Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 114804 |
|---|---|
| ensemblid | ENSG00000141576.16 |
| hgncid | 29402 |
| symbol | RNF157 |
| name | ring finger protein 157 |
| refseq_nuc | NM_052916.3 |
| refseq_prot | NP_443148.1 |
| ensembl_nuc | ENST00000269391.11 |
| ensembl_prot | ENSP00000269391.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 76142474 |
| end | 76240493 |
| strand | - |
| ver | v1.2 |
| region | chr17:76142474-76240493 |
| region5000 | chr17:76137474-76245493 |
| regionname0 | RNF157_chr17_76142474_76240493 |
| regionname5000 | RNF157_chr17_76137474_76245493 |
| 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 | 1/0 | 679 | 221 | 79 | 51 | 62 | 8 | 20 | 45 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0002 | 0/0 | 679 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0003 | 0/0 | 679 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0004 | 0/0 | 679 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0005 | 0/0 | 679 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0006 | 0/1 | 679 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0007 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0008 | 0/0 | 679 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0009 | 0/0 | 679 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2040 | 99 | 31 | 23 | 31 | 3 | 10 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0002 | 0/0 | 2040 | 50 | 21 | 15 | 12 | 1 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0003 | 0/0 | 2040 | 32 | 3 | 9 | 12 | 3 | 5 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0004 | 0/0 | 2040 | 26 | 14 | 4 | 5 | 1 | 2 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0005 | 0/0 | 2040 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0006 | 0/0 | 2040 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0007 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0008 | 0/0 | 2040 | 2 | 0 | 0 | 0 | 0 | 2 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0009 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0010 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0011 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0012 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0013 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0014 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0015 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0016 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0017 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0018 | 0/1 | 2040 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0019 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0020 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0021 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| c0022 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| 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 | 3015 | 106 | 22 | 23 | 39 | 5 | 15 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0002 | 0/0 | 3015 | 73 | 28 | 22 | 18 | 2 | 3 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0003 | 0/0 | 3015 | 12 | 11 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0004 | 0/0 | 3016 | 5 | 5 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0005 | 0/0 | 3015 | 4 | 0 | 2 | 0 | 1 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0006 | 0/0 | 3015 | 4 | 3 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0007 | 0/0 | 3016 | 4 | 4 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0008 | 0/0 | 3015 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0009 | 0/0 | 3015 | 3 | 0 | 3 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0010 | 0/0 | 3016 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0011 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0012 | 0/0 | 3016 | 2 | 0 | 1 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0013 | 0/0 | 3015 | 2 | 0 | 0 | 2 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0014 | 0/0 | 3015 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0015 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0016 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0017 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0018 | 0/0 | 3015 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0019 | 0/0 | 3015 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0020 | 0/0 | 3015 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0021 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0022 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0023 | 0/0 | 3015 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| t0024 | 0/0 | 3015 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| 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 | 2 | 0 | 1 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2040 | 99 | 31 | 23 | 31 | 3 | 10 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002 | 0/0 | 2040 | 50 | 21 | 15 | 12 | 1 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003 | 0/0 | 2040 | 32 | 3 | 9 | 12 | 3 | 5 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0004 | 0/0 | 2040 | 26 | 14 | 4 | 5 | 1 | 2 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0005 | 0/0 | 2040 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0006 | 0/0 | 2040 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0007 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0008 | 0/0 | 2040 | 2 | 0 | 0 | 0 | 0 | 2 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0012 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0015 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0016 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0021 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0002c0009 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0002c0010 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0003c0019 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0003c0020 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0004c0011 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0005c0013 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0006c0018 | 0/1 | 2040 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0007c0017 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0008c0014 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0009c0022 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5054 | 75 | 16 | 19 | 27 | 3 | 9 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0002 | 0/0 | 5054 | 6 | 4 | 0 | 1 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0003 | 0/0 | 5054 | 5 | 5 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0006 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0009 | 0/0 | 5054 | 2 | 0 | 2 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0010 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0014 | 0/0 | 5054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0015 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0016 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0018 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0020 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0021 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0023 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0001t0024 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0001 | 0/0 | 5054 | 13 | 3 | 3 | 6 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0002 | 0/0 | 5054 | 24 | 9 | 10 | 4 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0003 | 0/0 | 5054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0004 | 0/0 | 5055 | 5 | 5 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0007 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0009 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0011 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0013 | 0/0 | 5054 | 2 | 0 | 0 | 2 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0002t0017 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003t0001 | 0/0 | 5054 | 3 | 0 | 0 | 0 | 1 | 2 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003t0002 | 0/0 | 5054 | 22 | 3 | 6 | 11 | 1 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003t0003 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003t0005 | 0/0 | 5054 | 4 | 0 | 2 | 0 | 1 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003t0012 | 0/0 | 5055 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0003t0019 | 0/0 | 5054 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0004t0001 | 0/0 | 5054 | 5 | 1 | 0 | 2 | 1 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0004t0002 | 0/0 | 5054 | 14 | 7 | 4 | 2 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0004t0003 | 0/0 | 5054 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0004t0006 | 0/0 | 5054 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0004t0012 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0005t0008 | 0/0 | 5054 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0006t0007 | 0/0 | 5055 | 3 | 3 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0007t0001 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0007t0022 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0008t0001 | 0/0 | 5054 | 2 | 0 | 0 | 0 | 0 | 2 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0012t0011 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0015t0001 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0016t0001 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0001c0021t0001 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0002c0009t0002 | 0/0 | 5054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0002c0010t0003 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0002c0010t0010 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0003c0019t0002 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0003c0020t0002 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0004c0011t0002 | 0/0 | 5054 | 2 | 2 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0005c0013t0001 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0006c0018t0001 | 0/1 | 5054 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0007c0017t0002 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0008c0014t0001 | 0/0 | 5054 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| a0009c0022t0001 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | copy fasta | chr17 | 76137474 | 76245493 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0014g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0015g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0018g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0020g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0021g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0023g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0001t0024g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0002t0017g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0005g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0012g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0003t0019g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0004t0012g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0005t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0005t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0005t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0006t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0006t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0006t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0007t0022g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0008t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0012t0011g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0015t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0016t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0001c0021t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0002c0009t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0002c0009t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0002c0010t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0002c0010t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0003c0019t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0003c0020t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0004c0011t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0004c0011t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0005c0013t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0006c0018t0001g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0007c0017t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0008c0014t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| a0009c0022t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0136 | EUR | GBR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00438 | hp1 | a0001 | c0001 | t0023 | g0110 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00544 | hp2 | a0009 | c0022 | t0001 | g0070 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00597 | hp1 | a0001 | c0004 | t0002 | g0188 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0141 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0130 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01069 | hp1 | a0001 | c0004 | t0002 | g0199 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0057 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0066 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01169 | hp2 | a0001 | c0003 | t0005 | g0002 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01175 | hp1 | a0001 | c0002 | t0009 | g0100 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01175 | hp2 | a0001 | c0003 | t0012 | g0129 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01243 | hp1 | a0001 | c0004 | t0002 | g0168 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0090 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01261 | hp1 | a0003 | c0019 | t0002 | g0126 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01261 | hp2 | a0008 | c0014 | t0001 | g0161 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0175 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0102 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01361 | hp2 | a0001 | c0004 | t0002 | g0011 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01433 | hp1 | a0003 | c0020 | t0002 | g0123 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0091 | AMR | CLM | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0176 | EUR | IBS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01516 | hp2 | a0001 | c0003 | t0005 | g0002 | EUR | IBS | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01884 | hp2 | a0004 | c0011 | t0002 | g0185 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0208 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01934 | hp1 | a0001 | c0003 | t0005 | g0177 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01952 | hp2 | a0001 | c0003 | t0002 | g0073 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01981 | hp1 | a0001 | c0001 | t0009 | g0101 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01993 | hp1 | a0001 | c0002 | t0017 | g0138 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02055 | hp1 | a0001 | c0004 | t0006 | g0202 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02129 | hp1 | a0001 | c0003 | t0002 | g0174 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02132 | hp1 | a0001 | c0004 | t0001 | g0097 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0195 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02148 | hp2 | a0001 | c0001 | t0024 | g0081 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0040 | EAS | CDX | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0065 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02258 | hp1 | a0002 | c0010 | t0003 | g0213 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02258 | hp2 | a0001 | c0004 | t0002 | g0135 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02280 | hp1 | a0002 | c0009 | t0002 | g0211 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0115 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0064 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PEL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0162 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0025 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02622 | hp2 | a0001 | c0001 | t0021 | g0089 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0167 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0121 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02818 | hp2 | a0001 | c0007 | t0001 | g0194 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02886 | hp1 | a0001 | c0016 | t0001 | g0094 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0117 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02895 | hp2 | a0001 | c0004 | t0003 | g0027 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0119 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02922 | hp1 | a0001 | c0001 | t0014 | g0086 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0039 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02965 | hp2 | a0001 | c0006 | t0007 | g0016 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02976 | hp1 | a0004 | c0011 | t0002 | g0184 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02976 | hp2 | a0002 | c0010 | t0010 | g0220 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03017 | hp1 | a0001 | c0008 | t0001 | g0048 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0124 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0196 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0116 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0207 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0228 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03139 | hp2 | a0001 | c0006 | t0007 | g0015 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03195 | hp2 | a0001 | c0007 | t0022 | g0200 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0003 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03225 | hp2 | a0001 | c0004 | t0006 | g0019 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03453 | hp1 | a0001 | c0004 | t0003 | g0045 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03453 | hp2 | a0001 | c0004 | t0002 | g0133 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03486 | hp1 | a0001 | c0002 | t0011 | g0205 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03490 | hp1 | a0001 | c0003 | t0019 | g0227 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03516 | hp2 | a0001 | c0006 | t0007 | g0014 | AFR | ESN | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0118 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03540 | hp2 | a0001 | c0004 | t0002 | g0137 | AFR | GWD | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03579 | hp2 | a0001 | c0012 | t0011 | g0201 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0224 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0092 | SAS | PJL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03927 | hp2 | a0001 | c0003 | t0005 | g0204 | SAS | BEB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03942 | hp1 | a0001 | c0004 | t0002 | g0144 | SAS | BEB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG04115 | hp2 | a0001 | c0008 | t0001 | g0047 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0160 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18522 | hp1 | a0001 | c0005 | t0008 | g0197 | AFR | YRI | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18522 | hp2 | a0002 | c0009 | t0002 | g0212 | AFR | YRI | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18943 | hp2 | a0001 | c0004 | t0001 | g0104 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18947 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18956 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18962 | hp2 | a0001 | c0001 | t0020 | g0038 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18964 | hp1 | a0005 | c0013 | t0001 | g0223 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0111 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18979 | hp2 | a0001 | c0003 | t0002 | g0096 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18992 | hp1 | a0001 | c0004 | t0012 | g0106 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18993 | hp1 | a0001 | c0015 | t0001 | g0105 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19004 | hp1 | a0001 | c0001 | t0018 | g0225 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0030 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19007 | hp1 | a0001 | c0002 | t0013 | g0164 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0078 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19030 | hp1 | a0001 | c0005 | t0008 | g0017 | AFR | LWK | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0113 | AFR | LWK | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0033 | AFR | LWK | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19043 | hp2 | a0001 | c0004 | t0006 | g0018 | AFR | LWK | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19057 | hp1 | a0001 | c0021 | t0001 | g0043 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19070 | hp1 | a0001 | c0002 | t0013 | g0163 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19075 | hp2 | a0001 | c0003 | t0003 | g0020 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19240 | hp1 | a0001 | c0005 | t0008 | g0198 | AFR | YRI | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA19240 | hp2 | a0007 | c0017 | t0002 | g0150 | AFR | YRI | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ASW | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ASW | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0170 | EUR | TSI | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0122 | EUR | TSI | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | ACB | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0134 | AFR | MSL | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | USA | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0151 | AFR | USA | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | USA | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | LWK | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | LWK | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| homoSapiens_chm13v2 | hp1 | a0006 | c0018 | t0001 | g0026 | REF | REF | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0028 | REF | REF | RNF157_chr17_76137474_76245493 | RNF157 | chr17 | 76137474 | 76245493 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76154306
|
T | A | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1787A>T | p.Glu596Val | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/19 | 2040/5054 | 1787/2040 | 596/679 | chr17 | 76154306 | ||
| chr17:76158415
|
G | A | 1 | a0006 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1391C>T | p.Pro464Leu | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/19 | 1644/5054 | 1391/2040 | 464/679 | chr17 | 76158415 | ||
| chr17:76158441
|
C | A | 1 | a0002 | 4 | HG02258.hp1 HG02280.hp1 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.1365G>T | p.Glu455Asp | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/19 | 1618/5054 | 1365/2040 | 455/679 | chr17 | 76158441 | ||
| chr17:76166467
|
C | T | 1 | a0008 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.622G>A | p.Gly208Arg | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/19 | 875/5054 | 622/2040 | 208/679 | chr17 | 76166467 | ||
| chr17:76167011
|
C | T | 1 | a0005 | 1 | NA18964.hp1 | missense_variant&splice_region_variant | MODERATE | c.559G>A | p.Glu187Lys | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/19 | 812/5054 | 559/2040 | 187/679 | chr17 | 76167011 | ||
| chr17:76167043
|
T | A | 1 | a0005 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.527A>T | p.His176Leu | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/19 | 780/5054 | 527/2040 | 176/679 | chr17 | 76167043 | ||
| chr17:76167073
|
C | T | 1 | a0005 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.497G>A | p.Gly166Glu | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/19 | 750/5054 | 497/2040 | 166/679 | chr17 | 76167073 | ||
| chr17:76167076
|
C | T | 1 | a0004 | 2 | HG01884.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.494G>A | p.Arg165Gln | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/19 | 747/5054 | 494/2040 | 165/679 | chr17 | 76167076 | ||
| chr17:76167678
|
G | A | 1 | a0003 | 2 | HG01261.hp1 HG01433.hp1 |
missense_variant | MODERATE | c.416C>T | p.Thr139Met | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/19 | 669/5054 | 416/2040 | 139/679 | chr17 | 76167678 | ||
| chr17:76173781
|
C | A | 1 | a0009 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.217G>T | p.Ala73Ser | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/19 | 470/5054 | 217/2040 | 73/679 | chr17 | 76173781 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76152455
|
C | A | 1 | a0001c0016 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1821G>T | p.Thr607Thr | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/19 | 2074/5054 | 1821/2040 | 607/679 | chr17 | 76152455 | ||
| chr17:76154290
|
C | T | 1 | a0001c0015 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.1803G>A | p.Thr601Thr | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/19 | 2056/5054 | 1803/2040 | 601/679 | chr17 | 76154290 | ||
| chr17:76155315
|
C | A | 1 | a0001c0005 | 3 | NA18522.hp1 NA19030.hp1 NA19240.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1701G>T | p.Gly567Gly | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 16/19 | 1954/5054 | 1701/2040 | 567/679 | chr17 | 76155315 | ||
| chr17:76155610
|
A | C | 1 | a0001c0008 | 2 | HG03017.hp1 HG04115.hp2 |
synonymous_variant | LOW | c.1650T>G | p.Ala550Ala | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 15/19 | 1903/5054 | 1650/2040 | 550/679 | chr17 | 76155610 | ||
| chr17:76156285
|
A | G | 7 | a0001c0002a0001c0003a0001c0006others(4): Show | 90 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(87): Show |
synonymous_variant | LOW | c.1450T>C | p.Leu484Leu | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 14/19 | 1703/5054 | 1450/2040 | 484/679 | chr17 | 76156285 | ||
| chr17:76166480
|
G | A | 1 | a0001c0006 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.609C>T | p.Ala203Ala | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/19 | 862/5054 | 609/2040 | 203/679 | chr17 | 76166480 | ||
| chr17:76167740
|
G | A | 5 | a0001c0003a0001c0004a0003c0019others(2): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
synonymous_variant | LOW | c.354C>T | p.Tyr118Tyr | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/19 | 607/5054 | 354/2040 | 118/679 | chr17 | 76167740 | ||
| chr17:76167779
|
C | T | 2 | a0001c0007a0001c0012 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.315G>A | p.Lys105Lys | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/19 | 568/5054 | 315/2040 | 105/679 | chr17 | 76167779 | ||
| chr17:76173779
|
G | A | 1 | a0001c0021 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.219C>T | p.Ala73Ala | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/19 | 472/5054 | 219/2040 | 73/679 | chr17 | 76173779 | ||
| chr17:76212388
|
G | A | 1 | a0001c0006 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.183C>T | p.Asn61Asn | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/19 | 436/5054 | 183/2040 | 61/679 | chr17 | 76212388 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76142632
|
A | C | 1 | a0001c0002t0013 | 2 | NA19007.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2603T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2603 | chr17 | 76142632 | |||||
| chr17:76142711
|
C | A | 1 | a0001c0001t0021 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2524G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2524 | chr17 | 76142711 | |||||
| chr17:76142904
|
A | G | 1 | a0001c0001t0020 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2331T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2331 | chr17 | 76142904 | |||||
| chr17:76142937
|
C | G | 2 | a0001c0001t0009a0001c0002t0009 | 3 | HG01175.hp1 HG01358.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2298G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2298 | chr17 | 76142937 | |||||
| chr17:76143119
|
G | T | 1 | a0001c0005t0008 | 3 | NA18522.hp1 NA19030.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2116C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2116 | chr17 | 76143119 | |||||
| chr17:76143179
|
C | T | 2 | a0001c0001t0006a0001c0004t0006 | 4 | HG00639.hp2 HG02055.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2056G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2056 | chr17 | 76143179 | |||||
| chr17:76143183
|
G | A | 19 | a0001c0001t0002a0001c0001t0006a0001c0001t0020others(16): Show | 91 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2052C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 2052 | chr17 | 76143183 | |||||
| chr17:76143267
|
T | C | 1 | a0001c0007t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1968A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 1968 | chr17 | 76143267 | |||||
| chr17:76143271
|
C | T | 1 | a0001c0003t0019 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1964G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 1964 | chr17 | 76143271 | |||||
| chr17:76143545
|
G | T | 1 | a0001c0005t0008 | 3 | NA18522.hp1 NA19030.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1690C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 1690 | chr17 | 76143545 | |||||
| chr17:76143613
|
A | G | 32 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(29): Show | 117 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1622T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 1622 | chr17 | 76143613 | |||||
| chr17:76143761
|
A | AT | 6 | a0001c0001t0010a0001c0002t0007a0001c0003t0012others(3): Show | 8 | HG01175.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1473dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 1473 | chr17 | 76143761 | |||||
| chr17:76144095
|
G | C | 1 | a0001c0001t0016 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1140C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 1140 | chr17 | 76144095 | |||||
| chr17:76144292
|
A | C | 2 | a0001c0001t0016a0001c0002t0004 | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*943T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 943 | chr17 | 76144292 | |||||
| chr17:76144324
|
C | CT | 1 | a0001c0002t0004 | 5 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*910dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 910 | chr17 | 76144324 | |||||
| chr17:76144369
|
G | A | 1 | a0001c0001t0023 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*866C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 866 | chr17 | 76144369 | |||||
| chr17:76144382
|
A | T | 1 | a0001c0001t0018 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*853T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 853 | chr17 | 76144382 | |||||
| chr17:76144520
|
G | C | 1 | a0001c0001t0015 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*715C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 715 | chr17 | 76144520 | |||||
| chr17:76144525
|
T | G | 1 | a0001c0001t0014 | 2 | HG02922.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*710A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 710 | chr17 | 76144525 | |||||
| chr17:76144602
|
C | T | 1 | a0001c0002t0017 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*633G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 633 | chr17 | 76144602 | |||||
| chr17:76144668
|
G | A | 2 | a0001c0002t0007a0001c0006t0007 | 4 | HG02965.hp2 HG03139.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*567C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 567 | chr17 | 76144668 | |||||
| chr17:76144764
|
G | T | 1 | a0001c0003t0005 | 4 | HG01169.hp2 HG01516.hp2 HG01934.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*471C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 471 | chr17 | 76144764 | |||||
| chr17:76144794
|
C | T | 5 | a0001c0001t0010a0001c0001t0015a0001c0002t0011others(2): Show | 5 | HG02965.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*441G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 441 | chr17 | 76144794 | |||||
| chr17:76144810
|
C | T | 1 | a0001c0001t0016 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 425 | chr17 | 76144810 | |||||
| chr17:76145102
|
T | G | 1 | a0001c0001t0024 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 133 | chr17 | 76145102 | |||||
| chr17:76145104
|
C | T | 5 | a0001c0001t0010a0001c0001t0015a0001c0002t0011others(2): Show | 5 | HG02965.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*131G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 131 | chr17 | 76145104 | |||||
| chr17:76145140
|
T | C | 1 | a0001c0002t0004 | 5 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*95A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 19/19 | 95 | chr17 | 76145140 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76145404
|
A | T | 53 | a0001c0001t0002g0036a0001c0001t0002g0149a0001c0001t0002g0203others(50): Show | 53 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1922-51T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145404 | ||||||
| chr17:76145441
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1922-88G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145441 | ||||||
| chr17:76145442
|
G | A | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1922-89C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145442 | ||||||
| chr17:76145491
|
A | C | 11 | a0001c0001t0003g0012a0001c0001t0003g0217a0001c0002t0003g0032others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1922-138T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145491 | ||||||
| chr17:76145525
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1922-172A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145525 | ||||||
| chr17:76145549
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1922-196G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145549 | ||||||
| chr17:76145881
|
G | A | 4 | a0001c0001t0006g0141a0001c0004t0006g0018a0001c0004t0006g0019others(1): Show | 4 | HG00639.hp2 HG02055.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-528C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145881 | ||||||
| chr17:76145884
|
T | G | 2 | a0001c0001t0003g0012a0002c0010t0003g0213 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1922-531A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76145884 | ||||||
| chr17:76146066
|
T | G | 1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1922-713A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146066 | ||||||
| chr17:76146137
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1922-784C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146137 | ||||||
| chr17:76146141
|
C | A | 34 | a0001c0001t0002g0154a0001c0001t0002g0187a0001c0001t0006g0141others(31): Show | 35 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1922-788G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146141 | ||||||
| chr17:76146163
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1922-810C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146163 | ||||||
| chr17:76146531
|
A | G | 1 | a0001c0015t0001g0105 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1922-1178T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146531 | ||||||
| chr17:76146639
|
G | A | 1 | a0001c0008t0001g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1922-1286C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146639 | ||||||
| chr17:76146810
|
C | T | 93 | a0001c0001t0002g0036a0001c0001t0002g0149a0001c0001t0002g0154others(90): Show | 94 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1922-1457G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146810 | ||||||
| chr17:76146841
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1922-1488G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146841 | ||||||
| chr17:76146907
|
C | A | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1922-1554G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146907 | ||||||
| chr17:76146909
|
C | A | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1922-1556G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146909 | ||||||
| chr17:76146911
|
T | G | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1922-1558A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146911 | ||||||
| chr17:76146912
|
T | A | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1922-1559A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146912 | ||||||
| chr17:76146913
|
A | C | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1922-1560T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76146913 | ||||||
| chr17:76147381
|
C | G | 1 | a0001c0003t0019g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1922-2028G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76147381 | ||||||
| chr17:76147586
|
C | T | 2 | a0001c0001t0003g0217a0001c0004t0003g0027 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1922-2233G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76147586 | ||||||
| chr17:76147697
|
C | G | 7 | a0001c0001t0002g0203a0001c0001t0010g0039a0001c0001t0015g0196others(4): Show | 7 | HG02257.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1922-2344G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76147697 | ||||||
| chr17:76147881
|
A | G | 4 | a0001c0001t0003g0012a0001c0001t0014g0003a0001c0001t0014g0086others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1922-2528T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76147881 | ||||||
| chr17:76147967
|
T | C | 3 | a0001c0001t0003g0217a0001c0002t0004g0121a0001c0004t0003g0027 | 3 | HG02809.hp2 HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1922-2614A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76147967 | ||||||
| chr17:76148245
|
T | C | 3 | a0001c0001t0003g0217a0001c0002t0004g0121a0001c0004t0003g0027 | 3 | HG02809.hp2 HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1922-2892A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148245 | ||||||
| chr17:76148254
|
T | A | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1922-2901A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148254 | ||||||
| chr17:76148255
|
C | T | 3 | a0001c0001t0003g0217a0001c0002t0004g0121a0001c0004t0003g0027 | 3 | HG02809.hp2 HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1922-2902G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148255 | ||||||
| chr17:76148261
|
C | CT | 19 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0049others(16): Show | 19 | HG01070.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1922-2909dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148261 | ||||||
| chr17:76148261
|
C | CTT | 29 | a0001c0001t0002g0154a0001c0001t0002g0187a0001c0001t0010g0039others(26): Show | 30 | HG00639.hp1 HG00735.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.1922-2910_1922-290 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148261 | ||||||
| chr17:76148261
|
CT | C | 28 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0002g0036others(25): Show | 28 | HG00621.hp1 HG01069.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.1922-2909delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148261 | ||||||
| chr17:76148291
|
GTC | G | 3 | a0001c0001t0003g0217a0001c0002t0004g0121a0001c0004t0003g0027 | 3 | HG02809.hp2 HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1922-2940_1922-293 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148291 | ||||||
| chr17:76148303
|
G | A | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1922-2950C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148303 | ||||||
| chr17:76148335
|
C | T | 3 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG01891.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1922-2982G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148335 | ||||||
| chr17:76148566
|
C | CT | 5 | a0001c0001t0001g0006a0001c0001t0001g0193a0001c0001t0016g0113others(2): Show | 5 | HG00597.hp2 HG02055.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1922-3214dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148566 | ||||||
| chr17:76148566
|
CT | C | 89 | a0001c0001t0002g0036a0001c0001t0002g0149a0001c0001t0002g0154others(86): Show | 90 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.1922-3214delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148566 | ||||||
| chr17:76148567
|
T | G | 1 | a0001c0002t0002g0063 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1922-3214A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148567 | ||||||
| chr17:76148852
|
G | A | 1 | a0008c0014t0001g0161 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1922-3499C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148852 | ||||||
| chr17:76148906
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1921+3449G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76148906 | ||||||
| chr17:76149194
|
C | G | 5 | a0001c0001t0003g0217a0001c0004t0003g0027a0001c0005t0008g0017others(2): Show | 5 | HG02895.hp2 NA18522.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1921+3161G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149194 | ||||||
| chr17:76149236
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1921+3119C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149236 | ||||||
| chr17:76149420
|
C | T | 5 | a0001c0002t0004g0116a0001c0002t0004g0117a0001c0002t0004g0118others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1921+2935G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149420 | ||||||
| chr17:76149460
|
G | A | 3 | a0001c0005t0008g0017a0001c0005t0008g0197a0001c0005t0008g0198 | 3 | NA18522.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1921+2895C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149460 | ||||||
| chr17:76149786
|
C | A | 2 | a0001c0001t0010g0039a0002c0010t0010g0220 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1921+2569G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149786 | ||||||
| chr17:76149859
|
C | A | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1921+2496G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149859 | ||||||
| chr17:76149861
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1921+2494G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149861 | ||||||
| chr17:76149862
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1921+2493G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149862 | ||||||
| chr17:76149864
|
T | G | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1921+2491A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149864 | ||||||
| chr17:76149865
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1921+2490G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149865 | ||||||
| chr17:76149907
|
G | A | 2 | a0001c0001t0003g0217a0001c0004t0003g0027 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1921+2448C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76149907 | ||||||
| chr17:76150139
|
AT | A | 26 | a0001c0001t0002g0154a0001c0001t0002g0187a0001c0002t0002g0031others(23): Show | 27 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1921+2215delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76150139 | ||||||
| chr17:76150583
|
C | T | 10 | a0001c0001t0003g0125a0001c0001t0003g0217a0001c0001t0010g0039others(7): Show | 10 | HG01891.hp2 HG02895.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1921+1772G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76150583 | ||||||
| chr17:76150622
|
AAG | A | 24 | a0001c0001t0002g0036a0001c0002t0002g0067a0001c0002t0002g0068others(21): Show | 24 | HG01069.hp1 HG01081.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1921+1731_1921+173 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76150622 | ||||||
| chr17:76150652
|
A | G | 111 | a0001c0001t0002g0036a0001c0001t0002g0149a0001c0001t0002g0154others(108): Show | 112 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.1921+1703T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76150652 | ||||||
| chr17:76150997
|
T | C | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1921+1358A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76150997 | ||||||
| chr17:76151037
|
G | A | 2 | a0001c0001t0014g0003a0001c0001t0014g0086 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1921+1318C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151037 | ||||||
| chr17:76151088
|
C | T | 3 | a0001c0002t0002g0103a0001c0004t0002g0057a0001c0004t0002g0162 | 3 | HG01081.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1921+1267G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151088 | ||||||
| chr17:76151435
|
A | G | 1 | a0001c0008t0001g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1921+920T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151435 | ||||||
| chr17:76151525
|
G | A | 2 | a0001c0001t0014g0003a0001c0001t0014g0086 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1921+830C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151525 | ||||||
| chr17:76151543
|
T | G | 102 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(99): Show | 103 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.1921+812A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151543 | ||||||
| chr17:76151607
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1921+748C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151607 | ||||||
| chr17:76151643
|
A | C | 5 | a0001c0001t0010g0039a0001c0001t0015g0196a0001c0002t0011g0205others(2): Show | 5 | HG02965.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1921+712T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76151643 | ||||||
| chr17:76152082
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1921+273C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76152082 | ||||||
| chr17:76152197
|
T | C | 2 | a0001c0001t0003g0012a0002c0010t0003g0213 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1921+158A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 18/18 | chr17 | 76152197 | ||||||
| chr17:76152554
|
C | CA | 9 | a0001c0001t0003g0125a0001c0001t0016g0113a0001c0002t0003g0032others(6): Show | 9 | HG01891.hp2 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1811-90dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152554 | ||||||
| chr17:76152554
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1811-89G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152554 | ||||||
| chr17:76152598
|
C | T | 5 | a0001c0001t0003g0012a0001c0005t0008g0017a0001c0005t0008g0197others(2): Show | 5 | HG02109.hp2 HG02258.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1811-133G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152598 | ||||||
| chr17:76152680
|
C | G | 4 | a0001c0003t0002g0130a0001c0003t0012g0129a0003c0019t0002g0126others(1): Show | 4 | HG00735.hp2 HG01175.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1811-215G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152680 | ||||||
| chr17:76152773
|
A | T | 2 | a0001c0001t0010g0039a0002c0010t0010g0220 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1811-308T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152773 | ||||||
| chr17:76152778
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1811-313G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152778 | ||||||
| chr17:76152885
|
G | C | 1 | a0001c0003t0002g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1811-420C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152885 | ||||||
| chr17:76152910
|
A | C | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1811-445T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152910 | ||||||
| chr17:76152997
|
T | C | 98 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(95): Show | 99 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.1811-532A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76152997 | ||||||
| chr17:76153122
|
CA | C | 81 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(78): Show | 82 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.1811-658delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153122 | ||||||
| chr17:76153124
|
G | C | 81 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(78): Show | 82 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.1811-659C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153124 | ||||||
| chr17:76153219
|
A | G | 97 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(94): Show | 98 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1811-754T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153219 | ||||||
| chr17:76153230
|
A | G | 8 | a0001c0001t0003g0012a0001c0001t0003g0217a0001c0002t0007g0228others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1811-765T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153230 | ||||||
| chr17:76153301
|
T | C | 1 | a0001c0004t0002g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1811-836A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153301 | ||||||
| chr17:76153443
|
T | C | 102 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(99): Show | 103 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.1810+840A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153443 | ||||||
| chr17:76153531
|
G | C | 1 | a0001c0002t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1810+752C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153531 | ||||||
| chr17:76153608
|
C | T | 113 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(110): Show | 114 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.1810+675G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153608 | ||||||
| chr17:76153677
|
G | C | 2 | a0001c0001t0003g0012a0002c0010t0003g0213 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1810+606C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153677 | ||||||
| chr17:76153781
|
C | T | 2 | a0001c0001t0014g0003a0001c0001t0014g0086 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1810+502G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153781 | ||||||
| chr17:76153866
|
G | A | 3 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033 | 3 | HG01891.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1810+417C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153866 | ||||||
| chr17:76153888
|
C | T | 103 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(100): Show | 104 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1810+395G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153888 | ||||||
| chr17:76153956
|
G | A | 2 | a0001c0001t0003g0012a0002c0010t0003g0213 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1810+327C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76153956 | ||||||
| chr17:76154032
|
T | C | 79 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(76): Show | 80 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.1810+251A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76154032 | ||||||
| chr17:76154067
|
C | T | 101 | a0001c0001t0002g0036a0001c0001t0002g0114a0001c0001t0002g0149others(98): Show | 102 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1810+216G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 17/18 | chr17 | 76154067 | ||||||
| chr17:76154377
|
A | C | 7 | a0001c0001t0003g0217a0001c0002t0004g0121a0001c0002t0007g0228others(4): Show | 7 | HG02809.hp2 HG02895.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1765-49T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 16/18 | chr17 | 76154377 | ||||||
| chr17:76154544
|
A | G | 1 | a0001c0002t0002g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1765-216T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 16/18 | chr17 | 76154544 | ||||||
| chr17:76154627
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1765-299T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 16/18 | chr17 | 76154627 | ||||||
| chr17:76154712
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1765-384A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 16/18 | chr17 | 76154712 | ||||||
| chr17:76155144
|
G | C | 2 | a0001c0005t0008g0197a0001c0005t0008g0198 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1764+108C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 16/18 | chr17 | 76155144 | ||||||
| chr17:76155375
|
C | T | 26 | a0001c0001t0002g0154a0001c0001t0002g0187a0001c0002t0002g0031others(23): Show | 27 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1699-58G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 15/18 | chr17 | 76155375 | ||||||
| chr17:76155396
|
T | C | 2 | a0001c0001t0003g0012a0002c0010t0003g0213 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1699-79A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 15/18 | chr17 | 76155396 | ||||||
| chr17:76155523
|
G | A | 2 | a0001c0001t0003g0217a0001c0004t0003g0027 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1698+39C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 15/18 | chr17 | 76155523 | ||||||
| chr17:76156015
|
A | G | 1 | a0001c0004t0001g0104 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1525+195T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 14/18 | chr17 | 76156015 | ||||||
| chr17:76156145
|
G | A | 1 | a0001c0001t0020g0038 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1525+65C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 14/18 | chr17 | 76156145 | ||||||
| chr17:76156196
|
C | T | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1525+14G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 14/18 | chr17 | 76156196 | ||||||
| chr17:76156481
|
T | C | 2 | a0001c0003t0002g0111a0001c0015t0001g0105 | 2 | NA18968.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1414-160A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76156481 | ||||||
| chr17:76156724
|
G | A | 2 | a0001c0001t0003g0012a0001c0002t0001g0186 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1414-403C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76156724 | ||||||
| chr17:76156826
|
G | C | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1414-505C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76156826 | ||||||
| chr17:76157000
|
T | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(46): Show | 49 | HG00639.hp1 HG01106.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.1414-679A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157000 | ||||||
| chr17:76157031
|
G | A | 2 | a0001c0001t0002g0114a0001c0004t0003g0027 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-710C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157031 | ||||||
| chr17:76157059
|
T | C | 2 | a0001c0001t0002g0114a0001c0004t0003g0027 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-738A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157059 | ||||||
| chr17:76157080
|
C | T | 2 | a0001c0001t0002g0114a0001c0004t0003g0027 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-759G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157080 | ||||||
| chr17:76157111
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1414-790A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157111 | ||||||
| chr17:76157112
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1414-791C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157112 | ||||||
| chr17:76157114
|
A | C | 3 | a0001c0001t0002g0114a0001c0001t0002g0203a0001c0004t0003g0027 | 3 | HG02257.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-793T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157114 | ||||||
| chr17:76157115
|
T | C | 3 | a0001c0001t0002g0114a0001c0001t0002g0203a0001c0004t0003g0027 | 3 | HG02257.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-794A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157115 | ||||||
| chr17:76157140
|
G | C | 2 | a0001c0001t0002g0114a0001c0004t0003g0027 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-819C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157140 | ||||||
| chr17:76157233
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1414-912G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157233 | ||||||
| chr17:76157245
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1414-924G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157245 | ||||||
| chr17:76157266
|
A | T | 2 | a0001c0001t0002g0114a0001c0004t0003g0027 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1414-945T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157266 | ||||||
| chr17:76157304
|
C | G | 1 | a0001c0001t0002g0114 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1414-983G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157304 | ||||||
| chr17:76157304
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1414-983G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157304 | ||||||
| chr17:76157315
|
G | A | 5 | a0001c0003t0002g0078a0001c0003t0002g0095a0001c0003t0002g0096others(2): Show | 5 | HG02132.hp1 NA18956.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-994C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157315 | ||||||
| chr17:76157348
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1414-1027G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157348 | ||||||
| chr17:76157409
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1413+984C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157409 | ||||||
| chr17:76157411
|
C | A | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1413+982G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157411 | ||||||
| chr17:76157585
|
G | A | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1413+808C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157585 | ||||||
| chr17:76157883
|
C | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(22): Show | 25 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.1413+510G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76157883 | ||||||
| chr17:76158119
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1413+274G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76158119 | ||||||
| chr17:76158143
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1413+250A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76158143 | ||||||
| chr17:76158230
|
A | C | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1413+163T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76158230 | ||||||
| chr17:76158269
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1413+124G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 13/18 | chr17 | 76158269 | ||||||
| chr17:76158641
|
G | A | 1 | a0001c0002t0002g0071 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1305-140C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76158641 | ||||||
| chr17:76158682
|
C | T | 1 | a0001c0008t0001g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1305-181G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76158682 | ||||||
| chr17:76158763
|
A | G | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1305-262T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76158763 | ||||||
| chr17:76158970
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1304+365C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76158970 | ||||||
| chr17:76159018
|
G | A | 61 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(58): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1304+317C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76159018 | ||||||
| chr17:76159060
|
A | C | 10 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0003g0217others(7): Show | 10 | HG01884.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1304+275T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76159060 | ||||||
| chr17:76159179
|
T | C | 10 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0003g0217others(7): Show | 10 | HG01884.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1304+156A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76159179 | ||||||
| chr17:76159204
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1304+131C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 12/18 | chr17 | 76159204 | ||||||
| chr17:76160137
|
C | T | 1 | a0001c0003t0002g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1066-564G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160137 | ||||||
| chr17:76160147
|
G | C | 1 | a0001c0003t0002g0030 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1066-574C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160147 | ||||||
| chr17:76160251
|
A | C | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(101): Show | 105 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1066-678T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160251 | ||||||
| chr17:76160315
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0002g0151others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-742A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160315 | ||||||
| chr17:76160374
|
GT | G | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(101): Show | 105 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1066-802delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160374 | ||||||
| chr17:76160542
|
T | C | 1 | a0006c0018t0001g0026 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1066-969A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160542 | ||||||
| chr17:76160616
|
A | C | 62 | a0001c0001t0006g0141a0001c0003t0001g0124a0001c0003t0001g0176others(59): Show | 63 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1065+919T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160616 | ||||||
| chr17:76160654
|
T | C | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065+881A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160654 | ||||||
| chr17:76160671
|
G | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(102): Show | 106 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1065+864C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160671 | ||||||
| chr17:76160700
|
A | G | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(26): Show | 29 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.1065+835T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160700 | ||||||
| chr17:76160764
|
G | A | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+771C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160764 | ||||||
| chr17:76160824
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1065+711T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76160824 | ||||||
| chr17:76161514
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1065+21C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 11/18 | chr17 | 76161514 | ||||||
| chr17:76161700
|
A | T | 1 | a0001c0002t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.953-53T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 10/18 | chr17 | 76161700 | ||||||
| chr17:76162425
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179 | 3 | NA18948.hp1 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.792+127G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 9/18 | chr17 | 76162425 | ||||||
| chr17:76162486
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0109a0001c0001t0001g0172others(5): Show | 8 | HG00438.hp2 HG00597.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+66C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 9/18 | chr17 | 76162486 | ||||||
| chr17:76162655
|
G | A | 6 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-32C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76162655 | ||||||
| chr17:76162720
|
C | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(29): Show | 32 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.721-97G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76162720 | ||||||
| chr17:76162953
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.721-330A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76162953 | ||||||
| chr17:76163031
|
AAAG | A | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-411_721-409del others(3): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163031 | ||||||
| chr17:76163048
|
C | T | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.721-425G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163048 | ||||||
| chr17:76163060
|
T | C | 62 | a0001c0001t0006g0141a0001c0003t0001g0124a0001c0003t0001g0176others(59): Show | 63 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.721-437A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163060 | ||||||
| chr17:76163168
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.721-545A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163168 | ||||||
| chr17:76163190
|
C | CT | 12 | a0001c0001t0001g0013a0001c0001t0001g0219a0001c0001t0003g0125others(9): Show | 12 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-568dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163190 | ||||||
| chr17:76163190
|
C | CTT | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(30): Show | 33 | HG01106.hp1 HG01928.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.721-569_721-568dup others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163190 | ||||||
| chr17:76163190
|
C | CTTT | 64 | a0001c0001t0002g0203a0001c0001t0016g0113a0001c0002t0002g0071others(61): Show | 65 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.721-570_721-568dup others(3): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163190 | ||||||
| chr17:76163190
|
C | CTTTT | 6 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0002g0151others(3): Show | 6 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-571_721-568dup others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163190 | ||||||
| chr17:76163247
|
C | T | 1 | a0001c0002t0004g0117 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.721-624G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163247 | ||||||
| chr17:76163489
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(38): Show | 41 | HG00639.hp1 HG01106.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.721-866G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163489 | ||||||
| chr17:76163671
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.721-1048G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163671 | ||||||
| chr17:76163682
|
T | G | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(101): Show | 105 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.721-1059A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76163682 | ||||||
| chr17:76164345
|
T | C | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.720+403A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76164345 | ||||||
| chr17:76164465
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.720+283G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76164465 | ||||||
| chr17:76164611
|
TA | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0072a0001c0001t0001g0127others(12): Show | 15 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+136delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 8/18 | chr17 | 76164611 | ||||||
| chr17:76164833
|
G | C | 61 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(58): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.673-38C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 7/18 | chr17 | 76164833 | ||||||
| chr17:76165301
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.672+201A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 7/18 | chr17 | 76165301 | ||||||
| chr17:76165452
|
C | T | 61 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(58): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.672+50G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 7/18 | chr17 | 76165452 | ||||||
| chr17:76165565
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.629-20C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76165565 | ||||||
| chr17:76165683
|
C | CT | 40 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0029others(37): Show | 40 | HG00438.hp1 HG00597.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.629-139dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76165683 | ||||||
| chr17:76165770
|
C | T | 1 | a0001c0003t0002g0066 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.629-225G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76165770 | ||||||
| chr17:76165817
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.629-272A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76165817 | ||||||
| chr17:76165969
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.629-424G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76165969 | ||||||
| chr17:76166156
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG01069.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628+305C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76166156 | ||||||
| chr17:76166267
|
GC | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+193delG | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76166267 | ||||||
| chr17:76166357
|
A | C | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.628+104T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76166357 | ||||||
| chr17:76166425
|
G | A | 60 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(57): Show | 61 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.628+36C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76166425 | ||||||
| chr17:76166436
|
C | T | 3 | a0001c0003t0001g0176a0001c0003t0001g0224a0001c0003t0005g0204 | 3 | HG01515.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.628+25G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 6/18 | chr17 | 76166436 | ||||||
| chr17:76166559
|
A | C | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.562-32T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166559 | ||||||
| chr17:76166682
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.562-155C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166682 | ||||||
| chr17:76166738
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.562-211A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166738 | ||||||
| chr17:76166914
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.561+95C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166914 | ||||||
| chr17:76166916
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(102): Show | 106 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.561+93T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166916 | ||||||
| chr17:76166920
|
G | A | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.561+89C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166920 | ||||||
| chr17:76166995
|
C | G | 1 | a0001c0002t0002g0063 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.561+14G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 5/18 | chr17 | 76166995 | ||||||
| chr17:76167166
|
C | T | 12 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(9): Show | 12 | HG00140.hp2 HG00735.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.444-40G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167166 | ||||||
| chr17:76167184
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444-58G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167184 | ||||||
| chr17:76167229
|
G | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.444-103C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167229 | ||||||
| chr17:76167284
|
G | A | 4 | a0001c0001t0009g0101a0001c0001t0009g0102a0001c0002t0002g0098others(1): Show | 4 | HG01081.hp2 HG01175.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-158C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167284 | ||||||
| chr17:76167368
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.444-242A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167368 | ||||||
| chr17:76167397
|
C | T | 61 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(58): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.443+254G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167397 | ||||||
| chr17:76167409
|
G | A | 110 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(107): Show | 111 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.443+242C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 4/18 | chr17 | 76167409 | ||||||
| chr17:76167851
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.297-54A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76167851 | ||||||
| chr17:76167884
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.297-87G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76167884 | ||||||
| chr17:76168017
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.297-220A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168017 | ||||||
| chr17:76168056
|
C | T | 1 | a0001c0001t0015g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297-259G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168056 | ||||||
| chr17:76168193
|
T | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.297-396A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168193 | ||||||
| chr17:76168428
|
A | AT | 15 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.297-632dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168428 | ||||||
| chr17:76168428
|
A | ATT | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.297-633_297-632dup others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168428 | ||||||
| chr17:76168463
|
A | G | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0016g0113others(5): Show | 8 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.297-666T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168463 | ||||||
| chr17:76168580
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.297-783G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168580 | ||||||
| chr17:76168619
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.297-822G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168619 | ||||||
| chr17:76168739
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.297-942T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168739 | ||||||
| chr17:76168770
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0221a0001c0001t0001g0229others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.297-973G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168770 | ||||||
| chr17:76168865
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.297-1068A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76168865 | ||||||
| chr17:76169063
|
G | T | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.297-1266C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169063 | ||||||
| chr17:76169108
|
C | T | 130 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(127): Show | 131 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.297-1311G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169108 | ||||||
| chr17:76169279
|
CCT | C | 63 | a0001c0001t0003g0218a0001c0003t0001g0124a0001c0003t0001g0176others(60): Show | 64 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.297-1484_297-1483d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169279 | ||||||
| chr17:76169290
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0003g0218 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.297-1493A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169290 | ||||||
| chr17:76169425
|
G | C | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.297-1628C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169425 | ||||||
| chr17:76169428
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0003g0218 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.297-1631A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169428 | ||||||
| chr17:76169520
|
T | C | 110 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(107): Show | 111 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.297-1723A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169520 | ||||||
| chr17:76169579
|
G | GT | 13 | a0001c0001t0001g0029a0001c0001t0001g0148a0001c0001t0002g0149others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.297-1783dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169579 | ||||||
| chr17:76169579
|
GT | G | 8 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0002g0203others(5): Show | 8 | HG01081.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.297-1783delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169579 | ||||||
| chr17:76169579
|
GTT | G | 61 | a0001c0001t0006g0141a0001c0003t0001g0124a0001c0003t0001g0176others(58): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.297-1784_297-1783d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169579 | ||||||
| chr17:76169725
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0003g0218 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.297-1928C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169725 | ||||||
| chr17:76169849
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.297-2052C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169849 | ||||||
| chr17:76169870
|
C | T | 1 | a0001c0021t0001g0043 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.297-2073G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169870 | ||||||
| chr17:76169968
|
T | G | 62 | a0001c0001t0006g0141a0001c0003t0001g0124a0001c0003t0001g0176others(59): Show | 63 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.297-2171A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169968 | ||||||
| chr17:76169983
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.297-2186C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76169983 | ||||||
| chr17:76170038
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.297-2241C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170038 | ||||||
| chr17:76170105
|
C | G | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.297-2308G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170105 | ||||||
| chr17:76170182
|
A | G | 113 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(110): Show | 114 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.297-2385T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170182 | ||||||
| chr17:76170216
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.297-2419A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170216 | ||||||
| chr17:76170788
|
G | A | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(99): Show | 103 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.296+2914C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170788 | ||||||
| chr17:76170931
|
C | T | 5 | a0001c0001t0001g0219a0001c0001t0003g0125a0001c0002t0003g0032others(2): Show | 5 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.296+2771G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170931 | ||||||
| chr17:76170969
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.296+2733A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76170969 | ||||||
| chr17:76171024
|
C | T | 61 | a0001c0001t0006g0141a0001c0003t0001g0124a0001c0003t0001g0176others(58): Show | 62 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.296+2678G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171024 | ||||||
| chr17:76171077
|
G | A | 1 | a0001c0003t0005g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.296+2625C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171077 | ||||||
| chr17:76171207
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.296+2495A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171207 | ||||||
| chr17:76171241
|
T | C | 107 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0077others(104): Show | 108 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.296+2461A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171241 | ||||||
| chr17:76171434
|
C | T | 63 | a0001c0001t0002g0203a0001c0001t0006g0141a0001c0003t0001g0124others(60): Show | 64 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.296+2268G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171434 | ||||||
| chr17:76171746
|
C | A | 8 | a0001c0002t0002g0209a0001c0002t0002g0214a0001c0002t0002g0215others(5): Show | 8 | HG01106.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.296+1956G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171746 | ||||||
| chr17:76171880
|
G | A | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.296+1822C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76171880 | ||||||
| chr17:76172039
|
C | G | 2 | a0001c0005t0008g0197a0001c0005t0008g0198 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.296+1663G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172039 | ||||||
| chr17:76172050
|
C | T | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0016g0113others(5): Show | 8 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.296+1652G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172050 | ||||||
| chr17:76172053
|
G | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0079 | 2 | NA19066.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.296+1649C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172053 | ||||||
| chr17:76172268
|
C | T | 2 | a0001c0004t0002g0207a0001c0004t0002g0208 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.296+1434G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172268 | ||||||
| chr17:76172448
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.296+1254C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172448 | ||||||
| chr17:76172478
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.296+1224G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172478 | ||||||
| chr17:76172550
|
T | G | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.296+1152A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172550 | ||||||
| chr17:76172556
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(22): Show | 25 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.296+1146C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172556 | ||||||
| chr17:76172607
|
C | CA | 14 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0109others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.296+1094dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172607
|
C | CAAAAAA | 5 | a0001c0001t0001g0148a0001c0002t0002g0151a0001c0002t0004g0121others(2): Show | 5 | HG02809.hp2 HG02818.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.296+1089_296+1094d others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172607
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.296+1083_296+1094d others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172607
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0219a0001c0001t0003g0218 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.296+1082_296+1094d others(15): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172607
|
CA | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(24): Show | 27 | HG00639.hp1 HG01928.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.296+1094delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172607
|
CAAAAA | C | 9 | a0001c0003t0002g0096a0001c0003t0002g0130a0001c0003t0002g0182others(6): Show | 9 | HG00621.hp1 HG00735.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.296+1090_296+1094d others(7): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172607
|
CAAAAAA | C | 52 | a0001c0001t0006g0141a0001c0003t0001g0124a0001c0003t0001g0176others(49): Show | 53 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.296+1089_296+1094d others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172607 | ||||||
| chr17:76172634
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.296+1068C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172634 | ||||||
| chr17:76172651
|
A | AAT | 6 | a0001c0001t0003g0125a0001c0002t0011g0205a0001c0006t0007g0014others(3): Show | 6 | HG02965.hp2 HG03139.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.296+1049_296+1050d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172651 | ||||||
| chr17:76172750
|
A | T | 29 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(26): Show | 29 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.296+952T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172750 | ||||||
| chr17:76172837
|
C | T | 1 | a0001c0007t0001g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.296+865G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172837 | ||||||
| chr17:76172906
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.296+796T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76172906 | ||||||
| chr17:76173012
|
C | T | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(101): Show | 105 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.296+690G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173012 | ||||||
| chr17:76173015
|
G | A | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.296+687C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173015 | ||||||
| chr17:76173015
|
G | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.296+687C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173015 | ||||||
| chr17:76173142
|
C | T | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(101): Show | 105 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.296+560G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173142 | ||||||
| chr17:76173254
|
C | G | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.296+448G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173254 | ||||||
| chr17:76173261
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.296+441C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173261 | ||||||
| chr17:76173346
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296+356C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173346 | ||||||
| chr17:76173531
|
C | T | 1 | a0001c0004t0003g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.296+171G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173531 | ||||||
| chr17:76173572
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0018g0225 | 3 | NA18993.hp2 NA19004.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.296+130C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173572 | ||||||
| chr17:76173601
|
C | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0059others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.296+101G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 3/18 | chr17 | 76173601 | ||||||
| chr17:76173808
|
CAGG | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(18): Show | 21 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.208-21_208-19delCC others(1): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76173808 | ||||||
| chr17:76173862
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-72A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76173862 | ||||||
| chr17:76174029
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0210 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.208-239T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174029 | ||||||
| chr17:76174039
|
T | G | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-249A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174039 | ||||||
| chr17:76174073
|
T | TA | 4 | a0001c0002t0002g0180a0001c0003t0002g0195a0001c0004t0002g0040others(1): Show | 4 | HG02145.hp1 HG02155.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-284dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174073 | ||||||
| chr17:76174076
|
T | A | 110 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0148others(107): Show | 111 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.208-286A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174076 | ||||||
| chr17:76174084
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-294T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174084 | ||||||
| chr17:76174126
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-336C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174126 | ||||||
| chr17:76174196
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208-406G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174196 | ||||||
| chr17:76174450
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-660A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174450 | ||||||
| chr17:76174544
|
T | C | 1 | a0004c0011t0002g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.208-754A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174544 | ||||||
| chr17:76174909
|
T | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(27): Show | 30 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.208-1119A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174909 | ||||||
| chr17:76174969
|
T | C | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.208-1179A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76174969 | ||||||
| chr17:76175161
|
A | T | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-1371T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175161 | ||||||
| chr17:76175274
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-1484G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175274 | ||||||
| chr17:76175371
|
G | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-1581C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175371 | ||||||
| chr17:76175513
|
C | A | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-1723G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175513 | ||||||
| chr17:76175542
|
A | G | 1 | a0001c0004t0002g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.208-1752T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175542 | ||||||
| chr17:76175666
|
T | C | 1 | a0001c0002t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208-1876A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175666 | ||||||
| chr17:76175769
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-1979G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175769 | ||||||
| chr17:76175845
|
GA | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179others(18): Show | 21 | HG00639.hp1 HG01106.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.208-2056delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175845 | ||||||
| chr17:76175982
|
T | A | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-2192A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175982 | ||||||
| chr17:76175986
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-2196G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76175986 | ||||||
| chr17:76176053
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0221a0001c0001t0001g0229others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-2263C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176053 | ||||||
| chr17:76176182
|
G | C | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.208-2392C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176182 | ||||||
| chr17:76176323
|
T | G | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-2533A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176323 | ||||||
| chr17:76176426
|
T | A | 5 | a0001c0001t0001g0006a0001c0001t0003g0217a0001c0004t0001g0104others(2): Show | 5 | HG00597.hp1 HG03927.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2636A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176426 | ||||||
| chr17:76176511
|
T | A | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-2721A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176511 | ||||||
| chr17:76176788
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-2998G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176788 | ||||||
| chr17:76176837
|
C | T | 1 | a0001c0003t0002g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.208-3047G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176837 | ||||||
| chr17:76176838
|
G | A | 1 | a0001c0004t0002g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.208-3048C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176838 | ||||||
| chr17:76176884
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-3094G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176884 | ||||||
| chr17:76176954
|
G | A | 8 | a0001c0001t0002g0154a0001c0001t0002g0187a0001c0002t0002g0071others(5): Show | 8 | HG00639.hp1 HG01928.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-3164C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76176954 | ||||||
| chr17:76177027
|
T | C | 69 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.208-3237A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177027 | ||||||
| chr17:76177054
|
T | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(34): Show | 37 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.208-3264A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177054 | ||||||
| chr17:76177092
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.208-3302G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177092 | ||||||
| chr17:76177125
|
ACTGGCCC others(5): Show |
A | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-3347_208-3336d others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177125 | ||||||
| chr17:76177193
|
T | C | 1 | a0001c0001t0015g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208-3403A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177193 | ||||||
| chr17:76177249
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-3459C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177249 | ||||||
| chr17:76177293
|
C | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(32): Show | 35 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.208-3503G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177293 | ||||||
| chr17:76177313
|
C | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(28): Show | 31 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.208-3523G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177313 | ||||||
| chr17:76177314
|
C | G | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-3524G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177314 | ||||||
| chr17:76177612
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-3822G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177612 | ||||||
| chr17:76177717
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.208-3927T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177717 | ||||||
| chr17:76177749
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.208-3959G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177749 | ||||||
| chr17:76177825
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-4035G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177825 | ||||||
| chr17:76177961
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.208-4171G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177961 | ||||||
| chr17:76177981
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-4191C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76177981 | ||||||
| chr17:76178024
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-4234G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178024 | ||||||
| chr17:76178048
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-4258A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178048 | ||||||
| chr17:76178195
|
G | A | 3 | a0001c0001t0009g0101a0001c0001t0009g0102a0001c0002t0002g0098 | 3 | HG01081.hp2 HG01358.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.208-4405C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178195 | ||||||
| chr17:76178279
|
C | T | 2 | a0001c0001t0003g0218a0001c0004t0003g0027 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.208-4489G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178279 | ||||||
| chr17:76178319
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-4529G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178319 | ||||||
| chr17:76178498
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-4708C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178498 | ||||||
| chr17:76178503
|
T | C | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-4713A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178503 | ||||||
| chr17:76178532
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-4742A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178532 | ||||||
| chr17:76178804
|
G | C | 34 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(31): Show | 34 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.208-5014C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178804 | ||||||
| chr17:76178936
|
G | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(30): Show | 33 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.208-5146C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178936 | ||||||
| chr17:76178964
|
G | A | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-5174C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76178964 | ||||||
| chr17:76179023
|
G | A | 2 | a0003c0019t0002g0126a0003c0020t0002g0123 | 2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.208-5233C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179023 | ||||||
| chr17:76179042
|
T | C | 2 | a0001c0002t0002g0067a0001c0002t0002g0090 | 2 | HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.208-5252A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179042 | ||||||
| chr17:76179077
|
T | C | 1 | a0001c0003t0019g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.208-5287A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179077 | ||||||
| chr17:76179169
|
A | G | 4 | a0001c0001t0001g0219a0001c0001t0002g0203a0001c0001t0006g0141others(1): Show | 4 | HG00639.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-5379T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179169 | ||||||
| chr17:76179173
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0143a0001c0002t0001g0037 | 3 | HG01169.hp1 HG02148.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.208-5383G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179173 | ||||||
| chr17:76179273
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208-5483T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179273 | ||||||
| chr17:76179297
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-5507G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179297 | ||||||
| chr17:76179306
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-5516T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179306 | ||||||
| chr17:76179349
|
G | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-5559C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179349 | ||||||
| chr17:76179350
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-5560G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179350 | ||||||
| chr17:76179370
|
G | T | 1 | a0001c0003t0012g0129 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.208-5580C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179370 | ||||||
| chr17:76179585
|
A | C | 78 | a0001c0001t0001g0148a0001c0001t0001g0219a0001c0001t0002g0149others(75): Show | 79 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.208-5795T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179585 | ||||||
| chr17:76179585
|
A | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(29): Show | 32 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.208-5795T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179585 | ||||||
| chr17:76179657
|
C | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(29): Show | 32 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.208-5867G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179657 | ||||||
| chr17:76179709
|
A | G | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-5919T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179709 | ||||||
| chr17:76179791
|
G | A | 7 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(4): Show | 7 | HG01891.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-6001C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179791 | ||||||
| chr17:76179864
|
T | C | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-6074A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76179864 | ||||||
| chr17:76180374
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.208-6584G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76180374 | ||||||
| chr17:76180383
|
C | A | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-6593G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76180383 | ||||||
| chr17:76180477
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-6687T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76180477 | ||||||
| chr17:76180654
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.208-6864T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76180654 | ||||||
| chr17:76180888
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-7098G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76180888 | ||||||
| chr17:76180933
|
G | A | 63 | a0001c0001t0001g0219a0001c0001t0003g0125a0001c0002t0003g0032others(60): Show | 64 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.208-7143C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76180933 | ||||||
| chr17:76181037
|
C | T | 1 | a0001c0003t0002g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.208-7247G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181037 | ||||||
| chr17:76181091
|
G | A | 1 | a0001c0001t0015g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208-7301C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181091 | ||||||
| chr17:76181301
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-7511C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181301 | ||||||
| chr17:76181305
|
T | C | 59 | a0001c0001t0001g0219a0001c0003t0001g0124a0001c0003t0001g0176others(56): Show | 60 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.208-7515A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181305 | ||||||
| chr17:76181341
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-7551C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181341 | ||||||
| chr17:76181536
|
C | T | 3 | a0001c0001t0002g0203a0001c0001t0006g0141a0001c0004t0003g0027 | 3 | HG00639.hp2 HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.208-7746G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181536 | ||||||
| chr17:76181631
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0003g0218 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208-7841G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181631 | ||||||
| chr17:76181646
|
A | C | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-7856T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181646 | ||||||
| chr17:76181845
|
T | C | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-8055A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181845 | ||||||
| chr17:76181888
|
A | G | 1 | a0001c0002t0004g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.208-8098T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181888 | ||||||
| chr17:76181891
|
G | A | 58 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(55): Show | 59 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.208-8101C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181891 | ||||||
| chr17:76181907
|
C | CA | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 46 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.208-8118dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181907 | ||||||
| chr17:76181907
|
CA | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0131a0001c0001t0002g0149others(6): Show | 9 | HG00735.hp2 HG01261.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-8118delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181907 | ||||||
| chr17:76181918
|
A | AG | 2 | a0001c0001t0016g0113a0001c0005t0008g0017 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208-8129_208-8128i others(3): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181918 | ||||||
| chr17:76181953
|
A | C | 1 | a0001c0002t0004g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.208-8163T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76181953 | ||||||
| chr17:76182036
|
A | C | 58 | a0001c0003t0001g0124a0001c0003t0001g0176a0001c0003t0001g0224others(55): Show | 59 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.208-8246T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182036 | ||||||
| chr17:76182036
|
A | G | 1 | a0001c0002t0004g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.208-8246T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182036 | ||||||
| chr17:76182113
|
C | T | 1 | a0001c0001t0018g0225 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.208-8323G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182113 | ||||||
| chr17:76182129
|
G | C | 9 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0016g0113others(6): Show | 9 | HG01884.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-8339C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182129 | ||||||
| chr17:76182257
|
C | T | 59 | a0001c0001t0001g0219a0001c0003t0001g0124a0001c0003t0001g0176others(56): Show | 60 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.208-8467G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182257 | ||||||
| chr17:76182265
|
CTG | C | 3 | a0001c0002t0002g0180a0001c0002t0013g0163a0001c0002t0013g0164 | 3 | NA19007.hp1 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.208-8477_208-8476d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182265 | ||||||
| chr17:76182431
|
T | G | 1 | a0001c0001t0003g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-8641A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182431 | ||||||
| chr17:76182451
|
C | CTG | 43 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0035others(40): Show | 43 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.208-8663_208-8662d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTG | 26 | a0001c0001t0001g0007a0001c0001t0001g0152a0001c0001t0001g0159others(23): Show | 26 | HG00140.hp2 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-8665_208-8662d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTGTG | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(42): Show | 46 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.208-8667_208-8662d others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTGTGT others(1): Show |
19 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0021g0089others(16): Show | 19 | HG01069.hp1 HG01361.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.208-8669_208-8662d others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTGTGT others(3): Show |
11 | a0001c0001t0003g0012a0001c0001t0003g0217a0001c0002t0001g0186others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-8671_208-8662d others(12): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTGTGT others(5): Show |
1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-8673_208-8662d others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-8675_208-8662d others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
C | CTGTGTGT others(9): Show |
1 | a0001c0003t0002g0111 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.208-8677_208-8662d others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
CTG | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0210others(2): Show | 5 | HG02922.hp2 HG03130.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-8663_208-8662d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182451
|
CTGTG | C | 2 | a0001c0001t0002g0203a0001c0002t0002g0068 | 2 | HG01106.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.208-8665_208-8662d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182451 | ||||||
| chr17:76182535
|
C | T | 1 | a0001c0002t0002g0183 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.208-8745G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182535 | ||||||
| chr17:76182546
|
C | T | 9 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0016g0113others(6): Show | 9 | HG01884.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-8756G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182546 | ||||||
| chr17:76182632
|
C | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-8842G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182632 | ||||||
| chr17:76182760
|
C | CAT | 28 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0088others(25): Show | 28 | HG00621.hp2 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.208-8972_208-8971d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATAT | 29 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0029others(26): Show | 29 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.208-8974_208-8971d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATAT | 18 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0072others(15): Show | 18 | HG00738.hp1 HG01109.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.208-8976_208-8971d others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(1): Show |
9 | a0001c0001t0001g0109a0001c0001t0001g0152a0001c0001t0001g0191others(6): Show | 9 | HG00438.hp2 HG00597.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-8978_208-8971d others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(5): Show |
2 | a0001c0002t0003g0032a0001c0002t0003g0033 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208-8982_208-8971d others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(7): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0179others(7): Show | 10 | HG01169.hp1 HG02080.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-8984_208-8971d others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(9): Show |
2 | a0001c0001t0002g0036a0001c0002t0002g0183 | 2 | HG02300.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.208-8986_208-8971d others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(11): Show |
11 | a0001c0001t0001g0008a0001c0001t0014g0003a0001c0002t0002g0180others(8): Show | 11 | HG01106.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-8988_208-8971d others(20): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(13): Show |
2 | a0001c0002t0004g0116a0001c0002t0004g0119 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.208-8990_208-8971d others(22): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(15): Show |
3 | a0001c0002t0002g0214a0001c0002t0004g0117a0001c0012t0011g0201 | 3 | HG02886.hp2 HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208-8992_208-8971d others(24): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(17): Show |
3 | a0001c0001t0003g0012a0001c0001t0014g0086a0001c0007t0001g0194 | 3 | HG02109.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.208-8994_208-8971d others(26): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(21): Show |
1 | a0001c0007t0022g0200 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208-8998_208-8971d others(30): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(23): Show |
5 | a0001c0001t0001g0143a0001c0002t0001g0186a0001c0002t0002g0071others(2): Show | 5 | HG00639.hp1 HG01928.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-8971_208-8970i others(32): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(25): Show |
5 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0003g0125others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-8971_208-8970i others(34): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(27): Show |
2 | a0001c0001t0016g0113a0001c0005t0008g0017 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208-8971_208-8970i others(36): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(29): Show |
1 | a0001c0002t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.208-8971_208-8970i others(38): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(31): Show |
2 | a0001c0002t0011g0205a0001c0005t0008g0198 | 2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.208-8971_208-8970i others(40): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(33): Show |
2 | a0001c0005t0008g0197a0007c0017t0002g0150 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.208-8971_208-8970i others(42): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
C | CATATATA others(35): Show |
1 | a0001c0001t0021g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.208-8971_208-8970i others(44): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182760
|
CATATATA others(101): Show |
C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-9078_208-8971d others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182760 | ||||||
| chr17:76182771
|
A | G | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-8981T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182771 | ||||||
| chr17:76182773
|
A | G | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-8983T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182773 | ||||||
| chr17:76182789
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-8999C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182789 | ||||||
| chr17:76182791
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-9001C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182791 | ||||||
| chr17:76182793
|
G | T | 2 | a0001c0001t0001g0219a0001c0004t0003g0027 | 2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.208-9003C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182793 | ||||||
| chr17:76182795
|
T | G | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0016g0113others(5): Show | 8 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-9005A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182795 | ||||||
| chr17:76182810
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-9020C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182810 | ||||||
| chr17:76182810
|
GATATATA others(40): Show |
G | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-9067_208-9021d others(49): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182810 | ||||||
| chr17:76182818
|
TCCTATAT others(3): Show |
T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-9038_208-9029d others(12): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182818 | ||||||
| chr17:76182819
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-9029G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182819 | ||||||
| chr17:76182820
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-9030G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182820 | ||||||
| chr17:76182829
|
C | A | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-9039G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182829 | ||||||
| chr17:76182836
|
TGATATAT others(2): Show |
T | 62 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(59): Show | 63 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.208-9055_208-9047d others(11): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182836 | ||||||
| chr17:76182837
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-9047C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182837 | ||||||
| chr17:76182838
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-9048T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182838 | ||||||
| chr17:76182845
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0006g0141 | 2 | HG00639.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.208-9055C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182845 | ||||||
| chr17:76182848
|
T | G | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-9058A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182848 | ||||||
| chr17:76182857
|
T | G | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-9067A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182857 | ||||||
| chr17:76182871
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-9081T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182871 | ||||||
| chr17:76182951
|
T | C | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-9161A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76182951 | ||||||
| chr17:76183022
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0179 | 3 | NA18948.hp1 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.208-9232G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183022 | ||||||
| chr17:76183078
|
G | A | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-9288C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183078 | ||||||
| chr17:76183125
|
T | C | 4 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(1): Show | 4 | HG01891.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-9335A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183125 | ||||||
| chr17:76183232
|
C | T | 1 | a0001c0002t0002g0183 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.208-9442G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183232 | ||||||
| chr17:76183233
|
G | A | 2 | a0001c0008t0001g0047a0001c0008t0001g0048 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.208-9443C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183233 | ||||||
| chr17:76183674
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.208-9884T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183674 | ||||||
| chr17:76183733
|
CATTCAAT others(1): Show |
C | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(29): Show | 32 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.208-9951_208-9944d others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76183733 | ||||||
| chr17:76184160
|
C | T | 3 | a0001c0001t0001g0148a0001c0001t0002g0149a0007c0017t0002g0150 | 3 | HG01884.hp1 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.208-10370G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76184160 | ||||||
| chr17:76184189
|
T | G | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-10399A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76184189 | ||||||
| chr17:76184189
|
T | TA | 64 | a0001c0001t0001g0082a0001c0001t0001g0109a0001c0001t0001g0219others(61): Show | 65 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.208-10400dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76184189 | ||||||
| chr17:76184389
|
T | G | 1 | a0001c0004t0002g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.208-10599A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76184389 | ||||||
| chr17:76184745
|
A | C | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.208-10955T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76184745 | ||||||
| chr17:76185006
|
C | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(31): Show | 34 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.208-11216G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185006 | ||||||
| chr17:76185020
|
C | T | 2 | a0001c0001t0014g0003a0001c0001t0014g0086 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.208-11230G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185020 | ||||||
| chr17:76185164
|
T | C | 3 | a0001c0003t0001g0224a0001c0003t0005g0204a0001c0004t0002g0057 | 3 | HG01081.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.208-11374A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185164 | ||||||
| chr17:76185184
|
A | G | 13 | a0001c0004t0002g0011a0001c0004t0002g0133a0001c0004t0002g0134others(10): Show | 13 | HG01069.hp1 HG01361.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.208-11394T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185184 | ||||||
| chr17:76185185
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.208-11395G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185185 | ||||||
| chr17:76185381
|
G | A | 63 | a0001c0001t0001g0219a0001c0001t0003g0125a0001c0002t0003g0032others(60): Show | 64 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.208-11591C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185381 | ||||||
| chr17:76185421
|
T | C | 1 | a0001c0004t0002g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.208-11631A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185421 | ||||||
| chr17:76185468
|
G | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(34): Show | 37 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.208-11678C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185468 | ||||||
| chr17:76185473
|
T | C | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11683A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185473 | ||||||
| chr17:76185475
|
C | CTTTTTTT others(7): Show |
29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(26): Show | 29 | HG01169.hp1 HG02109.hp2 HG02148.hp1 others(26): Show |
intron_variant | MODIFIER | c.208-11686_208-1168 others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185475 | ||||||
| chr17:76185475
|
C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0154others(12): Show | 15 | HG00639.hp1 HG01106.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-11686_208-1168 others(19): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185475 | ||||||
| chr17:76185475
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-11686_208-1168 others(21): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185475 | ||||||
| chr17:76185498
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11708G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185498 | ||||||
| chr17:76185500
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11710G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185500 | ||||||
| chr17:76185501
|
G | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11711C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185501 | ||||||
| chr17:76185502
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11712G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185502 | ||||||
| chr17:76185504
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11714G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185504 | ||||||
| chr17:76185506
|
G | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11716C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185506 | ||||||
| chr17:76185512
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11722G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185512 | ||||||
| chr17:76185513
|
A | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-11723T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185513 | ||||||
| chr17:76185533
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.208-11743C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185533 | ||||||
| chr17:76185621
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0023g0110others(2): Show | 5 | HG00438.hp1 HG00544.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-11831A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185621 | ||||||
| chr17:76185650
|
C | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(43): Show | 46 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.208-11860G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185650 | ||||||
| chr17:76185675
|
T | C | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-11885A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185675 | ||||||
| chr17:76185691
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0131 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.208-11901C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185691 | ||||||
| chr17:76185712
|
G | A | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-11922C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185712 | ||||||
| chr17:76185728
|
C | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(28): Show | 31 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.208-11938G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185728 | ||||||
| chr17:76185768
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | HG01069.hp2 HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.208-11978G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185768 | ||||||
| chr17:76185769
|
G | A | 1 | a0001c0002t0002g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.208-11979C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185769 | ||||||
| chr17:76185867
|
A | G | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.208-12077T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76185867 | ||||||
| chr17:76186399
|
C | T | 1 | a0001c0004t0002g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.208-12609G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186399 | ||||||
| chr17:76186524
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-12734G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186524 | ||||||
| chr17:76186660
|
G | C | 7 | a0001c0001t0001g0072a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG01109.hp1 HG01952.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-12870C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186660 | ||||||
| chr17:76186662
|
G | T | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-12872C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186662 | ||||||
| chr17:76186810
|
C | T | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-13020G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186810 | ||||||
| chr17:76186939
|
CAAAATAA others(5): Show |
C | 9 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0016g0113others(6): Show | 9 | HG01884.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-13161_208-1315 others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186939 | ||||||
| chr17:76186940
|
A | AAAAT | 58 | a0001c0001t0001g0010a0001c0001t0001g0058a0001c0001t0001g0083others(55): Show | 59 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.208-13154_208-1315 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186940 | ||||||
| chr17:76186940
|
A | AAAATAAA others(1): Show |
17 | a0001c0001t0001g0181a0001c0001t0001g0219a0001c0001t0002g0203others(14): Show | 17 | HG01109.hp2 HG01496.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.208-13158_208-1315 others(12): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186940 | ||||||
| chr17:76186940
|
A | AAAATAAA others(5): Show |
2 | a0001c0003t0002g0111a0001c0004t0002g0168 | 2 | HG01243.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.208-13162_208-1315 others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186940 | ||||||
| chr17:76186940
|
A | AAAATAAA others(9): Show |
1 | a0001c0004t0003g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.208-13166_208-1315 others(20): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186940 | ||||||
| chr17:76186940
|
AAAAT | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(24): Show | 27 | HG00639.hp1 HG00639.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.208-13154_208-1315 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186940 | ||||||
| chr17:76186940
|
AAAATAAA others(5): Show |
A | 1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-13162_208-1315 others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76186940 | ||||||
| chr17:76187120
|
G | A | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-13330C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187120 | ||||||
| chr17:76187214
|
C | T | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-13424G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187214 | ||||||
| chr17:76187220
|
G | A | 2 | a0001c0001t0002g0203a0001c0001t0006g0141 | 2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.208-13430C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187220 | ||||||
| chr17:76187270
|
G | A | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.208-13480C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187270 | ||||||
| chr17:76187436
|
A | G | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0022others(121): Show | 125 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.208-13646T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187436 | ||||||
| chr17:76187477
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(106): Show | 110 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.208-13687A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187477 | ||||||
| chr17:76187478
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-13688G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187478 | ||||||
| chr17:76187640
|
C | G | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-13850G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187640 | ||||||
| chr17:76187686
|
G | A | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.208-13896C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187686 | ||||||
| chr17:76187799
|
T | C | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-14009A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187799 | ||||||
| chr17:76187815
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-14025G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187815 | ||||||
| chr17:76187889
|
C | T | 2 | a0001c0001t0014g0003a0001c0001t0014g0086 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.208-14099G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187889 | ||||||
| chr17:76187963
|
T | C | 1 | a0001c0003t0005g0177 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.208-14173A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187963 | ||||||
| chr17:76187999
|
T | A | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-14209A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76187999 | ||||||
| chr17:76188026
|
T | C | 3 | a0001c0002t0003g0032a0001c0002t0003g0033a0001c0002t0011g0205 | 3 | HG01891.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.208-14236A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188026 | ||||||
| chr17:76188056
|
C | T | 2 | a0001c0001t0002g0203a0001c0001t0006g0141 | 2 | HG00639.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.208-14266G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188056 | ||||||
| chr17:76188190
|
C | T | 1 | a0001c0002t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208-14400G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188190 | ||||||
| chr17:76188213
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.208-14423T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188213 | ||||||
| chr17:76188230
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.208-14440C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188230 | ||||||
| chr17:76188252
|
G | A | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.208-14462C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188252 | ||||||
| chr17:76188289
|
T | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(27): Show | 30 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-14499A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188289 | ||||||
| chr17:76188343
|
C | T | 31 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(28): Show | 31 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.208-14553G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188343 | ||||||
| chr17:76188494
|
G | A | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.208-14704C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188494 | ||||||
| chr17:76188565
|
G | T | 1 | a0001c0002t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.208-14775C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188565 | ||||||
| chr17:76188580
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-14790A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188580 | ||||||
| chr17:76188589
|
C | T | 3 | a0001c0001t0016g0113a0001c0005t0008g0197a0001c0005t0008g0198 | 3 | NA18522.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-14799G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188589 | ||||||
| chr17:76188686
|
A | G | 1 | a0001c0002t0011g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208-14896T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188686 | ||||||
| chr17:76188739
|
T | C | 3 | a0001c0001t0003g0005a0001c0002t0001g0093a0001c0016t0001g0094 | 3 | HG02630.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.208-14949A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76188739 | ||||||
| chr17:76189061
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.208-15271A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189061 | ||||||
| chr17:76189209
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208-15419C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189209 | ||||||
| chr17:76189292
|
T | A | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.208-15502A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189292 | ||||||
| chr17:76189402
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-15612C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189402 | ||||||
| chr17:76189724
|
G | A | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.208-15934C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189724 | ||||||
| chr17:76189802
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-16012G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189802 | ||||||
| chr17:76189817
|
T | C | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-16027A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189817 | ||||||
| chr17:76189835
|
C | CAAACAAA others(1): Show |
110 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(107): Show | 111 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.208-16046_208-1604 others(12): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76189835 | ||||||
| chr17:76190045
|
T | C | 7 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(4): Show | 7 | HG01891.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-16255A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190045 | ||||||
| chr17:76190093
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-16303A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190093 | ||||||
| chr17:76190163
|
GCTCT | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0222a0001c0001t0001g0226others(5): Show | 8 | HG01106.hp2 HG01255.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-16377_208-1637 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190163 | ||||||
| chr17:76190170
|
C | CT | 7 | a0001c0001t0001g0171a0001c0001t0003g0125a0001c0001t0006g0141others(4): Show | 7 | HG00639.hp2 HG01346.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-16381dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190170 | ||||||
| chr17:76190170
|
C | CTT | 12 | a0001c0001t0002g0154a0001c0001t0002g0187a0001c0001t0020g0038others(9): Show | 12 | HG00639.hp1 HG01928.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-16382_208-1638 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190170 | ||||||
| chr17:76190170
|
C | CTTT | 10 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0179others(7): Show | 10 | HG01106.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-16383_208-1638 others(7): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190170 | ||||||
| chr17:76190171
|
T | TC | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-16382_208-1638 others(5): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190171 | ||||||
| chr17:76190178
|
T | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-16388A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190178 | ||||||
| chr17:76190187
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-16397C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190187 | ||||||
| chr17:76190349
|
T | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(29): Show | 32 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.208-16559A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190349 | ||||||
| chr17:76190376
|
A | G | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208-16586T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190376 | ||||||
| chr17:76190602
|
C | CA | 7 | a0001c0001t0001g0128a0001c0001t0003g0125a0001c0002t0003g0032others(4): Show | 7 | HG01109.hp1 HG01361.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-16813dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190602 | ||||||
| chr17:76190688
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0109others(6): Show | 9 | HG00438.hp2 HG00621.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-16898C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76190688 | ||||||
| chr17:76191048
|
T | C | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208-17258A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191048 | ||||||
| chr17:76191573
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208-17783G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191573 | ||||||
| chr17:76191575
|
T | C | 1 | a0001c0004t0003g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.208-17785A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191575 | ||||||
| chr17:76191579
|
C | T | 1 | a0001c0005t0008g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.208-17789G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191579 | ||||||
| chr17:76191595
|
C | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0143others(24): Show | 27 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.208-17805G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191595 | ||||||
| chr17:76191600
|
C | CA | 19 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(16): Show | 19 | HG00438.hp2 HG00639.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.208-17811dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191600 | ||||||
| chr17:76191600
|
CA | C | 90 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(87): Show | 91 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.208-17811delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191600 | ||||||
| chr17:76191612
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208-17822T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191612 | ||||||
| chr17:76191615
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.208-17825T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191615 | ||||||
| chr17:76191718
|
G | T | 62 | a0001c0001t0003g0125a0001c0002t0003g0032a0001c0002t0003g0033others(59): Show | 63 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.208-17928C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191718 | ||||||
| chr17:76191906
|
C | T | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.208-18116G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191906 | ||||||
| chr17:76191993
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0221a0001c0001t0001g0229others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-18203C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76191993 | ||||||
| chr17:76192026
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-18236A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192026 | ||||||
| chr17:76192285
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-18495C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192285 | ||||||
| chr17:76192506
|
G | A | 1 | a0001c0002t0001g0044 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.208-18716C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192506 | ||||||
| chr17:76192673
|
GT | G | 6 | a0001c0003t0002g0073a0001c0003t0002g0182a0001c0003t0002g0190others(3): Show | 6 | HG00597.hp1 HG00621.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-18884delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192673 | ||||||
| chr17:76192841
|
C | CT | 9 | a0001c0001t0001g0053a0001c0001t0001g0152a0001c0001t0006g0141others(6): Show | 9 | HG00639.hp2 HG01346.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-19052dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192841 | ||||||
| chr17:76192841
|
CT | C | 47 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0143others(44): Show | 47 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.208-19052delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192841 | ||||||
| chr17:76192940
|
C | A | 4 | a0001c0002t0004g0116a0001c0002t0004g0117a0001c0002t0004g0118others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-19150G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192940 | ||||||
| chr17:76192971
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0222a0001c0001t0001g0226others(6): Show | 9 | HG01106.hp2 HG01255.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-19181C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76192971 | ||||||
| chr17:76193009
|
C | T | 2 | a0001c0004t0006g0018a0001c0004t0006g0019 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.208-19219G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193009 | ||||||
| chr17:76193010
|
G | A | 11 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0006g0141others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-19220C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193010 | ||||||
| chr17:76193107
|
G | C | 14 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(11): Show | 14 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+19257C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193107 | ||||||
| chr17:76193229
|
T | C | 1 | a0001c0002t0002g0216 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.207+19135A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193229 | ||||||
| chr17:76193397
|
G | C | 8 | a0001c0002t0002g0209a0001c0002t0002g0214a0001c0002t0002g0215others(5): Show | 8 | HG01106.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+18967C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193397 | ||||||
| chr17:76193444
|
G | A | 97 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0143others(94): Show | 98 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.207+18920C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193444 | ||||||
| chr17:76193466
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.207+18898G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193466 | ||||||
| chr17:76193552
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.207+18812G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193552 | ||||||
| chr17:76193561
|
C | A | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+18803G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193561 | ||||||
| chr17:76193613
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.207+18751C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193613 | ||||||
| chr17:76193636
|
A | G | 63 | a0001c0002t0004g0121a0001c0003t0001g0124a0001c0003t0001g0176others(60): Show | 64 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.207+18728T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193636 | ||||||
| chr17:76193651
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0221a0001c0001t0001g0229others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+18713C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193651 | ||||||
| chr17:76193751
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.207+18613G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193751 | ||||||
| chr17:76193824
|
A | T | 1 | a0006c0018t0001g0026 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.207+18540T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193824 | ||||||
| chr17:76193937
|
G | A | 1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.207+18427C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193937 | ||||||
| chr17:76193952
|
G | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0143others(31): Show | 34 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.207+18412C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76193952 | ||||||
| chr17:76194149
|
A | C | 7 | a0001c0001t0003g0012a0001c0006t0007g0014a0001c0006t0007g0015others(4): Show | 7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+18215T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194149 | ||||||
| chr17:76194340
|
G | T | 4 | a0001c0001t0001g0088a0001c0006t0007g0014a0001c0006t0007g0015others(1): Show | 4 | HG02717.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+18024C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194340 | ||||||
| chr17:76194367
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+17997G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194367 | ||||||
| chr17:76194377
|
C | A | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+17987G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194377 | ||||||
| chr17:76194402
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+17962G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194402 | ||||||
| chr17:76194450
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0152a0001c0001t0023g0110others(1): Show | 4 | HG00438.hp1 HG02129.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+17914T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194450 | ||||||
| chr17:76194722
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.207+17642T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194722 | ||||||
| chr17:76194739
|
G | A | 1 | a0001c0001t0010g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.207+17625C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194739 | ||||||
| chr17:76194742
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0002g0180 | 3 | HG02109.hp2 HG02145.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.207+17622T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194742 | ||||||
| chr17:76194743
|
C | T | 1 | a0001c0002t0002g0180 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.207+17621G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194743 | ||||||
| chr17:76194744
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.207+17620C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194744 | ||||||
| chr17:76194754
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(91): Show | 95 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.207+17610T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194754 | ||||||
| chr17:76194782
|
A | C | 1 | a0001c0004t0002g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.207+17582T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194782 | ||||||
| chr17:76194782
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+17582T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194782 | ||||||
| chr17:76194783
|
A | C | 1 | a0001c0002t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+17581T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194783 | ||||||
| chr17:76194786
|
T | C | 2 | a0001c0001t0015g0196a0001c0002t0001g0080 | 2 | HG00621.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.207+17578A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194786 | ||||||
| chr17:76194787
|
G | A | 1 | a0001c0002t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+17577C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194787 | ||||||
| chr17:76194790
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+17574G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194790 | ||||||
| chr17:76194791
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+17573T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194791 | ||||||
| chr17:76194803
|
C | G | 3 | a0001c0003t0002g0095a0001c0003t0002g0112a0001c0004t0001g0097 | 3 | HG02132.hp1 NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.207+17561G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194803 | ||||||
| chr17:76194821
|
C | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0029others(84): Show | 88 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.207+17543G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194821 | ||||||
| chr17:76194826
|
T | C | 1 | a0001c0003t0005g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.207+17538A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194826 | ||||||
| chr17:76194831
|
T | C | 4 | a0001c0002t0011g0205a0001c0003t0002g0095a0001c0003t0002g0112others(1): Show | 4 | HG02132.hp1 HG03486.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+17533A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194831 | ||||||
| chr17:76194871
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.207+17493G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194871 | ||||||
| chr17:76194872
|
A | G | 3 | a0001c0001t0001g0029a0001c0002t0002g0067a0001c0002t0002g0090 | 3 | HG01255.hp2 HG03688.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.207+17492T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194872 | ||||||
| chr17:76194876
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.207+17488C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194876 | ||||||
| chr17:76194923
|
C | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(228): Show | 233 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.207+17441G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76194923 | ||||||
| chr17:76195133
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0003g0012 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.207+17231T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76195133 | ||||||
| chr17:76195306
|
GATCACCT others(14): Show |
G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+17037_207+1705 others(25): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76195306 | ||||||
| chr17:76195474
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.207+16890C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76195474 | ||||||
| chr17:76195548
|
A | G | 71 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(68): Show | 71 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.207+16816T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76195548 | ||||||
| chr17:76195613
|
A | C | 11 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+16751T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76195613 | ||||||
| chr17:76195742
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+16622C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76195742 | ||||||
| chr17:76196038
|
G | A | 50 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(47): Show | 50 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.207+16326C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196038 | ||||||
| chr17:76196143
|
G | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+16221C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196143 | ||||||
| chr17:76196144
|
C | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+16220G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196144 | ||||||
| chr17:76196309
|
A | G | 11 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+16055T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196309 | ||||||
| chr17:76196504
|
T | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+15860A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196504 | ||||||
| chr17:76196683
|
C | CT | 39 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(36): Show | 39 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.207+15680dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196683 | ||||||
| chr17:76196711
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+15653T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196711 | ||||||
| chr17:76196746
|
C | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(36): Show | 39 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.207+15618G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196746 | ||||||
| chr17:76196908
|
G | A | 1 | a0001c0008t0001g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.207+15456C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76196908 | ||||||
| chr17:76197110
|
A | AC | 69 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(66): Show | 69 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.207+15253dupG | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197110 | ||||||
| chr17:76197329
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+15035T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197329 | ||||||
| chr17:76197475
|
C | A | 4 | a0001c0001t0016g0113a0001c0007t0001g0194a0001c0007t0022g0200others(1): Show | 4 | HG02818.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+14889G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197475 | ||||||
| chr17:76197593
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.207+14771C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197593 | ||||||
| chr17:76197638
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.207+14726A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197638 | ||||||
| chr17:76197693
|
C | T | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.207+14671G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197693 | ||||||
| chr17:76197701
|
G | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(36): Show | 39 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.207+14663C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197701 | ||||||
| chr17:76197899
|
A | G | 1 | a0001c0021t0001g0043 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.207+14465T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76197899 | ||||||
| chr17:76198199
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+14165T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198199 | ||||||
| chr17:76198278
|
C | T | 160 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0013others(157): Show | 161 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.207+14086G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198278 | ||||||
| chr17:76198279
|
A | G | 69 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(66): Show | 69 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.207+14085T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198279 | ||||||
| chr17:76198280
|
G | A | 11 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+14084C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198280 | ||||||
| chr17:76198281
|
G | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+14083C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198281 | ||||||
| chr17:76198393
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+13971T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198393 | ||||||
| chr17:76198445
|
T | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+13919A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198445 | ||||||
| chr17:76198446
|
C | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+13918G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198446 | ||||||
| chr17:76198480
|
G | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+13884C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198480 | ||||||
| chr17:76198508
|
G | A | 8 | a0001c0001t0015g0196a0001c0002t0011g0205a0001c0003t0002g0195others(5): Show | 8 | HG02145.hp1 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+13856C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198508 | ||||||
| chr17:76198509
|
G | T | 21 | a0001c0001t0001g0192a0001c0003t0001g0176a0001c0003t0002g0066others(18): Show | 22 | HG00597.hp1 HG00621.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.207+13855C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198509 | ||||||
| chr17:76198532
|
A | G | 1 | a0001c0002t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.207+13832T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198532 | ||||||
| chr17:76198666
|
T | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+13698A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198666 | ||||||
| chr17:76198667
|
C | T | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+13697G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198667 | ||||||
| chr17:76198688
|
C | T | 8 | a0001c0001t0015g0196a0001c0002t0011g0205a0001c0003t0002g0195others(5): Show | 8 | HG02145.hp1 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+13676G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198688 | ||||||
| chr17:76198700
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(36): Show | 39 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.207+13664G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76198700 | ||||||
| chr17:76199016
|
T | C | 1 | a0001c0004t0002g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.207+13348A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199016 | ||||||
| chr17:76199020
|
A | G | 19 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.207+13344T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199020 | ||||||
| chr17:76199054
|
A | G | 11 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+13310T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199054 | ||||||
| chr17:76199070
|
C | T | 152 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0013others(149): Show | 153 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.207+13294G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199070 | ||||||
| chr17:76199099
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+13265T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199099 | ||||||
| chr17:76199148
|
GA | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0219 | 2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.207+13215delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199148 | ||||||
| chr17:76199171
|
G | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(36): Show | 39 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.207+13193C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199171 | ||||||
| chr17:76199296
|
G | C | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.207+13068C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199296 | ||||||
| chr17:76199570
|
T | TA | 12 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0056others(9): Show | 12 | HG00140.hp1 HG01081.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+12793dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199570 | ||||||
| chr17:76199570
|
TA | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0024others(98): Show | 101 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.207+12793delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199570 | ||||||
| chr17:76199570
|
TAA | T | 18 | a0001c0001t0001g0088a0001c0001t0001g0148a0001c0001t0001g0219others(15): Show | 18 | HG00639.hp2 HG01069.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+12792_207+1279 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199570 | ||||||
| chr17:76199721
|
G | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+12643C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199721 | ||||||
| chr17:76199722
|
C | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+12642G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199722 | ||||||
| chr17:76199778
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+12586T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199778 | ||||||
| chr17:76199959
|
C | T | 1 | a0001c0002t0011g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.207+12405G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76199959 | ||||||
| chr17:76200174
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0085 | 2 | HG01346.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.207+12190C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200174 | ||||||
| chr17:76200191
|
A | G | 69 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(66): Show | 69 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.207+12173T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200191 | ||||||
| chr17:76200199
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.207+12165C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200199 | ||||||
| chr17:76200206
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.207+12158G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200206 | ||||||
| chr17:76200237
|
G | A | 4 | a0001c0001t0016g0113a0001c0007t0001g0194a0001c0007t0022g0200others(1): Show | 4 | HG02818.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+12127C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200237 | ||||||
| chr17:76200250
|
A | AC | 2 | a0001c0001t0001g0013a0001c0001t0003g0012 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.207+12113_207+1211 others(5): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200250 | ||||||
| chr17:76200255
|
A | C | 1 | a0001c0004t0012g0106 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.207+12109T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200255 | ||||||
| chr17:76200368
|
G | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(66): Show | 69 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.207+11996C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200368 | ||||||
| chr17:76200692
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+11672T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200692 | ||||||
| chr17:76200812
|
T | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+11552A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200812 | ||||||
| chr17:76200904
|
C | G | 70 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(67): Show | 70 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.207+11460G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76200904 | ||||||
| chr17:76201101
|
A | G | 1 | a0005c0013t0001g0223 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.207+11263T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201101 | ||||||
| chr17:76201162
|
C | T | 68 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(65): Show | 68 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.207+11202G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201162 | ||||||
| chr17:76201189
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+11175A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201189 | ||||||
| chr17:76201235
|
C | T | 1 | a0001c0004t0002g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.207+11129G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201235 | ||||||
| chr17:76201251
|
T | C | 68 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(65): Show | 68 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.207+11113A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201251 | ||||||
| chr17:76201323
|
C | CA | 44 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(41): Show | 44 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.207+11040dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201323 | ||||||
| chr17:76201323
|
C | CAA | 16 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(13): Show | 16 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.207+11039_207+1104 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201323 | ||||||
| chr17:76201323
|
C | CAAA | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+11038_207+1104 others(7): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201323 | ||||||
| chr17:76201323
|
CA | C | 5 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | NA18993.hp2 NA19004.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+11040delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201323 | ||||||
| chr17:76201410
|
G | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+10954C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201410 | ||||||
| chr17:76201510
|
T | TA | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+10853dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201510 | ||||||
| chr17:76201608
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+10756T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201608 | ||||||
| chr17:76201813
|
T | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+10551A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201813 | ||||||
| chr17:76201885
|
A | C | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+10479T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76201885 | ||||||
| chr17:76202038
|
A | T | 3 | a0001c0001t0003g0125a0001c0004t0002g0133a0001c0004t0002g0134 | 3 | HG03209.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.207+10326T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202038 | ||||||
| chr17:76202071
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+10293T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202071 | ||||||
| chr17:76202086
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.207+10278T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202086 | ||||||
| chr17:76202111
|
T | TTC | 35 | a0001c0001t0001g0010a0001c0001t0001g0128a0001c0001t0001g0142others(32): Show | 36 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.207+10251_207+1025 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202111 | ||||||
| chr17:76202111
|
T | TTCTC | 13 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(10): Show | 13 | HG00738.hp1 HG02572.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.207+10249_207+1025 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202111 | ||||||
| chr17:76202111
|
T | TTCTCTC | 5 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0002g0154others(2): Show | 5 | HG02559.hp1 HG02976.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+10247_207+1025 others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202111 | ||||||
| chr17:76202111
|
T | TTCTCTCT others(3): Show |
2 | a0001c0001t0003g0218a0001c0001t0021g0089 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.207+10243_207+1025 others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202111 | ||||||
| chr17:76202111
|
TTC | T | 5 | a0001c0001t0006g0141a0001c0001t0009g0102a0001c0001t0016g0113others(2): Show | 5 | HG00639.hp2 HG01358.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+10251_207+1025 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202111 | ||||||
| chr17:76202124
|
T | TCA | 2 | a0001c0002t0002g0151a0007c0017t0002g0150 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.207+10239_207+1024 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202124 | ||||||
| chr17:76202126
|
T | A | 5 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0001g0186others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+10238A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202126 | ||||||
| chr17:76202126
|
TCTCA | T | 3 | a0001c0001t0001g0041a0001c0004t0002g0040a0001c0007t0022g0200 | 3 | HG02155.hp1 HG03195.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.207+10234_207+1023 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202126 | ||||||
| chr17:76202128
|
T | A | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+10236A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCA | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(1): Show | 4 | HG02155.hp2 HG03927.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+10234_207+1023 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCACA | 4 | a0001c0001t0001g0022a0001c0002t0001g0080a0001c0002t0003g0032others(1): Show | 4 | HG00621.hp2 HG01891.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+10232_207+1023 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCACACAC others(3): Show |
1 | a0001c0002t0002g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.207+10226_207+1023 others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCA | 3 | a0001c0001t0001g0147a0001c0001t0023g0110a0001c0003t0002g0122 | 3 | HG00438.hp1 NA19088.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.207+10235_207+1023 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(1): Show |
2 | a0001c0003t0002g0195a0001c0004t0002g0057 | 2 | HG01081.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.207+10235_207+1023 others(12): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(3): Show |
2 | a0001c0002t0004g0117a0001c0003t0005g0204 | 2 | HG02895.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.207+10235_207+1023 others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(5): Show |
3 | a0001c0001t0002g0114a0001c0002t0004g0118a0001c0003t0001g0224 | 3 | HG03486.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.207+10235_207+1023 others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(7): Show |
1 | a0001c0001t0001g0226 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.207+10235_207+1023 others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(9): Show |
4 | a0001c0001t0001g0088a0001c0002t0002g0120a0001c0002t0004g0116others(1): Show | 4 | HG02559.hp2 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+10235_207+1023 others(20): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(11): Show |
1 | a0001c0002t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.207+10235_207+1023 others(22): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(3): Show |
1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.207+10235_207+1023 others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(9): Show |
1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.207+10235_207+1023 others(20): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(5): Show |
8 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0002t0002g0209others(5): Show | 8 | HG02280.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+10235_207+1023 others(16): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(7): Show |
1 | a0001c0002t0002g0216 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.207+10235_207+1023 others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(9): Show |
2 | a0001c0001t0003g0217a0002c0010t0003g0213 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.207+10235_207+1023 others(20): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(7): Show |
1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.207+10235_207+1023 others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(9): Show |
1 | a0001c0001t0003g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+10235_207+1023 others(20): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
T | TCTCTCTC others(11): Show |
1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+10235_207+1023 others(22): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
TCA | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0082others(13): Show | 16 | HG00544.hp2 HG01069.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.207+10234_207+1023 others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
TCACA | T | 15 | a0001c0001t0001g0077a0001c0001t0001g0107a0001c0001t0001g0206others(12): Show | 15 | HG01070.hp2 HG01106.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+10232_207+1023 others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202128
|
TCACACAC others(17): Show |
T | 1 | a0001c0003t0002g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.207+10212_207+1023 others(28): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202128 | ||||||
| chr17:76202130
|
A | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0046others(61): Show | 64 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.207+10234T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202130 | ||||||
| chr17:76202132
|
A | T | 10 | a0001c0001t0001g0131a0001c0001t0001g0181a0001c0002t0001g0042others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+10232T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202132 | ||||||
| chr17:76202134
|
A | T | 9 | a0001c0001t0001g0107a0001c0001t0001g0206a0001c0002t0002g0099others(6): Show | 9 | HG01070.hp2 HG01361.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+10230T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202134 | ||||||
| chr17:76202136
|
A | T | 2 | a0001c0002t0017g0138a0001c0004t0002g0011 | 2 | HG01361.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.207+10228T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202136 | ||||||
| chr17:76202138
|
A | T | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.207+10226T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202138 | ||||||
| chr17:76202154
|
A | T | 1 | a0001c0003t0002g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.207+10210T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202154 | ||||||
| chr17:76202305
|
C | T | 10 | a0001c0001t0014g0003a0001c0001t0014g0086a0001c0001t0015g0196others(7): Show | 10 | HG02145.hp1 HG02922.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+10059G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202305 | ||||||
| chr17:76202388
|
A | G | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+9976T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202388 | ||||||
| chr17:76202632
|
C | T | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+9732G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202632 | ||||||
| chr17:76202737
|
C | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0029others(81): Show | 85 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.207+9627G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202737 | ||||||
| chr17:76202790
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+9574A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202790 | ||||||
| chr17:76202843
|
A | T | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+9521T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202843 | ||||||
| chr17:76202852
|
A | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+9512T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202852 | ||||||
| chr17:76202906
|
GTCT | G | 3 | a0001c0004t0002g0137a0003c0019t0002g0126a0003c0020t0002g0123 | 3 | HG01261.hp1 HG01433.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.207+9455_207+9457d others(5): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202906 | ||||||
| chr17:76202989
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.207+9375A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76202989 | ||||||
| chr17:76203108
|
A | T | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+9256T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203108 | ||||||
| chr17:76203109
|
G | C | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+9255C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203109 | ||||||
| chr17:76203110
|
C | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+9254G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203110 | ||||||
| chr17:76203126
|
G | C | 1 | a0001c0003t0002g0178 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.207+9238C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203126 | ||||||
| chr17:76203182
|
G | T | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.207+9182C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203182 | ||||||
| chr17:76203292
|
T | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9072A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203292 | ||||||
| chr17:76203300
|
T | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9064A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203300 | ||||||
| chr17:76203302
|
A | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9062T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203302 | ||||||
| chr17:76203303
|
G | A | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9061C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203303 | ||||||
| chr17:76203304
|
T | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9060A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203304 | ||||||
| chr17:76203310
|
A | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9054T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203310 | ||||||
| chr17:76203317
|
C | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9047G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203317 | ||||||
| chr17:76203319
|
T | C | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9045A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203319 | ||||||
| chr17:76203327
|
A | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9037T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203327 | ||||||
| chr17:76203328
|
A | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9036T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203328 | ||||||
| chr17:76203329
|
T | A | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9035A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203329 | ||||||
| chr17:76203332
|
T | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9032A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203332 | ||||||
| chr17:76203334
|
T | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9030A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203334 | ||||||
| chr17:76203335
|
A | T | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9029T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203335 | ||||||
| chr17:76203344
|
A | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9020T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203344 | ||||||
| chr17:76203360
|
T | C | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.207+9004A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203360 | ||||||
| chr17:76203368
|
C | T | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+8996G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203368 | ||||||
| chr17:76203452
|
CT | C | 46 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0061others(43): Show | 46 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(43): Show |
intron_variant | MODIFIER | c.207+8911delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203452 | ||||||
| chr17:76203452
|
CTT | C | 23 | a0001c0001t0001g0034a0001c0001t0001g0148a0001c0001t0001g0210others(20): Show | 23 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.207+8910_207+8911d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203452 | ||||||
| chr17:76203458
|
TTTTTTTT others(15): Show |
T | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+8884_207+8905d others(24): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203458 | ||||||
| chr17:76203482
|
T | G | 1 | a0001c0002t0002g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.207+8882A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203482 | ||||||
| chr17:76203559
|
T | C | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+8805A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203559 | ||||||
| chr17:76203612
|
C | G | 1 | a0001c0002t0001g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.207+8752G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203612 | ||||||
| chr17:76203640
|
C | T | 1 | a0009c0022t0001g0070 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.207+8724G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203640 | ||||||
| chr17:76203720
|
G | A | 4 | a0001c0001t0015g0196a0001c0002t0011g0205a0001c0005t0008g0197others(1): Show | 4 | HG03041.hp1 HG03486.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+8644C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203720 | ||||||
| chr17:76203769
|
C | CT | 32 | a0001c0001t0001g0082a0001c0001t0001g0148a0001c0001t0001g0165others(29): Show | 32 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.207+8594dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203769 | ||||||
| chr17:76203769
|
C | CTT | 27 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(24): Show | 27 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+8593_207+8594d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203769 | ||||||
| chr17:76203829
|
A | G | 41 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(38): Show | 41 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.207+8535T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203829 | ||||||
| chr17:76203860
|
C | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+8504G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203860 | ||||||
| chr17:76203875
|
C | T | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+8489G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203875 | ||||||
| chr17:76203988
|
C | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+8376G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76203988 | ||||||
| chr17:76204135
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0003g0012 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.207+8229T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204135 | ||||||
| chr17:76204212
|
CT | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+8151delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204212 | ||||||
| chr17:76204573
|
T | C | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+7791A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204573 | ||||||
| chr17:76204575
|
T | C | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+7789A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204575 | ||||||
| chr17:76204577
|
T | C | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+7787A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204577 | ||||||
| chr17:76204592
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+7772T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204592 | ||||||
| chr17:76204632
|
A | C | 41 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(38): Show | 41 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.207+7732T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204632 | ||||||
| chr17:76204766
|
TTTTC | T | 10 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0002g0114others(7): Show | 10 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+7594_207+7597d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204766 | ||||||
| chr17:76204782
|
C | CTTTCT | 27 | a0001c0001t0001g0034a0001c0001t0001g0148a0001c0001t0001g0210others(24): Show | 27 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.207+7581_207+7582i others(7): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76204782 | ||||||
| chr17:76205066
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02080.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.207+7298G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205066 | ||||||
| chr17:76205133
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.207+7214_207+7230d others(19): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205133 | ||||||
| chr17:76205145
|
C | CT | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+7218dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205145 | ||||||
| chr17:76205322
|
C | G | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+7042G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205322 | ||||||
| chr17:76205703
|
G | A | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+6661C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205703 | ||||||
| chr17:76205723
|
C | CTAAA | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0107others(16): Show | 19 | HG00438.hp2 HG01069.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.207+6637_207+6640d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205723
|
C | CTAAATAA others(1): Show |
19 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0210others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.207+6633_207+6640d others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205723
|
C | CTAAATAA others(5): Show |
5 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0006g0141others(2): Show | 5 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6629_207+6640d others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205723
|
C | CTAAATAA others(9): Show |
4 | a0001c0001t0001g0148a0001c0001t0003g0218a0001c0002t0002g0151others(1): Show | 4 | HG02818.hp1 HG03471.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6625_207+6640d others(18): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205723
|
CTAAA | C | 24 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0131others(21): Show | 24 | HG00140.hp2 HG00735.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.207+6637_207+6640d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205723
|
CTAAATAA others(1): Show |
C | 32 | a0001c0001t0001g0013a0001c0001t0001g0088a0001c0001t0001g0219others(29): Show | 32 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.207+6633_207+6640d others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205723
|
CTAAATAA others(5): Show |
C | 2 | a0001c0004t0001g0104a0001c0004t0002g0040 | 2 | HG02155.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.207+6629_207+6640d others(14): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205723 | ||||||
| chr17:76205912
|
AGC | A | 5 | a0001c0001t0014g0003a0001c0001t0014g0086a0001c0006t0007g0014others(2): Show | 5 | HG02922.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+6450_207+6451d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76205912 | ||||||
| chr17:76206014
|
G | C | 4 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0002g0151others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6350C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76206014 | ||||||
| chr17:76206164
|
G | A | 40 | a0001c0001t0001g0013a0001c0001t0001g0088a0001c0001t0001g0219others(37): Show | 40 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.207+6200C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76206164 | ||||||
| chr17:76206167
|
G | A | 27 | a0001c0001t0001g0013a0001c0001t0001g0088a0001c0001t0001g0219others(24): Show | 27 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+6197C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76206167 | ||||||
| chr17:76206481
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.207+5883G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76206481 | ||||||
| chr17:76206787
|
A | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0003g0217others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+5577T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76206787 | ||||||
| chr17:76206900
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0002g0036a0001c0001t0003g0012 | 3 | HG02109.hp2 HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.207+5464G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76206900 | ||||||
| chr17:76207053
|
C | T | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+5311G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207053 | ||||||
| chr17:76207137
|
C | T | 10 | a0001c0001t0014g0003a0001c0001t0014g0086a0001c0001t0015g0196others(7): Show | 10 | HG02145.hp1 HG02922.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+5227G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207137 | ||||||
| chr17:76207158
|
G | A | 5 | a0001c0003t0002g0182a0001c0003t0002g0190a0001c0004t0001g0104others(2): Show | 5 | HG00597.hp1 HG00621.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+5206C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207158 | ||||||
| chr17:76207265
|
T | A | 3 | a0001c0007t0001g0194a0001c0007t0022g0200a0001c0012t0011g0201 | 3 | HG02818.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.207+5099A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207265 | ||||||
| chr17:76207366
|
T | G | 1 | a0001c0003t0005g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.207+4998A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207366 | ||||||
| chr17:76207379
|
C | T | 1 | a0001c0003t0005g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.207+4985G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207379 | ||||||
| chr17:76207440
|
T | A | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+4924A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207440 | ||||||
| chr17:76207441
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0004t0006g0018others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+4923A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207441 | ||||||
| chr17:76207454
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+4910A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207454 | ||||||
| chr17:76207569
|
T | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0035others(5): Show | 8 | HG01069.hp1 HG01069.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+4795A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207569 | ||||||
| chr17:76207977
|
G | A | 2 | a0001c0002t0002g0063a0009c0022t0001g0070 | 2 | HG00544.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.207+4387C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76207977 | ||||||
| chr17:76208081
|
A | C | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+4283T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208081 | ||||||
| chr17:76208105
|
A | G | 12 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+4259T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208105 | ||||||
| chr17:76208115
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+4249C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208115 | ||||||
| chr17:76208119
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0023g0110 | 2 | HG00438.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.207+4245G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208119 | ||||||
| chr17:76208276
|
A | G | 5 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+4088T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208276 | ||||||
| chr17:76208318
|
C | G | 1 | a0001c0002t0002g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.207+4046G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208318 | ||||||
| chr17:76208370
|
T | C | 68 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(65): Show | 68 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.207+3994A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208370 | ||||||
| chr17:76208414
|
C | T | 27 | a0001c0001t0001g0034a0001c0001t0001g0148a0001c0001t0001g0210others(24): Show | 27 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.207+3950G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208414 | ||||||
| chr17:76208421
|
T | C | 68 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0054others(65): Show | 68 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.207+3943A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208421 | ||||||
| chr17:76208511
|
T | G | 84 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0029others(81): Show | 85 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.207+3853A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208511 | ||||||
| chr17:76208698
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+3666C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208698 | ||||||
| chr17:76208861
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+3503G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208861 | ||||||
| chr17:76208861
|
C | T | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+3503G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208861 | ||||||
| chr17:76208896
|
C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0222a0001c0001t0001g0226others(5): Show | 8 | HG01081.hp1 HG03688.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3468G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208896 | ||||||
| chr17:76208942
|
C | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0029others(81): Show | 85 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.207+3422G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208942 | ||||||
| chr17:76208973
|
C | CA | 17 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0148others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.207+3390dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208973 | ||||||
| chr17:76208973
|
C | CAA | 16 | a0001c0001t0001g0034a0001c0001t0001g0210a0001c0001t0002g0203others(13): Show | 16 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.207+3389_207+3390d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208973 | ||||||
| chr17:76208973
|
CA | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0230a0001c0004t0006g0018others(2): Show | 5 | HG02572.hp2 HG03225.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+3390delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208973 | ||||||
| chr17:76208991
|
C | A | 1 | a0001c0002t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.207+3373G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76208991 | ||||||
| chr17:76209068
|
C | CT | 5 | a0001c0003t0002g0182a0001c0003t0002g0190a0001c0004t0001g0104others(2): Show | 5 | HG00597.hp1 HG00621.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3295dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209068 | ||||||
| chr17:76209068
|
CT | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0127others(14): Show | 17 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+3295delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209068 | ||||||
| chr17:76209201
|
G | A | 2 | a0001c0008t0001g0047a0001c0008t0001g0048 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.207+3163C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209201 | ||||||
| chr17:76209235
|
C | T | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+3129G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209235 | ||||||
| chr17:76209482
|
G | GT | 61 | a0001c0001t0001g0034a0001c0001t0001g0085a0001c0001t0001g0088others(58): Show | 61 | HG00621.hp1 HG00639.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.207+2881dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209482 | ||||||
| chr17:76209482
|
G | GTT | 8 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0001t0014g0003others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+2880_207+2881d others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209482 | ||||||
| chr17:76209555
|
ATTC | A | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+2806_207+2808d others(5): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209555 | ||||||
| chr17:76209651
|
A | T | 9 | a0001c0001t0001g0072a0001c0001t0002g0187a0001c0002t0002g0071others(6): Show | 9 | HG00639.hp1 HG01928.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+2713T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209651 | ||||||
| chr17:76209658
|
T | A | 10 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0002g0203others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+2706A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209658 | ||||||
| chr17:76209783
|
G | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0002t0007g0228 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.207+2581C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209783 | ||||||
| chr17:76209792
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.207+2572G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209792 | ||||||
| chr17:76209809
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.207+2555C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76209809 | ||||||
| chr17:76210009
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.207+2355G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210009 | ||||||
| chr17:76210036
|
A | G | 156 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0013others(153): Show | 157 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.207+2328T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210036 | ||||||
| chr17:76210183
|
G | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0004t0003g0025 | 3 | HG01069.hp2 HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.207+2181C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210183 | ||||||
| chr17:76210259
|
T | C | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 82 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.207+2105A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210259 | ||||||
| chr17:76210320
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.207+2044C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210320 | ||||||
| chr17:76210321
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0015g0196a0001c0004t0002g0199others(2): Show | 5 | HG01069.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+2043G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210321 | ||||||
| chr17:76210322
|
A | G | 8 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0001t0015g0196others(5): Show | 8 | HG01069.hp1 HG01884.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+2042T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210322 | ||||||
| chr17:76210331
|
T | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 146 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.207+2033A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210331 | ||||||
| chr17:76210360
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.207+2004T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210360 | ||||||
| chr17:76210364
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.207+2000A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210364 | ||||||
| chr17:76210375
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.207+1989G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210375 | ||||||
| chr17:76210381
|
C | CAGG | 2 | a0001c0001t0001g0076a0001c0002t0002g0063 | 2 | HG02132.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.207+1982_207+1983i others(5): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210381 | ||||||
| chr17:76210386
|
C | T | 1 | a0001c0001t0010g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.207+1978G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210386 | ||||||
| chr17:76210406
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0002g0151others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1958G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210406 | ||||||
| chr17:76210407
|
A | G | 3 | a0001c0001t0001g0181a0001c0002t0001g0084a0001c0004t0002g0011 | 3 | HG01361.hp2 NA18964.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.207+1957T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210407 | ||||||
| chr17:76210450
|
T | C | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+1914A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210450 | ||||||
| chr17:76210453
|
A | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(142): Show | 146 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.207+1911T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210453 | ||||||
| chr17:76210459
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.207+1905C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210459 | ||||||
| chr17:76210462
|
T | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0219a0001c0001t0003g0012others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+1902A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210462 | ||||||
| chr17:76210463
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+1901C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210463 | ||||||
| chr17:76210477
|
C | T | 24 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0127others(21): Show | 24 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.207+1887G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210477 | ||||||
| chr17:76210483
|
A | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0127others(20): Show | 23 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.207+1881T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210483 | ||||||
| chr17:76210511
|
A | G | 30 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0127others(27): Show | 30 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.207+1853T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210511 | ||||||
| chr17:76210514
|
C | T | 30 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0127others(27): Show | 30 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.207+1850G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210514 | ||||||
| chr17:76210522
|
A | G | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(137): Show | 141 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.207+1842T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210522 | ||||||
| chr17:76210529
|
T | G | 30 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0127others(27): Show | 30 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.207+1835A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210529 | ||||||
| chr17:76210557
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(88): Show | 92 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.207+1807A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210557 | ||||||
| chr17:76210584
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.207+1780G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210584 | ||||||
| chr17:76210588
|
C | CAAAAA | 5 | a0001c0001t0001g0219a0001c0003t0019g0227a0001c0006t0007g0014others(2): Show | 5 | HG02965.hp2 HG03139.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+1771_207+1775d others(7): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210588 | ||||||
| chr17:76210588
|
C | CAAAAAA | 30 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0050others(27): Show | 30 | HG00738.hp1 HG01106.hp1 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.207+1770_207+1775d others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210588 | ||||||
| chr17:76210588
|
C | CAAAAAAA | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(66): Show | 71 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.207+1769_207+1775d others(9): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210588 | ||||||
| chr17:76210588
|
C | CAAAAAAA others(1): Show |
80 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(77): Show | 80 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.207+1768_207+1775d others(10): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210588 | ||||||
| chr17:76210588
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0082others(10): Show | 13 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.207+1767_207+1775d others(11): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210588 | ||||||
| chr17:76210605
|
G | A | 2 | a0001c0001t0016g0113a0001c0002t0011g0205 | 2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.207+1759C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210605 | ||||||
| chr17:76210898
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.207+1466C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210898 | ||||||
| chr17:76210945
|
T | C | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(100): Show | 104 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.207+1419A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76210945 | ||||||
| chr17:76211041
|
G | A | 5 | a0001c0001t0009g0101a0001c0001t0009g0102a0001c0002t0002g0098others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+1323C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211041 | ||||||
| chr17:76211046
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0159 | 2 | NA18947.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.207+1318G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211046 | ||||||
| chr17:76211054
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.207+1310G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211054 | ||||||
| chr17:76211066
|
A | G | 2 | a0001c0007t0022g0200a0001c0012t0011g0201 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.207+1298T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211066 | ||||||
| chr17:76211271
|
G | A | 1 | a0001c0003t0002g0122 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.207+1093C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211271 | ||||||
| chr17:76211355
|
C | T | 1 | a0001c0004t0003g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.207+1009G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211355 | ||||||
| chr17:76211379
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0210a0001c0001t0002g0114others(17): Show | 20 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.207+985C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211379 | ||||||
| chr17:76211422
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.207+942T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211422 | ||||||
| chr17:76211736
|
C | T | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.207+628G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211736 | ||||||
| chr17:76211803
|
C | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(49): Show | 53 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.207+561G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211803 | ||||||
| chr17:76211851
|
T | C | 1 | a0001c0003t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.207+513A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211851 | ||||||
| chr17:76211862
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.207+502T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211862 | ||||||
| chr17:76211898
|
A | G | 1 | a0001c0002t0004g0116 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.207+466T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76211898 | ||||||
| chr17:76212102
|
A | G | 4 | a0001c0001t0014g0003a0001c0004t0006g0018a0001c0004t0006g0019others(1): Show | 4 | HG03209.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+262T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76212102 | ||||||
| chr17:76212287
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0004t0002g0011 | 3 | HG01361.hp2 HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.207+77G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76212287 | ||||||
| chr17:76212343
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(45): Show | 49 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.207+21C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 2/18 | chr17 | 76212343 | ||||||
| chr17:76212541
|
T | TA | 54 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(51): Show | 55 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.89-60dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76212541 | ||||||
| chr17:76212682
|
C | T | 6 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(3): Show | 6 | HG01069.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-200G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76212682 | ||||||
| chr17:76212772
|
G | A | 28 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(25): Show | 28 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-290C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76212772 | ||||||
| chr17:76212988
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.89-506G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76212988 | ||||||
| chr17:76213227
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.89-745A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213227 | ||||||
| chr17:76213292
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-810G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213292 | ||||||
| chr17:76213305
|
C | T | 1 | a0001c0007t0022g0200 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-823G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213305 | ||||||
| chr17:76213569
|
C | CAA | 40 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(37): Show | 40 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.89-1089_89-1088dup others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213569 | ||||||
| chr17:76213588
|
T | A | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-1106A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213588 | ||||||
| chr17:76213588
|
T | C | 7 | a0001c0001t0002g0114a0001c0002t0002g0120a0001c0002t0004g0116others(4): Show | 7 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1106A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213588 | ||||||
| chr17:76213651
|
C | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-1169G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213651 | ||||||
| chr17:76213858
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-1376T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76213858 | ||||||
| chr17:76214018
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.89-1536C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214018 | ||||||
| chr17:76214097
|
A | G | 2 | a0001c0007t0022g0200a0001c0012t0011g0201 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.89-1615T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214097 | ||||||
| chr17:76214141
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0018g0225 | 2 | NA18968.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.89-1659A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214141 | ||||||
| chr17:76214328
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.89-1846C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214328 | ||||||
| chr17:76214472
|
C | A | 1 | a0001c0021t0001g0043 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.89-1990G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214472 | ||||||
| chr17:76214667
|
A | G | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.89-2185T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214667 | ||||||
| chr17:76214782
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-2300A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214782 | ||||||
| chr17:76214852
|
G | A | 1 | a0001c0004t0002g0199 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.89-2370C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214852 | ||||||
| chr17:76214971
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-2489G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76214971 | ||||||
| chr17:76215010
|
T | C | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-2528A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215010 | ||||||
| chr17:76215111
|
T | G | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-2629A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215111 | ||||||
| chr17:76215127
|
A | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-2645T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215127 | ||||||
| chr17:76215140
|
T | C | 2 | a0001c0008t0001g0047a0001c0008t0001g0048 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.89-2658A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215140 | ||||||
| chr17:76215147
|
T | G | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-2665A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215147 | ||||||
| chr17:76215540
|
TA | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(39): Show | 42 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.89-3059delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215540 | ||||||
| chr17:76215540
|
TAA | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(60): Show | 64 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.89-3060_89-3059del others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215540 | ||||||
| chr17:76215555
|
AAT | A | 6 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(3): Show | 6 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3075_89-3074del others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215555 | ||||||
| chr17:76215653
|
T | C | 1 | a0001c0002t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-3171A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215653 | ||||||
| chr17:76215763
|
T | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-3281A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215763 | ||||||
| chr17:76215788
|
G | A | 129 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(126): Show | 130 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.89-3306C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215788 | ||||||
| chr17:76215871
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 5 | HG01346.hp2 HG01496.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3389G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215871 | ||||||
| chr17:76215979
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-3497C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76215979 | ||||||
| chr17:76216111
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.89-3629C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216111 | ||||||
| chr17:76216184
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.89-3702A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216184 | ||||||
| chr17:76216219
|
C | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-3737G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216219 | ||||||
| chr17:76216301
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-3819G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216301 | ||||||
| chr17:76216361
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-3879G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216361 | ||||||
| chr17:76216362
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3880C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216362 | ||||||
| chr17:76216579
|
T | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-4097A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216579 | ||||||
| chr17:76216592
|
A | AAAT | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-4113_89-4111dup others(3): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216592 | ||||||
| chr17:76216707
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(108): Show | 112 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.89-4225A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216707 | ||||||
| chr17:76216708
|
A | T | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-4226T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216708 | ||||||
| chr17:76216723
|
T | G | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-4241A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216723 | ||||||
| chr17:76216894
|
A | C | 2 | a0001c0001t0001g0147a0001c0016t0001g0094 | 2 | HG02886.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.89-4412T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76216894 | ||||||
| chr17:76217694
|
G | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(108): Show | 112 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.89-5212C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76217694 | ||||||
| chr17:76217701
|
G | A | 1 | a0001c0004t0002g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.89-5219C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76217701 | ||||||
| chr17:76217760
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-5278C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76217760 | ||||||
| chr17:76217821
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.89-5339A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76217821 | ||||||
| chr17:76217865
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-5383T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76217865 | ||||||
| chr17:76218067
|
G | A | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.89-5585C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218067 | ||||||
| chr17:76218195
|
C | T | 48 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0127others(45): Show | 48 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-5713G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218195 | ||||||
| chr17:76218246
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-5764G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218246 | ||||||
| chr17:76218298
|
T | C | 2 | a0001c0004t0006g0018a0001c0004t0006g0019 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.89-5816A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218298 | ||||||
| chr17:76218414
|
G | C | 2 | a0001c0003t0002g0182a0001c0003t0002g0190 | 2 | HG00621.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.89-5932C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218414 | ||||||
| chr17:76218471
|
T | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-5989A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218471 | ||||||
| chr17:76218736
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.89-6254G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218736 | ||||||
| chr17:76218895
|
C | T | 6 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(3): Show | 6 | HG01069.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-6413G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76218895 | ||||||
| chr17:76219386
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0002g0036 | 2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.89-6904A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76219386 | ||||||
| chr17:76219528
|
A | G | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-7046T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76219528 | ||||||
| chr17:76220108
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.89-7626G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220108 | ||||||
| chr17:76220331
|
T | C | 7 | a0001c0001t0002g0114a0001c0002t0002g0120a0001c0002t0004g0116others(4): Show | 7 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-7849A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220331 | ||||||
| chr17:76220334
|
G | C | 6 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7852C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220334 | ||||||
| chr17:76220385
|
TA | T | 61 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0051others(58): Show | 62 | HG00597.hp1 HG00597.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.89-7904delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220385 | ||||||
| chr17:76220385
|
TAA | T | 27 | a0001c0001t0001g0013a0001c0001t0001g0191a0001c0001t0001g0219others(24): Show | 27 | HG00738.hp1 HG01361.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-7905_89-7904del others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220385 | ||||||
| chr17:76220385
|
TAAA | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-7906_89-7904del others(3): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220385 | ||||||
| chr17:76220435
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-7953A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220435 | ||||||
| chr17:76220597
|
C | T | 6 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(3): Show | 6 | HG01069.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-8115G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220597 | ||||||
| chr17:76220655
|
A | ATT | 7 | a0001c0001t0002g0203a0001c0003t0002g0195a0001c0004t0006g0202others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-8175_89-8174dup others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220655 | ||||||
| chr17:76220658
|
T | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(70): Show | 74 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.89-8176A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220658 | ||||||
| chr17:76220957
|
C | CA | 5 | a0001c0002t0001g0044a0001c0002t0001g0079a0001c0002t0001g0080others(2): Show | 5 | HG00621.hp2 NA19007.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-8476dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220957 | ||||||
| chr17:76220957
|
CA | C | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(90): Show | 94 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.89-8476delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220957 | ||||||
| chr17:76220957
|
CAA | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0206a0001c0001t0003g0012others(6): Show | 9 | HG01070.hp2 HG01361.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-8477_89-8476del others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76220957 | ||||||
| chr17:76221008
|
C | T | 8 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0004t0002g0199others(5): Show | 8 | HG01069.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-8526G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221008 | ||||||
| chr17:76221083
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.89-8601A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221083 | ||||||
| chr17:76221509
|
G | A | 14 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-9027C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221509 | ||||||
| chr17:76221665
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.89-9183T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221665 | ||||||
| chr17:76221798
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-9316A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221798 | ||||||
| chr17:76221801
|
G | C | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.89-9319C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221801 | ||||||
| chr17:76221963
|
G | A | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-9481C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76221963 | ||||||
| chr17:76222156
|
G | C | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-9674C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222156 | ||||||
| chr17:76222174
|
C | T | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.89-9692G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222174 | ||||||
| chr17:76222323
|
G | C | 1 | a0001c0003t0002g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.89-9841C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222323 | ||||||
| chr17:76222384
|
G | A | 1 | a0001c0002t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-9902C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222384 | ||||||
| chr17:76222399
|
T | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-9917A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222399 | ||||||
| chr17:76222459
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0003g0012 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.89-9977G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222459 | ||||||
| chr17:76222480
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-9998G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222480 | ||||||
| chr17:76222525
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.89-10043A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222525 | ||||||
| chr17:76222721
|
T | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0004t0003g0025 | 3 | HG01069.hp2 HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.89-10239A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222721 | ||||||
| chr17:76222767
|
T | C | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.89-10285A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222767 | ||||||
| chr17:76222895
|
C | CT | 7 | a0001c0001t0002g0114a0001c0002t0002g0120a0001c0002t0004g0116others(4): Show | 7 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-10414dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222895 | ||||||
| chr17:76222916
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-10434T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222916 | ||||||
| chr17:76222922
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.89-10440C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222922 | ||||||
| chr17:76222969
|
C | T | 2 | a0001c0003t0002g0130a0001c0003t0012g0129 | 2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.89-10487G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222969 | ||||||
| chr17:76222994
|
C | T | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-10512G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76222994 | ||||||
| chr17:76223011
|
C | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-10529G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223011 | ||||||
| chr17:76223016
|
G | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG00597.hp2 HG01070.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-10534C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223016 | ||||||
| chr17:76223189
|
C | CT | 10 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0049others(7): Show | 10 | HG01255.hp1 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-10708dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223189 | ||||||
| chr17:76223211
|
G | C | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-10729C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223211 | ||||||
| chr17:76223348
|
T | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0140others(2): Show | 5 | HG01109.hp1 HG01952.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-10866A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223348 | ||||||
| chr17:76223386
|
C | G | 1 | a0001c0003t0002g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.89-10904G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223386 | ||||||
| chr17:76223439
|
C | T | 3 | a0001c0003t0002g0095a0001c0003t0002g0096a0001c0004t0001g0097 | 3 | HG02132.hp1 NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.89-10957G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223439 | ||||||
| chr17:76223440
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-10958C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223440 | ||||||
| chr17:76223516
|
A | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0018g0225others(1): Show | 4 | NA18964.hp1 NA18968.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-11034T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223516 | ||||||
| chr17:76223581
|
C | T | 14 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-11099G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223581 | ||||||
| chr17:76223761
|
T | C | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.89-11279A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76223761 | ||||||
| chr17:76224223
|
C | A | 7 | a0001c0001t0002g0114a0001c0002t0002g0120a0001c0002t0004g0116others(4): Show | 7 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-11741G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224223 | ||||||
| chr17:76224386
|
TTTTCTA | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-11910_89-11905d others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224386 | ||||||
| chr17:76224444
|
T | G | 9 | a0001c0001t0001g0210a0001c0001t0003g0217a0001c0001t0003g0218others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-11962A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224444 | ||||||
| chr17:76224461
|
A | T | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.89-11979T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224461 | ||||||
| chr17:76224510
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-12028T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224510 | ||||||
| chr17:76224682
|
T | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-12200A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224682 | ||||||
| chr17:76224719
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-12237A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224719 | ||||||
| chr17:76224719
|
T | TA | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.89-12238dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224719 | ||||||
| chr17:76224728
|
AAAAG | A | 6 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-12250_89-12247d others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224728 | ||||||
| chr17:76224830
|
A | G | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(109): Show | 113 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.89-12348T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76224830 | ||||||
| chr17:76225040
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-12558G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225040 | ||||||
| chr17:76225125
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-12643A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225125 | ||||||
| chr17:76225215
|
A | T | 4 | a0001c0002t0011g0205a0001c0006t0007g0014a0001c0006t0007g0015others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-12733T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225215 | ||||||
| chr17:76225381
|
A | T | 1 | a0002c0009t0002g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.89-12899T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225381 | ||||||
| chr17:76225444
|
G | C | 3 | a0002c0009t0002g0211a0002c0009t0002g0212a0002c0010t0003g0213 | 3 | HG02258.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.89-12962C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225444 | ||||||
| chr17:76225604
|
A | ATCTT | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0127others(40): Show | 43 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-13123_89-13122i others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225604 | ||||||
| chr17:76225795
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.89-13313A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225795 | ||||||
| chr17:76225989
|
A | G | 2 | a0001c0005t0008g0197a0001c0005t0008g0198 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.89-13507T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76225989 | ||||||
| chr17:76226089
|
C | G | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-13607G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226089 | ||||||
| chr17:76226203
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.89-13721G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226203 | ||||||
| chr17:76226239
|
C | T | 153 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(150): Show | 154 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.89-13757G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226239 | ||||||
| chr17:76226266
|
C | G | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0127others(40): Show | 43 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-13784G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226266 | ||||||
| chr17:76226401
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.88+13752C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226401 | ||||||
| chr17:76226409
|
A | G | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(108): Show | 112 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.88+13744T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226409 | ||||||
| chr17:76226418
|
G | A | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+13735C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226418 | ||||||
| chr17:76226432
|
G | A | 14 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+13721C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226432 | ||||||
| chr17:76226829
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.88+13324C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226829 | ||||||
| chr17:76226875
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.88+13278G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226875 | ||||||
| chr17:76226912
|
C | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.88+13241G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226912 | ||||||
| chr17:76226922
|
G | A | 5 | a0001c0002t0011g0205a0001c0004t0002g0011a0001c0006t0007g0014others(2): Show | 5 | HG01361.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+13231C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226922 | ||||||
| chr17:76226927
|
G | A | 6 | a0001c0002t0002g0120a0001c0002t0004g0116a0001c0002t0004g0117others(3): Show | 6 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+13226C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76226927 | ||||||
| chr17:76227117
|
G | GT | 28 | a0001c0001t0001g0127a0001c0001t0001g0210a0001c0001t0002g0114others(25): Show | 28 | HG01069.hp1 HG01261.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.88+13035dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227117 | ||||||
| chr17:76227307
|
G | A | 1 | a0001c0001t0018g0225 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.88+12846C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227307 | ||||||
| chr17:76227373
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(127): Show | 131 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.88+12780T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227373 | ||||||
| chr17:76227522
|
AT | A | 6 | a0001c0002t0002g0120a0001c0002t0004g0116a0001c0002t0004g0117others(3): Show | 6 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+12630delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227522 | ||||||
| chr17:76227600
|
C | T | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+12553G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227600 | ||||||
| chr17:76227605
|
T | C | 1 | a0001c0002t0002g0183 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.88+12548A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227605 | ||||||
| chr17:76227643
|
C | T | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.88+12510G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227643 | ||||||
| chr17:76227839
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.88+12314A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227839 | ||||||
| chr17:76227988
|
A | G | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.88+12165T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76227988 | ||||||
| chr17:76228221
|
C | T | 4 | a0001c0002t0011g0205a0001c0006t0007g0014a0001c0006t0007g0015others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+11932G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228221 | ||||||
| chr17:76228324
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(108): Show | 112 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.88+11829A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228324 | ||||||
| chr17:76228420
|
T | G | 1 | a0001c0001t0024g0081 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.88+11733A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228420 | ||||||
| chr17:76228466
|
C | T | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+11687G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228466 | ||||||
| chr17:76228557
|
C | G | 1 | a0001c0002t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.88+11596G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228557 | ||||||
| chr17:76228778
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.88+11375C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228778 | ||||||
| chr17:76228830
|
C | T | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+11323G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228830 | ||||||
| chr17:76228896
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.88+11257G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228896 | ||||||
| chr17:76228942
|
C | CA | 10 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0001t0016g0113others(7): Show | 10 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+11210dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228942 | ||||||
| chr17:76228984
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88+11169C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76228984 | ||||||
| chr17:76229038
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.88+11115A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229038 | ||||||
| chr17:76229512
|
T | C | 1 | a0001c0002t0001g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.88+10641A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229512 | ||||||
| chr17:76229643
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.88+10510C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229643 | ||||||
| chr17:76229746
|
G | A | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+10407C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229746 | ||||||
| chr17:76229795
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+10358G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229795 | ||||||
| chr17:76229854
|
A | G | 1 | a0001c0003t0003g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.88+10299T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229854 | ||||||
| chr17:76229898
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.88+10255C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229898 | ||||||
| chr17:76229998
|
T | C | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.88+10155A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76229998 | ||||||
| chr17:76230261
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.88+9892G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230261 | ||||||
| chr17:76230379
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+9774A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230379 | ||||||
| chr17:76230396
|
A | T | 2 | a0001c0001t0001g0041a0001c0004t0002g0040 | 2 | HG02155.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.88+9757T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230396 | ||||||
| chr17:76230473
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88+9680C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230473 | ||||||
| chr17:76230474
|
G | A | 6 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(3): Show | 6 | HG01069.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+9679C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230474 | ||||||
| chr17:76230499
|
A | G | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+9654T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230499 | ||||||
| chr17:76230515
|
G | A | 3 | a0001c0001t0010g0039a0001c0001t0014g0086a0001c0002t0002g0087 | 3 | HG02622.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.88+9638C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230515 | ||||||
| chr17:76230716
|
C | T | 129 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(126): Show | 130 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.88+9437G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230716 | ||||||
| chr17:76230836
|
TA | T | 11 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(8): Show | 11 | HG01069.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+9316delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230836 | ||||||
| chr17:76230836
|
TAA | T | 8 | a0001c0001t0001g0022a0001c0002t0003g0032a0001c0002t0003g0033others(5): Show | 8 | HG01891.hp2 HG02895.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+9315_88+9316del others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230836 | ||||||
| chr17:76230851
|
AAAAAAAA others(4): Show |
A | 2 | a0004c0011t0002g0184a0004c0011t0002g0185 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.88+9291_88+9301del others(11): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230851 | ||||||
| chr17:76230855
|
AAAAAGAG | A | 49 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(46): Show | 50 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.88+9291_88+9297del others(7): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230855 | ||||||
| chr17:76230855
|
AAAAAGAG others(4): Show |
A | 1 | a0001c0003t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+9287_88+9297del others(11): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230855 | ||||||
| chr17:76230855
|
AAAAAGAG others(6): Show |
A | 40 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(37): Show | 40 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.88+9285_88+9297del others(13): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230855 | ||||||
| chr17:76230857
|
AAAG | A | 5 | a0001c0001t0001g0229a0001c0001t0014g0003a0001c0004t0006g0018others(2): Show | 5 | HG03195.hp1 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+9293_88+9295del others(3): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230857 | ||||||
| chr17:76230857
|
AAAGAG | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0088a0001c0001t0003g0012others(7): Show | 10 | HG01361.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+9291_88+9295del others(5): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230857 | ||||||
| chr17:76230858
|
AAG | A | 6 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0230others(3): Show | 6 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+9293_88+9294del others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230858 | ||||||
| chr17:76230858
|
AAGAGAG | A | 6 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0018g0225others(3): Show | 6 | HG03490.hp1 HG03704.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+9289_88+9294del others(6): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230858 | ||||||
| chr17:76230878
|
GAAAGAGA others(1): Show |
G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+9267_88+9274del others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230878 | ||||||
| chr17:76230880
|
AAGAGAAA others(1): Show |
A | 4 | a0001c0002t0001g0186a0001c0007t0001g0194a0004c0011t0002g0184others(1): Show | 4 | HG01884.hp2 HG02818.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9265_88+9272del others(8): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230880 | ||||||
| chr17:76230886
|
AAGAGAGA others(5): Show |
A | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+9255_88+9266del others(12): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230886 | ||||||
| chr17:76230894
|
AAGAG | A | 4 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(1): Show | 4 | HG01069.hp1 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9255_88+9258del others(4): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230894 | ||||||
| chr17:76230935
|
C | CT | 14 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+9217dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230935 | ||||||
| chr17:76230935
|
CT | C | 100 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 101 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.88+9217delA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230935 | ||||||
| chr17:76230965
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0003g0012 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.88+9188C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76230965 | ||||||
| chr17:76231041
|
C | T | 4 | a0001c0001t0014g0003a0001c0004t0006g0018a0001c0004t0006g0019others(1): Show | 4 | HG03209.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9112G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231041 | ||||||
| chr17:76231058
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+9095G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231058 | ||||||
| chr17:76231146
|
G | A | 4 | a0001c0001t0014g0003a0001c0004t0006g0018a0001c0004t0006g0019others(1): Show | 4 | HG03209.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9007C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231146 | ||||||
| chr17:76231199
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+8954C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231199 | ||||||
| chr17:76231249
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.88+8904C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231249 | ||||||
| chr17:76231287
|
G | A | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+8866C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231287 | ||||||
| chr17:76231350
|
G | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.88+8803C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231350 | ||||||
| chr17:76231447
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88+8706G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231447 | ||||||
| chr17:76231452
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+8701T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231452 | ||||||
| chr17:76231538
|
T | C | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+8615A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231538 | ||||||
| chr17:76231570
|
T | C | 10 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0001t0014g0003others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+8583A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231570 | ||||||
| chr17:76231583
|
G | C | 4 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0002g0151others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+8570C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231583 | ||||||
| chr17:76231722
|
T | C | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.88+8431A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231722 | ||||||
| chr17:76231749
|
G | A | 3 | a0001c0004t0006g0018a0001c0004t0006g0019a0001c0005t0008g0017 | 3 | HG03225.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.88+8404C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231749 | ||||||
| chr17:76231799
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+8354A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76231799 | ||||||
| chr17:76232109
|
G | A | 1 | a0001c0003t0002g0091 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.88+8044C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232109 | ||||||
| chr17:76232191
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+7962T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232191 | ||||||
| chr17:76232200
|
T | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+7953A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232200 | ||||||
| chr17:76232242
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.88+7911C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232242 | ||||||
| chr17:76232339
|
G | C | 1 | a0001c0002t0011g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+7814C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232339 | ||||||
| chr17:76232389
|
TA | T | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+7763delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232389 | ||||||
| chr17:76232520
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88+7633G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232520 | ||||||
| chr17:76232547
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0002g0149a0001c0002t0002g0151others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+7606G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232547 | ||||||
| chr17:76232596
|
T | C | 4 | a0001c0001t0014g0003a0001c0004t0006g0018a0001c0004t0006g0019others(1): Show | 4 | HG03209.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+7557A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232596 | ||||||
| chr17:76232750
|
T | C | 1 | a0001c0004t0002g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.88+7403A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232750 | ||||||
| chr17:76232765
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.88+7388G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232765 | ||||||
| chr17:76232808
|
T | C | 14 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+7345A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232808 | ||||||
| chr17:76232844
|
C | G | 4 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(1): Show | 4 | HG01069.hp1 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+7309G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232844 | ||||||
| chr17:76232926
|
A | AT | 56 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(53): Show | 57 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.88+7226dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76232926 | ||||||
| chr17:76233065
|
T | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0127others(45): Show | 48 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+7088A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233065 | ||||||
| chr17:76233157
|
T | C | 6 | a0001c0002t0002g0120a0001c0002t0004g0116a0001c0002t0004g0117others(3): Show | 6 | HG02559.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+6996A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233157 | ||||||
| chr17:76233200
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+6953C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233200 | ||||||
| chr17:76233224
|
G | C | 1 | a0001c0003t0002g0190 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.88+6929C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233224 | ||||||
| chr17:76233267
|
G | T | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+6886C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233267 | ||||||
| chr17:76233569
|
A | C | 4 | a0001c0001t0014g0003a0001c0004t0006g0018a0001c0004t0006g0019others(1): Show | 4 | HG03209.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+6584T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233569 | ||||||
| chr17:76233651
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.88+6502G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233651 | ||||||
| chr17:76233761
|
G | A | 1 | a0001c0003t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.88+6392C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233761 | ||||||
| chr17:76233845
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.88+6308A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233845 | ||||||
| chr17:76233895
|
T | C | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.88+6258A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233895 | ||||||
| chr17:76233908
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0011g0205others(4): Show | 7 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+6245C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76233908 | ||||||
| chr17:76234022
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(228): Show | 233 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.88+6131A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234022 | ||||||
| chr17:76234101
|
T | C | 12 | a0001c0001t0001g0210a0001c0001t0003g0217a0001c0001t0003g0218others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+6052A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234101 | ||||||
| chr17:76234188
|
C | T | 1 | a0001c0004t0003g0027 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.88+5965G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234188 | ||||||
| chr17:76234261
|
T | G | 2 | a0001c0002t0001g0093a0001c0016t0001g0094 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.88+5892A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234261 | ||||||
| chr17:76234362
|
T | C | 4 | a0001c0003t0002g0095a0001c0003t0002g0096a0001c0003t0002g0112others(1): Show | 4 | HG02132.hp1 NA18956.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+5791A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234362 | ||||||
| chr17:76234448
|
G | A | 5 | a0001c0001t0009g0101a0001c0001t0009g0102a0001c0002t0002g0098others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+5705C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234448 | ||||||
| chr17:76234554
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+5599A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234554 | ||||||
| chr17:76234740
|
C | T | 8 | a0001c0001t0001g0210a0001c0002t0002g0209a0001c0002t0002g0214others(5): Show | 8 | HG01106.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+5413G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234740 | ||||||
| chr17:76234776
|
T | C | 9 | a0001c0001t0002g0203a0001c0001t0015g0196a0001c0003t0002g0195others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+5377A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234776 | ||||||
| chr17:76234924
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0003g0012 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.88+5229G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76234924 | ||||||
| chr17:76235083
|
C | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+5070G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235083 | ||||||
| chr17:76235101
|
G | A | 1 | a0001c0001t0016g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88+5052C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235101 | ||||||
| chr17:76235199
|
C | CT | 40 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(37): Show | 40 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.88+4953dupA | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235199 | ||||||
| chr17:76235267
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+4886C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235267 | ||||||
| chr17:76235349
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.88+4804G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235349 | ||||||
| chr17:76235372
|
G | T | 1 | a0006c0018t0001g0026 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.88+4781C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235372 | ||||||
| chr17:76235389
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+4764C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235389 | ||||||
| chr17:76235444
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+4709G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235444 | ||||||
| chr17:76235489
|
C | T | 14 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 14 | HG00738.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+4664G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235489 | ||||||
| chr17:76235510
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.88+4643A>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235510 | ||||||
| chr17:76235737
|
G | A | 3 | a0001c0006t0007g0014a0001c0006t0007g0015a0001c0006t0007g0016 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+4416C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76235737 | ||||||
| chr17:76236190
|
C | T | 1 | a0003c0020t0002g0123 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.88+3963G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236190 | ||||||
| chr17:76236737
|
G | T | 2 | a0001c0004t0002g0207a0001c0004t0002g0208 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.88+3416C>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236737 | ||||||
| chr17:76236874
|
G | C | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+3279C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236874 | ||||||
| chr17:76236877
|
C | T | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+3276G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236877 | ||||||
| chr17:76236880
|
T | C | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+3273A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236880 | ||||||
| chr17:76236881
|
C | A | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+3272G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236881 | ||||||
| chr17:76236882
|
T | A | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+3271A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236882 | ||||||
| chr17:76236883
|
A | C | 1 | a0001c0003t0002g0195 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+3270T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76236883 | ||||||
| chr17:76237003
|
GC | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0004t0003g0025 | 3 | HG01069.hp2 HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.88+3149delG | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237003 | ||||||
| chr17:76237093
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.88+3060G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237093 | ||||||
| chr17:76237170
|
G | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+2983C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237170 | ||||||
| chr17:76237242
|
T | C | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.88+2911A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237242 | ||||||
| chr17:76237306
|
G | C | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+2847C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237306 | ||||||
| chr17:76237436
|
C | T | 1 | a0001c0003t0002g0122 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.88+2717G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237436 | ||||||
| chr17:76237442
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.88+2711A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237442 | ||||||
| chr17:76237503
|
A | G | 1 | a0001c0002t0001g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88+2650T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237503 | ||||||
| chr17:76237554
|
A | G | 6 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(3): Show | 6 | HG01069.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+2599T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237554 | ||||||
| chr17:76237770
|
T | C | 1 | a0001c0002t0002g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+2383A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237770 | ||||||
| chr17:76237847
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(38): Show | 41 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+2306C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237847 | ||||||
| chr17:76237993
|
A | T | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.88+2160T>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76237993 | ||||||
| chr17:76238071
|
G | C | 6 | a0001c0001t0015g0196a0001c0004t0002g0199a0001c0005t0008g0197others(3): Show | 6 | HG01069.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+2082C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238071 | ||||||
| chr17:76238085
|
C | CA | 19 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0191others(16): Show | 19 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+2067dupT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238085 | ||||||
| chr17:76238085
|
CA | C | 20 | a0001c0001t0001g0013a0001c0001t0002g0114a0001c0001t0003g0005others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+2067delT | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238085 | ||||||
| chr17:76238167
|
T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(51): Show | 55 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.88+1986A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238167 | ||||||
| chr17:76238251
|
A | G | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.88+1902T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238251 | ||||||
| chr17:76238418
|
A | AAG | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(99): Show | 103 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.88+1734_88+1735ins others(2): Show |
RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238418 | ||||||
| chr17:76238451
|
G | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(2): Show | 5 | HG00738.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+1702C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238451 | ||||||
| chr17:76238514
|
T | C | 2 | a0001c0001t0002g0203a0001c0004t0006g0202 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.88+1639A>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238514 | ||||||
| chr17:76238577
|
A | G | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(109): Show | 113 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.88+1576T>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238577 | ||||||
| chr17:76238850
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88+1303G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76238850 | ||||||
| chr17:76239124
|
A | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(50): Show | 54 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.88+1029T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239124 | ||||||
| chr17:76239347
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0146others(61): Show | 65 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.88+806C>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239347 | ||||||
| chr17:76239379
|
C | T | 1 | a0001c0004t0002g0011 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.88+774G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239379 | ||||||
| chr17:76239497
|
T | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0127others(118): Show | 122 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.88+656A>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239497 | ||||||
| chr17:76239539
|
A | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | NA18947.hp2 NA18948.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.88+614T>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239539 | ||||||
| chr17:76239541
|
C | A | 1 | a0001c0002t0011g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+612G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239541 | ||||||
| chr17:76239550
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0003g0005 | 3 | HG01255.hp1 HG03225.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.88+603G>C | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239550 | ||||||
| chr17:76239722
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.88+431G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239722 | ||||||
| chr17:76239761
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.88+392G>T | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239761 | ||||||
| chr17:76239822
|
C | T | 1 | a0001c0001t0014g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88+331G>A | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76239822 | ||||||
| chr17:76240034
|
G | C | 26 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0221others(23): Show | 26 | HG00738.hp1 HG01106.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+119C>G | RNF157 | ENSG00000141576.16 | transcript | ENST00000269391.11 | protein_coding | 1/18 | chr17 | 76240034 |