288
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2056-585C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806288 | ||||||
| chr2:97806482
|
A | G | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2056-779T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806482 | ||||||
| chr2:97806518
|
G | T | 2 | a0001c0002t0001g0217a0001c0002t0001g0277 | 2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.2056-815C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806518 | ||||||
| chr2:97806672
|
G | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2056-969C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806672 | ||||||
| chr2:97806837
|
G | A | 1 | a0002c0003t0004g0197 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2056-1134C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97806837 | ||||||
| chr2:97807004
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2056-1301G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807004 | ||||||
| chr2:97807325
|
T | C | 1 | a0001c0001t0007g0020 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2056-1622A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807325 | ||||||
| chr2:97807477
|
G | A | 2 | a0002c0003t0004g0191a0002c0003t0004g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2056-1774C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807477 | ||||||
| chr2:97807516
|
C | T | 1 | a0001c0001t0003g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2056-1813G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807516 | ||||||
| chr2:97807611
|
C | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2056-1908G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807611 | ||||||
| chr2:97807751
|
C | A | 1 | a0001c0001t0007g0018 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2055+1937G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807751 | ||||||
| chr2:97807761
|
C | T | 1 | a0004c0008t0002g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2055+1927G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807761 | ||||||
| chr2:97807781
|
T | C | 1 | a0001c0002t0001g0282 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2055+1907A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807781 | ||||||
| chr2:97807793
|
G | A | 1 | a0001c0001t0005g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2055+1895C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807793 | ||||||
| chr2:97807823
|
G | T | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2055+1865C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807823 | ||||||
| chr2:97807833
|
G | GAAGTC | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2055+1854_2055+185 others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97807833 | ||||||
| chr2:97808027
|
T | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0072 | 2 | HG02040.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2055+1661A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808027 | ||||||
| chr2:97808047
|
A | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2055+1641T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808047 | ||||||
| chr2:97808166
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2055+1522C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808166 | ||||||
| chr2:97808184
|
T | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.2055+1504A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808184 | ||||||
| chr2:97808254
|
G | C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2055+1434C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808254 | ||||||
| chr2:97808339
|
A | G | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.2055+1349T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808339 | ||||||
| chr2:97808672
|
G | A | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055+1016C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808672 | ||||||
| chr2:97808695
|
G | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG00423.hp1 NA18949.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.2055+993C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808695 | ||||||
| chr2:97808713
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2055+975C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97808713 | ||||||
| chr2:97809097
|
A | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2055+591T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97809097 | ||||||
| chr2:97809540
|
T | C | 1 | a0001c0002t0001g0282 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2055+148A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97809540 | ||||||
| chr2:97809577
|
A | G | 1 | a0002c0003t0004g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2055+111T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97809577 | ||||||
| chr2:97809605
|
TTACTC | T | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2055+78_2055+82del others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97809605 | ||||||
| chr2:97809645
|
C | CA | 9 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2055+42dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 19/40 | chr2 | 97809645 | ||||||
| chr2:97809837
|
T | C | 1 | a0001c0001t0004g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1969-63A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97809837 | ||||||
| chr2:97809872
|
C | T | 4 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1969-98G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97809872 | ||||||
| chr2:97809918
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1969-144A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97809918 | ||||||
| chr2:97810028
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1969-254C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97810028 | ||||||
| chr2:97810191
|
G | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1969-417C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97810191 | ||||||
| chr2:97810251
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1969-477A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97810251 | ||||||
| chr2:97810531
|
A | G | 278 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1968+597T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97810531 | ||||||
| chr2:97810919
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1968+209A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97810919 | ||||||
| chr2:97810945
|
C | T | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1968+183G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97810945 | ||||||
| chr2:97811022
|
T | C | 1 | a0001c0002t0001g0254 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1968+106A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 18/40 | chr2 | 97811022 | ||||||
| chr2:97811274
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1864-42A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 17/40 | chr2 | 97811274 | ||||||
| chr2:97811621
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1864-389T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 17/40 | chr2 | 97811621 | ||||||
| chr2:97811684
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1864-452G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 17/40 | chr2 | 97811684 | ||||||
| chr2:97811763
|
C | G | 1 | a0001c0002t0001g0241 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1864-531G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 17/40 | chr2 | 97811763 | ||||||
| chr2:97812346
|
T | C | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1863+75A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 17/40 | chr2 | 97812346 | ||||||
| chr2:97812843
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-94A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97812843 | ||||||
| chr2:97812975
|
C | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1618-226G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97812975 | ||||||
| chr2:97813113
|
G | A | 1 | a0001c0002t0001g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1618-364C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813113 | ||||||
| chr2:97813163
|
T | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1618-414A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813163 | ||||||
| chr2:97813170
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1618-421C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813170 | ||||||
| chr2:97813525
|
C | T | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1617+446G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813525 | ||||||
| chr2:97813615
|
G | A | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+356C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813615 | ||||||
| chr2:97813647
|
T | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1617+324A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813647 | ||||||
| chr2:97813656
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1617+315G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813656 | ||||||
| chr2:97813942
|
T | TA | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617+28dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 15/40 | chr2 | 97813942 | ||||||
| chr2:97814527
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1293-139A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 13/40 | chr2 | 97814527 | ||||||
| chr2:97814552
|
C | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1293-164G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 13/40 | chr2 | 97814552 | ||||||
| chr2:97814757
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1293-369A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 13/40 | chr2 | 97814757 | ||||||
| chr2:97814876
|
A | G | 1 | a0001c0001t0005g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1292+323T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 13/40 | chr2 | 97814876 | ||||||
| chr2:97814995
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292+204A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 13/40 | chr2 | 97814995 | ||||||
| chr2:97815174
|
G | T | 3 | a0002c0003t0004g0190a0002c0003t0004g0191a0002c0003t0004g0192 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1292+25C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 13/40 | chr2 | 97815174 | ||||||
| chr2:97815390
|
TA | T | 7 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0002t0001g0260others(4): Show | 7 | HG01069.hp2 HG01070.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184-84delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815390 | ||||||
| chr2:97815391
|
A | T | 2 | a0001c0002t0001g0232a0001c0002t0001g0256 | 2 | HG02027.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1184-84T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815391 | ||||||
| chr2:97815575
|
T | C | 2 | a0001c0002t0001g0244a0001c0002t0010g0243 | 2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1184-268A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815575 | ||||||
| chr2:97815627
|
G | A | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1184-320C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815627 | ||||||
| chr2:97815858
|
G | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1184-551C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815858 | ||||||
| chr2:97815958
|
T | C | 1 | a0004c0008t0002g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1184-651A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815958 | ||||||
| chr2:97815959
|
G | A | 7 | a0001c0002t0001g0237a0001c0002t0001g0238a0001c0002t0001g0239others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184-652C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97815959 | ||||||
| chr2:97816003
|
TC | T | 3 | a0002c0003t0004g0190a0002c0003t0004g0191a0002c0003t0004g0192 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1184-697delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816003 | ||||||
| chr2:97816490
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1184-1183G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816490 | ||||||
| chr2:97816508
|
A | G | 2 | a0005c0006t0005g0136a0005c0006t0005g0137 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1184-1201T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816508 | ||||||
| chr2:97816541
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1184-1234G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816541 | ||||||
| chr2:97816596
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184-1289C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816596 | ||||||
| chr2:97816784
|
A | C | 2 | a0003c0004t0002g0108a0003c0004t0002g0109 | 2 | NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1184-1477T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816784 | ||||||
| chr2:97816890
|
A | G | 2 | a0001c0001t0003g0043a0001c0001t0003g0072 | 2 | HG02040.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1184-1583T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97816890 | ||||||
| chr2:97817124
|
A | G | 2 | a0002c0003t0004g0179a0002c0003t0004g0193 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1183+1489T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817124 | ||||||
| chr2:97817161
|
G | GA | 12 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(9): Show | 12 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1183+1451dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817161 | ||||||
| chr2:97817204
|
G | C | 1 | a0001c0007t0003g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1183+1409C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817204 | ||||||
| chr2:97817207
|
TAGCTCTT others(14): Show |
T | 12 | a0001c0001t0005g0122a0001c0005t0005g0132a0001c0005t0005g0133others(9): Show | 12 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1183+1385_1183+140 others(25): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817207 | ||||||
| chr2:97817347
|
C | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1183+1266G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817347 | ||||||
| chr2:97817445
|
G | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1183+1168C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817445 | ||||||
| chr2:97817449
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1183+1164G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817449 | ||||||
| chr2:97817530
|
C | G | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1183+1083G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817530 | ||||||
| chr2:97817583
|
A | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183+1030T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817583 | ||||||
| chr2:97817723
|
T | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1183+890A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817723 | ||||||
| chr2:97817743
|
T | G | 1 | a0001c0002t0001g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1183+870A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817743 | ||||||
| chr2:97817808
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1183+805C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97817808 | ||||||
| chr2:97818021
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183+592G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818021 | ||||||
| chr2:97818109
|
C | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183+504G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818109 | ||||||
| chr2:97818280
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183+333G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818280 | ||||||
| chr2:97818463
|
C | CG | 47 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0002t0001g0204others(44): Show | 47 | HG01070.hp1 HG01169.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.1183+149dupC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818463 | ||||||
| chr2:97818466
|
G | C | 12 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(9): Show | 12 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1183+147C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818466 | ||||||
| chr2:97818468
|
GGGGGC | G | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1183+140_1183+144d others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818468 | ||||||
| chr2:97818470
|
GGGC | G | 22 | a0001c0001t0005g0023a0001c0001t0005g0026a0001c0001t0005g0027others(19): Show | 22 | HG01074.hp1 HG01192.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1183+140_1183+142d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818470 | ||||||
| chr2:97818471
|
GGC | G | 20 | a0001c0001t0005g0024a0001c0001t0005g0028a0001c0001t0005g0031others(17): Show | 20 | HG00544.hp2 HG00597.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1183+140_1183+141d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818471 | ||||||
| chr2:97818472
|
GC | G | 10 | a0001c0001t0002g0121a0001c0001t0005g0029a0001c0001t0005g0030others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+140delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818472 | ||||||
| chr2:97818473
|
C | G | 76 | a0001c0001t0002g0014a0001c0001t0002g0125a0001c0001t0002g0126others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1183+140G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818473 | ||||||
| chr2:97818480
|
G | A | 26 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0005g0023others(23): Show | 26 | HG00099.hp2 HG00597.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1183+133C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818480 | ||||||
| chr2:97818481
|
G | A | 133 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1183+132C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GA | 4 | a0001c0005t0005g0145a0001c0007t0003g0034a0004c0008t0002g0092others(1): Show | 4 | HG02818.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183+131dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0003g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1183+131_1183+132i others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0003g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1183+131_1183+132i others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(4): Show |
1 | a0001c0001t0003g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1183+131_1183+132i others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(5): Show |
2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1183+131_1183+132i others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(6): Show |
2 | a0005c0006t0005g0131a0005c0006t0005g0137 | 2 | HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1183+131_1183+132i others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(7): Show |
1 | a0001c0001t0003g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1183+131_1183+132i others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(7): Show |
1 | a0005c0006t0005g0136 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1183+131_1183+132i others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(9): Show |
1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1183+131_1183+132i others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(9): Show |
3 | a0001c0023t0003g0061a0005c0006t0005g0138a0005c0006t0005g0142 | 3 | HG01175.hp2 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1183+131_1183+132i others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(12): Show |
1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1183+131_1183+132i others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818481
|
G | GGGGGGGG others(16): Show |
1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1183+131_1183+132i others(25): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 12/40 | chr2 | 97818481 | ||||||
| chr2:97818956
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075-235C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97818956 | ||||||
| chr2:97819121
|
G | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-400C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97819121 | ||||||
| chr2:97819519
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1075-798G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97819519 | ||||||
| chr2:97819554
|
G | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1075-833C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97819554 | ||||||
| chr2:97819745
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1075-1024G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97819745 | ||||||
| chr2:97819914
|
T | A | 1 | a0004c0008t0002g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1075-1193A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97819914 | ||||||
| chr2:97820192
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1075-1471G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820192 | ||||||
| chr2:97820227
|
G | C | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1075-1506C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820227 | ||||||
| chr2:97820512
|
T | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-1791A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820512 | ||||||
| chr2:97820529
|
T | A | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1075-1808A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820529 | ||||||
| chr2:97820555
|
T | G | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-1834A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820555 | ||||||
| chr2:97820583
|
G | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-1862C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820583 | ||||||
| chr2:97820780
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-2059G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820780 | ||||||
| chr2:97820855
|
A | G | 5 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0029others(2): Show | 5 | HG00099.hp2 HG01099.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-2134T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820855 | ||||||
| chr2:97820951
|
C | T | 201 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1075-2230G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97820951 | ||||||
| chr2:97821266
|
T | C | 6 | a0001c0002t0001g0207a0001c0002t0001g0221a0001c0002t0001g0223others(3): Show | 6 | HG02074.hp2 NA18966.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-2545A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821266 | ||||||
| chr2:97821280
|
A | C | 1 | a0001c0002t0001g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1075-2559T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821280 | ||||||
| chr2:97821418
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075-2697G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821418 | ||||||
| chr2:97821510
|
T | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1075-2789A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821510 | ||||||
| chr2:97821615
|
C | T | 27 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(24): Show | 27 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1075-2894G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821615 | ||||||
| chr2:97821650
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-2929A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821650 | ||||||
| chr2:97821748
|
A | G | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1075-3027T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821748 | ||||||
| chr2:97821828
|
G | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-3107C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821828 | ||||||
| chr2:97821863
|
T | C | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1075-3142A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821863 | ||||||
| chr2:97821912
|
C | G | 1 | a0001c0001t0006g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1075-3191G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97821912 | ||||||
| chr2:97822002
|
T | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1075-3281A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822002 | ||||||
| chr2:97822224
|
CCAAT | C | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1075-3507_1075-350 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822224 | ||||||
| chr2:97822260
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1075-3539C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822260 | ||||||
| chr2:97822371
|
T | A | 215 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1075-3650A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822371 | ||||||
| chr2:97822445
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1075-3724G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822445 | ||||||
| chr2:97822540
|
C | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1075-3819G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822540 | ||||||
| chr2:97822973
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075-4252G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97822973 | ||||||
| chr2:97823289
|
G | T | 2 | a0002c0003t0004g0179a0002c0003t0004g0193 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1075-4568C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97823289 | ||||||
| chr2:97823395
|
T | C | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1075-4674A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97823395 | ||||||
| chr2:97823489
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1075-4768T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97823489 | ||||||
| chr2:97823555
|
A | G | 1 | a0001c0001t0003g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1075-4834T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97823555 | ||||||
| chr2:97823771
|
C | T | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1075-5050G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97823771 | ||||||
| chr2:97823784
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1075-5063G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97823784 | ||||||
| chr2:97824000
|
C | T | 28 | a0001c0001t0002g0121a0001c0001t0003g0089a0003c0004t0002g0096others(25): Show | 28 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.1075-5279G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824000 | ||||||
| chr2:97824153
|
A | G | 1 | a0001c0012t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1075-5432T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824153 | ||||||
| chr2:97824329
|
C | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075-5608G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824329 | ||||||
| chr2:97824410
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-5689G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824410 | ||||||
| chr2:97824430
|
T | C | 5 | a0003c0004t0002g0098a0003c0004t0002g0100a0003c0004t0002g0102others(2): Show | 5 | NA18957.hp1 NA18977.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-5709A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824430 | ||||||
| chr2:97824432
|
C | T | 10 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0001t0003g0067others(7): Show | 10 | HG00423.hp1 NA18939.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075-5711G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824432 | ||||||
| chr2:97824526
|
C | T | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1075-5805G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824526 | ||||||
| chr2:97824899
|
A | T | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1075-6178T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97824899 | ||||||
| chr2:97825022
|
C | G | 2 | a0001c0001t0006g0158a0001c0001t0006g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1075-6301G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825022 | ||||||
| chr2:97825070
|
CT | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-6350delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825070 | ||||||
| chr2:97825080
|
G | A | 1 | a0001c0001t0004g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1075-6359C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825080 | ||||||
| chr2:97825097
|
C | A | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1075-6376G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825097 | ||||||
| chr2:97825250
|
G | A | 1 | a0001c0027t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1075-6529C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825250 | ||||||
| chr2:97825325
|
G | A | 1 | a0001c0002t0001g0240 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1075-6604C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825325 | ||||||
| chr2:97825453
|
G | A | 1 | a0002c0003t0004g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1075-6732C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825453 | ||||||
| chr2:97825463
|
T | C | 1 | a0015c0013t0005g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1075-6742A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825463 | ||||||
| chr2:97825501
|
A | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075-6780T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825501 | ||||||
| chr2:97825671
|
G | A | 4 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-6950C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825671 | ||||||
| chr2:97825738
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1075-7017G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825738 | ||||||
| chr2:97825739
|
G | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1075-7018C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825739 | ||||||
| chr2:97825893
|
G | C | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1075-7172C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97825893 | ||||||
| chr2:97826024
|
T | C | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1075-7303A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826024 | ||||||
| chr2:97826049
|
T | C | 201 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1074+7316A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826049 | ||||||
| chr2:97826157
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074+7208C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826157 | ||||||
| chr2:97826214
|
C | T | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1074+7151G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826214 | ||||||
| chr2:97826283
|
A | G | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1074+7082T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826283 | ||||||
| chr2:97826315
|
A | G | 1 | a0001c0002t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1074+7050T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826315 | ||||||
| chr2:97826576
|
G | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1074+6789C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826576 | ||||||
| chr2:97826600
|
C | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+6765G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826600 | ||||||
| chr2:97826618
|
GA | G | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1074+6746delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826618 | ||||||
| chr2:97826810
|
A | G | 5 | a0002c0003t0004g0200a0002c0003t0004g0201a0002c0009t0004g0182others(2): Show | 5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074+6555T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97826810 | ||||||
| chr2:97827068
|
C | CA | 17 | a0001c0002t0001g0207a0001c0002t0001g0213a0001c0002t0001g0232others(14): Show | 17 | HG01070.hp1 HG01243.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+6296dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827068 | ||||||
| chr2:97827068
|
CA | C | 148 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0015others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1074+6296delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827068 | ||||||
| chr2:97827068
|
CAA | C | 18 | a0001c0001t0002g0126a0001c0001t0003g0041a0001c0001t0003g0089others(15): Show | 18 | HG01069.hp1 HG01069.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1074+6295_1074+629 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827068 | ||||||
| chr2:97827092
|
T | A | 27 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(24): Show | 27 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+6273A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827092 | ||||||
| chr2:97827195
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1074+6170G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827195 | ||||||
| chr2:97827231
|
C | T | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1074+6134G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827231 | ||||||
| chr2:97827355
|
G | A | 1 | a0001c0001t0003g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1074+6010C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827355 | ||||||
| chr2:97827420
|
C | A | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1074+5945G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827420 | ||||||
| chr2:97827795
|
G | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074+5570C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827795 | ||||||
| chr2:97827892
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+5473C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827892 | ||||||
| chr2:97827944
|
T | C | 1 | a0002c0003t0004g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1074+5421A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97827944 | ||||||
| chr2:97828229
|
G | A | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1074+5136C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97828229 | ||||||
| chr2:97828506
|
T | C | 1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1074+4859A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97828506 | ||||||
| chr2:97829092
|
G | T | 1 | a0001c0002t0001g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1074+4273C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829092 | ||||||
| chr2:97829097
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074+4268A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829097 | ||||||
| chr2:97829110
|
G | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074+4255C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829110 | ||||||
| chr2:97829168
|
G | A | 1 | a0015c0013t0005g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1074+4197C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829168 | ||||||
| chr2:97829321
|
A | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1074+4044T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829321 | ||||||
| chr2:97829359
|
TGCACCAA others(18): Show |
T | 2 | a0001c0002t0001g0242a0001c0002t0001g0254 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1074+3981_1074+400 others(29): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829359 | ||||||
| chr2:97829527
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074+3838G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829527 | ||||||
| chr2:97829550
|
AGAACATG others(3): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+3805_1074+381 others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829550 | ||||||
| chr2:97829552
|
A | G | 209 | a0001c0001t0001g0202a0001c0001t0002g0002a0001c0001t0002g0003others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1074+3813T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829552 | ||||||
| chr2:97829639
|
T | C | 1 | a0001c0007t0011g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1074+3726A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829639 | ||||||
| chr2:97829691
|
A | G | 1 | a0001c0002t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1074+3674T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97829691 | ||||||
| chr2:97830118
|
C | T | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1074+3247G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830118 | ||||||
| chr2:97830132
|
T | TA | 72 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1074+3232dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830132 | ||||||
| chr2:97830132
|
T | TAA | 32 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0016others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1074+3231_1074+323 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830132 | ||||||
| chr2:97830132
|
T | TAAA | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074+3230_1074+323 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830132 | ||||||
| chr2:97830132
|
T | TAAAAA | 39 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0150others(36): Show | 39 | HG00280.hp1 HG00733.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.1074+3228_1074+323 others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830132 | ||||||
| chr2:97830132
|
T | TAAAAAA | 11 | a0001c0001t0004g0149a0001c0001t0004g0151a0001c0001t0006g0163others(8): Show | 11 | HG01070.hp2 HG01993.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1074+3227_1074+323 others(10): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830132 | ||||||
| chr2:97830475
|
T | C | 9 | a0002c0003t0004g0179a0002c0003t0004g0183a0002c0003t0004g0184others(6): Show | 9 | HG00642.hp2 HG01496.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074+2890A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830475 | ||||||
| chr2:97830541
|
T | C | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1074+2824A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830541 | ||||||
| chr2:97830592
|
A | C | 1 | a0001c0002t0001g0255 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1074+2773T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97830592 | ||||||
| chr2:97831004
|
T | A | 1 | a0001c0001t0003g0067 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1074+2361A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831004 | ||||||
| chr2:97831058
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+2307C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831058 | ||||||
| chr2:97831164
|
C | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074+2201G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831164 | ||||||
| chr2:97831213
|
T | C | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+2152A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831213 | ||||||
| chr2:97831431
|
A | C | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1074+1934T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831431 | ||||||
| chr2:97831451
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1074+1914T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831451 | ||||||
| chr2:97831457
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+1908C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831457 | ||||||
| chr2:97831628
|
G | A | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1074+1737C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831628 | ||||||
| chr2:97831664
|
C | CT | 62 | a0001c0001t0002g0121a0001c0001t0002g0127a0001c0002t0001g0207others(59): Show | 62 | HG00280.hp1 HG00544.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1074+1700dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831664
|
C | CTTT | 44 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1074+1698_1074+170 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831664
|
C | CTTTT | 9 | a0001c0001t0003g0044a0001c0001t0003g0054a0001c0001t0003g0059others(6): Show | 9 | HG01255.hp2 HG01934.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074+1697_1074+170 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831664
|
CT | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(14): Show | 17 | HG01257.hp2 HG01884.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+1700delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831664
|
CTTT | C | 22 | a0001c0001t0004g0148a0001c0001t0004g0149a0001c0001t0004g0150others(19): Show | 22 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1074+1698_1074+170 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831664
|
CTTTTTTT | C | 17 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(14): Show | 17 | HG00099.hp2 HG01074.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1074+1694_1074+170 others(11): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831664
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1074+1688_1074+170 others(17): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831664 | ||||||
| chr2:97831700
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1074+1665G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831700 | ||||||
| chr2:97831932
|
G | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1074+1433C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97831932 | ||||||
| chr2:97832004
|
C | CA | 95 | a0001c0001t0002g0121a0001c0001t0002g0127a0001c0001t0004g0147others(92): Show | 95 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1074+1360dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAA | 13 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140others(10): Show | 13 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074+1359_1074+136 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAAAA | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074+1357_1074+136 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAAAAA | 14 | a0001c0001t0002g0011a0001c0001t0002g0015a0001c0001t0003g0060others(11): Show | 14 | HG01074.hp1 HG01261.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+1356_1074+136 others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAAAAAA | 28 | a0001c0001t0002g0016a0001c0001t0003g0032a0001c0001t0003g0033others(25): Show | 28 | HG00099.hp2 HG00597.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074+1355_1074+136 others(10): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAAAAAAA | 27 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0045others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1074+1354_1074+136 others(11): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0053others(4): Show | 7 | HG00280.hp2 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074+1353_1074+136 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1074+1351_1074+136 others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832004
|
CAAAAAAA others(4): Show |
C | 1 | a0010c0018t0003g0063 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1074+1350_1074+136 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832004 | ||||||
| chr2:97832077
|
A | G | 1 | a0003c0004t0002g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1074+1288T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832077 | ||||||
| chr2:97832236
|
G | A | 1 | a0001c0001t0003g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1074+1129C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832236 | ||||||
| chr2:97832269
|
T | C | 9 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074+1096A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832269 | ||||||
| chr2:97832323
|
C | A | 1 | a0001c0002t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1074+1042G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832323 | ||||||
| chr2:97832384
|
T | C | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+981A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832384 | ||||||
| chr2:97832561
|
G | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1074+804C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832561 | ||||||
| chr2:97832576
|
G | T | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1074+789C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832576 | ||||||
| chr2:97832719
|
G | A | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074+646C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832719 | ||||||
| chr2:97832769
|
C | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+596G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832769 | ||||||
| chr2:97832792
|
C | T | 1 | a0001c0002t0001g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074+573G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832792 | ||||||
| chr2:97832793
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+572C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832793 | ||||||
| chr2:97832811
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074+554C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97832811 | ||||||
| chr2:97833006
|
C | T | 4 | a0004c0008t0002g0091a0004c0008t0002g0093a0004c0008t0002g0094others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+359G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97833006 | ||||||
| chr2:97833255
|
C | A | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1074+110G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 11/40 | chr2 | 97833255 | ||||||
| chr2:97833654
|
CT | C | 182 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1013-229delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97833654 | ||||||
| chr2:97833654
|
CTT | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1013-230_1013-229d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97833654 | ||||||
| chr2:97833670
|
T | A | 1 | a0001c0002t0001g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1013-244A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97833670 | ||||||
| chr2:97834371
|
C | G | 1 | a0001c0005t0005g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1012+250G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97834371 | ||||||
| chr2:97834484
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012+137C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97834484 | ||||||
| chr2:97834573
|
T | TA | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(20): Show | 23 | HG00597.hp1 HG01884.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.1012+47dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97834573 | ||||||
| chr2:97834573
|
TA | T | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1012+47delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97834573 | ||||||
| chr2:97834590
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1012+31G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 10/40 | chr2 | 97834590 | ||||||
| chr2:97835168
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.805-243T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97835168 | ||||||
| chr2:97835254
|
T | C | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.805-329A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97835254 | ||||||
| chr2:97835454
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-529A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97835454 | ||||||
| chr2:97835744
|
C | A | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-819G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97835744 | ||||||
| chr2:97835760
|
T | C | 2 | a0001c0002t0001g0226a0001c0002t0001g0273 | 2 | NA18974.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.805-835A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97835760 | ||||||
| chr2:97835896
|
A | T | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-971T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97835896 | ||||||
| chr2:97836356
|
G | C | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.804+721C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97836356 | ||||||
| chr2:97836525
|
C | G | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+552G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97836525 | ||||||
| chr2:97836633
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+444A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97836633 | ||||||
| chr2:97836729
|
T | A | 1 | a0001c0002t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.804+348A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97836729 | ||||||
| chr2:97836804
|
A | T | 1 | a0002c0003t0004g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+273T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97836804 | ||||||
| chr2:97836808
|
T | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.804+269A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97836808 | ||||||
| chr2:97837064
|
G | C | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.804+13C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 8/40 | chr2 | 97837064 | ||||||
| chr2:97837357
|
G | A | 4 | a0003c0004t0002g0098a0003c0004t0002g0100a0003c0004t0002g0102others(1): Show | 4 | NA18957.hp1 NA18977.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-200C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97837357 | ||||||
| chr2:97837685
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-528A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97837685 | ||||||
| chr2:97837762
|
T | C | 1 | a0003c0004t0002g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.724-605A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97837762 | ||||||
| chr2:97837794
|
T | C | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.724-637A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97837794 | ||||||
| chr2:97837795
|
G | A | 2 | a0001c0001t0005g0081a0001c0001t0005g0082 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.724-638C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97837795 | ||||||
| chr2:97837813
|
G | A | 3 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070 | 3 | HG01884.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.724-656C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97837813 | ||||||
| chr2:97838009
|
G | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.724-852C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838009 | ||||||
| chr2:97838010
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.724-853G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838010 | ||||||
| chr2:97838082
|
C | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.724-925G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838082 | ||||||
| chr2:97838084
|
C | T | 1 | a0001c0002t0001g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.724-927G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838084 | ||||||
| chr2:97838109
|
G | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.724-952C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838109 | ||||||
| chr2:97838256
|
TA | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.724-1100delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838256 | ||||||
| chr2:97838342
|
C | T | 12 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(9): Show | 12 | HG00597.hp1 HG00642.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.724-1185G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838342 | ||||||
| chr2:97838388
|
A | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-1231T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838388 | ||||||
| chr2:97838420
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724-1264_724-1263i others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838420 | ||||||
| chr2:97838420
|
CTTAAACT others(12): Show |
C | 2 | a0001c0001t0002g0007a0001c0001t0002g0013 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.724-1282_724-1264d others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838420 | ||||||
| chr2:97838420
|
CTTAAACT others(13): Show |
C | 10 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-1283_724-1264d others(22): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838420 | ||||||
| chr2:97838423
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724-1266T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838423 | ||||||
| chr2:97838424
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724-1267T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838424 | ||||||
| chr2:97838425
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724-1268T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838425 | ||||||
| chr2:97838426
|
C | CT | 20 | a0001c0002t0001g0225a0001c0002t0001g0234a0001c0002t0001g0237others(17): Show | 20 | HG00642.hp1 HG01070.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.724-1270dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTT | 6 | a0001c0001t0002g0016a0001c0002t0001g0213a0001c0002t0001g0214others(3): Show | 6 | HG02027.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-1272_724-1270d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0001g0211 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.724-1280_724-1270d others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0007g0020a0001c0001t0007g0022 | 2 | HG00597.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.724-1286_724-1270d others(19): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.724-1287_724-1270d others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0007g0021 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.724-1288_724-1270d others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.724-1289_724-1270d others(22): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.724-1292_724-1270d others(25): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724-1269G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CT | C | 30 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0002t0001g0206others(27): Show | 30 | HG00423.hp2 HG01123.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.724-1270delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(2): Show |
C | 24 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(21): Show | 24 | HG00544.hp2 HG02129.hp2 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.724-1278_724-1270d others(11): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(3): Show |
C | 7 | a0002c0003t0004g0184a0002c0003t0004g0197a0002c0003t0004g0198others(4): Show | 7 | HG01123.hp2 HG01192.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-1279_724-1270d others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(4): Show |
C | 47 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(44): Show | 47 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.724-1280_724-1270d others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0006g0159a0002c0003t0004g0190 | 2 | HG02897.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.724-1281_724-1270d others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(8): Show |
C | 9 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(6): Show | 9 | HG01346.hp1 HG01981.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.724-1284_724-1270d others(17): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(9): Show |
C | 16 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.724-1285_724-1270d others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838426
|
CTTTTTTT others(10): Show |
C | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.724-1286_724-1270d others(19): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838426 | ||||||
| chr2:97838468
|
G | A | 82 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.724-1311C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838468 | ||||||
| chr2:97838626
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.724-1469C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838626 | ||||||
| chr2:97838689
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.724-1532G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838689 | ||||||
| chr2:97838691
|
T | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.724-1534A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838691 | ||||||
| chr2:97838711
|
G | A | 1 | a0001c0010t0005g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.724-1554C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838711 | ||||||
| chr2:97838760
|
G | T | 4 | a0001c0001t0003g0062a0001c0002t0001g0268a0001c0002t0001g0269others(1): Show | 4 | HG02040.hp1 HG03486.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-1603C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97838760 | ||||||
| chr2:97839047
|
G | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.724-1890C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839047 | ||||||
| chr2:97839073
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-1916G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839073 | ||||||
| chr2:97839098
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-1941C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839098 | ||||||
| chr2:97839127
|
C | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.724-1970G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839127 | ||||||
| chr2:97839240
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.724-2083A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839240 | ||||||
| chr2:97839312
|
AAACC | A | 62 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(59): Show | 62 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.724-2159_724-2156d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839312 | ||||||
| chr2:97839312
|
AAACCAAC others(1): Show |
A | 51 | a0001c0001t0002g0121a0001c0001t0003g0062a0001c0001t0003g0064others(48): Show | 51 | HG00544.hp2 HG00597.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.724-2163_724-2156d others(10): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839312 | ||||||
| chr2:97839312
|
AAACCAAC others(5): Show |
A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.724-2167_724-2156d others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839312 | ||||||
| chr2:97839312
|
AAACCAAC others(17): Show |
A | 1 | a0001c0001t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.724-2179_724-2156d others(26): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839312 | ||||||
| chr2:97839335
|
C | T | 1 | a0002c0003t0004g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.724-2178G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839335 | ||||||
| chr2:97839382
|
A | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.724-2225T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839382 | ||||||
| chr2:97839650
|
G | A | 1 | a0003c0004t0002g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.723+2165C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839650 | ||||||
| chr2:97839656
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.723+2159A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839656 | ||||||
| chr2:97839666
|
C | T | 1 | a0001c0001t0005g0083 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.723+2149G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839666 | ||||||
| chr2:97839677
|
T | C | 1 | a0001c0002t0009g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.723+2138A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839677 | ||||||
| chr2:97839705
|
A | G | 210 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.723+2110T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97839705 | ||||||
| chr2:97840346
|
G | C | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.723+1469C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97840346 | ||||||
| chr2:97840374
|
G | T | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.723+1441C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97840374 | ||||||
| chr2:97840710
|
AG | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.723+1104delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97840710 | ||||||
| chr2:97840898
|
C | T | 3 | a0003c0004t0002g0099a0003c0004t0002g0106a0003c0004t0002g0107 | 3 | NA18941.hp2 NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.723+917G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97840898 | ||||||
| chr2:97840916
|
CT | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+898delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97840916 | ||||||
| chr2:97840945
|
T | A | 3 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070 | 3 | HG01884.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.723+870A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97840945 | ||||||
| chr2:97841189
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.723+626G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841189 | ||||||
| chr2:97841193
|
G | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.723+622C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841193 | ||||||
| chr2:97841386
|
T | C | 1 | a0001c0001t0004g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.723+429A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841386 | ||||||
| chr2:97841539
|
T | C | 210 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.723+276A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841539 | ||||||
| chr2:97841580
|
G | T | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.723+235C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841580 | ||||||
| chr2:97841594
|
T | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.723+221A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841594 | ||||||
| chr2:97841610
|
CCAGACTG others(15): Show |
C | 210 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.723+183_723+204del others(22): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 7/40 | chr2 | 97841610 | ||||||
| chr2:97842012
|
T | C | 2 | a0001c0005t0005g0133a0001c0005t0005g0134 | 2 | HG00642.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.601-75A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842012 | ||||||
| chr2:97842019
|
A | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-82T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842019 | ||||||
| chr2:97842032
|
A | G | 1 | a0005c0006t0005g0131 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.601-95T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842032 | ||||||
| chr2:97842517
|
T | TA | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.601-581dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842517 | ||||||
| chr2:97842686
|
T | C | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.601-749A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842686 | ||||||
| chr2:97842730
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-793A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842730 | ||||||
| chr2:97842852
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601-915G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97842852 | ||||||
| chr2:97843066
|
T | TA | 121 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0015others(118): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.600+1078dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843066 | ||||||
| chr2:97843066
|
T | TAAA | 11 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.600+1076_600+1078d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843066 | ||||||
| chr2:97843093
|
TGTAAA | T | 46 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.600+1047_600+1051d others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843093 | ||||||
| chr2:97843278
|
G | A | 32 | a0001c0001t0002g0121a0001c0001t0003g0073a0001c0001t0003g0074others(29): Show | 32 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.600+867C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843278 | ||||||
| chr2:97843322
|
T | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+823A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843322 | ||||||
| chr2:97843349
|
A | G | 1 | a0001c0001t0005g0026 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.600+796T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843349 | ||||||
| chr2:97843531
|
G | A | 46 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.600+614C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843531 | ||||||
| chr2:97843758
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.600+387T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843758 | ||||||
| chr2:97843881
|
TAA | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+262_600+263del others(2): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843881 | ||||||
| chr2:97843978
|
TAG | T | 66 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.600+165_600+166del others(2): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 6/40 | chr2 | 97843978 | ||||||
| chr2:97844279
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.484-18C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97844279 | ||||||
| chr2:97844392
|
G | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.484-131C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97844392 | ||||||
| chr2:97844577
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-316C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97844577 | ||||||
| chr2:97844689
|
CA | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-429delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97844689 | ||||||
| chr2:97844751
|
G | A | 2 | a0001c0001t0003g0045a0001c0001t0003g0046 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.484-490C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97844751 | ||||||
| chr2:97844873
|
C | G | 1 | a0003c0004t0002g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.484-612G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97844873 | ||||||
| chr2:97845110
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-849G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845110 | ||||||
| chr2:97845339
|
T | C | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.484-1078A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845339 | ||||||
| chr2:97845358
|
C | T | 95 | a0001c0001t0002g0121a0001c0001t0003g0073a0001c0001t0003g0074others(92): Show | 95 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.484-1097G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845358 | ||||||
| chr2:97845490
|
C | A | 1 | a0001c0001t0003g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.484-1229G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845490 | ||||||
| chr2:97845490
|
C | T | 95 | a0001c0001t0002g0121a0001c0001t0003g0073a0001c0001t0003g0074others(92): Show | 95 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.484-1229G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845490 | ||||||
| chr2:97845759
|
C | CA | 39 | a0001c0001t0002g0121a0001c0001t0003g0073a0001c0001t0003g0074others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.484-1499dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845759 | ||||||
| chr2:97845759
|
C | CAA | 59 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.484-1500_484-1499d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845759 | ||||||
| chr2:97845759
|
C | CAAA | 14 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(11): Show | 14 | HG01516.hp2 HG01517.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.484-1501_484-1499d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845759 | ||||||
| chr2:97845759
|
CA | C | 14 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-1499delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845759 | ||||||
| chr2:97845995
|
C | T | 15 | a0001c0001t0003g0071a0001c0005t0005g0132a0001c0005t0005g0133others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.484-1734G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97845995 | ||||||
| chr2:97846195
|
G | A | 69 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.484-1934C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846195 | ||||||
| chr2:97846453
|
C | A | 1 | a0001c0005t0005g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.484-2192G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846453 | ||||||
| chr2:97846580
|
C | T | 3 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019 | 3 | NA18965.hp1 NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.484-2319G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846580 | ||||||
| chr2:97846584
|
CTGCAGCC others(11): Show |
C | 2 | a0001c0002t0001g0219a0001c0002t0001g0225 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.484-2341_484-2324d others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846584 | ||||||
| chr2:97846722
|
A | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-2461T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846722 | ||||||
| chr2:97846891
|
T | C | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-2630A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846891 | ||||||
| chr2:97846955
|
C | T | 1 | a0001c0002t0001g0216 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.484-2694G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97846955 | ||||||
| chr2:97847048
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.484-2787C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847048 | ||||||
| chr2:97847070
|
T | TG | 39 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0062others(36): Show | 39 | HG00423.hp2 HG00597.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.484-2810dupC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847070
|
T | TGG | 26 | a0001c0001t0001g0202a0001c0001t0003g0077a0001c0001t0004g0149others(23): Show | 26 | HG00544.hp1 HG01346.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.484-2811_484-2810d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847070
|
T | TGGGGGGG others(3): Show |
1 | a0002c0003t0004g0194 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.484-2819_484-2810d others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847070
|
T | TGGGGGGG others(5): Show |
2 | a0002c0009t0004g0182a0002c0009t0004g0187 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.484-2821_484-2810d others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847070
|
TG | T | 56 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(53): Show | 56 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.484-2810delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847070
|
TGG | T | 30 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0007others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-2811_484-2810d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847070
|
TGGG | T | 22 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0009others(19): Show | 22 | HG01099.hp1 HG01261.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-2812_484-2810d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847070 | ||||||
| chr2:97847075
|
G | C | 9 | a0001c0002t0001g0239a0001c0002t0001g0241a0003c0004t0002g0101others(6): Show | 9 | HG00597.hp2 HG01243.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-2814C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847075 | ||||||
| chr2:97847076
|
G | C | 27 | a0001c0001t0002g0121a0001c0001t0003g0088a0001c0002t0001g0224others(24): Show | 27 | HG00544.hp2 HG01070.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.484-2815C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847076 | ||||||
| chr2:97847081
|
G | T | 1 | a0003c0004t0002g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.484-2820C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847081 | ||||||
| chr2:97847145
|
C | T | 1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.484-2884G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847145 | ||||||
| chr2:97847363
|
A | G | 14 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.484-3102T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847363 | ||||||
| chr2:97847943
|
C | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-3682G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97847943 | ||||||
| chr2:97848310
|
A | C | 1 | a0001c0001t0005g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.484-4049T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97848310 | ||||||
| chr2:97848516
|
A | C | 1 | a0001c0002t0010g0243 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.484-4255T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97848516 | ||||||
| chr2:97848827
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-4566A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97848827 | ||||||
| chr2:97849223
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.484-4962C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849223 | ||||||
| chr2:97849413
|
C | G | 3 | a0005c0006t0005g0136a0005c0006t0005g0137a0005c0006t0005g0138 | 3 | HG01257.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.484-5152G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849413 | ||||||
| chr2:97849439
|
A | T | 1 | a0002c0003t0004g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.484-5178T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849439 | ||||||
| chr2:97849622
|
A | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.484-5361T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849622 | ||||||
| chr2:97849642
|
T | C | 2 | a0002c0003t0004g0191a0002c0003t0004g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.484-5381A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849642 | ||||||
| chr2:97849705
|
ATC | A | 8 | a0001c0001t0002g0014a0001c0001t0007g0017a0001c0001t0007g0018others(5): Show | 8 | HG00597.hp1 HG02055.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-5446_484-5445d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849705 | ||||||
| chr2:97849714
|
T | A | 9 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-5453A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849714 | ||||||
| chr2:97849715
|
C | A | 9 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-5454G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849715 | ||||||
| chr2:97849717
|
C | CT | 6 | a0001c0002t0001g0219a0001c0002t0001g0224a0001c0002t0001g0257others(3): Show | 6 | HG01243.hp1 HG02602.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-5457dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849717 | ||||||
| chr2:97849717
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.484-5456G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849717 | ||||||
| chr2:97849717
|
CT | C | 149 | a0001c0001t0002g0121a0001c0001t0003g0033a0001c0001t0003g0040others(146): Show | 149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.484-5457delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849717 | ||||||
| chr2:97849717
|
CTT | C | 10 | a0001c0001t0003g0032a0001c0001t0003g0050a0001c0001t0003g0054others(7): Show | 10 | HG00099.hp1 HG01255.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-5458_484-5457d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849717 | ||||||
| chr2:97849737
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.484-5476A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97849737 | ||||||
| chr2:97850094
|
C | T | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.484-5833G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850094 | ||||||
| chr2:97850102
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484-5841A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850102 | ||||||
| chr2:97850184
|
C | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.484-5923G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850184 | ||||||
| chr2:97850345
|
G | A | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.484-6084C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850345 | ||||||
| chr2:97850565
|
A | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.484-6304T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850565 | ||||||
| chr2:97850834
|
T | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-6573A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850834 | ||||||
| chr2:97850878
|
A | C | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.484-6617T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97850878 | ||||||
| chr2:97851309
|
G | A | 3 | a0001c0002t0001g0236a0001c0002t0001g0242a0001c0002t0001g0254 | 3 | HG01175.hp1 HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.484-7048C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97851309 | ||||||
| chr2:97851334
|
C | T | 2 | a0003c0004t0002g0119a0003c0004t0002g0120 | 2 | NA18991.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.484-7073G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97851334 | ||||||
| chr2:97851659
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-7398A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97851659 | ||||||
| chr2:97851712
|
A | G | 2 | a0001c0001t0003g0043a0001c0001t0003g0072 | 2 | HG02040.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.484-7451T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97851712 | ||||||
| chr2:97851836
|
C | T | 1 | a0001c0002t0001g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483+7468G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97851836 | ||||||
| chr2:97852161
|
CT | C | 14 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(11): Show | 14 | HG00597.hp1 HG01123.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.483+7142delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852161 | ||||||
| chr2:97852161
|
CTT | C | 188 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.483+7141_483+7142d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852161 | ||||||
| chr2:97852264
|
C | T | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.483+7040G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852264 | ||||||
| chr2:97852346
|
T | C | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.483+6958A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852346 | ||||||
| chr2:97852360
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.483+6944C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852360 | ||||||
| chr2:97852413
|
C | T | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.483+6891G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852413 | ||||||
| chr2:97852429
|
AC | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.483+6874delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852429 | ||||||
| chr2:97852508
|
C | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.483+6796G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852508 | ||||||
| chr2:97852633
|
G | A | 2 | a0002c0003t0004g0180a0002c0003t0004g0181 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.483+6671C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852633 | ||||||
| chr2:97852671
|
A | G | 2 | a0001c0011t0001g0229a0001c0011t0001g0248 | 2 | HG01934.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.483+6633T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852671 | ||||||
| chr2:97852952
|
A | G | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.483+6352T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852952 | ||||||
| chr2:97852973
|
T | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.483+6331A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97852973 | ||||||
| chr2:97853357
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.483+5947C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853357 | ||||||
| chr2:97853366
|
G | A | 1 | a0003c0004t0002g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.483+5938C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853366 | ||||||
| chr2:97853420
|
T | C | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.483+5884A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853420 | ||||||
| chr2:97853432
|
T | TA | 6 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG00544.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+5871dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853432 | ||||||
| chr2:97853432
|
TA | T | 141 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.483+5871delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853432 | ||||||
| chr2:97853432
|
TAA | T | 10 | a0001c0001t0003g0040a0001c0001t0003g0068a0001c0001t0003g0069others(7): Show | 10 | HG01069.hp2 HG01070.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+5870_483+5871d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853432 | ||||||
| chr2:97853483
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.483+5821T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853483 | ||||||
| chr2:97853523
|
T | C | 1 | a0003c0004t0002g0096 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.483+5781A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853523 | ||||||
| chr2:97853607
|
G | GA | 31 | a0001c0001t0006g0161a0001c0002t0001g0211a0001c0005t0005g0132others(28): Show | 31 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.483+5696dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853607 | ||||||
| chr2:97853607
|
GA | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.483+5696delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853607 | ||||||
| chr2:97853607
|
GAA | G | 7 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(4): Show | 7 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+5695_483+5696d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97853607 | ||||||
| chr2:97854126
|
GC | G | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.483+5177delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97854126 | ||||||
| chr2:97854520
|
A | G | 2 | a0004c0008t0002g0091a0004c0008t0002g0093 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483+4784T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97854520 | ||||||
| chr2:97854682
|
T | G | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.483+4622A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97854682 | ||||||
| chr2:97854915
|
T | C | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.483+4389A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97854915 | ||||||
| chr2:97855005
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.483+4299A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855005 | ||||||
| chr2:97855081
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.483+4223A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855081 | ||||||
| chr2:97855175
|
A | G | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.483+4129T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855175 | ||||||
| chr2:97855227
|
A | G | 9 | a0001c0002t0001g0205a0001c0002t0001g0212a0001c0002t0001g0217others(6): Show | 9 | HG01257.hp2 HG01943.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+4077T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855227 | ||||||
| chr2:97855516
|
A | G | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.483+3788T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855516 | ||||||
| chr2:97855535
|
A | G | 1 | a0002c0003t0004g0185 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.483+3769T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855535 | ||||||
| chr2:97855699
|
C | CA | 6 | a0001c0001t0002g0014a0001c0002t0001g0205a0001c0002t0001g0212others(3): Show | 6 | HG01257.hp2 HG01943.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+3604dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855699 | ||||||
| chr2:97855699
|
CA | C | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.483+3604delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855699 | ||||||
| chr2:97855785
|
T | C | 1 | a0001c0001t0003g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.483+3519A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855785 | ||||||
| chr2:97855902
|
A | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.483+3402T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97855902 | ||||||
| chr2:97856147
|
T | C | 32 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.483+3157A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856147 | ||||||
| chr2:97856157
|
T | C | 3 | a0001c0002t0001g0205a0001c0002t0001g0212a0001c0002t0001g0231 | 3 | HG01257.hp2 HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.483+3147A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856157 | ||||||
| chr2:97856265
|
T | G | 76 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.483+3039A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856265 | ||||||
| chr2:97856495
|
T | C | 1 | a0003c0004t0002g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.483+2809A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856495 | ||||||
| chr2:97856597
|
C | T | 4 | a0001c0002t0001g0227a0001c0002t0001g0276a0001c0011t0001g0229others(1): Show | 4 | HG01169.hp2 HG01934.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+2707G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856597 | ||||||
| chr2:97856618
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.483+2686A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856618 | ||||||
| chr2:97856766
|
A | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.483+2538T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856766 | ||||||
| chr2:97856809
|
T | C | 1 | a0001c0002t0010g0243 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.483+2495A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97856809 | ||||||
| chr2:97857074
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+2230G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97857074 | ||||||
| chr2:97857168
|
A | G | 5 | a0001c0007t0003g0034a0001c0007t0003g0035a0001c0007t0003g0036others(2): Show | 5 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+2136T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97857168 | ||||||
| chr2:97857267
|
C | T | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.483+2037G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97857267 | ||||||
| chr2:97857474
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.483+1830T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97857474 | ||||||
| chr2:97858121
|
G | A | 2 | a0001c0001t0003g0066a0001c0001t0003g0067 | 2 | NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.483+1183C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858121 | ||||||
| chr2:97858122
|
G | A | 1 | a0001c0002t0001g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.483+1182C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858122 | ||||||
| chr2:97858256
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.483+1048C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858256 | ||||||
| chr2:97858272
|
T | C | 1 | a0001c0002t0001g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.483+1032A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858272 | ||||||
| chr2:97858428
|
T | C | 1 | a0001c0002t0001g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.483+876A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858428 | ||||||
| chr2:97858623
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+681A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858623 | ||||||
| chr2:97858644
|
A | G | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.483+660T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97858644 | ||||||
| chr2:97859284
|
T | C | 1 | a0001c0002t0001g0252 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.483+20A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 5/40 | chr2 | 97859284 | ||||||
| chr2:97859452
|
A | G | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.360-25T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97859452 | ||||||
| chr2:97859516
|
C | T | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.360-89G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97859516 | ||||||
| chr2:97859696
|
G | A | 1 | a0001c0002t0010g0243 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.360-269C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97859696 | ||||||
| chr2:97859699
|
C | G | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.360-272G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97859699 | ||||||
| chr2:97859747
|
C | T | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.360-320G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97859747 | ||||||
| chr2:97860254
|
T | C | 1 | a0001c0002t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.360-827A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97860254 | ||||||
| chr2:97860527
|
G | T | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.360-1100C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97860527 | ||||||
| chr2:97860545
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.360-1118G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97860545 | ||||||
| chr2:97860640
|
G | A | 7 | a0001c0002t0001g0237a0001c0002t0001g0238a0001c0002t0001g0239others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.360-1213C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97860640 | ||||||
| chr2:97860753
|
C | T | 13 | a0003c0004t0002g0096a0003c0004t0002g0097a0003c0004t0002g0098others(10): Show | 13 | HG00597.hp2 HG02129.hp2 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.360-1326G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97860753 | ||||||
| chr2:97861104
|
T | G | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.360-1677A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861104 | ||||||
| chr2:97861227
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.360-1800G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861227 | ||||||
| chr2:97861280
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-1853A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861280 | ||||||
| chr2:97861496
|
A | C | 1 | a0001c0002t0001g0258 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.360-2069T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861496 | ||||||
| chr2:97861673
|
A | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.360-2246T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861673 | ||||||
| chr2:97861685
|
G | T | 1 | a0001c0005t0005g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.360-2258C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861685 | ||||||
| chr2:97861989
|
C | T | 1 | a0001c0002t0001g0216 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.360-2562G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97861989 | ||||||
| chr2:97862075
|
G | C | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-2648C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97862075 | ||||||
| chr2:97862217
|
C | G | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.360-2790G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97862217 | ||||||
| chr2:97862379
|
T | C | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-2952A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97862379 | ||||||
| chr2:97862488
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-3061A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97862488 | ||||||
| chr2:97862995
|
A | G | 1 | a0001c0001t0005g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.360-3568T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97862995 | ||||||
| chr2:97863055
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.360-3628A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863055 | ||||||
| chr2:97863109
|
C | CA | 5 | a0001c0002t0001g0250a0001c0005t0005g0135a0001c0005t0005g0139others(2): Show | 5 | HG01243.hp1 HG02074.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-3683dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863109 | ||||||
| chr2:97863118
|
C | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.360-3691G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863118 | ||||||
| chr2:97863148
|
C | A | 1 | a0001c0001t0002g0003 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-3721G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863148 | ||||||
| chr2:97863170
|
C | T | 1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.360-3743G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863170 | ||||||
| chr2:97863251
|
A | G | 1 | a0001c0002t0001g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.360-3824T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863251 | ||||||
| chr2:97863369
|
C | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.360-3942G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863369 | ||||||
| chr2:97863454
|
G | C | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.360-4027C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863454 | ||||||
| chr2:97863515
|
A | G | 1 | a0001c0001t0005g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.360-4088T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863515 | ||||||
| chr2:97863695
|
A | G | 1 | a0001c0024t0001g0263 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.360-4268T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863695 | ||||||
| chr2:97863912
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.360-4485C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863912 | ||||||
| chr2:97863915
|
T | A | 275 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.360-4488A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863915 | ||||||
| chr2:97863917
|
A | C | 275 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.360-4490T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97863917 | ||||||
| chr2:97864084
|
T | C | 1 | a0001c0002t0001g0225 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.360-4657A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864084 | ||||||
| chr2:97864124
|
C | T | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.360-4697G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864124 | ||||||
| chr2:97864144
|
T | C | 2 | a0001c0002t0001g0232a0001c0002t0001g0256 | 2 | HG02027.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.360-4717A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864144 | ||||||
| chr2:97864202
|
G | A | 1 | a0001c0001t0005g0028 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.360-4775C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864202 | ||||||
| chr2:97864241
|
G | A | 1 | a0001c0001t0004g0149 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.360-4814C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864241 | ||||||
| chr2:97864331
|
A | G | 8 | a0001c0002t0001g0205a0001c0002t0001g0212a0001c0002t0001g0217others(5): Show | 8 | HG01257.hp2 HG01943.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-4904T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864331 | ||||||
| chr2:97864333
|
A | G | 8 | a0001c0002t0001g0205a0001c0002t0001g0212a0001c0002t0001g0217others(5): Show | 8 | HG01257.hp2 HG01943.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-4906T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864333 | ||||||
| chr2:97864465
|
C | A | 1 | a0001c0001t0003g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.360-5038G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864465 | ||||||
| chr2:97864540
|
A | T | 9 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.360-5113T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864540 | ||||||
| chr2:97864571
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-5144A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864571 | ||||||
| chr2:97864709
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.360-5282C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864709 | ||||||
| chr2:97864725
|
A | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.360-5298T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864725 | ||||||
| chr2:97864757
|
T | G | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.360-5330A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864757 | ||||||
| chr2:97864785
|
A | T | 1 | a0001c0002t0001g0241 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.360-5358T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864785 | ||||||
| chr2:97864810
|
C | G | 1 | a0001c0001t0005g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.360-5383G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864810 | ||||||
| chr2:97864814
|
C | T | 1 | a0002c0003t0004g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.360-5387G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97864814 | ||||||
| chr2:97865234
|
T | C | 1 | a0001c0002t0001g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.360-5807A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865234 | ||||||
| chr2:97865248
|
T | C | 3 | a0001c0002t0001g0227a0001c0011t0001g0229a0001c0011t0001g0248 | 3 | HG01169.hp2 HG01934.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.360-5821A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865248 | ||||||
| chr2:97865336
|
G | A | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.360-5909C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865336 | ||||||
| chr2:97865430
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.360-6003G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865430 | ||||||
| chr2:97865580
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-6153G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865580 | ||||||
| chr2:97865665
|
C | T | 1 | a0001c0002t0001g0245 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.360-6238G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865665 | ||||||
| chr2:97865666
|
G | A | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.360-6239C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865666 | ||||||
| chr2:97865835
|
A | G | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-6408T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865835 | ||||||
| chr2:97865892
|
T | C | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.360-6465A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865892 | ||||||
| chr2:97865983
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.360-6556G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97865983 | ||||||
| chr2:97866025
|
G | GGTGCCC | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.360-6604_360-6599d others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866025 | ||||||
| chr2:97866124
|
C | T | 2 | a0001c0002t0001g0251a0001c0002t0001g0257 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.360-6697G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866124 | ||||||
| chr2:97866150
|
G | C | 2 | a0001c0001t0006g0163a0006c0021t0006g0164 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.360-6723C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866150 | ||||||
| chr2:97866288
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-6861C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866288 | ||||||
| chr2:97866332
|
T | G | 1 | a0001c0001t0003g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.360-6905A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866332 | ||||||
| chr2:97866574
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-7147G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866574 | ||||||
| chr2:97866583
|
GT | G | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-7157delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866583 | ||||||
| chr2:97866622
|
T | C | 1 | a0002c0003t0004g0184 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.360-7195A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866622 | ||||||
| chr2:97866703
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.360-7276G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97866703 | ||||||
| chr2:97867029
|
G | C | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.360-7602C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867029 | ||||||
| chr2:97867038
|
G | C | 20 | a0001c0001t0003g0058a0001c0001t0005g0023a0001c0001t0005g0024others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.360-7611C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867038 | ||||||
| chr2:97867098
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.360-7671A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867098 | ||||||
| chr2:97867115
|
T | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.360-7688A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867115 | ||||||
| chr2:97867230
|
A | G | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360-7803T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867230 | ||||||
| chr2:97867257
|
G | A | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.360-7830C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867257 | ||||||
| chr2:97867265
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-7838A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867265 | ||||||
| chr2:97867400
|
A | G | 1 | a0001c0001t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.360-7973T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867400 | ||||||
| chr2:97867454
|
G | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.360-8027C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867454 | ||||||
| chr2:97867529
|
T | A | 1 | a0002c0003t0004g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.360-8102A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867529 | ||||||
| chr2:97867672
|
G | C | 1 | a0001c0002t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.360-8245C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867672 | ||||||
| chr2:97867680
|
G | A | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.360-8253C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867680 | ||||||
| chr2:97867826
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.360-8399T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867826 | ||||||
| chr2:97867980
|
A | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.360-8553T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97867980 | ||||||
| chr2:97868110
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.360-8683A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868110 | ||||||
| chr2:97868186
|
G | A | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.360-8759C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868186 | ||||||
| chr2:97868367
|
T | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.360-8940A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868367 | ||||||
| chr2:97868581
|
C | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-9154G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868581 | ||||||
| chr2:97868595
|
G | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.360-9168C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868595 | ||||||
| chr2:97868703
|
A | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0056 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.360-9276T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868703 | ||||||
| chr2:97868953
|
C | T | 200 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.360-9526G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97868953 | ||||||
| chr2:97869106
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.360-9679T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97869106 | ||||||
| chr2:97869122
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-9695G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97869122 | ||||||
| chr2:97869567
|
G | T | 1 | a0001c0001t0007g0022 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.360-10140C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97869567 | ||||||
| chr2:97869685
|
G | A | 3 | a0002c0003t0004g0183a0002c0003t0004g0185a0002c0003t0004g0186 | 3 | HG01975.hp1 HG01993.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.360-10258C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97869685 | ||||||
| chr2:97869870
|
G | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-10443C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97869870 | ||||||
| chr2:97870090
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.360-10663A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97870090 | ||||||
| chr2:97870353
|
C | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.360-10926G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97870353 | ||||||
| chr2:97870516
|
C | T | 277 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.360-11089G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97870516 | ||||||
| chr2:97870951
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.360-11524C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97870951 | ||||||
| chr2:97871025
|
A | G | 1 | a0003c0004t0002g0120 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.360-11598T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97871025 | ||||||
| chr2:97871270
|
A | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.360-11843T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97871270 | ||||||
| chr2:97871576
|
T | C | 1 | a0001c0001t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.360-12149A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97871576 | ||||||
| chr2:97871849
|
T | C | 10 | a0003c0004t0002g0108a0003c0004t0002g0109a0003c0004t0002g0110others(7): Show | 10 | HG00544.hp2 HG02602.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.360-12422A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97871849 | ||||||
| chr2:97871856
|
C | G | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.360-12429G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97871856 | ||||||
| chr2:97872126
|
C | T | 1 | a0001c0002t0001g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.360-12699G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872126 | ||||||
| chr2:97872344
|
C | T | 2 | a0001c0001t0003g0073a0001c0001t0003g0074 | 2 | NA18949.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.360-12917G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872344 | ||||||
| chr2:97872388
|
C | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0053 | 2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.360-12961G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872388 | ||||||
| chr2:97872486
|
G | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.360-13059C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872486 | ||||||
| chr2:97872533
|
A | G | 1 | a0002c0003t0004g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.360-13106T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872533 | ||||||
| chr2:97872716
|
C | T | 2 | a0001c0002t0001g0251a0001c0002t0001g0257 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.360-13289G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872716 | ||||||
| chr2:97872773
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.360-13346G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872773 | ||||||
| chr2:97872835
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.360-13408G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872835 | ||||||
| chr2:97872849
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.360-13422A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872849 | ||||||
| chr2:97872864
|
ATTGGCAC others(30): Show |
A | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.360-13474_360-1343 others(41): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872864 | ||||||
| chr2:97872927
|
A | G | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.360-13500T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97872927 | ||||||
| chr2:97873008
|
T | C | 2 | a0005c0006t0005g0136a0005c0006t0005g0137 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.360-13581A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873008 | ||||||
| chr2:97873043
|
C | T | 1 | a0002c0003t0004g0186 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.360-13616G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873043 | ||||||
| chr2:97873386
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.360-13959C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873386 | ||||||
| chr2:97873404
|
G | A | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-13977C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873404 | ||||||
| chr2:97873412
|
GCCT | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.360-13988_360-1398 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873412 | ||||||
| chr2:97873451
|
T | C | 4 | a0004c0008t0002g0091a0004c0008t0002g0093a0004c0008t0002g0094others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-14024A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873451 | ||||||
| chr2:97873489
|
T | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.360-14062A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873489 | ||||||
| chr2:97873818
|
C | T | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.359+14234G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873818 | ||||||
| chr2:97873894
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+14158A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873894 | ||||||
| chr2:97873992
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.359+14060A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97873992 | ||||||
| chr2:97874059
|
G | A | 26 | a0003c0004t0002g0096a0003c0004t0002g0097a0003c0004t0002g0098others(23): Show | 26 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.359+13993C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874059 | ||||||
| chr2:97874116
|
G | A | 1 | a0001c0001t0003g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.359+13936C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874116 | ||||||
| chr2:97874182
|
TA | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.359+13869delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874182 | ||||||
| chr2:97874222
|
T | C | 1 | a0001c0002t0001g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.359+13830A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874222 | ||||||
| chr2:97874241
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+13811G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874241 | ||||||
| chr2:97874393
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+13659C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874393 | ||||||
| chr2:97874460
|
A | G | 1 | a0001c0001t0004g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.359+13592T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874460 | ||||||
| chr2:97874657
|
T | C | 1 | a0001c0001t0006g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.359+13395A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874657 | ||||||
| chr2:97874661
|
G | C | 1 | a0001c0001t0004g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.359+13391C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874661 | ||||||
| chr2:97874960
|
G | A | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.359+13092C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97874960 | ||||||
| chr2:97875287
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.359+12765A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875287 | ||||||
| chr2:97875372
|
T | C | 2 | a0003c0004t0002g0106a0003c0004t0002g0107 | 2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.359+12680A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875372 | ||||||
| chr2:97875386
|
A | T | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.359+12666T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875386 | ||||||
| chr2:97875389
|
C | G | 1 | a0001c0002t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.359+12663G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875389 | ||||||
| chr2:97875608
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+12444G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875608 | ||||||
| chr2:97875780
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.359+12272G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875780 | ||||||
| chr2:97875964
|
A | T | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.359+12088T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97875964 | ||||||
| chr2:97876166
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.359+11886C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876166 | ||||||
| chr2:97876187
|
A | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+11865T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876187 | ||||||
| chr2:97876206
|
C | G | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.359+11846G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876206 | ||||||
| chr2:97876343
|
C | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+11709G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876343 | ||||||
| chr2:97876465
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.359+11587G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876465 | ||||||
| chr2:97876591
|
T | C | 1 | a0001c0002t0001g0281 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.359+11461A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876591 | ||||||
| chr2:97876716
|
C | G | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.359+11336G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876716 | ||||||
| chr2:97876879
|
G | A | 2 | a0001c0002t0001g0242a0001c0002t0001g0254 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.359+11173C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876879 | ||||||
| chr2:97876896
|
A | G | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.359+11156T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876896 | ||||||
| chr2:97876941
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.359+11111C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97876941 | ||||||
| chr2:97877112
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.359+10940C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97877112 | ||||||
| chr2:97877544
|
C | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.359+10508G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97877544 | ||||||
| chr2:97877800
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.359+10252T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97877800 | ||||||
| chr2:97877865
|
T | C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.359+10187A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97877865 | ||||||
| chr2:97878163
|
C | T | 1 | a0001c0007t0003g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.359+9889G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878163 | ||||||
| chr2:97878176
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.359+9876G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878176 | ||||||
| chr2:97878223
|
G | C | 1 | a0001c0002t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.359+9829C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878223 | ||||||
| chr2:97878667
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+9385C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878667 | ||||||
| chr2:97878735
|
G | A | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.359+9317C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878735 | ||||||
| chr2:97878788
|
T | TGTAC | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.359+9260_359+9263d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878788 | ||||||
| chr2:97878789
|
G | A | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.359+9263C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878789 | ||||||
| chr2:97878880
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.359+9172T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878880 | ||||||
| chr2:97878969
|
T | C | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.359+9083A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97878969 | ||||||
| chr2:97879117
|
C | G | 1 | a0001c0002t0001g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.359+8935G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879117 | ||||||
| chr2:97879166
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.359+8886C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879166 | ||||||
| chr2:97879198
|
T | G | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.359+8854A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879198 | ||||||
| chr2:97879203
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.359+8849C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879203 | ||||||
| chr2:97879585
|
T | G | 1 | a0001c0002t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.359+8467A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879585 | ||||||
| chr2:97879598
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.359+8454C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879598 | ||||||
| chr2:97879772
|
A | G | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.359+8280T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879772 | ||||||
| chr2:97879806
|
G | A | 26 | a0003c0004t0002g0096a0003c0004t0002g0097a0003c0004t0002g0098others(23): Show | 26 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.359+8246C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879806 | ||||||
| chr2:97879851
|
AG | A | 9 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(6): Show | 9 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.359+8200delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97879851 | ||||||
| chr2:97880138
|
A | AAAAAACT others(311): Show |
1 | a0005c0006t0005g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.359+7913_359+7914i others(320): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(316): Show |
2 | a0001c0005t0005g0139a0001c0005t0005g0140 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.359+7913_359+7914i others(325): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(317): Show |
1 | a0001c0005t0005g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.359+7913_359+7914i others(326): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(323): Show |
1 | a0005c0006t0005g0137 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.359+7913_359+7914i others(332): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(324): Show |
2 | a0005c0006t0005g0136a0005c0006t0005g0138 | 2 | HG01257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.359+7913_359+7914i others(333): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(325): Show |
2 | a0005c0006t0005g0131a0005c0006t0005g0142 | 2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.359+7913_359+7914i others(334): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(333): Show |
1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.359+7913_359+7914i others(342): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(334): Show |
1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.359+7913_359+7914i others(343): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(338): Show |
1 | a0001c0005t0005g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.359+7913_359+7914i others(347): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(339): Show |
2 | a0001c0005t0005g0132a0001c0005t0005g0133 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.359+7913_359+7914i others(348): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880138
|
A | AAAAAACT others(341): Show |
1 | a0001c0005t0005g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.359+7913_359+7914i others(350): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880138 | ||||||
| chr2:97880162
|
C | T | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.359+7890G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880162 | ||||||
| chr2:97880180
|
C | T | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.359+7872G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880180 | ||||||
| chr2:97880998
|
G | C | 1 | a0001c0001t0004g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.359+7054C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97880998 | ||||||
| chr2:97881090
|
C | A | 2 | a0002c0003t0004g0200a0002c0003t0004g0201 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.359+6962G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881090 | ||||||
| chr2:97881148
|
C | A | 1 | a0001c0012t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.359+6904G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881148 | ||||||
| chr2:97881242
|
CT | C | 72 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.359+6809delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881242 | ||||||
| chr2:97881242
|
CTT | C | 14 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(11): Show | 14 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.359+6808_359+6809d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881242 | ||||||
| chr2:97881254
|
T | C | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.359+6798A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881254 | ||||||
| chr2:97881295
|
C | G | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.359+6757G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881295 | ||||||
| chr2:97881296
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+6756A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881296 | ||||||
| chr2:97881391
|
A | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+6661T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881391 | ||||||
| chr2:97881538
|
C | T | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.359+6514G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881538 | ||||||
| chr2:97881707
|
C | CAA | 8 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0049others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.359+6343_359+6344d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881707 | ||||||
| chr2:97881722
|
A | G | 7 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(4): Show | 7 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.359+6330T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881722 | ||||||
| chr2:97881723
|
A | AAAG | 31 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0041others(28): Show | 31 | HG00099.hp1 HG01069.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.359+6328_359+6329i others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881723 | ||||||
| chr2:97881723
|
A | AAAGG | 9 | a0001c0001t0003g0043a0001c0001t0003g0059a0001c0001t0003g0067others(6): Show | 9 | HG00423.hp1 HG01934.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.359+6328_359+6329i others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881723 | ||||||
| chr2:97881723
|
A | AG | 55 | a0001c0001t0001g0202a0001c0001t0002g0007a0001c0001t0002g0126others(52): Show | 55 | HG01070.hp2 HG01106.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.359+6328dupC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881723 | ||||||
| chr2:97881723
|
A | AGG | 29 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(26): Show | 29 | HG00423.hp2 HG01070.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.359+6327_359+6328d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881723 | ||||||
| chr2:97881723
|
A | G | 12 | a0001c0001t0001g0203a0001c0001t0002g0015a0001c0001t0002g0016others(9): Show | 12 | HG00597.hp1 HG01123.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.359+6329T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881723 | ||||||
| chr2:97881723
|
AG | A | 35 | a0001c0001t0004g0148a0001c0001t0004g0149a0001c0001t0004g0154others(32): Show | 35 | HG00099.hp2 HG00597.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.359+6328delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881723 | ||||||
| chr2:97881724
|
G | A | 1 | a0003c0004t0002g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.359+6328C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881724 | ||||||
| chr2:97881732
|
G | C | 1 | a0001c0001t0007g0018 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.359+6320C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881732 | ||||||
| chr2:97881734
|
C | G | 1 | a0001c0002t0001g0247 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.359+6318G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97881734 | ||||||
| chr2:97882222
|
C | T | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.359+5830G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97882222 | ||||||
| chr2:97882277
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.359+5775G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97882277 | ||||||
| chr2:97882897
|
T | C | 4 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+5155A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97882897 | ||||||
| chr2:97882900
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.359+5152A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97882900 | ||||||
| chr2:97883070
|
T | C | 2 | a0001c0002t0001g0258a0001c0002t0001g0260 | 2 | HG00423.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.359+4982A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97883070 | ||||||
| chr2:97883228
|
G | A | 1 | a0001c0005t0005g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.359+4824C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97883228 | ||||||
| chr2:97883295
|
G | A | 5 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(2): Show | 5 | HG00642.hp1 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+4757C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97883295 | ||||||
| chr2:97883349
|
A | G | 8 | a0002c0003t0004g0176a0002c0003t0004g0177a0002c0003t0004g0180others(5): Show | 8 | HG00733.hp2 HG01070.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+4703T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97883349 | ||||||
| chr2:97883754
|
T | C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.359+4298A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97883754 | ||||||
| chr2:97884052
|
TTTA | T | 10 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0045others(7): Show | 10 | HG00733.hp1 HG01069.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.359+3997_359+3999d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884052 | ||||||
| chr2:97884058
|
GTT | G | 5 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(2): Show | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.359+3992_359+3993d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884058 | ||||||
| chr2:97884248
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.359+3804G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884248 | ||||||
| chr2:97884249
|
G | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.359+3803C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884249 | ||||||
| chr2:97884311
|
A | T | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359+3741T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884311 | ||||||
| chr2:97884344
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.359+3708G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884344 | ||||||
| chr2:97884410
|
A | G | 2 | a0001c0005t0005g0135a0001c0005t0005g0139 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.359+3642T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884410 | ||||||
| chr2:97884440
|
A | G | 1 | a0003c0004t0002g0100 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.359+3612T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884440 | ||||||
| chr2:97884441
|
G | C | 2 | a0001c0002t0001g0251a0001c0002t0001g0257 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.359+3611C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884441 | ||||||
| chr2:97884454
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+3598A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884454 | ||||||
| chr2:97884459
|
A | T | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.359+3593T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884459 | ||||||
| chr2:97884576
|
A | C | 2 | a0001c0002t0001g0232a0001c0002t0001g0256 | 2 | HG02027.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.359+3476T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884576 | ||||||
| chr2:97884608
|
A | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+3444T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884608 | ||||||
| chr2:97884612
|
G | C | 52 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.359+3440C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884612 | ||||||
| chr2:97884817
|
A | T | 1 | a0001c0001t0007g0020 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.359+3235T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884817 | ||||||
| chr2:97884896
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+3156G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97884896 | ||||||
| chr2:97885025
|
T | G | 1 | a0001c0001t0005g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.359+3027A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885025 | ||||||
| chr2:97885110
|
G | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.359+2942C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885110 | ||||||
| chr2:97885220
|
C | T | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.359+2832G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885220 | ||||||
| chr2:97885221
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+2831C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885221 | ||||||
| chr2:97885229
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.359+2823C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885229 | ||||||
| chr2:97885267
|
C | T | 1 | a0001c0001t0007g0018 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.359+2785G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885267 | ||||||
| chr2:97885290
|
C | CA | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+2761_359+2762i others(3): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885290 | ||||||
| chr2:97885292
|
G | GGTTCAC | 189 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.359+2759_359+2760i others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885292 | ||||||
| chr2:97885293
|
T | G | 189 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.359+2759A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885293 | ||||||
| chr2:97885293
|
T | TTCACG | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+2758_359+2759i others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885293 | ||||||
| chr2:97885340
|
C | T | 6 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0068others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.359+2712G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885340 | ||||||
| chr2:97885341
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359+2711C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885341 | ||||||
| chr2:97885353
|
A | G | 6 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0068others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.359+2699T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885353 | ||||||
| chr2:97885358
|
AT | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.359+2693delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885358 | ||||||
| chr2:97885421
|
C | T | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.359+2631G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885421 | ||||||
| chr2:97885438
|
C | CCTGCCT | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.359+2613_359+2614i others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885438 | ||||||
| chr2:97885440
|
C | CGCCTCG | 187 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.359+2611_359+2612i others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885440 | ||||||
| chr2:97885440
|
C | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.359+2612G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885440 | ||||||
| chr2:97885485
|
G | A | 1 | a0003c0004t0002g0103 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.359+2567C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885485 | ||||||
| chr2:97885579
|
TTGAG | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+2469_359+2472d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885579 | ||||||
| chr2:97885600
|
T | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.359+2452A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885600 | ||||||
| chr2:97885686
|
T | G | 1 | a0001c0001t0003g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359+2366A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885686 | ||||||
| chr2:97885738
|
T | C | 18 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.359+2314A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885738 | ||||||
| chr2:97885915
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.359+2137A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97885915 | ||||||
| chr2:97886259
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.359+1793A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886259 | ||||||
| chr2:97886344
|
G | A | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.359+1708C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886344 | ||||||
| chr2:97886372
|
G | A | 1 | a0003c0004t0002g0113 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.359+1680C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886372 | ||||||
| chr2:97886385
|
T | C | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+1667A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886385 | ||||||
| chr2:97886524
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.359+1528A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886524 | ||||||
| chr2:97886660
|
C | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.359+1392G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886660 | ||||||
| chr2:97886750
|
C | T | 159 | a0001c0001t0002g0121a0001c0001t0003g0032a0001c0001t0003g0033others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.359+1302G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886750 | ||||||
| chr2:97886842
|
C | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.359+1210G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886842 | ||||||
| chr2:97886843
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.359+1209C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886843 | ||||||
| chr2:97886936
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.359+1116G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886936 | ||||||
| chr2:97886957
|
A | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+1095T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97886957 | ||||||
| chr2:97887263
|
A | G | 210 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.359+789T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887263 | ||||||
| chr2:97887275
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+777A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887275 | ||||||
| chr2:97887392
|
T | A | 1 | a0001c0002t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.359+660A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887392 | ||||||
| chr2:97887429
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.359+623T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887429 | ||||||
| chr2:97887629
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.359+423A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887629 | ||||||
| chr2:97887731
|
AT | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.359+320delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887731 | ||||||
| chr2:97887994
|
A | G | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.359+58T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 4/40 | chr2 | 97887994 | ||||||
| chr2:97888143
|
A | G | 1 | a0005c0006t0005g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.291-23T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97888143 | ||||||
| chr2:97888582
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.291-462A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97888582 | ||||||
| chr2:97889221
|
C | T | 1 | a0001c0001t0003g0059 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.291-1101G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889221 | ||||||
| chr2:97889267
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.291-1147C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889267 | ||||||
| chr2:97889336
|
C | A | 3 | a0001c0001t0006g0158a0001c0001t0006g0159a0001c0001t0006g0160 | 3 | HG02451.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.291-1216G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889336 | ||||||
| chr2:97889548
|
TATA | T | 39 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0127others(36): Show | 39 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.291-1431_291-1429d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889548 | ||||||
| chr2:97889603
|
TATATATA | T | 7 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(4): Show | 7 | HG02074.hp1 HG02083.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1490_291-1484d others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889603 | ||||||
| chr2:97889768
|
C | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-1648G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889768 | ||||||
| chr2:97889821
|
A | G | 2 | a0002c0003t0004g0180a0002c0003t0004g0181 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.291-1701T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889821 | ||||||
| chr2:97889944
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.291-1824G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97889944 | ||||||
| chr2:97890443
|
C | T | 21 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.291-2323G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97890443 | ||||||
| chr2:97890447
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.291-2327A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97890447 | ||||||
| chr2:97891255
|
T | C | 2 | a0002c0003t0004g0191a0002c0003t0004g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.291-3135A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97891255 | ||||||
| chr2:97891288
|
G | A | 1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.291-3168C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97891288 | ||||||
| chr2:97891509
|
CA | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.291-3390delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97891509 | ||||||
| chr2:97891595
|
G | A | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-3475C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97891595 | ||||||
| chr2:97891881
|
TA | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.291-3762delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97891881 | ||||||
| chr2:97891930
|
CA | C | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-3811delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97891930 | ||||||
| chr2:97892206
|
T | C | 1 | a0002c0009t0004g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.291-4086A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97892206 | ||||||
| chr2:97892280
|
C | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-4160G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97892280 | ||||||
| chr2:97892357
|
G | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.291-4237C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97892357 | ||||||
| chr2:97892553
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.291-4433C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97892553 | ||||||
| chr2:97892728
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.291-4608A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97892728 | ||||||
| chr2:97892955
|
T | C | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.291-4835A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97892955 | ||||||
| chr2:97893037
|
T | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.291-4917A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893037 | ||||||
| chr2:97893044
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-4924G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893044 | ||||||
| chr2:97893120
|
T | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-5000A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893120 | ||||||
| chr2:97893123
|
T | C | 13 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0125others(10): Show | 13 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-5003A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893123 | ||||||
| chr2:97893169
|
G | T | 1 | a0004c0008t0002g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.291-5049C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893169 | ||||||
| chr2:97893219
|
A | G | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-5099T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893219 | ||||||
| chr2:97893289
|
CTTTGATG others(4): Show |
C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-5180_291-5170d others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893289 | ||||||
| chr2:97893513
|
G | A | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-5393C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893513 | ||||||
| chr2:97893670
|
G | C | 1 | a0001c0002t0001g0242 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.291-5550C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893670 | ||||||
| chr2:97893676
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.291-5556G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893676 | ||||||
| chr2:97893703
|
T | G | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.291-5583A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893703 | ||||||
| chr2:97893732
|
T | TGGTTTTT others(306): Show |
1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.291-5613_291-5612i others(315): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893732 | ||||||
| chr2:97893734
|
G | GT | 19 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.291-5615dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893734 | ||||||
| chr2:97893958
|
T | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.291-5838A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893958 | ||||||
| chr2:97893960
|
C | T | 3 | a0001c0002t0001g0277a0001c0002t0001g0281a0001c0002t0001g0282 | 3 | HG02129.hp1 NA18612.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.291-5840G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97893960 | ||||||
| chr2:97894096
|
T | C | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-5976A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894096 | ||||||
| chr2:97894220
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-6100A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894220 | ||||||
| chr2:97894265
|
C | G | 1 | a0003c0004t0002g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.291-6145G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894265 | ||||||
| chr2:97894448
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0005g0122 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291-6328A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894448 | ||||||
| chr2:97894467
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.291-6347A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894467 | ||||||
| chr2:97894653
|
G | A | 1 | a0001c0001t0005g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.291-6533C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894653 | ||||||
| chr2:97894720
|
A | T | 6 | a0001c0007t0003g0034a0001c0007t0003g0035a0001c0007t0003g0036others(3): Show | 6 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-6600T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894720 | ||||||
| chr2:97894869
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-6749A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97894869 | ||||||
| chr2:97895148
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.291-7028C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895148 | ||||||
| chr2:97895188
|
C | T | 109 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.291-7068G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895188 | ||||||
| chr2:97895235
|
T | C | 1 | a0001c0001t0007g0020 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.291-7115A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895235 | ||||||
| chr2:97895244
|
C | T | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-7124G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895244 | ||||||
| chr2:97895298
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-7178G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895298 | ||||||
| chr2:97895418
|
G | C | 9 | a0003c0004t0002g0096a0003c0004t0002g0097a0003c0004t0002g0098others(6): Show | 9 | HG00597.hp2 NA18942.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.291-7298C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895418 | ||||||
| chr2:97895726
|
C | T | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-7606G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895726 | ||||||
| chr2:97895783
|
G | C | 1 | a0001c0007t0003g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-7663C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895783 | ||||||
| chr2:97895840
|
A | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.291-7720T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895840 | ||||||
| chr2:97895877
|
C | T | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.291-7757G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97895877 | ||||||
| chr2:97896101
|
T | A | 9 | a0001c0002t0001g0205a0001c0002t0001g0212a0001c0002t0001g0217others(6): Show | 9 | HG01257.hp2 HG01943.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.291-7981A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896101 | ||||||
| chr2:97896292
|
A | G | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-8172T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896292 | ||||||
| chr2:97896343
|
T | C | 1 | a0001c0001t0005g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.291-8223A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896343 | ||||||
| chr2:97896378
|
T | C | 113 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.291-8258A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896378 | ||||||
| chr2:97896412
|
T | G | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-8292A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896412 | ||||||
| chr2:97896546
|
G | A | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.291-8426C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896546 | ||||||
| chr2:97896660
|
T | C | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | NA18949.hp2 NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.291-8540A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896660 | ||||||
| chr2:97896789
|
T | TA | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-8670_291-8669i others(3): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896789 | ||||||
| chr2:97896932
|
G | C | 1 | a0005c0006t0005g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.291-8812C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896932 | ||||||
| chr2:97896955
|
T | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.291-8835A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896955 | ||||||
| chr2:97896968
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-8848G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896968 | ||||||
| chr2:97896970
|
G | C | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-8850C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97896970 | ||||||
| chr2:97897003
|
T | G | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.291-8883A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897003 | ||||||
| chr2:97897008
|
C | CTAT | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.291-8891_291-8889d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897008 | ||||||
| chr2:97897042
|
T | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-8922A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897042 | ||||||
| chr2:97897285
|
G | A | 1 | a0001c0002t0001g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.291-9165C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897285 | ||||||
| chr2:97897344
|
C | T | 1 | a0004c0014t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.291-9224G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897344 | ||||||
| chr2:97897458
|
A | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.291-9338T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897458 | ||||||
| chr2:97897625
|
T | C | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-9505A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897625 | ||||||
| chr2:97897692
|
C | T | 1 | a0001c0002t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.291-9572G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897692 | ||||||
| chr2:97897960
|
T | C | 1 | a0001c0023t0003g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291-9840A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97897960 | ||||||
| chr2:97898195
|
G | T | 1 | a0002c0003t0004g0194 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.291-10075C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97898195 | ||||||
| chr2:97898459
|
T | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+10199A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97898459 | ||||||
| chr2:97898943
|
C | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+9715G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97898943 | ||||||
| chr2:97899072
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.290+9586C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899072 | ||||||
| chr2:97899230
|
G | T | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.290+9428C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899230 | ||||||
| chr2:97899236
|
T | C | 1 | a0001c0002t0001g0255 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.290+9422A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899236 | ||||||
| chr2:97899245
|
G | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+9413C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899245 | ||||||
| chr2:97899287
|
C | G | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+9371G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899287 | ||||||
| chr2:97899374
|
G | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.290+9284C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899374 | ||||||
| chr2:97899659
|
A | G | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290+8999T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899659 | ||||||
| chr2:97899709
|
C | T | 3 | a0002c0009t0004g0182a0002c0009t0004g0187a0002c0009t0004g0188 | 3 | HG01123.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.290+8949G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899709 | ||||||
| chr2:97899749
|
A | G | 4 | a0003c0004t0002g0108a0003c0004t0002g0109a0003c0004t0002g0111others(1): Show | 4 | NA18612.hp2 NA18952.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+8909T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899749 | ||||||
| chr2:97899901
|
C | T | 1 | a0001c0002t0010g0243 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.290+8757G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97899901 | ||||||
| chr2:97900215
|
A | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+8443T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900215 | ||||||
| chr2:97900236
|
T | C | 1 | a0001c0002t0001g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.290+8422A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900236 | ||||||
| chr2:97900353
|
T | G | 4 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+8305A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900353 | ||||||
| chr2:97900506
|
T | A | 1 | a0001c0001t0002g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.290+8152A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900506 | ||||||
| chr2:97900532
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.290+8126A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900532 | ||||||
| chr2:97900543
|
GGAATACT others(5): Show |
G | 1 | a0001c0002t0009g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.290+8103_290+8114d others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900543 | ||||||
| chr2:97900718
|
TG | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.290+7939delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900718 | ||||||
| chr2:97900814
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.290+7844G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900814 | ||||||
| chr2:97900957
|
T | C | 1 | a0003c0004t0002g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.290+7701A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900957 | ||||||
| chr2:97900992
|
C | A | 1 | a0001c0005t0005g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.290+7666G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97900992 | ||||||
| chr2:97901110
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.290+7548T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901110 | ||||||
| chr2:97901163
|
G | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.290+7495C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901163 | ||||||
| chr2:97901394
|
T | C | 2 | a0001c0002t0001g0216a0001c0002t0001g0252 | 2 | NA18952.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.290+7264A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901394 | ||||||
| chr2:97901410
|
T | G | 1 | a0001c0001t0005g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290+7248A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901410 | ||||||
| chr2:97901488
|
G | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.290+7170C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901488 | ||||||
| chr2:97901595
|
T | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+7063A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901595 | ||||||
| chr2:97901642
|
T | C | 3 | a0001c0001t0005g0024a0001c0001t0005g0027a0001c0001t0005g0028 | 3 | HG01261.hp1 HG01346.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290+7016A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901642 | ||||||
| chr2:97901703
|
C | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+6955G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901703 | ||||||
| chr2:97901813
|
G | C | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.290+6845C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901813 | ||||||
| chr2:97901900
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+6758A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97901900 | ||||||
| chr2:97902008
|
C | T | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+6650G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902008 | ||||||
| chr2:97902094
|
A | T | 1 | a0001c0002t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.290+6564T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902094 | ||||||
| chr2:97902495
|
T | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+6163A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902495 | ||||||
| chr2:97902551
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.290+6107A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902551 | ||||||
| chr2:97902647
|
T | G | 5 | a0002c0003t0004g0183a0002c0003t0004g0184a0002c0003t0004g0185others(2): Show | 5 | HG00642.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+6011A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902647 | ||||||
| chr2:97902743
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.290+5915C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902743 | ||||||
| chr2:97902888
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+5770G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902888 | ||||||
| chr2:97902897
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.290+5761C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97902897 | ||||||
| chr2:97903209
|
A | G | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+5449T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903209 | ||||||
| chr2:97903501
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.290+5157T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903501 | ||||||
| chr2:97903585
|
T | G | 9 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+5073A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903585 | ||||||
| chr2:97903676
|
GGTTT | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+4978_290+4981d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903676 | ||||||
| chr2:97903685
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.290+4973C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903685 | ||||||
| chr2:97903685
|
GTTTA | G | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.290+4969_290+4972d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903685 | ||||||
| chr2:97903759
|
A | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.290+4899T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903759 | ||||||
| chr2:97903909
|
G | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.290+4749C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97903909 | ||||||
| chr2:97904101
|
T | C | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.290+4557A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97904101 | ||||||
| chr2:97904368
|
G | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0056 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.290+4290C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97904368 | ||||||
| chr2:97904668
|
T | C | 1 | a0002c0003t0004g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290+3990A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97904668 | ||||||
| chr2:97904691
|
C | T | 6 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(3): Show | 6 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+3967G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97904691 | ||||||
| chr2:97904798
|
CT | C | 9 | a0001c0002t0001g0272a0002c0003t0004g0186a0003c0004t0002g0113others(6): Show | 9 | HG01975.hp1 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+3859delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97904798 | ||||||
| chr2:97904937
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.290+3721A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97904937 | ||||||
| chr2:97905085
|
A | G | 1 | a0001c0001t0004g0149 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.290+3573T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905085 | ||||||
| chr2:97905360
|
C | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.290+3298G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905360 | ||||||
| chr2:97905489
|
A | T | 5 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0029others(2): Show | 5 | HG00099.hp2 HG01099.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+3169T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905489 | ||||||
| chr2:97905579
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.290+3079G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905579 | ||||||
| chr2:97905674
|
C | A | 13 | a0003c0004t0002g0108a0003c0004t0002g0109a0003c0004t0002g0110others(10): Show | 13 | HG00544.hp2 HG02602.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+2984G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905674 | ||||||
| chr2:97905738
|
T | C | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+2920A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905738 | ||||||
| chr2:97905921
|
A | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.290+2737T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97905921 | ||||||
| chr2:97906032
|
G | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+2626C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97906032 | ||||||
| chr2:97906073
|
G | T | 12 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(9): Show | 12 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.290+2585C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97906073 | ||||||
| chr2:97906400
|
C | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.290+2258G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97906400 | ||||||
| chr2:97906420
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290+2238G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97906420 | ||||||
| chr2:97906454
|
A | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0228 | 2 | NA18942.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.290+2204T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97906454 | ||||||
| chr2:97907017
|
T | C | 2 | a0001c0001t0003g0043a0001c0001t0003g0072 | 2 | HG02040.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.290+1641A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97907017 | ||||||
| chr2:97907103
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1555A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97907103 | ||||||
| chr2:97907584
|
G | T | 1 | a0001c0002t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.290+1074C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97907584 | ||||||
| chr2:97907803
|
C | T | 2 | a0001c0001t0003g0062a0001c0023t0003g0061 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.290+855G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97907803 | ||||||
| chr2:97907917
|
A | C | 1 | a0001c0005t0005g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.290+741T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97907917 | ||||||
| chr2:97907996
|
T | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.290+662A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97907996 | ||||||
| chr2:97908047
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.290+611C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908047 | ||||||
| chr2:97908082
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+576A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908082 | ||||||
| chr2:97908105
|
A | C | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.290+553T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908105 | ||||||
| chr2:97908107
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.290+551C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908107 | ||||||
| chr2:97908113
|
A | C | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290+545T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908113 | ||||||
| chr2:97908310
|
C | T | 1 | a0001c0001t0005g0027 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.290+348G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908310 | ||||||
| chr2:97908311
|
C | G | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.290+347G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908311 | ||||||
| chr2:97908362
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+296G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908362 | ||||||
| chr2:97908396
|
A | C | 210 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.290+262T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908396 | ||||||
| chr2:97908542
|
T | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.290+116A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908542 | ||||||
| chr2:97908572
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290+86A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908572 | ||||||
| chr2:97908616
|
A | G | 1 | a0003c0004t0002g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.290+42T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908616 | ||||||
| chr2:97908644
|
T | C | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.290+14A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 3/40 | chr2 | 97908644 | ||||||
| chr2:97908839
|
A | T | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-141T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97908839 | ||||||
| chr2:97908875
|
A | C | 13 | a0003c0004t0002g0096a0003c0004t0002g0097a0003c0004t0002g0098others(10): Show | 13 | HG00597.hp2 HG02129.hp2 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-177T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97908875 | ||||||
| chr2:97908944
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.250-246G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97908944 | ||||||
| chr2:97908984
|
C | T | 2 | a0003c0004t0002g0097a0003c0004t0002g0146 | 2 | NA18942.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.250-286G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97908984 | ||||||
| chr2:97909080
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.250-382A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909080 | ||||||
| chr2:97909188
|
A | C | 1 | a0002c0003t0004g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.250-490T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909188 | ||||||
| chr2:97909281
|
A | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.250-583T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909281 | ||||||
| chr2:97909557
|
A | G | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-859T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909557 | ||||||
| chr2:97909865
|
A | G | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-1167T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909865 | ||||||
| chr2:97909960
|
G | A | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.250-1262C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909960 | ||||||
| chr2:97909999
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-1301A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97909999 | ||||||
| chr2:97910064
|
C | G | 1 | a0013c0028t0001g0246 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.250-1366G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910064 | ||||||
| chr2:97910149
|
G | C | 2 | a0001c0002t0001g0232a0001c0002t0001g0256 | 2 | HG02027.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.250-1451C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910149 | ||||||
| chr2:97910222
|
AAAAT | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.250-1528_250-1525d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910222 | ||||||
| chr2:97910306
|
T | C | 2 | a0001c0012t0001g0233a0001c0012t0001g0235 | 2 | HG02735.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.250-1608A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910306 | ||||||
| chr2:97910329
|
A | C | 1 | a0001c0002t0009g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.250-1631T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910329 | ||||||
| chr2:97910727
|
T | G | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-2029A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910727 | ||||||
| chr2:97910779
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-2081A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97910779 | ||||||
| chr2:97911003
|
A | C | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.250-2305T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97911003 | ||||||
| chr2:97911075
|
T | G | 1 | a0001c0002t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.250-2377A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97911075 | ||||||
| chr2:97911101
|
C | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0228 | 2 | NA18942.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.250-2403G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97911101 | ||||||
| chr2:97911408
|
T | C | 2 | a0001c0001t0004g0166a0001c0001t0008g0167 | 2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.250-2710A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97911408 | ||||||
| chr2:97912039
|
G | A | 2 | a0002c0003t0004g0179a0002c0003t0004g0193 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.250-3341C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912039 | ||||||
| chr2:97912152
|
G | A | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-3454C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912152 | ||||||
| chr2:97912177
|
T | C | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.250-3479A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912177 | ||||||
| chr2:97912201
|
T | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.250-3503A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912201 | ||||||
| chr2:97912226
|
G | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.250-3528C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912226 | ||||||
| chr2:97912342
|
A | C | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | NA19001.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.250-3644T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912342 | ||||||
| chr2:97912426
|
C | T | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-3728G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912426 | ||||||
| chr2:97912664
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.250-3966A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912664 | ||||||
| chr2:97912889
|
T | C | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.250-4191A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912889 | ||||||
| chr2:97912953
|
C | T | 1 | a0003c0004t0002g0098 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.250-4255G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97912953 | ||||||
| chr2:97913059
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250-4361G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913059 | ||||||
| chr2:97913200
|
T | C | 1 | a0001c0005t0005g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.250-4502A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913200 | ||||||
| chr2:97913296
|
A | G | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-4598T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913296 | ||||||
| chr2:97913306
|
A | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-4608T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913306 | ||||||
| chr2:97913509
|
C | T | 1 | a0001c0001t0005g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.250-4811G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913509 | ||||||
| chr2:97913603
|
G | A | 1 | a0001c0002t0001g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.250-4905C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913603 | ||||||
| chr2:97913803
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-5105G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97913803 | ||||||
| chr2:97914236
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-5538A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97914236 | ||||||
| chr2:97914345
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.250-5647C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97914345 | ||||||
| chr2:97914601
|
T | A | 2 | a0001c0010t0005g0079a0001c0010t0005g0080 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.250-5903A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97914601 | ||||||
| chr2:97914992
|
T | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.250-6294A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97914992 | ||||||
| chr2:97915163
|
C | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.250-6465G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915163 | ||||||
| chr2:97915171
|
CCT | C | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-6475_250-6474d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915171 | ||||||
| chr2:97915254
|
T | C | 1 | a0001c0001t0003g0066 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.250-6556A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915254 | ||||||
| chr2:97915320
|
TTTTG | T | 4 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-6626_250-6623d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915320 | ||||||
| chr2:97915582
|
T | C | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250-6884A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915582 | ||||||
| chr2:97915684
|
A | G | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-6986T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915684 | ||||||
| chr2:97915798
|
A | C | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.250-7100T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915798 | ||||||
| chr2:97915975
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250-7277C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97915975 | ||||||
| chr2:97916194
|
G | C | 2 | a0001c0001t0004g0166a0001c0001t0008g0167 | 2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.250-7496C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97916194 | ||||||
| chr2:97916289
|
T | C | 1 | a0002c0003t0004g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.250-7591A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97916289 | ||||||
| chr2:97916341
|
G | A | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.250-7643C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97916341 | ||||||
| chr2:97916579
|
G | T | 1 | a0001c0005t0005g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250-7881C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97916579 | ||||||
| chr2:97916676
|
A | G | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-7978T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97916676 | ||||||
| chr2:97917239
|
T | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.250-8541A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917239 | ||||||
| chr2:97917289
|
T | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.250-8591A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917289 | ||||||
| chr2:97917298
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-8600C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917298 | ||||||
| chr2:97917602
|
C | T | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.250-8904G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917602 | ||||||
| chr2:97917645
|
T | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-8947A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917645 | ||||||
| chr2:97917762
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.250-9064C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917762 | ||||||
| chr2:97917807
|
T | C | 3 | a0002c0003t0004g0190a0002c0003t0004g0191a0002c0003t0004g0192 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.250-9109A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917807 | ||||||
| chr2:97917862
|
A | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.250-9164T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917862 | ||||||
| chr2:97917895
|
G | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-9197C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917895 | ||||||
| chr2:97917928
|
A | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-9230T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917928 | ||||||
| chr2:97917941
|
T | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-9243A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917941 | ||||||
| chr2:97917949
|
T | C | 96 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(93): Show | 96 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.250-9251A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97917949 | ||||||
| chr2:97918068
|
C | T | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.249+9358G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918068 | ||||||
| chr2:97918240
|
G | A | 1 | a0001c0001t0003g0059 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.249+9186C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918240 | ||||||
| chr2:97918271
|
C | T | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+9155G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918271 | ||||||
| chr2:97918281
|
G | A | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.249+9145C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918281 | ||||||
| chr2:97918538
|
T | C | 1 | a0001c0001t0006g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.249+8888A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918538 | ||||||
| chr2:97918552
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.249+8874G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918552 | ||||||
| chr2:97918570
|
C | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+8856G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918570 | ||||||
| chr2:97918624
|
A | G | 5 | a0001c0001t0003g0062a0001c0001t0003g0124a0001c0022t0003g0123others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+8802T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918624 | ||||||
| chr2:97918850
|
A | AAAC | 210 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.249+8573_249+8575d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97918850 | ||||||
| chr2:97919151
|
CA | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+8274delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97919151 | ||||||
| chr2:97919897
|
T | C | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+7529A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97919897 | ||||||
| chr2:97920015
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.249+7411G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920015 | ||||||
| chr2:97920970
|
A | AGT | 97 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.249+6454_249+6455d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
A | AGTGT | 41 | a0001c0001t0002g0014a0001c0001t0003g0032a0001c0001t0003g0033others(38): Show | 41 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.249+6452_249+6455d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
A | AGTGTGT | 5 | a0001c0001t0003g0043a0001c0001t0003g0057a0001c0001t0003g0059others(2): Show | 5 | HG00280.hp2 HG01934.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+6450_249+6455d others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0003g0124a0001c0007t0003g0034a0001c0007t0003g0035others(1): Show | 4 | HG02818.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+6448_249+6455d others(10): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
A | AGTGTGTG others(3): Show |
2 | a0001c0007t0003g0036a0001c0007t0003g0037 | 2 | HG01261.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.249+6446_249+6455d others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
AGT | A | 10 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(7): Show | 10 | HG03471.hp2 NA18965.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+6454_249+6455d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
AGTGT | A | 52 | a0001c0001t0007g0022a0001c0002t0001g0272a0001c0005t0005g0130others(49): Show | 52 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.249+6452_249+6455d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97920970
|
AGTGTGT | A | 3 | a0002c0003t0004g0199a0005c0006t0005g0131a0005c0006t0005g0142 | 3 | HG01175.hp2 HG01515.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.249+6450_249+6455d others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97920970 | ||||||
| chr2:97921083
|
T | C | 2 | a0001c0012t0001g0233a0001c0012t0001g0235 | 2 | HG02735.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.249+6343A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921083 | ||||||
| chr2:97921127
|
G | A | 2 | a0001c0002t0001g0258a0001c0002t0001g0260 | 2 | HG00423.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.249+6299C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921127 | ||||||
| chr2:97921642
|
C | G | 186 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.249+5784G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921642 | ||||||
| chr2:97921731
|
C | G | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.249+5695G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921731 | ||||||
| chr2:97921893
|
G | T | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.249+5533C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921893 | ||||||
| chr2:97921956
|
C | G | 1 | a0001c0002t0001g0208 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.249+5470G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921956 | ||||||
| chr2:97921970
|
A | G | 17 | a0002c0003t0004g0176a0002c0003t0004g0177a0002c0003t0004g0179others(14): Show | 17 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+5456T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921970 | ||||||
| chr2:97921997
|
T | C | 1 | a0001c0002t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.249+5429A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97921997 | ||||||
| chr2:97922242
|
C | T | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+5184G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97922242 | ||||||
| chr2:97922379
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0009 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.249+5047T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97922379 | ||||||
| chr2:97922586
|
T | C | 2 | a0003c0004t0002g0106a0003c0004t0002g0107 | 2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.249+4840A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97922586 | ||||||
| chr2:97922916
|
A | T | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.249+4510T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97922916 | ||||||
| chr2:97922931
|
G | A | 2 | a0001c0002t0001g0219a0001c0002t0001g0225 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.249+4495C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97922931 | ||||||
| chr2:97923125
|
C | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.249+4301G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923125 | ||||||
| chr2:97923221
|
A | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+4205T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923221 | ||||||
| chr2:97923306
|
TAA | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4118_249+4119d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923306 | ||||||
| chr2:97923311
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4115G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923311 | ||||||
| chr2:97923312
|
A | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4114T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923312 | ||||||
| chr2:97923313
|
G | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4113C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923313 | ||||||
| chr2:97923314
|
G | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4112C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923314 | ||||||
| chr2:97923316
|
C | T | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4110G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923316 | ||||||
| chr2:97923322
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4104C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923322 | ||||||
| chr2:97923379
|
TTGGGAGG others(4): Show |
T | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.249+4036_249+4046d others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923379 | ||||||
| chr2:97923619
|
C | CT | 11 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+3806dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923619 | ||||||
| chr2:97923623
|
TTTTTTAA others(3): Show |
T | 3 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070 | 3 | HG01884.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.249+3793_249+3802d others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923623 | ||||||
| chr2:97923627
|
T | A | 2 | a0003c0004t0002g0096a0003c0004t0002g0104 | 2 | HG00597.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.249+3799A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.249+3799A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
T | TAA | 10 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(7): Show | 10 | HG02451.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+3798_249+3799i others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
T | TAAA | 5 | a0001c0005t0005g0140a0003c0004t0002g0098a0003c0004t0002g0099others(2): Show | 5 | HG02572.hp2 NA18939.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+3798_249+3799i others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
T | TAAAA | 20 | a0001c0001t0002g0121a0003c0004t0002g0097a0003c0004t0002g0100others(17): Show | 20 | HG00544.hp2 HG02129.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.249+3798_249+3799i others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
TTAAAA | T | 29 | a0001c0001t0003g0033a0001c0001t0005g0084a0002c0003t0004g0171others(26): Show | 29 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.249+3794_249+3798d others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
TTAAAAA | T | 45 | a0001c0001t0003g0032a0001c0001t0003g0043a0001c0001t0003g0045others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.249+3793_249+3798d others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923627
|
TTAAAAAA | T | 18 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(15): Show | 18 | HG00099.hp2 HG01069.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+3792_249+3798d others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923627 | ||||||
| chr2:97923628
|
T | A | 46 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(43): Show | 46 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.249+3798A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923628 | ||||||
| chr2:97923628
|
T | TA | 10 | a0001c0001t0004g0147a0001c0001t0006g0158a0001c0002t0001g0213others(7): Show | 10 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+3797dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923628 | ||||||
| chr2:97923628
|
T | TAA | 24 | a0001c0001t0004g0148a0001c0001t0004g0149a0001c0001t0004g0150others(21): Show | 24 | HG01123.hp1 HG01243.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.249+3796_249+3797d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923628 | ||||||
| chr2:97923628
|
T | TTA | 9 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(6): Show | 9 | HG00642.hp1 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+3797_249+3798i others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923628 | ||||||
| chr2:97923628
|
TA | T | 10 | a0001c0002t0001g0204a0001c0002t0001g0208a0001c0002t0001g0216others(7): Show | 10 | HG01070.hp1 HG01169.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.249+3797delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923628 | ||||||
| chr2:97923629
|
A | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0005 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.249+3797T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923629 | ||||||
| chr2:97923635
|
A | AAAAAAAA others(5): Show |
5 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(2): Show | 5 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+3790_249+3791i others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923635 | ||||||
| chr2:97923635
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0007g0021 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.249+3790_249+3791i others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923635 | ||||||
| chr2:97923637
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.249+3788_249+3789i others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923637 | ||||||
| chr2:97923654
|
G | A | 2 | a0001c0010t0005g0079a0001c0010t0005g0080 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.249+3772C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923654 | ||||||
| chr2:97923723
|
A | G | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.249+3703T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923723 | ||||||
| chr2:97923777
|
C | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.249+3649G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923777 | ||||||
| chr2:97923855
|
T | G | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.249+3571A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923855 | ||||||
| chr2:97923937
|
G | A | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.249+3489C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923937 | ||||||
| chr2:97923997
|
G | A | 51 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.249+3429C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97923997 | ||||||
| chr2:97924045
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.249+3381C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924045 | ||||||
| chr2:97924094
|
TAGATTAG | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.249+3325_249+3331d others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924094 | ||||||
| chr2:97924307
|
C | T | 1 | a0003c0004t0002g0118 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.249+3119G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924307 | ||||||
| chr2:97924538
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.249+2888A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924538 | ||||||
| chr2:97924655
|
G | T | 1 | a0002c0003t0004g0183 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.249+2771C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924655 | ||||||
| chr2:97924680
|
T | C | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+2746A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924680 | ||||||
| chr2:97924705
|
C | T | 8 | a0001c0001t0003g0060a0001c0001t0003g0088a0001c0007t0003g0034others(5): Show | 8 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+2721G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924705 | ||||||
| chr2:97924982
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.249+2444G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97924982 | ||||||
| chr2:97925020
|
C | G | 2 | a0001c0010t0005g0079a0001c0010t0005g0080 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.249+2406G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925020 | ||||||
| chr2:97925072
|
A | G | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.249+2354T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925072 | ||||||
| chr2:97925077
|
T | C | 1 | a0003c0004t0002g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.249+2349A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925077 | ||||||
| chr2:97925411
|
A | G | 3 | a0001c0001t0003g0041a0001c0001t0003g0045a0001c0001t0003g0046 | 3 | HG00733.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.249+2015T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925411 | ||||||
| chr2:97925562
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.249+1864G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925562 | ||||||
| chr2:97925714
|
T | C | 2 | a0001c0002t0001g0244a0001c0002t0010g0243 | 2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.249+1712A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925714 | ||||||
| chr2:97925788
|
T | C | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+1638A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925788 | ||||||
| chr2:97925803
|
G | A | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.249+1623C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925803 | ||||||
| chr2:97925886
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+1540C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97925886 | ||||||
| chr2:97926324
|
A | C | 1 | a0001c0001t0003g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.249+1102T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97926324 | ||||||
| chr2:97926402
|
T | G | 1 | a0001c0001t0003g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.249+1024A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97926402 | ||||||
| chr2:97926461
|
A | T | 1 | a0001c0002t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.249+965T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97926461 | ||||||
| chr2:97926590
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+836C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97926590 | ||||||
| chr2:97926656
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.249+770A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97926656 | ||||||
| chr2:97927049
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.249+377C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97927049 | ||||||
| chr2:97927099
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.249+327G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97927099 | ||||||
| chr2:97927115
|
T | G | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.249+311A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97927115 | ||||||
| chr2:97927260
|
C | T | 1 | a0004c0014t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.249+166G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 2/40 | chr2 | 97927260 | ||||||
| chr2:97927595
|
T | C | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-108A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97927595 | ||||||
| chr2:97927723
|
C | A | 1 | a0001c0002t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.188-236G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97927723 | ||||||
| chr2:97928065
|
G | A | 204 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.188-578C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97928065 | ||||||
| chr2:97928315
|
GAGATCAG others(3085): Show |
G | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-3920_188-829de others(1): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97928315 | ||||||
| chr2:97928321
|
A | C | 1 | a0005c0006t0005g0143 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.188-834T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97928321 | ||||||
| chr2:97928739
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.188-1252T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97928739 | ||||||
| chr2:97928833
|
A | G | 1 | a0001c0002t0001g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.188-1346T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97928833 | ||||||
| chr2:97928928
|
A | G | 10 | a0001c0002t0001g0207a0001c0002t0001g0216a0001c0002t0001g0221others(7): Show | 10 | HG02074.hp2 NA18949.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-1441T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97928928 | ||||||
| chr2:97929254
|
G | C | 1 | a0004c0008t0002g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.188-1767C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97929254 | ||||||
| chr2:97929347
|
A | C | 5 | a0001c0001t0003g0089a0001c0001t0004g0153a0001c0001t0004g0154others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-1860T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97929347 | ||||||
| chr2:97929378
|
C | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-1891G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97929378 | ||||||
| chr2:97929743
|
A | T | 1 | a0002c0003t0004g0197 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.188-2256T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97929743 | ||||||
| chr2:97930039
|
T | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188-2552A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930039 | ||||||
| chr2:97930084
|
G | C | 1 | a0001c0002t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.188-2597C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930084 | ||||||
| chr2:97930130
|
AC | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-2644delG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930130 | ||||||
| chr2:97930311
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-2824A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930311 | ||||||
| chr2:97930507
|
A | G | 3 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0009g0262 | 3 | HG00423.hp2 NA19072.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.188-3020T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930507 | ||||||
| chr2:97930606
|
AT | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-3120delA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930606 | ||||||
| chr2:97930629
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-3142A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930629 | ||||||
| chr2:97930950
|
T | TC | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-3464dupG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97930950 | ||||||
| chr2:97931173
|
C | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.188-3686G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97931173 | ||||||
| chr2:97931566
|
C | T | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-4079G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97931566 | ||||||
| chr2:97931659
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-4172G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97931659 | ||||||
| chr2:97931733
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.188-4246A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97931733 | ||||||
| chr2:97931750
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-4263C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97931750 | ||||||
| chr2:97932019
|
CATAAG | C | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-4537_188-4533d others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932019 | ||||||
| chr2:97932118
|
G | T | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-4631C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932118 | ||||||
| chr2:97932141
|
TA | T | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(84): Show | 87 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.188-4655delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932141 | ||||||
| chr2:97932395
|
G | A | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.188-4908C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932395 | ||||||
| chr2:97932544
|
C | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-5057G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932544 | ||||||
| chr2:97932563
|
G | C | 1 | a0002c0003t0004g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.188-5076C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932563 | ||||||
| chr2:97932664
|
T | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188-5177A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932664 | ||||||
| chr2:97932827
|
A | G | 1 | a0001c0001t0003g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.188-5340T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932827 | ||||||
| chr2:97932841
|
A | AAT | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-5356_188-5355d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932841 | ||||||
| chr2:97932847
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-5360G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932847 | ||||||
| chr2:97932848
|
T | TTATCTGT others(21): Show |
27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-5362_188-5361i others(30): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932848 | ||||||
| chr2:97932849
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-5362C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932849 | ||||||
| chr2:97932869
|
T | C | 2 | a0001c0001t0005g0083a0001c0001t0005g0086 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.188-5382A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97932869 | ||||||
| chr2:97933036
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-5549C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97933036 | ||||||
| chr2:97933191
|
C | T | 1 | a0002c0003t0004g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.188-5704G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97933191 | ||||||
| chr2:97933589
|
T | A | 1 | a0001c0001t0006g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.188-6102A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97933589 | ||||||
| chr2:97933780
|
C | G | 1 | a0001c0002t0001g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.188-6293G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97933780 | ||||||
| chr2:97933794
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.188-6307T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97933794 | ||||||
| chr2:97933897
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-6410G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97933897 | ||||||
| chr2:97934160
|
A | C | 1 | a0001c0002t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.188-6673T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934160 | ||||||
| chr2:97934172
|
T | G | 1 | a0002c0003t0004g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.188-6685A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934172 | ||||||
| chr2:97934273
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-6786G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934273 | ||||||
| chr2:97934535
|
A | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-7048T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934535 | ||||||
| chr2:97934599
|
C | T | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188-7112G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934599 | ||||||
| chr2:97934703
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-7216T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934703 | ||||||
| chr2:97934707
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-7220G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934707 | ||||||
| chr2:97934882
|
T | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188-7395A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934882 | ||||||
| chr2:97934993
|
G | GA | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.188-7507dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97934993 | ||||||
| chr2:97935050
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-7563G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935050 | ||||||
| chr2:97935307
|
T | C | 1 | a0001c0002t0001g0225 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.188-7820A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935307 | ||||||
| chr2:97935386
|
A | G | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.188-7899T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935386 | ||||||
| chr2:97935629
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0012 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.188-8142A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935629 | ||||||
| chr2:97935660
|
G | GA | 7 | a0001c0002t0001g0237a0001c0002t0001g0238a0001c0002t0001g0239others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-8174dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935660 | ||||||
| chr2:97935691
|
A | C | 1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.188-8204T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935691 | ||||||
| chr2:97935707
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188-8220C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935707 | ||||||
| chr2:97935808
|
G | C | 32 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.188-8321C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935808 | ||||||
| chr2:97935821
|
C | A | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-8334G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935821 | ||||||
| chr2:97935836
|
C | G | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.188-8349G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97935836 | ||||||
| chr2:97936222
|
T | C | 2 | a0001c0001t0005g0081a0001c0001t0005g0082 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.188-8735A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97936222 | ||||||
| chr2:97936691
|
T | G | 1 | a0001c0002t0001g0210 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.188-9204A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97936691 | ||||||
| chr2:97937108
|
C | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-9621G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937108 | ||||||
| chr2:97937165
|
T | C | 1 | a0001c0002t0001g0242 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.188-9678A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937165 | ||||||
| chr2:97937189
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-9702G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937189 | ||||||
| chr2:97937206
|
A | G | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.188-9719T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937206 | ||||||
| chr2:97937483
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.188-9996A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937483 | ||||||
| chr2:97937500
|
T | C | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.188-10013A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937500 | ||||||
| chr2:97937679
|
C | G | 1 | a0015c0013t0005g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.188-10192G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97937679 | ||||||
| chr2:97938062
|
A | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-10575T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938062 | ||||||
| chr2:97938085
|
T | C | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-10598A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938085 | ||||||
| chr2:97938095
|
C | G | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-10608G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938095 | ||||||
| chr2:97938158
|
G | C | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.188-10671C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938158 | ||||||
| chr2:97938171
|
T | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-10684A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938171 | ||||||
| chr2:97938237
|
T | C | 1 | a0002c0003t0004g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.188-10750A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938237 | ||||||
| chr2:97938361
|
A | C | 79 | a0001c0001t0002g0121a0001c0001t0003g0032a0001c0001t0003g0033others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.188-10874T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938361 | ||||||
| chr2:97938483
|
C | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.188-10996G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938483 | ||||||
| chr2:97938661
|
G | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-11174C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938661 | ||||||
| chr2:97938682
|
T | C | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-11195A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938682 | ||||||
| chr2:97938791
|
C | T | 9 | a0003c0004t0002g0108a0003c0004t0002g0109a0003c0004t0002g0110others(6): Show | 9 | HG00544.hp2 HG02602.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-11304G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938791 | ||||||
| chr2:97938905
|
G | C | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-11418C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938905 | ||||||
| chr2:97938942
|
G | A | 1 | a0001c0001t0004g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.188-11455C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97938942 | ||||||
| chr2:97939097
|
A | C | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.188-11610T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939097 | ||||||
| chr2:97939174
|
A | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-11687T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939174 | ||||||
| chr2:97939321
|
G | A | 1 | a0001c0001t0003g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.188-11834C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939321 | ||||||
| chr2:97939341
|
A | G | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.188-11854T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939341 | ||||||
| chr2:97939476
|
A | C | 1 | a0001c0002t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-11989T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939476 | ||||||
| chr2:97939562
|
C | T | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-12075G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939562 | ||||||
| chr2:97939635
|
A | G | 1 | a0001c0002t0001g0264 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.188-12148T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939635 | ||||||
| chr2:97939660
|
C | T | 1 | a0001c0001t0003g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-12173G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939660 | ||||||
| chr2:97939666
|
C | T | 3 | a0002c0009t0004g0182a0002c0009t0004g0187a0002c0009t0004g0188 | 3 | HG01123.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.188-12179G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939666 | ||||||
| chr2:97939726
|
AG | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-12240delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939726 | ||||||
| chr2:97939758
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-12271C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939758 | ||||||
| chr2:97939866
|
A | G | 1 | a0001c0002t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.188-12379T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97939866 | ||||||
| chr2:97940074
|
T | C | 1 | a0001c0001t0003g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.188-12587A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940074 | ||||||
| chr2:97940089
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.188-12602T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940089 | ||||||
| chr2:97940151
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-12664A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940151 | ||||||
| chr2:97940583
|
C | T | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188-13096G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940583 | ||||||
| chr2:97940584
|
G | A | 1 | a0010c0018t0003g0063 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.188-13097C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940584 | ||||||
| chr2:97940635
|
C | T | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.188-13148G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940635 | ||||||
| chr2:97940636
|
G | A | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.188-13149C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940636 | ||||||
| chr2:97940788
|
G | A | 1 | a0001c0001t0003g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.188-13301C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940788 | ||||||
| chr2:97940796
|
C | G | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-13309G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940796 | ||||||
| chr2:97940880
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-13393A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940880 | ||||||
| chr2:97940892
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.188-13405A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940892 | ||||||
| chr2:97940896
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-13409C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940896 | ||||||
| chr2:97940902
|
A | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-13415T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940902 | ||||||
| chr2:97940911
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-13424G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940911 | ||||||
| chr2:97940970
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-13483G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97940970 | ||||||
| chr2:97941102
|
C | T | 1 | a0001c0002t0001g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.188-13615G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941102 | ||||||
| chr2:97941112
|
G | T | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.188-13625C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941112 | ||||||
| chr2:97941267
|
C | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-13780G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941267 | ||||||
| chr2:97941325
|
A | C | 1 | a0001c0002t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-13838T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941325 | ||||||
| chr2:97941362
|
A | ATAAAAAC others(1): Show |
3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.188-13883_188-1387 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941362 | ||||||
| chr2:97941583
|
A | T | 2 | a0001c0002t0001g0251a0001c0002t0001g0257 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.188-14096T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941583 | ||||||
| chr2:97941601
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.188-14114G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941601 | ||||||
| chr2:97941660
|
C | T | 9 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-14173G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941660 | ||||||
| chr2:97941826
|
T | C | 9 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-14339A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941826 | ||||||
| chr2:97941914
|
G | T | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.188-14427C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941914 | ||||||
| chr2:97941982
|
C | T | 11 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(8): Show | 11 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-14495G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941982 | ||||||
| chr2:97941994
|
T | C | 9 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(6): Show | 9 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-14507A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97941994 | ||||||
| chr2:97942200
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-14713A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942200 | ||||||
| chr2:97942201
|
C | T | 1 | a0001c0024t0001g0263 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.188-14714G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942201 | ||||||
| chr2:97942205
|
C | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-14718G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942205 | ||||||
| chr2:97942339
|
G | T | 1 | a0001c0002t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.188-14852C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942339 | ||||||
| chr2:97942346
|
G | T | 5 | a0002c0003t0004g0183a0002c0003t0004g0184a0002c0003t0004g0185others(2): Show | 5 | HG00642.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-14859C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942346 | ||||||
| chr2:97942477
|
TA | T | 185 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(182): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.188-14991delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942477 | ||||||
| chr2:97942477
|
TAA | T | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-14992_188-1499 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942477 | ||||||
| chr2:97942479
|
A | T | 1 | a0001c0001t0006g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.188-14992T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942479 | ||||||
| chr2:97942492
|
C | CA | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(18): Show | 21 | HG00597.hp1 HG01884.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.188-15006dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942492 | ||||||
| chr2:97942499
|
AAAG | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-15015_188-1501 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942499 | ||||||
| chr2:97942506
|
A | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-15019T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942506 | ||||||
| chr2:97942507
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-15020C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942507 | ||||||
| chr2:97942633
|
GAACA | G | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-15150_188-1514 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942633 | ||||||
| chr2:97942949
|
C | A | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.188-15462G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942949 | ||||||
| chr2:97942998
|
G | GA | 4 | a0001c0002t0001g0237a0001c0002t0001g0240a0001c0002t0001g0241others(1): Show | 4 | HG01496.hp1 HG01993.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-15512dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942998 | ||||||
| chr2:97942998
|
G | GAAAAGAA others(4): Show |
1 | a0001c0002t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.188-15512_188-1551 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942998 | ||||||
| chr2:97942998
|
G | GAAAAGAA others(9): Show |
1 | a0001c0002t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.188-15512_188-1551 others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97942998 | ||||||
| chr2:97943007
|
G | GA | 10 | a0001c0002t0001g0218a0001c0002t0001g0237a0001c0002t0001g0238others(7): Show | 10 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-15521dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943007 | ||||||
| chr2:97943007
|
GAAAGAAA others(18): Show |
G | 13 | a0001c0001t0004g0155a0001c0001t0006g0156a0001c0001t0006g0157others(10): Show | 13 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-15545_188-1552 others(29): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943007 | ||||||
| chr2:97943012
|
AAAAGAAA others(22): Show |
A | 11 | a0001c0001t0004g0149a0001c0001t0004g0153a0001c0001t0006g0160others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.188-15554_188-1552 others(33): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943012 | ||||||
| chr2:97943012
|
AAAAGAAA others(26): Show |
A | 6 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0006g0161others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-15558_188-1552 others(37): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943012 | ||||||
| chr2:97943012
|
AAAAGAAA others(30): Show |
A | 14 | a0001c0001t0004g0166a0001c0001t0008g0167a0002c0003t0004g0172others(11): Show | 14 | HG01255.hp1 HG01943.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.188-15562_188-1552 others(41): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943012 | ||||||
| chr2:97943012
|
AAAAGAAA others(34): Show |
A | 7 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0007g0017others(4): Show | 7 | NA18951.hp2 NA18965.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-15566_188-1552 others(45): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943012 | ||||||
| chr2:97943012
|
AAAAGAAA others(38): Show |
A | 2 | a0002c0003t0004g0178a0003c0004t0002g0104 | 2 | HG00597.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.188-15570_188-1552 others(49): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943012 | ||||||
| chr2:97943016
|
GA | G | 39 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0121others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.188-15530delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943016 | ||||||
| chr2:97943016
|
GAAAAGA | G | 23 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0125others(20): Show | 23 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.188-15535_188-1553 others(10): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943016 | ||||||
| chr2:97943016
|
GAAAAGAA others(4): Show |
G | 8 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0012others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15540_188-1553 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943016 | ||||||
| chr2:97943016
|
GAAAAGAA others(9): Show |
G | 62 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.188-15545_188-1553 others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943016 | ||||||
| chr2:97943016
|
GAAAAGAA others(14): Show |
G | 7 | a0001c0001t0004g0154a0001c0001t0006g0158a0001c0001t0006g0159others(4): Show | 7 | HG01192.hp1 HG01978.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-15550_188-1553 others(25): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943016 | ||||||
| chr2:97943017
|
A | AAAGAAAA others(1): Show |
6 | a0001c0001t0005g0083a0001c0001t0005g0086a0001c0005t0005g0130others(3): Show | 6 | HG02109.hp2 HG02922.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-15531_188-1553 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943017 | ||||||
| chr2:97943019
|
AAGAAAAG others(10): Show |
A | 3 | a0001c0001t0004g0168a0001c0001t0006g0152a0001c0001t0006g0163 | 3 | HG03098.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.188-15549_188-1553 others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943019 | ||||||
| chr2:97943022
|
AAAAGAAA others(16): Show |
A | 9 | a0001c0001t0002g0121a0003c0004t0002g0108a0003c0004t0002g0109others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-15558_188-1553 others(27): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943022 | ||||||
| chr2:97943022
|
AAAAGAAA others(20): Show |
A | 5 | a0003c0004t0002g0110a0005c0006t0005g0131a0005c0006t0005g0138others(2): Show | 5 | HG00544.hp2 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-15562_188-1553 others(31): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943022 | ||||||
| chr2:97943022
|
AAAAGAAA others(24): Show |
A | 6 | a0001c0001t0007g0020a0001c0001t0007g0021a0001c0001t0007g0022others(3): Show | 6 | HG00597.hp1 NA18612.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-15566_188-1553 others(35): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943022 | ||||||
| chr2:97943022
|
AAAAGAAA others(28): Show |
A | 1 | a0003c0004t0002g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.188-15570_188-1553 others(39): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943022 | ||||||
| chr2:97943026
|
GA | G | 14 | a0001c0001t0002g0004a0001c0001t0005g0025a0001c0001t0005g0078others(11): Show | 14 | HG00099.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-15540delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943026 | ||||||
| chr2:97943027
|
A | AAAG | 5 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0085others(2): Show | 5 | HG02976.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-15541_188-1554 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943027
|
A | G | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.188-15540T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943027
|
AAAAGAAA others(7): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.188-15554_188-1554 others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943027
|
AAAAGAAA others(15): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.188-15562_188-1554 others(26): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943027
|
AAAAGAAA others(19): Show |
A | 1 | a0001c0027t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.188-15566_188-1554 others(30): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943027
|
AAAAGAAA others(23): Show |
A | 4 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-15570_188-1554 others(34): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943027
|
AAAAGAAA others(27): Show |
A | 1 | a0001c0026t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.188-15574_188-1554 others(38): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943027 | ||||||
| chr2:97943031
|
G | A | 9 | a0001c0001t0002g0005a0001c0001t0005g0082a0001c0001t0005g0083others(6): Show | 9 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-15544C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943031 | ||||||
| chr2:97943031
|
GA | G | 19 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0125others(16): Show | 19 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-15545delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943031 | ||||||
| chr2:97943032
|
A | G | 7 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0085others(4): Show | 7 | HG02976.hp2 HG03471.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-15545T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943032 | ||||||
| chr2:97943032
|
AAAAGAAA others(22): Show |
A | 2 | a0001c0001t0005g0025a0001c0010t0005g0080 | 2 | HG00099.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.188-15574_188-1554 others(33): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943032 | ||||||
| chr2:97943033
|
A | G | 2 | a0001c0001t0002g0005a0001c0005t0005g0139 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188-15546T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943033 | ||||||
| chr2:97943034
|
AAG | A | 9 | a0001c0001t0002g0004a0001c0002t0001g0268a0001c0005t0005g0144others(6): Show | 9 | HG01243.hp1 HG01496.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-15549_188-1554 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943034 | ||||||
| chr2:97943036
|
G | A | 2 | a0001c0001t0002g0005a0001c0005t0005g0139 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188-15549C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943036 | ||||||
| chr2:97943036
|
GA | G | 8 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0012others(5): Show | 8 | HG00544.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15550delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943036 | ||||||
| chr2:97943037
|
A | AAAAG | 7 | a0001c0002t0001g0206a0001c0002t0001g0214a0001c0002t0001g0220others(4): Show | 7 | HG01934.hp1 HG02280.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-15554_188-1555 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(7): Show |
1 | a0001c0002t0001g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.188-15551_188-1555 others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(12): Show |
1 | a0001c0002t0001g0222 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.188-15551_188-1555 others(23): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(11): Show |
1 | a0001c0012t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.188-15551_188-1555 others(22): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(15): Show |
1 | a0001c0002t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.188-15551_188-1555 others(26): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(19): Show |
2 | a0001c0002t0001g0247a0001c0002t0001g0259 | 2 | NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.188-15551_188-1555 others(30): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(6): Show |
1 | a0009c0025t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.188-15551_188-1555 others(17): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(10): Show |
1 | a0001c0002t0001g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.188-15551_188-1555 others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(14): Show |
1 | a0013c0028t0001g0246 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.188-15551_188-1555 others(25): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(1): Show |
7 | a0001c0002t0001g0215a0001c0002t0001g0221a0001c0002t0001g0228others(4): Show | 7 | HG00423.hp2 NA18950.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-15558_188-1555 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(5): Show |
4 | a0001c0002t0001g0211a0001c0002t0001g0213a0001c0002t0001g0216others(1): Show | 4 | HG01169.hp2 HG03516.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15562_188-1555 others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(9): Show |
6 | a0001c0002t0001g0219a0001c0002t0001g0226a0001c0002t0001g0245others(3): Show | 6 | HG02083.hp1 HG03239.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-15566_188-1555 others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(13): Show |
1 | a0001c0002t0001g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.188-15570_188-1555 others(24): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAAGAAA others(17): Show |
5 | a0001c0002t0001g0210a0001c0002t0001g0225a0001c0002t0001g0250others(2): Show | 5 | HG02074.hp2 HG02129.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-15574_188-1555 others(28): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAGAAAG others(8): Show |
1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.188-15551_188-1555 others(19): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | AAAGAAAG others(16): Show |
2 | a0001c0002t0001g0218a0001c0002t0001g0276 | 2 | HG03710.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.188-15551_188-1555 others(27): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
A | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0004g0168others(11): Show | 14 | HG01243.hp1 HG01496.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-15550T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943037
|
AAAAG | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0002t0001g0207others(10): Show | 13 | HG00642.hp1 HG01257.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-15554_188-1555 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943037 | ||||||
| chr2:97943040
|
A | G | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0005g0087others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-15553T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943040 | ||||||
| chr2:97943041
|
G | A | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0005g0087others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-15554C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943041 | ||||||
| chr2:97943041
|
G | GA | 6 | a0001c0002t0001g0237a0001c0002t0001g0239a0001c0002t0001g0240others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-15555dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943041 | ||||||
| chr2:97943044
|
A | AAGAAAAG others(5): Show |
1 | a0001c0012t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.188-15558_188-1555 others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943044 | ||||||
| chr2:97943045
|
G | A | 2 | a0001c0002t0001g0238a0001c0012t0001g0233 | 2 | HG01975.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.188-15558C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943045 | ||||||
| chr2:97943045
|
G | GA | 4 | a0001c0001t0002g0127a0001c0001t0003g0124a0001c0001t0005g0085others(1): Show | 4 | HG02486.hp1 HG02976.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-15559dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943045 | ||||||
| chr2:97943046
|
AAAG | A | 18 | a0001c0001t0003g0043a0001c0001t0003g0055a0001c0001t0003g0062others(15): Show | 18 | HG00423.hp1 HG01261.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.188-15562_188-1556 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943046 | ||||||
| chr2:97943046
|
AAAGAAAG | A | 33 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-15566_188-1556 others(11): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943046 | ||||||
| chr2:97943046
|
AAAGAAAG others(4): Show |
A | 7 | a0001c0001t0002g0128a0001c0001t0003g0066a0001c0001t0003g0067others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-15570_188-1556 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943046 | ||||||
| chr2:97943046
|
AAAGAAAG others(16): Show |
A | 3 | a0001c0001t0003g0040a0001c0001t0003g0052a0001c0001t0003g0056 | 3 | HG01256.hp1 HG01258.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.188-15582_188-1556 others(27): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943046 | ||||||
| chr2:97943048
|
A | AAG | 3 | a0001c0002t0001g0239a0001c0002t0001g0253a0001c0002t0001g0274 | 3 | HG01070.hp1 HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.188-15562_188-1556 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943048 | ||||||
| chr2:97943048
|
A | AAGAAAAG others(20): Show |
2 | a0001c0002t0001g0240a0001c0002t0001g0241 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.188-15562_188-1556 others(31): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943048 | ||||||
| chr2:97943049
|
G | A | 6 | a0001c0002t0001g0237a0001c0002t0001g0239a0001c0002t0001g0240others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-15562C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943049 | ||||||
| chr2:97943050
|
A | G | 1 | a0001c0002t0001g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.188-15563T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943050 | ||||||
| chr2:97943053
|
G | A | 2 | a0001c0002t0001g0237a0001c0002t0001g0238 | 2 | HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.188-15566C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943053 | ||||||
| chr2:97943054
|
A | G | 1 | a0001c0001t0005g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.188-15567T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943054 | ||||||
| chr2:97943055
|
A | G | 1 | a0001c0002t0001g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.188-15568T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943055 | ||||||
| chr2:97943056
|
A | AAG | 5 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(2): Show | 5 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-15570_188-1556 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943056 | ||||||
| chr2:97943057
|
G | A | 6 | a0001c0002t0001g0237a0001c0002t0001g0239a0001c0002t0001g0240others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-15570C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943057 | ||||||
| chr2:97943058
|
AAAG | A | 14 | a0001c0001t0003g0043a0001c0001t0003g0055a0001c0001t0003g0062others(11): Show | 14 | HG00423.hp1 HG01261.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.188-15574_188-1557 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943058 | ||||||
| chr2:97943060
|
A | G | 1 | a0001c0002t0001g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.188-15573T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943060 | ||||||
| chr2:97943061
|
G | A | 2 | a0001c0002t0001g0237a0001c0002t0001g0238 | 2 | HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.188-15574C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943061 | ||||||
| chr2:97943062
|
AAAG | A | 23 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0041others(20): Show | 23 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.188-15578_188-1557 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943062 | ||||||
| chr2:97943064
|
A | AAG | 5 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(2): Show | 5 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-15578_188-1557 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943064 | ||||||
| chr2:97943065
|
G | A | 5 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(2): Show | 5 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-15578C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943065 | ||||||
| chr2:97943083
|
AAG | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15598_188-1559 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943083 | ||||||
| chr2:97943090
|
A | C | 1 | a0004c0008t0002g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.188-15603T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943090 | ||||||
| chr2:97943094
|
A | C | 4 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15607T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943094 | ||||||
| chr2:97943098
|
A | C | 5 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(2): Show | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-15611T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943098 | ||||||
| chr2:97943101
|
G | GAAAGAAA others(10): Show |
1 | a0001c0011t0001g0248 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.188-15615_188-1561 others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943101 | ||||||
| chr2:97943101
|
G | GCAAGCAA others(3): Show |
1 | a0004c0014t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.188-15615_188-1561 others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943101 | ||||||
| chr2:97943248
|
T | C | 1 | a0001c0001t0004g0148 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.188-15761A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943248 | ||||||
| chr2:97943308
|
T | G | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.188-15821A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943308 | ||||||
| chr2:97943313
|
T | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15826A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943313 | ||||||
| chr2:97943335
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15848G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943335 | ||||||
| chr2:97943540
|
T | G | 1 | a0001c0001t0003g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.188-16053A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943540 | ||||||
| chr2:97943598
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.188-16111G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943598 | ||||||
| chr2:97943679
|
C | A | 6 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0068others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-16192G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943679 | ||||||
| chr2:97943701
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-16214T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943701 | ||||||
| chr2:97943951
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-16464C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943951 | ||||||
| chr2:97943953
|
G | A | 1 | a0002c0003t0004g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.188-16466C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943953 | ||||||
| chr2:97943974
|
T | C | 5 | a0002c0003t0004g0200a0002c0003t0004g0201a0002c0009t0004g0182others(2): Show | 5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-16487A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97943974 | ||||||
| chr2:97944024
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-16537C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944024 | ||||||
| chr2:97944140
|
G | A | 1 | a0001c0001t0003g0059 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.188-16653C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944140 | ||||||
| chr2:97944167
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.188-16680C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944167 | ||||||
| chr2:97944404
|
A | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-16917T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944404 | ||||||
| chr2:97944521
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188-17034C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944521 | ||||||
| chr2:97944600
|
G | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188-17113C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944600 | ||||||
| chr2:97944690
|
C | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-17203G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944690 | ||||||
| chr2:97944838
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-17351C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944838 | ||||||
| chr2:97944884
|
C | T | 72 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.188-17397G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97944884 | ||||||
| chr2:97945116
|
G | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-17629C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97945116 | ||||||
| chr2:97945258
|
A | G | 3 | a0001c0005t0005g0135a0001c0005t0005g0139a0001c0005t0005g0140 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.188-17771T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97945258 | ||||||
| chr2:97945354
|
A | G | 2 | a0003c0004t0002g0119a0003c0004t0002g0120 | 2 | NA18991.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.188-17867T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97945354 | ||||||
| chr2:97945653
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-18166C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97945653 | ||||||
| chr2:97946095
|
G | C | 1 | a0001c0001t0003g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.188-18608C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97946095 | ||||||
| chr2:97946154
|
C | A | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-18667G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97946154 | ||||||
| chr2:97946179
|
CATAT | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-18696_188-1869 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97946179 | ||||||
| chr2:97946683
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-19196C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97946683 | ||||||
| chr2:97946925
|
C | CA | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-19439dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97946925 | ||||||
| chr2:97946935
|
A | C | 2 | a0002c0003t0004g0179a0002c0003t0004g0193 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.188-19448T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97946935 | ||||||
| chr2:97947022
|
G | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-19535C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947022 | ||||||
| chr2:97947079
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-19592A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947079 | ||||||
| chr2:97947195
|
T | C | 283 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.188-19708A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947195 | ||||||
| chr2:97947636
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-20149C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947636 | ||||||
| chr2:97947703
|
G | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-20216C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947703 | ||||||
| chr2:97947779
|
T | C | 1 | a0001c0001t0003g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.188-20292A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947779 | ||||||
| chr2:97947886
|
T | C | 8 | a0001c0001t0005g0078a0001c0001t0005g0081a0001c0001t0005g0082others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-20399A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97947886 | ||||||
| chr2:97948153
|
G | A | 1 | a0001c0002t0001g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.188-20666C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948153 | ||||||
| chr2:97948270
|
G | C | 1 | a0001c0002t0001g0250 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.188-20783C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948270 | ||||||
| chr2:97948426
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-20939G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948426 | ||||||
| chr2:97948503
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-21016C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948503 | ||||||
| chr2:97948652
|
C | CT | 57 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(54): Show | 57 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.188-21166dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948652 | ||||||
| chr2:97948681
|
G | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-21194C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948681 | ||||||
| chr2:97948688
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.188-21201G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948688 | ||||||
| chr2:97948697
|
G | A | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.188-21210C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948697 | ||||||
| chr2:97948758
|
A | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-21271T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948758 | ||||||
| chr2:97948937
|
G | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-21450C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97948937 | ||||||
| chr2:97949027
|
T | C | 1 | a0001c0001t0004g0149 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.188-21540A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949027 | ||||||
| chr2:97949280
|
T | C | 36 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.188-21793A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949280 | ||||||
| chr2:97949298
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-21811A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949298 | ||||||
| chr2:97949396
|
TAGAG | T | 6 | a0001c0002t0001g0207a0001c0002t0001g0221a0001c0002t0001g0222others(3): Show | 6 | HG02074.hp2 NA18966.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-21913_188-2191 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949396 | ||||||
| chr2:97949641
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-22154C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949641 | ||||||
| chr2:97949681
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-22194C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949681 | ||||||
| chr2:97949689
|
G | A | 1 | a0001c0005t0005g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-22202C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949689 | ||||||
| chr2:97949817
|
C | CA | 85 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0121others(82): Show | 85 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.188-22331dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949817 | ||||||
| chr2:97949817
|
C | CAA | 31 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(28): Show | 31 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.188-22332_188-2233 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949817 | ||||||
| chr2:97949817
|
C | CAAA | 56 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.188-22333_188-2233 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949817 | ||||||
| chr2:97949817
|
C | CAAAA | 12 | a0001c0001t0003g0069a0001c0001t0003g0071a0001c0001t0005g0023others(9): Show | 12 | HG01074.hp1 HG01099.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.188-22334_188-2233 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949817 | ||||||
| chr2:97949817
|
CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-22338_188-2233 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949817 | ||||||
| chr2:97949905
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-22418G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97949905 | ||||||
| chr2:97950401
|
G | T | 1 | a0001c0001t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.188-22914C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950401 | ||||||
| chr2:97950561
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-23074C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950561 | ||||||
| chr2:97950580
|
C | G | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-23093G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950580 | ||||||
| chr2:97950652
|
C | T | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-23165G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950652 | ||||||
| chr2:97950899
|
A | G | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-23412T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950899 | ||||||
| chr2:97950905
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.188-23418A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950905 | ||||||
| chr2:97950944
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-23457C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97950944 | ||||||
| chr2:97951180
|
A | C | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.188-23693T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97951180 | ||||||
| chr2:97951304
|
T | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-23817A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97951304 | ||||||
| chr2:97951357
|
G | A | 55 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(52): Show | 55 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.188-23870C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97951357 | ||||||
| chr2:97951444
|
C | T | 10 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0001t0003g0067others(7): Show | 10 | HG00423.hp1 NA18939.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-23957G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97951444 | ||||||
| chr2:97951628
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-24141A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97951628 | ||||||
| chr2:97951944
|
A | G | 1 | a0001c0002t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.188-24457T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97951944 | ||||||
| chr2:97952025
|
C | T | 2 | a0001c0002t0001g0244a0001c0002t0010g0243 | 2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.188-24538G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952025 | ||||||
| chr2:97952157
|
C | CA | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-24671dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952157 | ||||||
| chr2:97952197
|
G | T | 6 | a0001c0007t0003g0034a0001c0007t0003g0035a0001c0007t0003g0036others(3): Show | 6 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-24710C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952197 | ||||||
| chr2:97952331
|
C | G | 1 | a0004c0014t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.188-24844G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952331 | ||||||
| chr2:97952331
|
C | T | 2 | a0001c0010t0005g0079a0001c0010t0005g0080 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.188-24844G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952331 | ||||||
| chr2:97952372
|
A | C | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-24885T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952372 | ||||||
| chr2:97952631
|
C | A | 1 | a0002c0003t0004g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.188-25144G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952631 | ||||||
| chr2:97952642
|
C | G | 1 | a0001c0001t0005g0083 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.188-25155G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952642 | ||||||
| chr2:97952648
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-25161C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952648 | ||||||
| chr2:97952956
|
C | A | 12 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(9): Show | 12 | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.188-25469G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97952956 | ||||||
| chr2:97953031
|
G | A | 1 | a0001c0001t0004g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.188-25544C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953031 | ||||||
| chr2:97953080
|
G | A | 1 | a0001c0001t0007g0021 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.188-25593C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953080 | ||||||
| chr2:97953128
|
A | G | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-25641T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953128 | ||||||
| chr2:97953156
|
T | C | 1 | a0001c0002t0001g0250 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.188-25669A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953156 | ||||||
| chr2:97953421
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.188-25934T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953421 | ||||||
| chr2:97953480
|
A | G | 1 | a0001c0002t0001g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.188-25993T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953480 | ||||||
| chr2:97953493
|
G | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.188-26006C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953493 | ||||||
| chr2:97953583
|
T | C | 1 | a0001c0001t0008g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.188-26096A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953583 | ||||||
| chr2:97953648
|
T | C | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.188-26161A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953648 | ||||||
| chr2:97953755
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.188-26268C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953755 | ||||||
| chr2:97953924
|
T | C | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.188-26437A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953924 | ||||||
| chr2:97953929
|
A | G | 1 | a0001c0001t0005g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.188-26442T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97953929 | ||||||
| chr2:97954100
|
T | A | 1 | a0001c0001t0006g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.188-26613A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954100 | ||||||
| chr2:97954183
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.188-26696A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954183 | ||||||
| chr2:97954378
|
T | C | 1 | a0003c0004t0002g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.188-26891A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954378 | ||||||
| chr2:97954536
|
G | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-27049C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954536 | ||||||
| chr2:97954621
|
A | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-27134T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954621 | ||||||
| chr2:97954621
|
A | G | 82 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-27134T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954621 | ||||||
| chr2:97954667
|
G | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(13): Show | 16 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-27180C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954667 | ||||||
| chr2:97954730
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-27243G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954730 | ||||||
| chr2:97954731
|
G | A | 1 | a0001c0012t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.188-27244C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954731 | ||||||
| chr2:97954742
|
G | A | 1 | a0001c0002t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.188-27255C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954742 | ||||||
| chr2:97954768
|
T | C | 2 | a0003c0004t0002g0106a0003c0004t0002g0107 | 2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.188-27281A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954768 | ||||||
| chr2:97954806
|
C | CA | 88 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 88 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.188-27320dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954806 | ||||||
| chr2:97954806
|
C | CAA | 6 | a0001c0001t0001g0202a0001c0001t0002g0013a0001c0001t0004g0153others(3): Show | 6 | HG00280.hp1 HG01346.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-27321_188-2732 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954806 | ||||||
| chr2:97954914
|
A | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-27427T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97954914 | ||||||
| chr2:97955138
|
G | A | 1 | a0002c0003t0004g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.188-27651C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955138 | ||||||
| chr2:97955358
|
C | T | 5 | a0005c0006t0005g0131a0005c0006t0005g0136a0005c0006t0005g0137others(2): Show | 5 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-27871G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955358 | ||||||
| chr2:97955385
|
TA | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-27899delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955385 | ||||||
| chr2:97955630
|
A | G | 2 | a0002c0003t0004g0179a0002c0003t0004g0193 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.188-28143T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955630 | ||||||
| chr2:97955766
|
A | G | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.188-28279T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955766 | ||||||
| chr2:97955895
|
A | G | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.188-28408T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955895 | ||||||
| chr2:97955967
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.188-28480G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97955967 | ||||||
| chr2:97956030
|
A | C | 1 | a0002c0003t0004g0175 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.188-28543T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956030 | ||||||
| chr2:97956082
|
T | C | 1 | a0001c0001t0004g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.188-28595A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956082 | ||||||
| chr2:97956131
|
A | T | 1 | a0001c0005t0005g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.188-28644T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956131 | ||||||
| chr2:97956166
|
T | C | 1 | a0001c0001t0003g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.188-28679A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956166 | ||||||
| chr2:97956692
|
T | TA | 91 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.188-29206_188-2920 others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956692 | ||||||
| chr2:97956857
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.188-29370C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956857 | ||||||
| chr2:97956865
|
G | A | 9 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0268others(6): Show | 9 | HG00544.hp1 HG01192.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-29378C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97956865 | ||||||
| chr2:97957081
|
C | A | 283 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.188-29594G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957081 | ||||||
| chr2:97957096
|
C | CA | 73 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.188-29610dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957096 | ||||||
| chr2:97957112
|
A | T | 86 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(83): Show | 86 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.188-29625T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957112 | ||||||
| chr2:97957144
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-29657C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957144 | ||||||
| chr2:97957339
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.188-29852A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957339 | ||||||
| chr2:97957548
|
G | A | 1 | a0001c0002t0001g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.188-30061C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957548 | ||||||
| chr2:97957722
|
A | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-30235T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957722 | ||||||
| chr2:97957759
|
C | A | 1 | a0001c0001t0005g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.188-30272G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957759 | ||||||
| chr2:97957797
|
A | G | 1 | a0001c0002t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.188-30310T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97957797 | ||||||
| chr2:97958017
|
C | T | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188-30530G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97958017 | ||||||
| chr2:97958191
|
G | A | 1 | a0002c0003t0004g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.188-30704C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97958191 | ||||||
| chr2:97958269
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-30782G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97958269 | ||||||
| chr2:97959068
|
T | C | 65 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.188-31581A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959068 | ||||||
| chr2:97959211
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-31724C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959211 | ||||||
| chr2:97959265
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.188-31778C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959265 | ||||||
| chr2:97959267
|
T | C | 4 | a0003c0004t0002g0113a0003c0004t0002g0114a0003c0004t0002g0115others(1): Show | 4 | HG02602.hp2 NA18982.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-31780A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959267 | ||||||
| chr2:97959428
|
G | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-31941C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959428 | ||||||
| chr2:97959482
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-31995A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959482 | ||||||
| chr2:97959558
|
C | CGT | 73 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.188-32073_188-3207 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959558 | ||||||
| chr2:97959820
|
T | G | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-32333A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97959820 | ||||||
| chr2:97960154
|
A | ATAAG | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-32668_188-3266 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960154 | ||||||
| chr2:97960484
|
A | G | 1 | a0001c0001t0007g0017 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.188-32997T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960484 | ||||||
| chr2:97960608
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-33121T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960608 | ||||||
| chr2:97960774
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-33287C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960774 | ||||||
| chr2:97960829
|
T | C | 1 | a0001c0001t0003g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.188-33342A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960829 | ||||||
| chr2:97960874
|
A | AT | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.188-33388dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960874 | ||||||
| chr2:97960901
|
T | C | 1 | a0001c0002t0009g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.188-33414A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97960901 | ||||||
| chr2:97961064
|
G | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-33577C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961064 | ||||||
| chr2:97961095
|
C | T | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188-33608G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961095 | ||||||
| chr2:97961136
|
T | TA | 7 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0064others(4): Show | 7 | HG00280.hp2 HG01074.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-33650dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961136 | ||||||
| chr2:97961136
|
TA | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-33650delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961136 | ||||||
| chr2:97961180
|
G | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.188-33693C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961180 | ||||||
| chr2:97961225
|
T | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0056 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.188-33738A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961225 | ||||||
| chr2:97961349
|
G | A | 26 | a0003c0004t0002g0096a0003c0004t0002g0097a0003c0004t0002g0098others(23): Show | 26 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.188-33862C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961349 | ||||||
| chr2:97961419
|
A | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.188-33932T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961419 | ||||||
| chr2:97961473
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.188-33986T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961473 | ||||||
| chr2:97961532
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.187+33944A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961532 | ||||||
| chr2:97961648
|
C | A | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+33828G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961648 | ||||||
| chr2:97961855
|
A | G | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+33621T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97961855 | ||||||
| chr2:97962114
|
A | G | 1 | a0001c0002t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.187+33362T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97962114 | ||||||
| chr2:97962139
|
T | C | 1 | a0001c0001t0005g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.187+33337A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97962139 | ||||||
| chr2:97962296
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0072 | 2 | HG02040.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.187+33180C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97962296 | ||||||
| chr2:97962591
|
A | G | 9 | a0003c0004t0002g0108a0003c0004t0002g0109a0003c0004t0002g0110others(6): Show | 9 | HG00544.hp2 HG02602.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+32885T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97962591 | ||||||
| chr2:97962592
|
C | G | 1 | a0001c0002t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.187+32884G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97962592 | ||||||
| chr2:97962773
|
G | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+32703C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97962773 | ||||||
| chr2:97963179
|
C | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.187+32297G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97963179 | ||||||
| chr2:97963266
|
T | C | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+32210A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97963266 | ||||||
| chr2:97963295
|
ATGTCACC others(7): Show |
A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+32167_187+3218 others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97963295 | ||||||
| chr2:97963324
|
T | C | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+32152A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97963324 | ||||||
| chr2:97963549
|
T | C | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+31927A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97963549 | ||||||
| chr2:97964022
|
C | T | 1 | a0002c0003t0004g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187+31454G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97964022 | ||||||
| chr2:97964167
|
A | G | 1 | a0001c0001t0004g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.187+31309T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97964167 | ||||||
| chr2:97964261
|
G | T | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+31215C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97964261 | ||||||
| chr2:97964542
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.187+30934T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97964542 | ||||||
| chr2:97964640
|
G | A | 1 | a0001c0002t0001g0205 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.187+30836C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97964640 | ||||||
| chr2:97964931
|
A | C | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.187+30545T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97964931 | ||||||
| chr2:97965337
|
T | C | 1 | a0001c0005t0005g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.187+30139A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965337 | ||||||
| chr2:97965338
|
G | C | 1 | a0002c0003t0004g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.187+30138C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965338 | ||||||
| chr2:97965439
|
T | C | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.187+30037A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965439 | ||||||
| chr2:97965446
|
C | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+30030G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965446 | ||||||
| chr2:97965484
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+29992C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965484 | ||||||
| chr2:97965567
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+29909G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965567 | ||||||
| chr2:97965683
|
T | TAAAAATT others(297): Show |
5 | a0002c0003t0004g0183a0002c0003t0004g0184a0002c0003t0004g0185others(2): Show | 5 | HG00642.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+29792_187+2979 others(308): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965683 | ||||||
| chr2:97965683
|
T | TAAAAATT others(297): Show |
1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.187+29792_187+2979 others(308): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965683 | ||||||
| chr2:97965683
|
T | TAAAAATT others(297): Show |
82 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(79): Show | 82 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+29792_187+2979 others(308): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965683 | ||||||
| chr2:97965767
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.187+29709A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97965767 | ||||||
| chr2:97966035
|
A | T | 3 | a0001c0001t0004g0168a0001c0005t0005g0130a0015c0013t0005g0001 | 3 | HG02922.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.187+29441T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97966035 | ||||||
| chr2:97966170
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+29306G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97966170 | ||||||
| chr2:97966295
|
T | A | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.187+29181A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97966295 | ||||||
| chr2:97966321
|
C | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+29155G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97966321 | ||||||
| chr2:97966534
|
G | GAC | 3 | a0001c0002t0001g0277a0001c0002t0001g0281a0001c0002t0001g0282 | 3 | HG02129.hp1 NA18612.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.187+28940_187+2894 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97966534 | ||||||
| chr2:97966725
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.187+28751G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97966725 | ||||||
| chr2:97967021
|
A | AAAAC | 11 | a0001c0001t0005g0028a0001c0001t0005g0078a0001c0001t0005g0083others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.187+28451_187+2845 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967021 | ||||||
| chr2:97967021
|
A | AAAACAAA others(1): Show |
10 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+28447_187+2845 others(12): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967021 | ||||||
| chr2:97967021
|
AAAACAAA others(5): Show |
A | 1 | a0006c0021t0006g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187+28443_187+2845 others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967021 | ||||||
| chr2:97967072
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+28404C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967072 | ||||||
| chr2:97967112
|
C | T | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.187+28364G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967112 | ||||||
| chr2:97967491
|
C | T | 1 | a0002c0003t0004g0175 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.187+27985G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967491 | ||||||
| chr2:97967516
|
GA | G | 6 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(3): Show | 6 | HG00642.hp1 HG01192.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+27959delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967516 | ||||||
| chr2:97967844
|
C | G | 3 | a0001c0002t0001g0277a0001c0002t0001g0281a0001c0002t0001g0282 | 3 | HG02129.hp1 NA18612.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.187+27632G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967844 | ||||||
| chr2:97967849
|
G | A | 11 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.187+27627C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967849 | ||||||
| chr2:97967861
|
G | A | 1 | a0002c0003t0004g0198 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.187+27615C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967861 | ||||||
| chr2:97967893
|
G | GT | 6 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(3): Show | 6 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+27582dupA | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967893 | ||||||
| chr2:97967982
|
T | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+27494A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97967982 | ||||||
| chr2:97968476
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+27000C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97968476 | ||||||
| chr2:97968803
|
G | A | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.187+26673C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97968803 | ||||||
| chr2:97968924
|
GA | G | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+26551delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97968924 | ||||||
| chr2:97968958
|
C | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+26518G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97968958 | ||||||
| chr2:97969086
|
C | CA | 180 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0126others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.187+26389dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969086 | ||||||
| chr2:97969086
|
C | CAAAA | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+26386_187+2638 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969086 | ||||||
| chr2:97969114
|
C | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+26362G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969114 | ||||||
| chr2:97969428
|
C | A | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.187+26048G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969428 | ||||||
| chr2:97969779
|
A | C | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+25697T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969779 | ||||||
| chr2:97969887
|
C | T | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+25589G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969887 | ||||||
| chr2:97969902
|
A | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+25574T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97969902 | ||||||
| chr2:97970007
|
T | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+25469A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970007 | ||||||
| chr2:97970007
|
T | C | 2 | a0001c0001t0005g0081a0001c0001t0005g0082 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.187+25469A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970007 | ||||||
| chr2:97970014
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | HG02027.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.187+25462C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970014 | ||||||
| chr2:97970063
|
C | T | 1 | a0003c0004t0002g0118 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.187+25413G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970063 | ||||||
| chr2:97970225
|
G | A | 1 | a0002c0003t0004g0198 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.187+25251C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970225 | ||||||
| chr2:97970306
|
TG | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+25169delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970306 | ||||||
| chr2:97970344
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+25132C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970344 | ||||||
| chr2:97970379
|
C | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+25097G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970379 | ||||||
| chr2:97970464
|
C | A | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.187+25012G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970464 | ||||||
| chr2:97970660
|
T | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+24816A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970660 | ||||||
| chr2:97970740
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.187+24736C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970740 | ||||||
| chr2:97970750
|
A | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.187+24726T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970750 | ||||||
| chr2:97970825
|
A | G | 32 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.187+24651T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970825 | ||||||
| chr2:97970939
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.187+24537C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970939 | ||||||
| chr2:97970967
|
G | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+24509C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970967 | ||||||
| chr2:97970973
|
G | T | 1 | a0001c0002t0001g0206 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.187+24503C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97970973 | ||||||
| chr2:97971214
|
G | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+24262C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971214 | ||||||
| chr2:97971295
|
T | C | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+24181A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971295 | ||||||
| chr2:97971302
|
C | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+24174G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971302 | ||||||
| chr2:97971426
|
C | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+24050G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971426 | ||||||
| chr2:97971463
|
A | T | 2 | a0001c0001t0003g0064a0011c0017t0003g0065 | 2 | NA18961.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.187+24013T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971463 | ||||||
| chr2:97971489
|
C | G | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.187+23987G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971489 | ||||||
| chr2:97971877
|
A | G | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.187+23599T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971877 | ||||||
| chr2:97971909
|
C | A | 88 | a0001c0001t0002g0121a0001c0001t0004g0147a0001c0001t0004g0148others(85): Show | 88 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+23567G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97971909 | ||||||
| chr2:97972042
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+23434A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972042 | ||||||
| chr2:97972156
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+23320G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972156 | ||||||
| chr2:97972307
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.187+23169T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972307 | ||||||
| chr2:97972371
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+23105A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972371 | ||||||
| chr2:97972434
|
A | AAGGGGAG others(10): Show |
1 | a0001c0001t0006g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.187+23025_187+2304 others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972434 | ||||||
| chr2:97972436
|
GGGGA | G | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.187+23036_187+2303 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972436 | ||||||
| chr2:97972453
|
G | GGGGAGGG others(13): Show |
1 | a0002c0003t0004g0197 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.187+23003_187+2302 others(24): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972453 | ||||||
| chr2:97972453
|
GGGGAGGG others(13): Show |
G | 2 | a0001c0002t0001g0264a0001c0002t0001g0267 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+23003_187+2302 others(24): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972453 | ||||||
| chr2:97972485
|
A | AAGGCGGG others(5): Show |
4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0003others(1): Show | 4 | HG01346.hp2 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+22979_187+2299 others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972485 | ||||||
| chr2:97972617
|
T | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+22859A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972617 | ||||||
| chr2:97972808
|
G | A | 1 | a0001c0002t0009g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.187+22668C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972808 | ||||||
| chr2:97972842
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.187+22634C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972842 | ||||||
| chr2:97972988
|
G | T | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+22488C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97972988 | ||||||
| chr2:97973191
|
A | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+22285T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973191 | ||||||
| chr2:97973461
|
T | C | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.187+22015A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973461 | ||||||
| chr2:97973502
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+21974C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973502 | ||||||
| chr2:97973526
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+21950G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973526 | ||||||
| chr2:97973560
|
T | C | 1 | a0001c0001t0003g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.187+21916A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973560 | ||||||
| chr2:97973593
|
T | C | 1 | a0001c0001t0003g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.187+21883A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973593 | ||||||
| chr2:97973620
|
T | A | 18 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.187+21856A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973620 | ||||||
| chr2:97973969
|
A | G | 3 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0255 | 3 | NA18949.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.187+21507T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973969 | ||||||
| chr2:97973979
|
T | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(3): Show | 6 | HG00597.hp1 NA18965.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+21497A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973979 | ||||||
| chr2:97973991
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+21485A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97973991 | ||||||
| chr2:97974032
|
C | T | 27 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0005g0023others(24): Show | 27 | HG00099.hp2 HG00597.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.187+21444G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97974032 | ||||||
| chr2:97974075
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.187+21401A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97974075 | ||||||
| chr2:97974231
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.187+21245A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97974231 | ||||||
| chr2:97974333
|
T | C | 1 | a0014c0015t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.187+21143A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97974333 | ||||||
| chr2:97974397
|
GGGA | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+21076_187+2107 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97974397 | ||||||
| chr2:97974738
|
G | GTAAT | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.187+20734_187+2073 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97974738 | ||||||
| chr2:97975031
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+20445G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975031 | ||||||
| chr2:97975244
|
GA | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+20231delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975244 | ||||||
| chr2:97975349
|
T | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187+20127A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975349 | ||||||
| chr2:97975398
|
C | T | 1 | a0001c0005t0005g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.187+20078G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975398 | ||||||
| chr2:97975656
|
C | T | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.187+19820G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975656 | ||||||
| chr2:97975811
|
G | GA | 50 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.187+19664dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975811 | ||||||
| chr2:97975811
|
GA | G | 120 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0121others(117): Show | 120 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.187+19664delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975811 | ||||||
| chr2:97975885
|
C | A | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+19591G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97975885 | ||||||
| chr2:97976033
|
C | G | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.187+19443G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976033 | ||||||
| chr2:97976343
|
T | C | 1 | a0001c0002t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.187+19133A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976343 | ||||||
| chr2:97976352
|
A | G | 7 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(4): Show | 7 | HG02074.hp1 HG02083.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+19124T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976352 | ||||||
| chr2:97976463
|
T | C | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.187+19013A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976463 | ||||||
| chr2:97976800
|
T | C | 1 | a0001c0002t0001g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.187+18676A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976800 | ||||||
| chr2:97976956
|
T | C | 1 | a0001c0007t0003g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.187+18520A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976956 | ||||||
| chr2:97976959
|
G | GC | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.187+18516dupG | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976959 | ||||||
| chr2:97976960
|
C | CA | 15 | a0001c0001t0001g0202a0001c0001t0003g0068a0001c0002t0001g0216others(12): Show | 15 | HG01346.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.187+18515dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976960 | ||||||
| chr2:97976960
|
C | CAA | 66 | a0001c0001t0001g0203a0001c0001t0003g0032a0001c0001t0003g0033others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.187+18514_187+1851 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976960 | ||||||
| chr2:97976960
|
CA | C | 54 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0125others(51): Show | 54 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.187+18515delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97976960 | ||||||
| chr2:97977711
|
T | C | 1 | a0001c0005t0005g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187+17765A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97977711 | ||||||
| chr2:97977761
|
T | G | 15 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(12): Show | 15 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.187+17715A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97977761 | ||||||
| chr2:97977793
|
T | G | 4 | a0001c0005t0005g0132a0001c0005t0005g0133a0001c0005t0005g0134others(1): Show | 4 | HG00642.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+17683A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97977793 | ||||||
| chr2:97978016
|
G | A | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+17460C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97978016 | ||||||
| chr2:97978036
|
G | A | 19 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+17440C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97978036 | ||||||
| chr2:97978044
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+17432C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97978044 | ||||||
| chr2:97978873
|
T | C | 1 | a0001c0002t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.187+16603A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97978873 | ||||||
| chr2:97978946
|
T | C | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+16530A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97978946 | ||||||
| chr2:97978974
|
G | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+16502C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97978974 | ||||||
| chr2:97979171
|
T | G | 1 | a0002c0003t0004g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.187+16305A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979171 | ||||||
| chr2:97979192
|
G | C | 1 | a0002c0003t0004g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.187+16284C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979192 | ||||||
| chr2:97979631
|
T | C | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.187+15845A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979631 | ||||||
| chr2:97979649
|
AG | A | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.187+15826delC | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979649 | ||||||
| chr2:97979682
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.187+15794A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979682 | ||||||
| chr2:97979749
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.187+15727G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979749 | ||||||
| chr2:97979847
|
G | A | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.187+15629C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979847 | ||||||
| chr2:97979868
|
T | A | 201 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.187+15608A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979868 | ||||||
| chr2:97979910
|
C | T | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+15566G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97979910 | ||||||
| chr2:97980000
|
A | C | 1 | a0001c0002t0001g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.187+15476T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980000 | ||||||
| chr2:97980037
|
G | A | 3 | a0002c0003t0004g0190a0002c0003t0004g0191a0002c0003t0004g0192 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.187+15439C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980037 | ||||||
| chr2:97980069
|
G | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.187+15407C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980069 | ||||||
| chr2:97980111
|
T | C | 1 | a0001c0002t0001g0236 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.187+15365A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980111 | ||||||
| chr2:97980162
|
CACT | C | 7 | a0001c0002t0001g0237a0001c0002t0001g0238a0001c0002t0001g0239others(4): Show | 7 | HG01070.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+15311_187+1531 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980162 | ||||||
| chr2:97980347
|
G | C | 2 | a0001c0002t0001g0242a0001c0002t0001g0254 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.187+15129C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980347 | ||||||
| chr2:97980473
|
T | C | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.187+15003A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980473 | ||||||
| chr2:97980566
|
T | A | 3 | a0002c0003t0004g0190a0002c0003t0004g0191a0002c0003t0004g0192 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.187+14910A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980566 | ||||||
| chr2:97980735
|
GACTA | G | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+14737_187+1474 others(8): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97980735 | ||||||
| chr2:97981028
|
C | CA | 34 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.187+14447dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
C | CAA | 12 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(9): Show | 12 | HG00423.hp1 HG02572.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+14446_187+1444 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
C | CAAA | 8 | a0001c0001t0002g0013a0002c0003t0004g0176a0002c0003t0004g0193others(5): Show | 8 | HG00733.hp2 HG01070.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+14445_187+1444 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
C | CAAAAA | 6 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+14443_187+1444 others(9): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0008g0167a0001c0005t0005g0144 | 2 | HG01243.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.187+14438_187+1444 others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
C | CAAAAAAA others(4): Show |
1 | a0002c0003t0004g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.187+14437_187+1444 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | NA19001.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.187+14433_187+1444 others(19): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CA | C | 42 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0001t0005g0023others(39): Show | 42 | HG01074.hp1 HG01169.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.187+14447delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAA | C | 7 | a0001c0001t0001g0203a0001c0001t0005g0083a0001c0002t0001g0217others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+14446_187+1444 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0002g0016a0001c0001t0002g0121a0003c0004t0002g0108others(11): Show | 14 | HG00544.hp2 HG02027.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.187+14439_187+1444 others(13): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0002g0015a0002c0003t0004g0177a0002c0003t0004g0178others(12): Show | 15 | HG00597.hp2 HG02071.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.187+14438_187+1444 others(14): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0007g0017a0001c0001t0007g0018a0001c0001t0007g0019others(5): Show | 8 | HG00597.hp1 HG02280.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+14437_187+1444 others(15): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0003g0060a0001c0001t0006g0165a0001c0002t0001g0216others(4): Show | 7 | HG00642.hp1 HG02970.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+14436_187+1444 others(16): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0006g0152a0001c0001t0006g0156a0001c0001t0006g0157others(9): Show | 12 | HG01515.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+14435_187+1444 others(17): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG02258.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.187+14434_187+1444 others(18): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(8): Show |
C | 21 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0043others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.187+14433_187+1444 others(19): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0003g0040a0001c0002t0001g0215 | 2 | HG01256.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.187+14432_187+1444 others(20): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.187+14431_187+1444 others(21): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(11): Show |
C | 7 | a0001c0001t0001g0202a0001c0001t0002g0125a0001c0001t0002g0126others(4): Show | 7 | HG01346.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+14430_187+1444 others(22): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0002t0001g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.187+14429_187+1444 others(23): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981028
|
CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0005g0081a0001c0001t0005g0082 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.187+14428_187+1444 others(24): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981028 | ||||||
| chr2:97981051
|
A | G | 1 | a0003c0004t0002g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.187+14425T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981051 | ||||||
| chr2:97981052
|
A | G | 13 | a0001c0001t0002g0121a0003c0004t0002g0108a0003c0004t0002g0109others(10): Show | 13 | HG00544.hp2 HG02602.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+14424T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981052 | ||||||
| chr2:97981053
|
A | G | 12 | a0003c0004t0002g0097a0003c0004t0002g0098a0003c0004t0002g0099others(9): Show | 12 | HG00597.hp2 HG02129.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+14423T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981053 | ||||||
| chr2:97981054
|
A | G | 1 | a0003c0004t0002g0096 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.187+14422T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981054 | ||||||
| chr2:97981068
|
G | A | 2 | a0002c0003t0004g0200a0002c0003t0004g0201 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.187+14408C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981068 | ||||||
| chr2:97981253
|
T | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+14223A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981253 | ||||||
| chr2:97981282
|
AATC | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+14191_187+1419 others(7): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981282 | ||||||
| chr2:97981699
|
G | C | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG00423.hp1 NA18949.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+13777C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97981699 | ||||||
| chr2:97982031
|
C | T | 7 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0268others(4): Show | 7 | HG00544.hp1 HG02040.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+13445G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982031 | ||||||
| chr2:97982032
|
G | A | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+13444C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982032 | ||||||
| chr2:97982067
|
G | C | 10 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0001t0003g0067others(7): Show | 10 | HG00423.hp1 NA18939.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+13409C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982067 | ||||||
| chr2:97982155
|
G | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+13321C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982155 | ||||||
| chr2:97982285
|
A | G | 4 | a0001c0007t0003g0034a0001c0007t0003g0035a0001c0007t0003g0036others(1): Show | 4 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+13191T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982285 | ||||||
| chr2:97982292
|
T | C | 1 | a0002c0003t0004g0175 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.187+13184A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982292 | ||||||
| chr2:97982692
|
T | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+12784A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982692 | ||||||
| chr2:97982926
|
A | G | 1 | a0002c0003t0004g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.187+12550T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97982926 | ||||||
| chr2:97983036
|
C | T | 5 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(2): Show | 5 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+12440G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983036 | ||||||
| chr2:97983163
|
C | A | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.187+12313G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983163 | ||||||
| chr2:97983249
|
T | C | 1 | a0001c0002t0001g0267 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.187+12227A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983249 | ||||||
| chr2:97983323
|
G | A | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.187+12153C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983323 | ||||||
| chr2:97983459
|
G | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+12017C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983459 | ||||||
| chr2:97983471
|
G | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.187+12005C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983471 | ||||||
| chr2:97983486
|
A | G | 1 | a0001c0001t0006g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.187+11990T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983486 | ||||||
| chr2:97983587
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.187+11889G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983587 | ||||||
| chr2:97983619
|
C | A | 71 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.187+11857G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983619 | ||||||
| chr2:97983770
|
T | C | 1 | a0001c0002t0009g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.187+11706A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983770 | ||||||
| chr2:97983824
|
G | C | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.187+11652C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97983824 | ||||||
| chr2:97984296
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.187+11180A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97984296 | ||||||
| chr2:97984398
|
T | C | 6 | a0001c0002t0001g0264a0001c0002t0001g0267a0001c0002t0001g0278others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+11078A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97984398 | ||||||
| chr2:97984577
|
G | C | 3 | a0003c0004t0002g0118a0003c0004t0002g0119a0003c0004t0002g0120 | 3 | NA18939.hp1 NA18991.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.187+10899C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97984577 | ||||||
| chr2:97984866
|
T | C | 3 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070 | 3 | HG01884.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.187+10610A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97984866 | ||||||
| chr2:97984873
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+10603C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97984873 | ||||||
| chr2:97985197
|
A | G | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.187+10279T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985197 | ||||||
| chr2:97985356
|
C | CAT | 68 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+10118_187+1011 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985356 | ||||||
| chr2:97985368
|
TAC | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+10106_187+1010 others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985368 | ||||||
| chr2:97985370
|
C | T | 274 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.187+10106G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985370 | ||||||
| chr2:97985459
|
T | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+10017A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985459 | ||||||
| chr2:97985474
|
A | T | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.187+10002T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985474 | ||||||
| chr2:97985657
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.187+9819C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985657 | ||||||
| chr2:97985695
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+9781G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985695 | ||||||
| chr2:97985702
|
A | G | 54 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0150others(51): Show | 54 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.187+9774T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985702 | ||||||
| chr2:97985781
|
G | T | 1 | a0012c0016t0003g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+9695C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985781 | ||||||
| chr2:97985887
|
A | AAATATTG others(25): Show |
1 | a0001c0001t0004g0147 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.187+9557_187+9588d others(34): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985887 | ||||||
| chr2:97985947
|
TA | T | 12 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(9): Show | 12 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+9528delT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985947 | ||||||
| chr2:97985948
|
A | T | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.187+9528T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97985948 | ||||||
| chr2:97986306
|
G | A | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+9170C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97986306 | ||||||
| chr2:97986378
|
A | G | 1 | a0008c0020t0004g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.187+9098T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97986378 | ||||||
| chr2:97986473
|
A | C | 6 | a0004c0008t0002g0091a0004c0008t0002g0092a0004c0008t0002g0093others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+9003T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97986473 | ||||||
| chr2:97986640
|
C | T | 27 | a0001c0001t0002g0121a0003c0004t0002g0096a0003c0004t0002g0097others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.187+8836G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97986640 | ||||||
| chr2:97986802
|
G | A | 1 | a0001c0001t0006g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.187+8674C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97986802 | ||||||
| chr2:97987014
|
G | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+8462C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987014 | ||||||
| chr2:97987196
|
A | G | 5 | a0001c0007t0003g0034a0001c0007t0003g0035a0001c0007t0003g0036others(2): Show | 5 | HG01261.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+8280T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987196 | ||||||
| chr2:97987240
|
C | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.187+8236G>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987240 | ||||||
| chr2:97987282
|
T | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+8194A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987282 | ||||||
| chr2:97987324
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.187+8152C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987324 | ||||||
| chr2:97987364
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.187+8112C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987364 | ||||||
| chr2:97987523
|
C | CA | 6 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0270others(3): Show | 6 | HG00544.hp1 HG02040.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+7952dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987523 | ||||||
| chr2:97987554
|
G | A | 17 | a0001c0005t0005g0130a0001c0005t0005g0132a0001c0005t0005g0133others(14): Show | 17 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+7922C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987554 | ||||||
| chr2:97987610
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+7866G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987610 | ||||||
| chr2:97987758
|
A | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+7718T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97987758 | ||||||
| chr2:97988107
|
GACAC | G | 54 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0150others(51): Show | 54 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.187+7365_187+7368d others(6): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988107 | ||||||
| chr2:97988150
|
C | T | 50 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.187+7326G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988150 | ||||||
| chr2:97988185
|
G | A | 1 | a0001c0002t0001g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.187+7291C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988185 | ||||||
| chr2:97988460
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.187+7016A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988460 | ||||||
| chr2:97988601
|
G | A | 1 | a0001c0002t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.187+6875C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988601 | ||||||
| chr2:97988610
|
G | A | 1 | a0001c0005t0005g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.187+6866C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988610 | ||||||
| chr2:97988819
|
T | C | 1 | a0001c0002t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.187+6657A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988819 | ||||||
| chr2:97988871
|
T | C | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG00423.hp1 NA18949.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+6605A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97988871 | ||||||
| chr2:97989277
|
C | CA | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(28): Show | 31 | HG00099.hp2 HG00597.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.187+6198dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989277 | ||||||
| chr2:97989277
|
C | CAA | 24 | a0001c0001t0005g0081a0001c0001t0005g0082a0001c0001t0005g0083others(21): Show | 24 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.187+6197_187+6198d others(4): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989277 | ||||||
| chr2:97989519
|
A | G | 89 | a0001c0001t0002g0121a0001c0001t0003g0088a0001c0001t0004g0147others(86): Show | 89 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.187+5957T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989519 | ||||||
| chr2:97989520
|
TGAA | T | 50 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.187+5953_187+5955d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989520 | ||||||
| chr2:97989735
|
G | A | 1 | a0001c0002t0001g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.187+5741C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989735 | ||||||
| chr2:97989924
|
ACTT | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+5549_187+5551d others(5): Show |
TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989924 | ||||||
| chr2:97989980
|
C | T | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.187+5496G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97989980 | ||||||
| chr2:97990307
|
T | C | 32 | a0002c0003t0004g0171a0002c0003t0004g0172a0002c0003t0004g0173others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.187+5169A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990307 | ||||||
| chr2:97990471
|
T | C | 1 | a0001c0002t0001g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+5005A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990471 | ||||||
| chr2:97990511
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.187+4965T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990511 | ||||||
| chr2:97990706
|
T | G | 1 | a0001c0001t0003g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.187+4770A>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990706 | ||||||
| chr2:97990799
|
T | C | 1 | a0001c0001t0005g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.187+4677A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990799 | ||||||
| chr2:97990817
|
T | C | 28 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0005g0023others(25): Show | 28 | HG00099.hp2 HG00597.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.187+4659A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990817 | ||||||
| chr2:97990874
|
T | C | 1 | a0001c0001t0005g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.187+4602A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990874 | ||||||
| chr2:97990875
|
G | A | 70 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.187+4601C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97990875 | ||||||
| chr2:97991276
|
T | A | 2 | a0001c0002t0001g0279a0001c0002t0001g0280 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.187+4200A>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97991276 | ||||||
| chr2:97991400
|
A | T | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.187+4076T>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97991400 | ||||||
| chr2:97991420
|
T | TA | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+4055dupT | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97991420 | ||||||
| chr2:97991733
|
C | T | 3 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149 | 3 | NA19001.hp1 NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.187+3743G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97991733 | ||||||
| chr2:97991888
|
G | A | 2 | a0001c0005t0005g0130a0015c0013t0005g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.187+3588C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97991888 | ||||||
| chr2:97992382
|
T | C | 2 | a0001c0002t0001g0281a0001c0002t0001g0282 | 2 | HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.187+3094A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97992382 | ||||||
| chr2:97992507
|
A | G | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0003g0032others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+2969T>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97992507 | ||||||
| chr2:97992717
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+2759A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97992717 | ||||||
| chr2:97992776
|
C | T | 9 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(6): Show | 9 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+2700G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97992776 | ||||||
| chr2:97993424
|
C | G | 1 | a0001c0002t0001g0205 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.187+2052G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97993424 | ||||||
| chr2:97993649
|
C | G | 8 | a0001c0001t0003g0088a0001c0001t0003g0089a0004c0008t0002g0091others(5): Show | 8 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+1827G>C | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97993649 | ||||||
| chr2:97993650
|
A | C | 69 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0040others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.187+1826T>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97993650 | ||||||
| chr2:97993810
|
G | A | 16 | a0001c0001t0002g0121a0001c0005t0005g0132a0001c0005t0005g0133others(13): Show | 16 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.187+1666C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97993810 | ||||||
| chr2:97993825
|
G | T | 23 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(20): Show | 23 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.187+1651C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97993825 | ||||||
| chr2:97994158
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+1318C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994158 | ||||||
| chr2:97994389
|
G | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0007g0017others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+1087C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994389 | ||||||
| chr2:97994461
|
C | T | 283 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0002others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.187+1015G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994461 | ||||||
| chr2:97994726
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.187+750A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994726 | ||||||
| chr2:97994806
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.187+670G>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994806 | ||||||
| chr2:97994949
|
T | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+527A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994949 | ||||||
| chr2:97994970
|
T | C | 1 | a0001c0022t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.187+506A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994970 | ||||||
| chr2:97994994
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.187+482C>T | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97994994 | ||||||
| chr2:97995161
|
T | C | 22 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(19): Show | 22 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+315A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97995161 | ||||||
| chr2:97995238
|
G | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+238C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97995238 | ||||||
| chr2:97995345
|
G | C | 1 | a0003c0004t0002g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.187+131C>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97995345 | ||||||
| chr2:97995370
|
T | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+106A>G | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97995370 | ||||||
| chr2:97995467
|
G | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+9C>A | TMEM131 | ENSG00000075568.17 | transcript | ENST00000186436.10 | protein_coding | 1/40 | chr2 | 97995467 |