Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84077 |
|---|---|
| ensemblid | ENSG00000131379.10 |
| hgncid | 25320 |
| symbol | C3orf20 |
| name | chromosome 3 open reading frame 20 |
| refseq_nuc | NM_032137.5 |
| refseq_prot | NP_115513.4 |
| ensembl_nuc | ENST00000253697.8 |
| ensembl_prot | ENSP00000253697.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 14675141 |
| end | 14773036 |
| strand | + |
| ver | v1.2 |
| region | chr3:14675141-14773036 |
| region5000 | chr3:14670141-14778036 |
| regionname0 | C3orf20_chr3_14675141_14773036 |
| regionname5000 | C3orf20_chr3_14670141_14778036 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 904 | 168 | 51 | 29 | 68 | 3 | 15 | 53 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0002 | 0/0 | 904 | 60 | 13 | 14 | 21 | 5 | 7 | 20 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0003 | 0/0 | 904 | 49 | 11 | 13 | 18 | 2 | 5 | 12 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0004 | 0/0 | 904 | 25 | 0 | 0 | 24 | 1 | 0 | 19 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0005 | 0/0 | 904 | 25 | 4 | 6 | 9 | 0 | 6 | 8 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0006 | 0/0 | 904 | 20 | 0 | 6 | 12 | 0 | 2 | 9 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0007 | 0/0 | 904 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0008 | 0/0 | 904 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0009 | 0/0 | 904 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0010 | 0/0 | 904 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0011 | 0/0 | 904 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0012 | 0/0 | 904 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0013 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0014 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0015 | 0/0 | 904 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0016 | 0/0 | 311 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0017 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0018 | 0/0 | 904 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0019 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0020 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0021 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0022 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0023 | 0/0 | 904 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0024 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0025 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0026 | 0/0 | 904 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0027 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2715 | 160 | 44 | 29 | 67 | 3 | 15 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0002 | 0/0 | 2715 | 60 | 13 | 14 | 21 | 5 | 7 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0003 | 0/0 | 2715 | 49 | 11 | 13 | 18 | 2 | 5 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0004 | 0/0 | 2715 | 25 | 4 | 6 | 9 | 0 | 6 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0005 | 0/0 | 2715 | 25 | 0 | 0 | 24 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0006 | 0/0 | 2715 | 20 | 0 | 6 | 12 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0007 | 0/0 | 2715 | 4 | 0 | 0 | 4 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0008 | 0/0 | 2715 | 4 | 0 | 2 | 0 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0009 | 0/0 | 2715 | 4 | 4 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0010 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0011 | 0/0 | 2715 | 3 | 1 | 0 | 2 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0012 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0013 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0014 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0015 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0016 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0017 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0018 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0019 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0020 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0021 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0022 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0023 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0024 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0025 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0026 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0027 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0028 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0029 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0030 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0031 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0032 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| c0033 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| 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 | 0/1 | 572 | 278 | 59 | 52 | 118 | 11 | 37 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| t0002 | 1/0 | 572 | 81 | 17 | 12 | 48 | 0 | 3 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| t0003 | 0/0 | 583 | 6 | 6 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| t0004 | 0/0 | 572 | 6 | 4 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| t0005 | 0/0 | 572 | 4 | 2 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| t0006 | 0/0 | 572 | 4 | 0 | 4 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| t0007 | 0/0 | 572 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| 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 | 3 | 2 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2715 | 160 | 44 | 29 | 67 | 3 | 15 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0009 | 0/0 | 2715 | 4 | 4 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0021 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0022 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0023 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0024 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0002c0002 | 0/0 | 2715 | 60 | 13 | 14 | 21 | 5 | 7 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0003c0003 | 0/0 | 2715 | 49 | 11 | 13 | 18 | 2 | 5 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0004c0005 | 0/0 | 2715 | 25 | 0 | 0 | 24 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0005c0004 | 0/0 | 2715 | 25 | 4 | 6 | 9 | 0 | 6 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0006c0006 | 0/0 | 2715 | 20 | 0 | 6 | 12 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0007c0007 | 0/0 | 2715 | 4 | 0 | 0 | 4 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0008c0008 | 0/0 | 2715 | 4 | 0 | 2 | 0 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0009c0011 | 0/0 | 2715 | 3 | 1 | 0 | 2 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0010c0010 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0011c0025 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0011c0026 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0012c0012 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0013c0014 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0014c0015 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0015c0032 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0016c0031 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0017c0027 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0018c0028 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0019c0029 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0020c0030 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0021c0033 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0022c0017 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0023c0018 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0024c0019 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0025c0020 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0026c0016 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0027c0013 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3286 | 101 | 29 | 9 | 46 | 3 | 13 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0001t0002 | 1/0 | 3286 | 40 | 4 | 12 | 21 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0001t0003 | 0/0 | 3297 | 6 | 6 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0001t0004 | 0/0 | 3286 | 6 | 4 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0001t0005 | 0/0 | 3286 | 3 | 1 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0001t0006 | 0/0 | 3286 | 4 | 0 | 4 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0009t0001 | 0/0 | 3286 | 4 | 4 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0021t0005 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0022t0001 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0023t0001 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0001c0024t0002 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0002c0002t0001 | 0/0 | 3286 | 47 | 3 | 14 | 19 | 4 | 7 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0002c0002t0002 | 0/0 | 3286 | 12 | 10 | 0 | 2 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0002c0002t0007 | 0/0 | 3286 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0003c0003t0001 | 0/0 | 3286 | 49 | 11 | 13 | 18 | 2 | 5 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0004c0005t0001 | 0/0 | 3286 | 3 | 0 | 0 | 2 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0004c0005t0002 | 0/0 | 3286 | 22 | 0 | 0 | 22 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0005c0004t0001 | 0/0 | 3286 | 25 | 4 | 6 | 9 | 0 | 6 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0006c0006t0001 | 0/0 | 3286 | 20 | 0 | 6 | 12 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0007c0007t0001 | 0/0 | 3286 | 4 | 0 | 0 | 4 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0008c0008t0001 | 0/0 | 3286 | 4 | 0 | 2 | 0 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0009c0011t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0009c0011t0002 | 0/0 | 3286 | 2 | 1 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0010c0010t0001 | 0/0 | 3286 | 3 | 3 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0011c0025t0001 | 0/0 | 3286 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0011c0026t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0012c0012t0002 | 0/0 | 3286 | 2 | 2 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0013c0014t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0014c0015t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0015c0032t0001 | 0/0 | 3286 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0016c0031t0001 | 0/0 | 3286 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0017c0027t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0018c0028t0002 | 0/0 | 3286 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0019c0029t0001 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0020c0030t0001 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0021c0033t0002 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0022c0017t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0023c0018t0001 | 0/0 | 3286 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0024c0019t0001 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0025c0020t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0026c0016t0001 | 0/0 | 3286 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| a0027c0013t0001 | 0/0 | 3286 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | copy fasta | chr3 | 14670141 | 14778036 |
| 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 | 3 | 2 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0001t0006g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0009t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0009t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0009t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0009t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0021t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0022t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0023t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0001c0024t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0002c0002t0007g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0004c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0005c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0006c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0007c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0007c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0007c0007t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0007c0007t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0008c0008t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0008c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0008c0008t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0008c0008t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0009c0011t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0009c0011t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0009c0011t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0010c0010t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0010c0010t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0010c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0011c0025t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0011c0026t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0012c0012t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0012c0012t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0013c0014t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0014c0015t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0015c0032t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0016c0031t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0017c0027t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0018c0028t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0019c0029t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0020c0030t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0021c0033t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0022c0017t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0023c0018t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0024c0019t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0025c0020t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0026c0016t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| a0027c0013t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0016 | c0031 | t0001 | g0361 | EUR | GBR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00099 | hp2 | a0002 | c0002 | t0007 | g0261 | EUR | GBR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0136 | EUR | GBR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00140 | hp2 | a0004 | c0005 | t0001 | g0004 | EUR | GBR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00423 | hp2 | a0006 | c0006 | t0001 | g0222 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00597 | hp2 | a0004 | c0005 | t0002 | g0093 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00621 | hp1 | a0004 | c0005 | t0002 | g0035 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00621 | hp2 | a0009 | c0011 | t0001 | g0304 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00639 | hp1 | a0008 | c0008 | t0001 | g0127 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0132 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00673 | hp1 | a0006 | c0006 | t0001 | g0173 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00673 | hp2 | a0004 | c0005 | t0002 | g0081 | EAS | CHS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00735 | hp1 | a0005 | c0004 | t0001 | g0182 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0169 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0354 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01074 | hp1 | a0006 | c0006 | t0001 | g0164 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0333 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0117 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01167 | hp1 | a0023 | c0018 | t0001 | g0116 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0337 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0183 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0336 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0184 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0140 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0280 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0207 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0168 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01255 | hp1 | a0008 | c0008 | t0001 | g0181 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0332 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0363 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0322 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01358 | hp2 | a0005 | c0004 | t0001 | g0131 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0308 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01433 | hp2 | a0026 | c0016 | t0001 | g0135 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0237 | EUR | IBS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0335 | EUR | IBS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0239 | EUR | IBS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0356 | EUR | IBS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0338 | EUR | IBS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | IBS | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01884 | hp2 | a0001 | c0009 | t0001 | g0235 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01891 | hp2 | a0001 | c0009 | t0001 | g0236 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01928 | hp1 | a0005 | c0004 | t0001 | g0217 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0118 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01934 | hp2 | a0006 | c0006 | t0001 | g0176 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01943 | hp1 | a0005 | c0004 | t0001 | g0195 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0139 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0167 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01952 | hp2 | a0006 | c0006 | t0001 | g0002 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0170 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01978 | hp1 | a0005 | c0004 | t0001 | g0196 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0128 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01993 | hp1 | a0005 | c0004 | t0001 | g0197 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02004 | hp1 | a0006 | c0006 | t0001 | g0002 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02055 | hp2 | a0001 | c0022 | t0001 | g0110 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0220 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02071 | hp1 | a0004 | c0005 | t0001 | g0241 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02080 | hp2 | a0004 | c0005 | t0002 | g0060 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | CDX | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02165 | hp2 | a0006 | c0006 | t0001 | g0223 | EAS | CDX | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02258 | hp2 | a0001 | c0009 | t0001 | g0233 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02273 | hp2 | a0006 | c0006 | t0001 | g0152 | AMR | PEL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02280 | hp1 | a0005 | c0004 | t0001 | g0205 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0049 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0334 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02451 | hp2 | a0005 | c0004 | t0001 | g0130 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0319 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02602 | hp2 | a0005 | c0004 | t0001 | g0229 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02615 | hp2 | a0020 | c0030 | t0001 | g0349 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0208 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0201 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0134 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02717 | hp2 | a0005 | c0004 | t0001 | g0202 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02735 | hp2 | a0008 | c0008 | t0001 | g0145 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02738 | hp2 | a0005 | c0004 | t0001 | g0215 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02809 | hp1 | a0024 | c0019 | t0001 | g0211 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02896 | hp1 | a0019 | c0029 | t0001 | g0054 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0175 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0206 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02970 | hp1 | a0001 | c0009 | t0001 | g0234 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03017 | hp1 | a0008 | c0008 | t0001 | g0225 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03041 | hp1 | a0010 | c0010 | t0001 | g0221 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03139 | hp1 | a0012 | c0012 | t0002 | g0040 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0199 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03195 | hp1 | a0009 | c0011 | t0002 | g0041 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0171 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03225 | hp2 | a0001 | c0023 | t0001 | g0109 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03490 | hp1 | a0006 | c0006 | t0001 | g0172 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03490 | hp2 | a0005 | c0004 | t0001 | g0006 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03491 | hp2 | a0011 | c0025 | t0001 | g0343 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03492 | hp1 | a0005 | c0004 | t0001 | g0006 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0200 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ESN | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0371 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0210 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0159 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03704 | hp1 | a0005 | c0004 | t0001 | g0228 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0318 | SAS | PJL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03831 | hp1 | a0005 | c0004 | t0001 | g0227 | SAS | BEB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0347 | SAS | BEB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03834 | hp2 | a0015 | c0032 | t0001 | g0004 | SAS | BEB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03942 | hp2 | a0006 | c0006 | t0001 | g0149 | SAS | BEB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0364 | SAS | STU | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0346 | SAS | STU | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0292 | SAS | STU | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG04204 | hp2 | a0018 | c0028 | t0002 | g0102 | SAS | STU | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18522 | hp1 | a0001 | c0021 | t0005 | g0120 | AFR | YRI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0048 | AFR | YRI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18612 | hp1 | a0005 | c0004 | t0001 | g0214 | EAS | CHB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18906 | hp2 | a0012 | c0012 | t0002 | g0039 | AFR | YRI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18940 | hp2 | a0006 | c0006 | t0001 | g0158 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18941 | hp2 | a0004 | c0005 | t0002 | g0068 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0373 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18943 | hp1 | a0006 | c0006 | t0001 | g0191 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18943 | hp2 | a0009 | c0011 | t0002 | g0034 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18945 | hp2 | a0005 | c0004 | t0001 | g0226 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18951 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18952 | hp1 | a0025 | c0020 | t0001 | g0016 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18952 | hp2 | a0004 | c0005 | t0002 | g0071 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18954 | hp1 | a0004 | c0005 | t0002 | g0103 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18956 | hp1 | a0011 | c0026 | t0001 | g0257 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18957 | hp1 | a0007 | c0007 | t0001 | g0218 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18959 | hp2 | a0004 | c0005 | t0002 | g0080 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18960 | hp1 | a0004 | c0005 | t0002 | g0077 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0219 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18968 | hp2 | a0006 | c0006 | t0001 | g0180 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18969 | hp1 | a0014 | c0015 | t0001 | g0178 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18969 | hp2 | a0004 | c0005 | t0002 | g0086 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18974 | hp1 | a0004 | c0005 | t0001 | g0296 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18974 | hp2 | a0004 | c0005 | t0002 | g0075 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18975 | hp1 | a0004 | c0005 | t0002 | g0087 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18975 | hp2 | a0003 | c0003 | t0001 | g0138 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18978 | hp1 | a0013 | c0014 | t0001 | g0194 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18978 | hp2 | a0004 | c0005 | t0002 | g0063 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18979 | hp1 | a0006 | c0006 | t0001 | g0147 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0368 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18982 | hp2 | a0006 | c0006 | t0001 | g0174 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18986 | hp2 | a0005 | c0004 | t0001 | g0185 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18990 | hp1 | a0004 | c0005 | t0002 | g0065 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18990 | hp2 | a0017 | c0027 | t0001 | g0366 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18992 | hp1 | a0005 | c0004 | t0001 | g0189 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18992 | hp2 | a0027 | c0013 | t0001 | g0248 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18999 | hp2 | a0004 | c0005 | t0002 | g0078 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19005 | hp1 | a0004 | c0005 | t0002 | g0079 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0372 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19007 | hp1 | a0007 | c0007 | t0001 | g0154 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19007 | hp2 | a0005 | c0004 | t0001 | g0187 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19010 | hp1 | a0004 | c0005 | t0002 | g0091 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0163 | AFR | LWK | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19030 | hp2 | a0010 | c0010 | t0001 | g0224 | AFR | LWK | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19043 | hp2 | a0010 | c0010 | t0001 | g0213 | AFR | LWK | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19054 | hp2 | a0005 | c0004 | t0001 | g0146 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19055 | hp1 | a0004 | c0005 | t0002 | g0067 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19062 | hp2 | a0007 | c0007 | t0001 | g0192 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19063 | hp1 | a0003 | c0003 | t0001 | g0230 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19063 | hp2 | a0005 | c0004 | t0001 | g0186 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19064 | hp1 | a0006 | c0006 | t0001 | g0129 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19064 | hp2 | a0001 | c0024 | t0002 | g0037 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19067 | hp1 | a0021 | c0033 | t0002 | g0026 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19067 | hp2 | a0007 | c0007 | t0001 | g0198 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19070 | hp1 | a0004 | c0005 | t0002 | g0076 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19070 | hp2 | a0006 | c0006 | t0001 | g0179 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19074 | hp1 | a0006 | c0006 | t0001 | g0177 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19077 | hp1 | a0004 | c0005 | t0002 | g0064 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19077 | hp2 | a0006 | c0006 | t0001 | g0209 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19079 | hp1 | a0005 | c0004 | t0001 | g0143 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19083 | hp1 | a0005 | c0004 | t0001 | g0188 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19086 | hp1 | a0004 | c0005 | t0002 | g0066 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19087 | hp1 | a0022 | c0017 | t0001 | g0190 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | YRI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ASW | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ASW | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0150 | EUR | TSI | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | GIH | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0137 | SAS | GIH | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0330 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG01123 | hp2 | a0006 | c0006 | t0001 | g0153 | AMR | CLM | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG02559 | hp2 | a0005 | c0004 | t0001 | g0216 | AFR | ACB | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA18955 | hp2 | a0004 | c0005 | t0002 | g0062 | EAS | JPT | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | USA | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | USA | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0275 | REF | REF | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0013 | REF | REF | C3orf20_chr3_14670141_14778036 | C3orf20 | chr3 | 14670141 | 14778036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14682763
|
T | C | 1 | a0027 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.50T>C | p.Met17Thr | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 460/3286 | 50/2715 | 17/904 | chr3 | 14682763 | ||
| chr3:14682838
|
G | A | 4 | a0006a0007a0013others(1): Show | 26 | HG00423.hp2 HG00673.hp1 HG01074.hp1 others(23): Show |
missense_variant | MODERATE | c.125G>A | p.Gly42Asp | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 535/3286 | 125/2715 | 42/904 | chr3 | 14682838 | ||
| chr3:14682906
|
G | A | 13 | a0003a0005a0006others(10): Show | 112 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(109): Show |
missense_variant | MODERATE | c.193G>A | p.Asp65Asn | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 603/3286 | 193/2715 | 65/904 | chr3 | 14682906 | ||
| chr3:14683051
|
C | T | 1 | a0021 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.338C>T | p.Ala113Val | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 748/3286 | 338/2715 | 113/904 | chr3 | 14683051 | ||
| chr3:14684301
|
C | T | 1 | a0015 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.544C>T | p.Leu182Phe | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/17 | 954/3286 | 544/2715 | 182/904 | chr3 | 14684301 | ||
| chr3:14684371
|
A | G | 1 | a0008 | 4 | HG00639.hp1 HG01255.hp1 HG02735.hp2 others(1): Show |
missense_variant | MODERATE | c.614A>G | p.Gln205Arg | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/17 | 1024/3286 | 614/2715 | 205/904 | chr3 | 14684371 | ||
| chr3:14704350
|
G | A | 10 | a0002a0003a0006others(7): Show | 143 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(140): Show |
missense_variant | MODERATE | c.892G>A | p.Ala298Thr | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/17 | 1302/3286 | 892/2715 | 298/904 | chr3 | 14704350 | ||
| chr3:14704392
|
C | T | 1 | a0016 | 1 | HG00099.hp1 | stop_gained | HIGH | c.934C>T | p.Arg312* | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/17 | 1344/3286 | 934/2715 | 312/904 | chr3 | 14704392 | ||
| chr3:14714065
|
A | G | 12 | a0002a0003a0006others(9): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
missense_variant | MODERATE | c.1219A>G | p.Ile407Val | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/17 | 1629/3286 | 1219/2715 | 407/904 | chr3 | 14714065 | ||
| chr3:14714110
|
C | G | 12 | a0002a0003a0006others(9): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
missense_variant | MODERATE | c.1264C>G | p.Leu422Val | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/17 | 1674/3286 | 1264/2715 | 422/904 | chr3 | 14714110 | ||
| chr3:14728525
|
C | T | 1 | a0017 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.1777C>T | p.Leu593Phe | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/17 | 2187/3286 | 1777/2715 | 593/904 | chr3 | 14728525 | ||
| chr3:14757441
|
C | T | 1 | a0014 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2011C>T | p.Arg671Trp | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/17 | 2421/3286 | 2011/2715 | 671/904 | chr3 | 14757441 | ||
| chr3:14757469
|
G | A | 5 | a0004a0007a0011others(2): Show | 33 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
missense_variant | MODERATE | c.2039G>A | p.Arg680His | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/17 | 2449/3286 | 2039/2715 | 680/904 | chr3 | 14757469 | ||
| chr3:14757496
|
C | T | 4 | a0010a0012a0020others(1): Show | 7 | HG02615.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
missense_variant | MODERATE | c.2066C>T | p.Ala689Val | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/17 | 2476/3286 | 2066/2715 | 689/904 | chr3 | 14757496 | ||
| chr3:14761501
|
G | C | 1 | a0018 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.2381G>C | p.Gly794Ala | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/17 | 2791/3286 | 2381/2715 | 794/904 | chr3 | 14761501 | ||
| chr3:14761507
|
G | A | 1 | a0023 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.2387G>A | p.Arg796His | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/17 | 2797/3286 | 2387/2715 | 796/904 | chr3 | 14761507 | ||
| chr3:14761609
|
A | T | 1 | a0019 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.2489A>T | p.Lys830Ile | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/17 | 2899/3286 | 2489/2715 | 830/904 | chr3 | 14761609 | ||
| chr3:14772071
|
C | G | 1 | a0026 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2500C>G | p.Pro834Ala | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/17 | 2910/3286 | 2500/2715 | 834/904 | chr3 | 14772071 | ||
| chr3:14772086
|
A | T | 1 | a0013 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.2515A>T | p.Ser839Cys | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/17 | 2925/3286 | 2515/2715 | 839/904 | chr3 | 14772086 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14683151
|
G | A | 1 | a0001c0021 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.438G>A | p.Thr146Thr | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 848/3286 | 438/2715 | 146/904 | chr3 | 14683151 | ||
| chr3:14683196
|
G | A | 1 | a0001c0009 | 4 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.483G>A | p.Ser161Ser | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 893/3286 | 483/2715 | 161/904 | chr3 | 14683196 | ||
| chr3:14684312
|
G | A | 2 | a0001c0022a0001c0023 | 2 | HG02055.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.555G>A | p.Lys185Lys | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/17 | 965/3286 | 555/2715 | 185/904 | chr3 | 14684312 | ||
| chr3:14684348
|
G | A | 1 | a0001c0024 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.591G>A | p.Gly197Gly | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/17 | 1001/3286 | 591/2715 | 197/904 | chr3 | 14684348 | ||
| chr3:14704610
|
C | G | 1 | a0001c0023 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1152C>G | p.Ser384Ser | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/17 | 1562/3286 | 1152/2715 | 384/904 | chr3 | 14704610 | ||
| chr3:14728524
|
G | C | 1 | a0017c0027 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1776G>C | p.Arg592Arg | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/17 | 2186/3286 | 1776/2715 | 592/904 | chr3 | 14728524 | ||
| chr3:14759980
|
G | A | 5 | a0004c0005a0007c0007a0011c0025others(2): Show | 32 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
synonymous_variant | LOW | c.2334G>A | p.Val778Val | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/17 | 2744/3286 | 2334/2715 | 778/904 | chr3 | 14759980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14675145
|
T | TAGC | 1 | a0001c0001t0003 | 6 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-406_-405insAGC | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/17 | 7568 | chr3 | 14675145 | |||||
| chr3:14675147
|
A | ACTCCAGC others(1): Show |
1 | a0001c0001t0003 | 6 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-404_-403insCTCCAG others(2): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/17 | 7566 | chr3 | 14675147 | |||||
| chr3:14682209
|
C | T | 1 | a0002c0002t0007 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 2/17 | 505 | chr3 | 14682209 | |||||
| chr3:14682217
|
A | G | 1 | a0001c0001t0006 | 4 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-251A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 2/17 | 497 | chr3 | 14682217 | |||||
| chr3:14682243
|
C | A | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(31): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
5_prime_UTR_variant | MODIFIER | c.-225C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 2/17 | 471 | chr3 | 14682243 | |||||
| chr3:14682312
|
C | T | 2 | a0001c0001t0005a0001c0021t0005 | 4 | HG01109.hp2 HG01934.hp1 NA18522.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 2/17 | chr3 | 14682312 | ||||||
| chr3:14682608
|
G | A | 1 | a0001c0001t0004 | 6 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-106G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/17 | 106 | chr3 | 14682608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14675349
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-299+97T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675349 | ||||||
| chr3:14675385
|
T | G | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-299+133T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675385 | ||||||
| chr3:14675433
|
A | G | 373 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(370): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.-299+181A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675433 | ||||||
| chr3:14675517
|
A | AC | 373 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(370): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.-299+267dupC | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14675517 | |||||
| chr3:14675529
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-299+277G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675529 | ||||||
| chr3:14675579
|
T | C | 2 | a0003c0003t0001g0015a0025c0020t0001g0016 | 2 | NA18944.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-299+327T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675579 | ||||||
| chr3:14675637
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-299+385G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675637 | ||||||
| chr3:14675653
|
A | G | 142 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-299+401A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675653 | ||||||
| chr3:14675690
|
GTTATTTA others(1): Show |
G | 272 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-299+457_-299+464d others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14675690 | |||||
| chr3:14675826
|
G | A | 2 | a0002c0002t0001g0237a0002c0002t0001g0238 | 2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-299+574G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675826 | ||||||
| chr3:14675935
|
A | G | 272 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-299+683A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675935 | ||||||
| chr3:14675936
|
T | C | 272 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-299+684T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675936 | ||||||
| chr3:14675976
|
G | T | 1 | a0002c0002t0001g0373 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-299+724G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14675976 | ||||||
| chr3:14676016
|
A | G | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0009t0001g0233others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-299+764A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14676016 | ||||||
| chr3:14676116
|
C | CT | 108 | a0002c0002t0001g0141a0003c0003t0001g0003a0003c0003t0001g0015others(105): Show | 110 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-299+875dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14676116 | |||||
| chr3:14676324
|
T | C | 1 | a0002c0002t0001g0239 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-299+1072T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14676324 | ||||||
| chr3:14676492
|
T | A | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-299+1240T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14676492 | ||||||
| chr3:14676673
|
A | T | 1 | a0002c0002t0001g0372 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-299+1421A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14676673 | ||||||
| chr3:14677108
|
G | A | 1 | a0008c0008t0001g0127 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-299+1856G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14677108 | ||||||
| chr3:14677113
|
C | T | 1 | a0003c0003t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-299+1861C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14677113 | ||||||
| chr3:14677346
|
G | A | 1 | a0003c0003t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-299+2094G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14677346 | ||||||
| chr3:14677369
|
C | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-299+2117C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14677369 | ||||||
| chr3:14677720
|
C | G | 6 | a0001c0001t0004g0121a0001c0001t0004g0122a0001c0001t0004g0123others(3): Show | 6 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-299+2468C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14677720 | ||||||
| chr3:14677871
|
C | G | 2 | a0001c0009t0001g0235a0001c0009t0001g0236 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-299+2619C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14677871 | ||||||
| chr3:14677969
|
G | GCCAACTT others(10): Show |
266 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-299+2721_-299+273 others(21): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14677969 | |||||
| chr3:14678061
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-299+2809G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678061 | ||||||
| chr3:14678111
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02572.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-299+2859T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678111 | ||||||
| chr3:14678220
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-299+2968G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678220 | ||||||
| chr3:14678292
|
C | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-299+3040C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678292 | ||||||
| chr3:14678353
|
C | T | 2 | a0001c0022t0001g0110a0001c0023t0001g0109 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-299+3101C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678353 | ||||||
| chr3:14678367
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-299+3115G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678367 | ||||||
| chr3:14678439
|
C | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0231a0001c0001t0001g0232others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-299+3187C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678439 | ||||||
| chr3:14678485
|
G | A | 6 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(3): Show | 6 | HG01255.hp2 HG01346.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-299+3233G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678485 | ||||||
| chr3:14678560
|
C | G | 1 | a0005c0004t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-299+3308C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678560 | ||||||
| chr3:14678592
|
C | T | 1 | a0001c0001t0001g0371 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-299+3340C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678592 | ||||||
| chr3:14678628
|
T | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-299+3376T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678628 | ||||||
| chr3:14678662
|
A | G | 6 | a0001c0001t0004g0121a0001c0001t0004g0122a0001c0001t0004g0123others(3): Show | 6 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-299+3410A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678662 | ||||||
| chr3:14678766
|
T | C | 1 | a0021c0033t0002g0026 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-298-3404T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678766 | ||||||
| chr3:14678970
|
G | A | 278 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(275): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-298-3200G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14678970 | ||||||
| chr3:14679090
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-298-3080G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679090 | ||||||
| chr3:14679284
|
A | G | 271 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-298-2886A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679284 | ||||||
| chr3:14679286
|
G | A | 4 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG01934.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-298-2884G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679286 | ||||||
| chr3:14679317
|
A | G | 1 | a0008c0008t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-298-2853A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679317 | ||||||
| chr3:14679512
|
G | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 8 | HG01081.hp2 HG01884.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-298-2658G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679512 | ||||||
| chr3:14679562
|
G | T | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-298-2608G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679562 | ||||||
| chr3:14679567
|
C | T | 266 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-298-2603C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679567 | ||||||
| chr3:14679647
|
C | CA | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-298-2511dupA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14679647 | |||||
| chr3:14679759
|
T | G | 272 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-298-2411T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679759 | ||||||
| chr3:14679781
|
A | T | 1 | a0010c0010t0001g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-298-2389A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679781 | ||||||
| chr3:14679919
|
C | T | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-298-2251C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14679919 | ||||||
| chr3:14680126
|
C | T | 272 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-298-2044C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680126 | ||||||
| chr3:14680235
|
AAAT | A | 6 | a0001c0001t0004g0121a0001c0001t0004g0122a0001c0001t0004g0123others(3): Show | 6 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-298-1932_-298-193 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14680235 | |||||
| chr3:14680305
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-298-1865A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680305 | ||||||
| chr3:14680549
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-298-1621A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680549 | ||||||
| chr3:14680564
|
A | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-298-1606A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680564 | ||||||
| chr3:14680567
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-298-1603G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680567 | ||||||
| chr3:14680625
|
G | T | 1 | a0010c0010t0001g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-298-1545G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680625 | ||||||
| chr3:14680647
|
CAAT | C | 11 | a0003c0003t0001g0132a0003c0003t0001g0133a0003c0003t0001g0134others(8): Show | 11 | HG00140.hp1 HG00642.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-298-1520_-298-151 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 14680647 | |||||
| chr3:14680685
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-298-1485A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680685 | ||||||
| chr3:14680735
|
G | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-298-1435G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680735 | ||||||
| chr3:14680868
|
A | C | 2 | a0002c0002t0002g0106a0002c0002t0002g0107 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-298-1302A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680868 | ||||||
| chr3:14680995
|
A | G | 6 | a0001c0001t0004g0121a0001c0001t0004g0122a0001c0001t0004g0123others(3): Show | 6 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-298-1175A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14680995 | ||||||
| chr3:14681063
|
T | C | 278 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(275): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-298-1107T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681063 | ||||||
| chr3:14681293
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG01496.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-298-877C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681293 | ||||||
| chr3:14681358
|
C | T | 2 | a0002c0002t0002g0106a0002c0002t0002g0107 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-298-812C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681358 | ||||||
| chr3:14681368
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-298-802T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681368 | ||||||
| chr3:14681383
|
G | A | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0009t0001g0233others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-298-787G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681383 | ||||||
| chr3:14681590
|
G | A | 2 | a0001c0001t0001g0242a0004c0005t0001g0241 | 2 | HG02071.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-298-580G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681590 | ||||||
| chr3:14681803
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-298-367A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681803 | ||||||
| chr3:14681835
|
T | C | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-298-335T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681835 | ||||||
| chr3:14681878
|
A | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-298-292A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681878 | ||||||
| chr3:14681886
|
A | G | 4 | a0001c0001t0001g0365a0001c0001t0001g0367a0002c0002t0001g0368others(1): Show | 4 | HG00597.hp1 NA18982.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-298-284A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681886 | ||||||
| chr3:14681937
|
A | G | 1 | a0001c0001t0001g0364 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-298-233A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 1/16 | chr3 | 14681937 | ||||||
| chr3:14682359
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-137+28A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 2/16 | chr3 | 14682359 | ||||||
| chr3:14682512
|
C | T | 1 | a0002c0002t0001g0363 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-136-66C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 2/16 | chr3 | 14682512 | ||||||
| chr3:14683412
|
A | G | 1 | a0001c0001t0001g0362 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.484+215A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14683412 | ||||||
| chr3:14683416
|
G | A | 152 | a0001c0001t0001g0007a0001c0001t0001g0231a0001c0001t0001g0232others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.484+219G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14683416 | ||||||
| chr3:14683445
|
C | G | 2 | a0006c0006t0001g0222a0006c0006t0001g0223 | 2 | HG00423.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.484+248C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14683445 | ||||||
| chr3:14683500
|
A | G | 1 | a0016c0031t0001g0361 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.484+303A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14683500 | ||||||
| chr3:14683778
|
A | G | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.485-464A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14683778 | ||||||
| chr3:14683875
|
C | CA | 117 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0244others(114): Show | 120 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.485-347dupA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 14683875 | |||||
| chr3:14683875
|
CA | C | 14 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(11): Show | 14 | HG01069.hp2 HG01496.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-347delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 14683875 | |||||
| chr3:14684084
|
A | G | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-158A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14684084 | ||||||
| chr3:14684161
|
G | A | 266 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.485-81G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 3/16 | chr3 | 14684161 | ||||||
| chr3:14684403
|
C | G | 1 | a0005c0004t0001g0217 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.625+21C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684403 | ||||||
| chr3:14684425
|
A | G | 1 | a0005c0004t0001g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.625+43A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684425 | ||||||
| chr3:14684519
|
A | G | 2 | a0001c0001t0002g0105a0018c0028t0002g0102 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.625+137A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684519 | ||||||
| chr3:14684678
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.625+296T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684678 | ||||||
| chr3:14684731
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.625+349G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684731 | ||||||
| chr3:14684833
|
T | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.625+451T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684833 | ||||||
| chr3:14684877
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.625+495G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684877 | ||||||
| chr3:14684941
|
T | C | 5 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249others(2): Show | 5 | NA18951.hp2 NA18962.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.625+559T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14684941 | ||||||
| chr3:14685027
|
T | C | 1 | a0001c0001t0005g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.625+645T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685027 | ||||||
| chr3:14685332
|
A | C | 10 | a0001c0001t0002g0033a0001c0001t0002g0094a0001c0001t0002g0095others(7): Show | 10 | HG00597.hp2 HG02056.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.625+950A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685332 | ||||||
| chr3:14685439
|
C | T | 1 | a0005c0004t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.625+1057C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685439 | ||||||
| chr3:14685460
|
T | TTC | 12 | a0001c0001t0002g0042a0001c0001t0003g0014a0002c0002t0002g0043others(9): Show | 13 | HG00423.hp1 HG01167.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.625+1098_625+1099d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685460 | |||||
| chr3:14685460
|
T | TTCTC | 113 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.625+1096_625+1099d others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685460 | |||||
| chr3:14685460
|
TTCTC | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02572.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.625+1096_625+1099d others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685460 | |||||
| chr3:14685481
|
TGTGC | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.625+1111_625+1114d others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685481 | |||||
| chr3:14685482
|
G | C | 165 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(162): Show | 167 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.625+1100G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685482 | ||||||
| chr3:14685483
|
TGC | T | 144 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(141): Show | 146 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.625+1103_625+1104d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685483 | |||||
| chr3:14685484
|
G | C | 21 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0320others(18): Show | 21 | HG01109.hp2 HG01123.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.625+1102G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685484 | ||||||
| chr3:14685485
|
C | T | 21 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0320others(18): Show | 21 | HG01109.hp2 HG01123.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.625+1103C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685485 | ||||||
| chr3:14685486
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1104G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685486 | ||||||
| chr3:14685488
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1106G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685488 | ||||||
| chr3:14685489
|
C | CGT | 9 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0254others(6): Show | 9 | HG02055.hp2 HG02129.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.625+1109_625+1110d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685489 | |||||
| chr3:14685489
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1107C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685489 | ||||||
| chr3:14685490
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1108G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685490 | ||||||
| chr3:14685491
|
TGC | T | 8 | a0001c0001t0004g0126a0002c0002t0002g0043a0003c0003t0001g0142others(5): Show | 9 | HG00423.hp1 HG01167.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.625+1111_625+1112d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685491 | |||||
| chr3:14685493
|
C | CGT | 18 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0320others(15): Show | 18 | HG01109.hp2 HG01346.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.625+1128_625+1129d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685493 | |||||
| chr3:14685493
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.625+1111C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685493 | ||||||
| chr3:14685497
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1115T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685497 | ||||||
| chr3:14685508
|
GTGTA | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG01891.hp1 HG02145.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+1130_625+1133d others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685508 | |||||
| chr3:14685510
|
GTA | G | 27 | a0001c0001t0002g0032a0003c0003t0001g0003a0003c0003t0001g0132others(24): Show | 28 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.625+1130_625+1131d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685510 | |||||
| chr3:14685512
|
A | G | 273 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0231others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.625+1130A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685512 | ||||||
| chr3:14685804
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1422A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685804 | ||||||
| chr3:14685856
|
C | CT | 10 | a0001c0001t0002g0033a0001c0001t0002g0092a0001c0001t0002g0094others(7): Show | 10 | HG02056.hp2 NA18942.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.625+1498dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685856 | |||||
| chr3:14685856
|
CT | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(77): Show | 83 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.625+1498delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685856 | |||||
| chr3:14685856
|
CTT | C | 208 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.625+1497_625+1498d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685856 | |||||
| chr3:14685856
|
CTTT | C | 26 | a0001c0001t0001g0255a0001c0001t0003g0014a0001c0001t0005g0117others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.625+1496_625+1498d others(5): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14685856 | |||||
| chr3:14685885
|
C | T | 4 | a0005c0004t0001g0195a0005c0004t0001g0196a0005c0004t0001g0197others(1): Show | 4 | HG01928.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+1503C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685885 | ||||||
| chr3:14685931
|
G | A | 1 | a0002c0002t0001g0332 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.625+1549G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14685931 | ||||||
| chr3:14686051
|
G | A | 9 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(6): Show | 9 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.625+1669G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686051 | ||||||
| chr3:14686155
|
C | T | 243 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.625+1773C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686155 | ||||||
| chr3:14686193
|
C | CGTGTGTG others(3): Show |
14 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(11): Show | 14 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.625+1821_625+1830d others(12): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686193
|
C | CGTGTGTG others(5): Show |
198 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.625+1819_625+1830d others(14): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686193
|
C | CGTGTGTG others(7): Show |
51 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0316others(48): Show | 52 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.625+1817_625+1830d others(16): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686193
|
C | CGTGTGTG others(9): Show |
12 | a0001c0001t0004g0122a0002c0002t0001g0141a0002c0002t0001g0308others(9): Show | 13 | HG01361.hp2 HG01934.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.625+1815_625+1830d others(18): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686193
|
C | CGTGTGTG others(11): Show |
1 | a0001c0022t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.625+1813_625+1830d others(20): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686193
|
C | CGTGTGTG others(17): Show |
2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.625+1830_625+1831i others(26): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686193
|
C | CGTGTGTG others(19): Show |
2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.625+1830_625+1831i others(28): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686193 | |||||
| chr3:14686196
|
G | GTGTGTGT others(5): Show |
3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01891.hp1 HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625+1825_625+1826i others(14): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14686196 | |||||
| chr3:14686250
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625+1868A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686250 | ||||||
| chr3:14686303
|
G | A | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.625+1921G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686303 | ||||||
| chr3:14686458
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+2076A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686458 | ||||||
| chr3:14686586
|
T | C | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0021t0005g0120 | 3 | HG01934.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.625+2204T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686586 | ||||||
| chr3:14686608
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01891.hp1 HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625+2226A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686608 | ||||||
| chr3:14686781
|
G | A | 284 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.625+2399G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686781 | ||||||
| chr3:14686832
|
C | T | 4 | a0002c0002t0001g0237a0002c0002t0001g0238a0002c0002t0001g0346others(1): Show | 4 | HG01106.hp2 HG01515.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+2450C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14686832 | ||||||
| chr3:14687058
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.625+2676A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687058 | ||||||
| chr3:14687087
|
G | A | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.625+2705G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687087 | ||||||
| chr3:14687191
|
T | A | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-2806T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687191 | ||||||
| chr3:14687373
|
A | C | 288 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.626-2624A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687373 | ||||||
| chr3:14687480
|
T | A | 1 | a0005c0004t0001g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.626-2517T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687480 | ||||||
| chr3:14687571
|
GC | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01891.hp1 HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.626-2425delC | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687571 | ||||||
| chr3:14687590
|
T | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.626-2407T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687590 | ||||||
| chr3:14687758
|
C | T | 1 | a0001c0024t0002g0037 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.626-2239C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687758 | ||||||
| chr3:14687798
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.626-2199T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687798 | ||||||
| chr3:14687922
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-2075C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687922 | ||||||
| chr3:14687961
|
G | T | 1 | a0002c0002t0001g0253 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626-2036G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14687961 | ||||||
| chr3:14688189
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.626-1808T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688189 | ||||||
| chr3:14688277
|
C | A | 2 | a0005c0004t0001g0006a0023c0018t0001g0116 | 3 | HG01167.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626-1720C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688277 | ||||||
| chr3:14688347
|
T | C | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.626-1650T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688347 | ||||||
| chr3:14688480
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.626-1517C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688480 | ||||||
| chr3:14688529
|
C | CA | 218 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.626-1451dupA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14688529 | |||||
| chr3:14688529
|
C | CAA | 14 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0365others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.626-1452_626-1451d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14688529 | |||||
| chr3:14688529
|
CA | C | 33 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(30): Show | 34 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.626-1451delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14688529 | |||||
| chr3:14688568
|
A | G | 119 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0001g0141others(116): Show | 121 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.626-1429A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688568 | ||||||
| chr3:14688685
|
C | T | 4 | a0001c0009t0001g0233a0001c0009t0001g0234a0001c0009t0001g0235others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1312C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688685 | ||||||
| chr3:14688873
|
A | C | 16 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(13): Show | 16 | HG01109.hp2 HG01891.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.626-1124A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688873 | ||||||
| chr3:14688895
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.626-1102A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688895 | ||||||
| chr3:14688950
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0027others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.626-1047G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688950 | ||||||
| chr3:14688987
|
A | G | 7 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0002g0043others(4): Show | 7 | HG02280.hp2 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.626-1010A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14688987 | ||||||
| chr3:14689085
|
G | GTA | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-901_626-900dup others(2): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 14689085 | |||||
| chr3:14689138
|
C | T | 116 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0001g0141others(113): Show | 118 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.626-859C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689138 | ||||||
| chr3:14689220
|
G | A | 11 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(8): Show | 11 | HG01109.hp2 HG01934.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.626-777G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689220 | ||||||
| chr3:14689465
|
T | A | 5 | a0001c0001t0001g0112a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-532T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689465 | ||||||
| chr3:14689518
|
T | C | 1 | a0025c0020t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.626-479T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689518 | ||||||
| chr3:14689596
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0351a0001c0001t0002g0090 | 3 | NA18961.hp2 NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.626-401C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689596 | ||||||
| chr3:14689752
|
C | T | 244 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.626-245C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689752 | ||||||
| chr3:14689878
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.626-119C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 4/16 | chr3 | 14689878 | ||||||
| chr3:14690133
|
G | A | 2 | a0006c0006t0001g0222a0006c0006t0001g0223 | 2 | HG00423.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.745+17G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690133 | ||||||
| chr3:14690301
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.745+185C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690301 | ||||||
| chr3:14690444
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745+328C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690444 | ||||||
| chr3:14690545
|
T | A | 284 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.745+429T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690545 | ||||||
| chr3:14690601
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745+485A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690601 | ||||||
| chr3:14690804
|
G | C | 1 | a0005c0004t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.745+688G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690804 | ||||||
| chr3:14690828
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745+712G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690828 | ||||||
| chr3:14690927
|
C | T | 4 | a0001c0009t0001g0233a0001c0009t0001g0234a0001c0009t0001g0235others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+811C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14690927 | ||||||
| chr3:14691042
|
G | A | 244 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0231others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.745+926G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691042 | ||||||
| chr3:14691146
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0356 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.745+1030G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691146 | ||||||
| chr3:14691187
|
C | T | 31 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(28): Show | 32 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.745+1071C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691187 | ||||||
| chr3:14691223
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.745+1107C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691223 | ||||||
| chr3:14691452
|
G | A | 1 | a0002c0002t0001g0333 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.745+1336G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691452 | ||||||
| chr3:14691524
|
C | G | 1 | a0003c0003t0001g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.745+1408C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691524 | ||||||
| chr3:14691557
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.745+1441C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691557 | ||||||
| chr3:14691667
|
G | A | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.745+1551G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691667 | ||||||
| chr3:14691723
|
G | T | 27 | a0001c0001t0001g0316a0005c0004t0001g0006a0005c0004t0001g0130others(24): Show | 28 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.745+1607G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691723 | ||||||
| chr3:14691799
|
A | G | 32 | a0002c0002t0001g0239a0002c0002t0001g0332a0002c0002t0001g0333others(29): Show | 33 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.745+1683A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691799 | ||||||
| chr3:14691827
|
T | C | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.745+1711T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691827 | ||||||
| chr3:14691854
|
T | C | 1 | a0006c0006t0001g0147 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.745+1738T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14691854 | ||||||
| chr3:14692075
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745+1959A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692075 | ||||||
| chr3:14692108
|
C | T | 6 | a0003c0003t0001g0128a0003c0003t0001g0166a0003c0003t0001g0167others(3): Show | 6 | HG01069.hp1 HG01243.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+1992C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692108 | ||||||
| chr3:14692109
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0352a0001c0001t0001g0362 | 3 | NA18950.hp2 NA18968.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.745+1993G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692109 | ||||||
| chr3:14692208
|
G | A | 1 | a0001c0022t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.745+2092G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692208 | ||||||
| chr3:14692283
|
G | A | 31 | a0001c0001t0001g0027a0001c0001t0001g0316a0001c0001t0002g0042others(28): Show | 32 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.745+2167G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692283 | ||||||
| chr3:14692284
|
C | T | 248 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0113others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.745+2168C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692284 | ||||||
| chr3:14692390
|
A | G | 7 | a0001c0001t0001g0244a0001c0001t0001g0297a0001c0001t0001g0298others(4): Show | 7 | NA18944.hp2 NA18960.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+2274A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692390 | ||||||
| chr3:14692550
|
A | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG00735.hp2 HG01109.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.745+2434A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692550 | ||||||
| chr3:14692765
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 6 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+2649G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692765 | ||||||
| chr3:14692885
|
A | G | 4 | a0001c0009t0001g0233a0001c0009t0001g0234a0001c0009t0001g0235others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+2769A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692885 | ||||||
| chr3:14692913
|
G | A | 4 | a0005c0004t0001g0006a0005c0004t0001g0130a0005c0004t0001g0131others(1): Show | 5 | HG01167.hp1 HG01358.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+2797G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14692913 | ||||||
| chr3:14693030
|
G | A | 1 | a0020c0030t0001g0349 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.745+2914G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693030 | ||||||
| chr3:14693036
|
G | A | 1 | a0005c0004t0001g0143 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.745+2920G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693036 | ||||||
| chr3:14693091
|
T | A | 1 | a0002c0002t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.745+2975T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693091 | ||||||
| chr3:14693195
|
G | A | 11 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(8): Show | 11 | HG01109.hp2 HG01934.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.745+3079G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693195 | ||||||
| chr3:14693197
|
C | G | 243 | a0001c0001t0001g0007a0001c0001t0001g0231a0001c0001t0001g0232others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.745+3081C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693197 | ||||||
| chr3:14693281
|
C | T | 116 | a0001c0001t0001g0321a0001c0001t0002g0032a0001c0001t0002g0050others(113): Show | 118 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.745+3165C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693281 | ||||||
| chr3:14693358
|
G | A | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.745+3242G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693358 | ||||||
| chr3:14693471
|
C | G | 1 | a0001c0001t0001g0295 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.745+3355C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693471 | ||||||
| chr3:14693838
|
G | A | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+3722G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693838 | ||||||
| chr3:14693855
|
A | C | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | NA19011.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.745+3739A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14693855 | ||||||
| chr3:14694139
|
T | C | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249others(1): Show | 4 | NA18951.hp2 NA18962.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+4023T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14694139 | ||||||
| chr3:14694197
|
T | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.745+4081T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14694197 | ||||||
| chr3:14694349
|
T | C | 121 | a0001c0001t0001g0321a0001c0001t0002g0032a0001c0001t0002g0050others(118): Show | 123 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.745+4233T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14694349 | ||||||
| chr3:14694415
|
A | G | 248 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.745+4299A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14694415 | ||||||
| chr3:14694499
|
T | C | 30 | a0001c0001t0001g0316a0001c0001t0002g0042a0005c0004t0001g0006others(27): Show | 31 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.745+4383T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14694499 | ||||||
| chr3:14694671
|
T | G | 2 | a0002c0002t0002g0106a0002c0002t0002g0107 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.745+4555T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14694671 | ||||||
| chr3:14695026
|
A | G | 244 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0231others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.745+4910A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695026 | ||||||
| chr3:14695229
|
T | C | 32 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(29): Show | 33 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.745+5113T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695229 | ||||||
| chr3:14695481
|
A | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01891.hp1 HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.745+5365A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695481 | ||||||
| chr3:14695569
|
G | A | 21 | a0002c0002t0001g0243a0002c0002t0001g0253a0002c0002t0001g0259others(18): Show | 21 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+5453G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695569 | ||||||
| chr3:14695667
|
C | T | 1 | a0002c0002t0001g0330 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.745+5551C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695667 | ||||||
| chr3:14695675
|
G | T | 32 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(29): Show | 33 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.745+5559G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695675 | ||||||
| chr3:14695704
|
T | C | 1 | a0003c0003t0001g0148 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.745+5588T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695704 | ||||||
| chr3:14695792
|
A | G | 1 | a0002c0002t0001g0317 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.745+5676A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695792 | ||||||
| chr3:14695826
|
C | T | 282 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.745+5710C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695826 | ||||||
| chr3:14695846
|
T | C | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+5730T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695846 | ||||||
| chr3:14695873
|
C | T | 1 | a0001c0023t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.745+5757C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14695873 | ||||||
| chr3:14696119
|
G | GT | 124 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(121): Show | 127 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.745+6015dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696119 | |||||
| chr3:14696119
|
GT | G | 119 | a0001c0001t0002g0032a0001c0001t0002g0050a0001c0021t0005g0120others(116): Show | 121 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.745+6015delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696119 | |||||
| chr3:14696131
|
T | A | 1 | a0003c0003t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.745+6015T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696131 | ||||||
| chr3:14696132
|
A | T | 1 | a0003c0003t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.745+6016A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696132 | ||||||
| chr3:14696272
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745+6156A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696272 | ||||||
| chr3:14696345
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.745+6229G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696345 | ||||||
| chr3:14696371
|
C | CATT | 173 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0246others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.745+6289_745+6291d others(5): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696371 | |||||
| chr3:14696371
|
C | CATTATT | 77 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0112others(74): Show | 79 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.745+6286_745+6291d others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696371 | |||||
| chr3:14696371
|
C | CATTATTA others(2): Show |
19 | a0001c0001t0001g0251a0001c0001t0001g0306a0001c0001t0001g0328others(16): Show | 19 | HG00639.hp1 HG00673.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.745+6283_745+6291d others(11): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696371 | |||||
| chr3:14696371
|
C | CATTATTA others(5): Show |
9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.745+6280_745+6291d others(14): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696371 | |||||
| chr3:14696371
|
CATT | C | 13 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0240others(10): Show | 13 | HG01109.hp2 HG01934.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.745+6289_745+6291d others(5): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14696371 | |||||
| chr3:14696497
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0027others(293): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.745+6381C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696497 | ||||||
| chr3:14696499
|
T | C | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+6383T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696499 | ||||||
| chr3:14696597
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745+6481C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696597 | ||||||
| chr3:14696630
|
G | A | 1 | a0001c0001t0001g0311 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.746-6500G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696630 | ||||||
| chr3:14696669
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.746-6461T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696669 | ||||||
| chr3:14696694
|
A | G | 6 | a0002c0002t0002g0044a0002c0002t0002g0045a0002c0002t0002g0046others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.746-6436A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14696694 | ||||||
| chr3:14697057
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.746-6073T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697057 | ||||||
| chr3:14697405
|
C | T | 4 | a0003c0003t0001g0148a0003c0003t0001g0165a0003c0003t0001g0193others(1): Show | 4 | HG00544.hp1 HG00609.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-5725C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697405 | ||||||
| chr3:14697556
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.746-5574T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697556 | ||||||
| chr3:14697606
|
G | T | 1 | a0005c0004t0001g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.746-5524G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697606 | ||||||
| chr3:14697652
|
C | G | 122 | a0001c0001t0001g0321a0001c0001t0002g0032a0001c0001t0002g0050others(119): Show | 124 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.746-5478C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697652 | ||||||
| chr3:14697709
|
A | AC | 264 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(261): Show | 269 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.746-5415dupC | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14697709 | |||||
| chr3:14697714
|
C | CT | 109 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.746-5416_746-5415i others(3): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697714 | ||||||
| chr3:14697769
|
T | C | 1 | a0002c0002t0007g0261 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.746-5361T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697769 | ||||||
| chr3:14697871
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.746-5259C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14697871 | ||||||
| chr3:14698015
|
A | T | 4 | a0003c0003t0001g0212a0010c0010t0001g0213a0010c0010t0001g0221others(1): Show | 4 | HG02886.hp1 HG03041.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.746-5115A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698015 | ||||||
| chr3:14698096
|
A | G | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.746-5034A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698096 | ||||||
| chr3:14698134
|
A | C | 249 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.746-4996A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698134 | ||||||
| chr3:14698136
|
T | A | 2 | a0002c0002t0001g0341a0002c0002t0001g0345 | 2 | NA18953.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.746-4994T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698136 | ||||||
| chr3:14698136
|
T | G | 247 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.746-4994T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698136 | ||||||
| chr3:14698222
|
AT | A | 109 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.746-4904delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14698222 | |||||
| chr3:14698280
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.746-4850G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698280 | ||||||
| chr3:14698529
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.746-4601A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698529 | ||||||
| chr3:14698671
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0003g0010others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-4459A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698671 | ||||||
| chr3:14698806
|
A | T | 30 | a0001c0001t0001g0112a0001c0001t0002g0042a0001c0001t0003g0008others(27): Show | 31 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.746-4324A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698806 | ||||||
| chr3:14698885
|
A | G | 1 | a0019c0029t0001g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.746-4245A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14698885 | ||||||
| chr3:14699272
|
C | T | 127 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0001g0141others(124): Show | 129 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.746-3858C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699272 | ||||||
| chr3:14699463
|
C | T | 7 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249others(4): Show | 7 | NA18951.hp2 NA18962.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.746-3667C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699463 | ||||||
| chr3:14699581
|
C | T | 1 | a0003c0003t0001g0170 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.746-3549C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699581 | ||||||
| chr3:14699697
|
C | A | 6 | a0001c0001t0001g0357a0001c0001t0003g0014a0001c0009t0001g0233others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.746-3433C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699697 | ||||||
| chr3:14699732
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.746-3398G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699732 | ||||||
| chr3:14699869
|
G | A | 6 | a0001c0001t0001g0357a0001c0001t0003g0014a0001c0009t0001g0233others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.746-3261G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699869 | ||||||
| chr3:14699929
|
CT | C | 280 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(277): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.746-3199delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14699929 | |||||
| chr3:14699945
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.746-3185C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699945 | ||||||
| chr3:14699989
|
C | T | 39 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(36): Show | 40 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.746-3141C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14699989 | ||||||
| chr3:14700047
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.746-3083A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14700047 | ||||||
| chr3:14700249
|
C | CT | 150 | a0001c0001t0001g0321a0001c0001t0002g0032a0001c0001t0002g0050others(147): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.746-2874dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14700249 | |||||
| chr3:14700263
|
G | A | 235 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0231others(232): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.746-2867G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14700263 | ||||||
| chr3:14700334
|
C | T | 6 | a0001c0001t0001g0357a0001c0001t0003g0014a0001c0009t0001g0233others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.746-2796C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14700334 | ||||||
| chr3:14700495
|
G | T | 8 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(5): Show | 8 | HG01109.hp2 HG01934.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.746-2635G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14700495 | ||||||
| chr3:14701006
|
C | T | 89 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0001g0141others(86): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.746-2124C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701006 | ||||||
| chr3:14701296
|
T | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0061 | 2 | HG00639.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.746-1834T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701296 | ||||||
| chr3:14701485
|
A | AG | 281 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0111others(278): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.746-1645_746-1644i others(3): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701485 | ||||||
| chr3:14701579
|
C | T | 1 | a0003c0003t0001g0137 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.746-1551C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701579 | ||||||
| chr3:14701583
|
G | T | 1 | a0001c0023t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.746-1547G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701583 | ||||||
| chr3:14701657
|
T | C | 4 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG01934.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-1473T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701657 | ||||||
| chr3:14701800
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG01496.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.746-1330C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701800 | ||||||
| chr3:14701824
|
C | T | 1 | a0005c0004t0001g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.746-1306C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701824 | ||||||
| chr3:14701884
|
G | A | 1 | a0003c0003t0001g0138 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.746-1246G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14701884 | ||||||
| chr3:14702313
|
C | T | 234 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0231others(231): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.746-817C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702313 | ||||||
| chr3:14702440
|
C | CTT | 8 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(5): Show | 8 | HG01109.hp2 HG01934.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.746-673_746-672dup others(2): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14702440 | |||||
| chr3:14702440
|
CT | C | 226 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0231others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.746-672delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 14702440 | |||||
| chr3:14702486
|
G | A | 6 | a0001c0001t0001g0357a0001c0001t0003g0014a0001c0009t0001g0233others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.746-644G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702486 | ||||||
| chr3:14702534
|
G | A | 2 | a0001c0009t0001g0235a0001c0009t0001g0236 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.746-596G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702534 | ||||||
| chr3:14702554
|
C | G | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.746-576C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702554 | ||||||
| chr3:14702694
|
G | A | 1 | a0003c0003t0001g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.746-436G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702694 | ||||||
| chr3:14702770
|
G | A | 23 | a0002c0002t0001g0318a0002c0002t0001g0319a0002c0002t0001g0327others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.746-360G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702770 | ||||||
| chr3:14702977
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.746-153G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14702977 | ||||||
| chr3:14703002
|
C | T | 4 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG01934.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-128C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14703002 | ||||||
| chr3:14703003
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.746-127G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14703003 | ||||||
| chr3:14703005
|
G | A | 8 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.746-125G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 5/16 | chr3 | 14703005 | ||||||
| chr3:14703492
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.878+230C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14703492 | ||||||
| chr3:14703876
|
G | A | 141 | a0002c0002t0001g0141a0002c0002t0001g0237a0002c0002t0001g0238others(138): Show | 143 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.879-461G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14703876 | ||||||
| chr3:14703958
|
G | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(76): Show | 80 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.879-379G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14703958 | ||||||
| chr3:14704064
|
C | T | 31 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(28): Show | 32 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.879-273C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14704064 | ||||||
| chr3:14704076
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879-261C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14704076 | ||||||
| chr3:14704113
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.879-224C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14704113 | ||||||
| chr3:14704153
|
T | G | 1 | a0001c0001t0002g0096 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.879-184T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14704153 | ||||||
| chr3:14704154
|
T | G | 1 | a0001c0001t0002g0096 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.879-183T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 6/16 | chr3 | 14704154 | ||||||
| chr3:14704703
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1160+85T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14704703 | ||||||
| chr3:14704854
|
A | G | 1 | a0004c0005t0002g0062 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1160+236A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14704854 | ||||||
| chr3:14705017
|
C | G | 1 | a0003c0003t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1160+399C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14705017 | ||||||
| chr3:14705297
|
G | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG01516.hp2 HG01517.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1160+679G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14705297 | ||||||
| chr3:14705493
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0001g0288a0008c0008t0001g0225others(1): Show | 4 | HG00099.hp1 HG02698.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+875C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14705493 | ||||||
| chr3:14705610
|
A | G | 5 | a0003c0003t0001g0212a0009c0011t0002g0041a0010c0010t0001g0213others(2): Show | 5 | HG02886.hp1 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160+992A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14705610 | ||||||
| chr3:14705905
|
C | T | 28 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1160+1287C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14705905 | ||||||
| chr3:14706002
|
A | T | 1 | a0003c0003t0001g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1160+1384A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706002 | ||||||
| chr3:14706366
|
T | C | 77 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0244others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1160+1748T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706366 | ||||||
| chr3:14706588
|
T | C | 5 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160+1970T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706588 | ||||||
| chr3:14706634
|
C | T | 1 | a0025c0020t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1160+2016C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706634 | ||||||
| chr3:14706734
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1160+2116C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706734 | ||||||
| chr3:14706791
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1160+2173G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706791 | ||||||
| chr3:14706830
|
T | G | 3 | a0005c0004t0001g0227a0005c0004t0001g0228a0005c0004t0001g0229 | 3 | HG02602.hp2 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1160+2212T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706830 | ||||||
| chr3:14706984
|
T | G | 15 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0002g0043others(12): Show | 15 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1160+2366T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706984 | ||||||
| chr3:14706985
|
C | G | 15 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0002g0043others(12): Show | 15 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1160+2367C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706985 | ||||||
| chr3:14706986
|
G | A | 1 | a0010c0010t0001g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1160+2368G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706986 | ||||||
| chr3:14706987
|
T | C | 15 | a0001c0001t0002g0032a0001c0001t0002g0050a0002c0002t0002g0043others(12): Show | 15 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1160+2369T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14706987 | ||||||
| chr3:14707094
|
A | G | 1 | a0005c0004t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1160+2476A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707094 | ||||||
| chr3:14707118
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1160+2500G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707118 | ||||||
| chr3:14707248
|
C | CA | 19 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(16): Show | 19 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1160+2649dupA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707248 | |||||
| chr3:14707248
|
C | CAA | 11 | a0001c0001t0001g0242a0001c0001t0001g0329a0001c0001t0003g0009others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1160+2648_1160+264 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707248 | |||||
| chr3:14707248
|
C | CAAA | 239 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0112others(236): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1160+2647_1160+264 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707248 | |||||
| chr3:14707248
|
C | CAAAA | 31 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0114others(28): Show | 31 | HG01891.hp1 HG01978.hp2 HG01981.hp2 others(28): Show |
intron_variant | MODIFIER | c.1160+2646_1160+264 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707248 | |||||
| chr3:14707304
|
C | T | 5 | a0003c0003t0001g0128a0003c0003t0001g0167a0003c0003t0001g0168others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160+2686C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707304 | ||||||
| chr3:14707316
|
A | T | 281 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(278): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1160+2698A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707316 | ||||||
| chr3:14707318
|
C | T | 4 | a0001c0001t0001g0365a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | HG00597.hp1 NA18983.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+2700C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707318 | ||||||
| chr3:14707368
|
C | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02280.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160+2750C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707368 | ||||||
| chr3:14707429
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1160+2811C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707429 | ||||||
| chr3:14707445
|
T | TTG | 50 | a0001c0001t0001g0242a0001c0001t0001g0247a0001c0001t0001g0249others(47): Show | 51 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1160+2873_1160+287 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
T | TTGTG | 18 | a0001c0001t0001g0246a0001c0001t0001g0255a0001c0001t0001g0273others(15): Show | 18 | HG01496.hp1 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1160+2871_1160+287 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
T | TTGTGTG | 13 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0244others(10): Show | 13 | HG01934.hp1 HG02055.hp2 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.1160+2869_1160+287 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTG | T | 63 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0027others(60): Show | 64 | HG00639.hp1 HG00735.hp1 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.1160+2873_1160+287 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTGTG | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0028others(90): Show | 96 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1160+2871_1160+287 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTGTGTG | T | 48 | a0001c0001t0001g0112a0002c0002t0001g0239a0002c0002t0001g0243others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.1160+2869_1160+287 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0111a0002c0002t0001g0341a0002c0002t0001g0345others(1): Show | 4 | HG02559.hp1 HG02896.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+2867_1160+287 others(12): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTGTGTGT others(3): Show |
T | 4 | a0003c0003t0001g0139a0003c0003t0001g0140a0003c0003t0001g0150others(1): Show | 4 | HG01175.hp1 HG01943.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+2865_1160+287 others(14): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTGTGTGT others(11): Show |
T | 1 | a0022c0017t0001g0190 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1160+2857_1160+287 others(22): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707445
|
TTGTGTGT others(13): Show |
T | 5 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160+2855_1160+287 others(24): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707445 | |||||
| chr3:14707492
|
T | TG | 4 | a0001c0001t0001g0323a0004c0005t0002g0066a0005c0004t0001g0214others(1): Show | 4 | HG04204.hp2 NA18612.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+2874_1160+287 others(5): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707492 | ||||||
| chr3:14707732
|
C | T | 30 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(27): Show | 31 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1160+3114C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707732 | ||||||
| chr3:14707741
|
C | T | 277 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1160+3123C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707741 | ||||||
| chr3:14707820
|
C | CTTTT | 10 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249others(7): Show | 10 | HG01069.hp1 HG01168.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160+3215_1160+321 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707820 | |||||
| chr3:14707820
|
C | CTTTTT | 236 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1160+3214_1160+321 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707820 | |||||
| chr3:14707820
|
C | CTTTTTT | 29 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0001g0232others(26): Show | 29 | HG00140.hp2 HG01109.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.1160+3213_1160+321 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14707820 | |||||
| chr3:14707849
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0030a0024c0019t0001g0211 | 5 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160+3231C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707849 | ||||||
| chr3:14707852
|
T | G | 1 | a0005c0004t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1160+3234T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707852 | ||||||
| chr3:14707922
|
C | A | 29 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(26): Show | 30 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1160+3304C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14707922 | ||||||
| chr3:14708021
|
T | C | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1160+3403T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14708021 | ||||||
| chr3:14708111
|
C | T | 1 | a0002c0002t0002g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1160+3493C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14708111 | ||||||
| chr3:14708286
|
A | G | 1 | a0002c0002t0001g0243 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1160+3668A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14708286 | ||||||
| chr3:14708537
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1160+3919T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14708537 | ||||||
| chr3:14708887
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1160+4269G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14708887 | ||||||
| chr3:14709011
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1160+4393A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14709011 | ||||||
| chr3:14709133
|
CAAATT | C | 40 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(37): Show | 41 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1160+4524_1160+452 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14709133 | |||||
| chr3:14709156
|
A | G | 1 | a0023c0018t0001g0116 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1160+4538A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14709156 | ||||||
| chr3:14709340
|
T | C | 1 | a0003c0003t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1161-4667T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14709340 | ||||||
| chr3:14709407
|
A | G | 242 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0113others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1161-4600A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14709407 | ||||||
| chr3:14709789
|
G | A | 314 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(311): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1161-4218G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14709789 | ||||||
| chr3:14709836
|
T | C | 25 | a0002c0002t0001g0243a0002c0002t0001g0253a0002c0002t0001g0259others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.1161-4171T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14709836 | ||||||
| chr3:14710006
|
T | A | 8 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161-4001T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710006 | ||||||
| chr3:14710057
|
C | G | 143 | a0001c0001t0001g0321a0002c0002t0001g0141a0002c0002t0001g0237others(140): Show | 145 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1161-3950C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710057 | ||||||
| chr3:14710129
|
G | A | 3 | a0001c0001t0001g0271a0008c0008t0001g0225a0016c0031t0001g0361 | 3 | HG00099.hp1 HG03017.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1161-3878G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710129 | ||||||
| chr3:14710151
|
A | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-3856A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710151 | ||||||
| chr3:14710239
|
G | A | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161-3768G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710239 | ||||||
| chr3:14710305
|
T | C | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161-3702T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710305 | ||||||
| chr3:14710369
|
C | T | 282 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1161-3638C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710369 | ||||||
| chr3:14710381
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1161-3626T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710381 | ||||||
| chr3:14710664
|
T | G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1161-3343T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14710664 | ||||||
| chr3:14710897
|
CT | C | 279 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(276): Show | 283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1161-3096delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14710897 | |||||
| chr3:14711097
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1161-2910A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14711097 | ||||||
| chr3:14711141
|
A | G | 283 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0111others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1161-2866A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14711141 | ||||||
| chr3:14711245
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 9 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161-2762T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14711245 | ||||||
| chr3:14711627
|
C | A | 1 | a0001c0001t0002g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1161-2380C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14711627 | ||||||
| chr3:14711627
|
C | CT | 132 | a0001c0001t0001g0029a0001c0001t0001g0111a0001c0001t0001g0115others(129): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1161-2354dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14711627 | |||||
| chr3:14711627
|
C | CTT | 13 | a0001c0001t0001g0272a0001c0001t0001g0286a0001c0001t0001g0302others(10): Show | 13 | HG00639.hp1 HG01069.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1161-2355_1161-235 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14711627 | |||||
| chr3:14711667
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1161-2340G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14711667 | ||||||
| chr3:14711710
|
G | A | 7 | a0005c0004t0001g0146a0005c0004t0001g0185a0005c0004t0001g0186others(4): Show | 7 | NA18945.hp2 NA18986.hp2 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161-2297G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14711710 | ||||||
| chr3:14712088
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 9 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161-1919A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712088 | ||||||
| chr3:14712172
|
ACG | A | 3 | a0003c0003t0001g0166a0005c0004t0001g0202a0005c0004t0001g0205 | 3 | HG02280.hp1 HG02717.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1161-1825_1161-182 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712172 | |||||
| chr3:14712172
|
ACGCG | A | 5 | a0002c0002t0001g0290a0002c0002t0007g0261a0003c0003t0001g0015others(2): Show | 5 | HG00099.hp2 HG01978.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-1827_1161-182 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712172 | |||||
| chr3:14712176
|
G | A | 92 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0231others(89): Show | 93 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1161-1831G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712176 | ||||||
| chr3:14712177
|
C | T | 139 | a0001c0001t0001g0321a0002c0002t0001g0141a0002c0002t0001g0237others(136): Show | 141 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1161-1830C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712177 | ||||||
| chr3:14712178
|
GCGCGCA | G | 137 | a0001c0001t0001g0321a0002c0002t0001g0141a0002c0002t0001g0237others(134): Show | 139 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1161-1827_1161-182 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712178 | |||||
| chr3:14712179
|
C | T | 1 | a0003c0003t0001g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1161-1828C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712179 | ||||||
| chr3:14712180
|
GCGCA | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG01109.hp1 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161-1825_1161-182 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712180 | |||||
| chr3:14712180
|
GCGCACA | G | 7 | a0001c0001t0001g0306a0001c0001t0001g0310a0001c0001t0001g0324others(4): Show | 7 | HG01516.hp2 HG01517.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161-1825_1161-182 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712180 | |||||
| chr3:14712180
|
GCGCACAC others(1): Show |
G | 86 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1161-1825_1161-181 others(12): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712180 | |||||
| chr3:14712180
|
GCGCACAC others(3): Show |
G | 21 | a0001c0001t0001g0111a0001c0001t0001g0246a0001c0001t0001g0247others(18): Show | 21 | HG01109.hp2 HG01934.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161-1825_1161-181 others(14): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712180 | |||||
| chr3:14712180
|
GCGCACAC others(7): Show |
G | 1 | a0001c0001t0001g0275 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1161-1825_1161-181 others(18): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712180 | |||||
| chr3:14712181
|
C | T | 5 | a0002c0002t0001g0290a0002c0002t0007g0261a0003c0003t0001g0015others(2): Show | 5 | HG00099.hp2 HG01978.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-1826C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712181 | ||||||
| chr3:14712182
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161-1825G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712182 | ||||||
| chr3:14712182
|
G | GCA | 9 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(6): Show | 9 | HG02056.hp2 HG03831.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161-1792_1161-179 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712182 | |||||
| chr3:14712182
|
G | T | 1 | a0003c0003t0001g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1161-1825G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712182 | ||||||
| chr3:14712182
|
GCA | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0031others(10): Show | 15 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-1792_1161-179 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712182 | |||||
| chr3:14712182
|
GCACACA | G | 17 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(14): Show | 17 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.1161-1796_1161-179 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr3 | 14712182 | |||||
| chr3:14712184
|
A | T | 5 | a0002c0002t0001g0290a0002c0002t0007g0261a0003c0003t0001g0015others(2): Show | 5 | HG00099.hp2 HG01978.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-1823A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712184 | ||||||
| chr3:14712186
|
A | T | 137 | a0001c0001t0001g0321a0002c0002t0001g0141a0002c0002t0001g0237others(134): Show | 139 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1161-1821A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712186 | ||||||
| chr3:14712188
|
A | T | 2 | a0003c0003t0001g0159a0006c0006t0001g0172 | 2 | HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1161-1819A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712188 | ||||||
| chr3:14712226
|
T | C | 40 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(37): Show | 41 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1161-1781T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712226 | ||||||
| chr3:14712356
|
C | T | 145 | a0001c0001t0001g0321a0002c0002t0001g0141a0002c0002t0001g0237others(142): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1161-1651C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712356 | ||||||
| chr3:14712518
|
T | C | 282 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1161-1489T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712518 | ||||||
| chr3:14712980
|
G | A | 4 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG01934.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161-1027G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14712980 | ||||||
| chr3:14713062
|
T | C | 2 | a0005c0004t0001g0143a0022c0017t0001g0190 | 2 | NA19079.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1161-945T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713062 | ||||||
| chr3:14713386
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1161-621G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713386 | ||||||
| chr3:14713693
|
G | C | 1 | a0001c0001t0002g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1161-314G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713693 | ||||||
| chr3:14713695
|
T | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1161-312T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713695 | ||||||
| chr3:14713713
|
C | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1161-294C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713713 | ||||||
| chr3:14713739
|
G | C | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1161-268G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713739 | ||||||
| chr3:14713756
|
G | C | 23 | a0002c0002t0001g0243a0002c0002t0001g0253a0002c0002t0001g0259others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-251G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713756 | ||||||
| chr3:14713828
|
C | T | 39 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(36): Show | 40 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1161-179C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 7/16 | chr3 | 14713828 | ||||||
| chr3:14714190
|
G | A | 2 | a0001c0001t0001g0350a0020c0030t0001g0349 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1313+31G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14714190 | ||||||
| chr3:14714293
|
G | A | 1 | a0003c0003t0001g0210 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1313+134G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14714293 | ||||||
| chr3:14714304
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1313+145G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14714304 | ||||||
| chr3:14714476
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1313+317T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14714476 | ||||||
| chr3:14714622
|
G | T | 1 | a0001c0001t0001g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1313+463G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14714622 | ||||||
| chr3:14714685
|
C | T | 144 | a0002c0002t0001g0141a0002c0002t0001g0237a0002c0002t0001g0238others(141): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1313+526C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14714685 | ||||||
| chr3:14715042
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1314-247A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14715042 | ||||||
| chr3:14715071
|
A | C | 245 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0113others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1314-218A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14715071 | ||||||
| chr3:14715223
|
A | G | 285 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(282): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1314-66A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 8/16 | chr3 | 14715223 | ||||||
| chr3:14715851
|
A | G | 1 | a0001c0001t0004g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1434+442A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14715851 | ||||||
| chr3:14715867
|
TGATA | T | 28 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1434+465_1434+468d others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14715867 | |||||
| chr3:14715902
|
G | A | 28 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1434+493G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14715902 | ||||||
| chr3:14715994
|
CAACT | C | 148 | a0001c0001t0001g0310a0001c0001t0001g0321a0001c0001t0001g0356others(145): Show | 150 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1434+590_1434+593d others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14715994 | |||||
| chr3:14716186
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1434+777G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14716186 | ||||||
| chr3:14716227
|
A | C | 1 | a0001c0001t0001g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1434+818A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14716227 | ||||||
| chr3:14716548
|
T | C | 267 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1434+1139T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14716548 | ||||||
| chr3:14716599
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1434+1190T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14716599 | ||||||
| chr3:14716632
|
A | G | 4 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(1): Show | 4 | HG01109.hp2 HG01934.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1434+1223A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14716632 | ||||||
| chr3:14717056
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1434+1647C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14717056 | ||||||
| chr3:14717334
|
A | AG | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1434+1926dupG | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14717334 | |||||
| chr3:14717528
|
G | C | 1 | a0002c0002t0001g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1434+2119G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14717528 | ||||||
| chr3:14717679
|
T | G | 21 | a0002c0002t0001g0327a0002c0002t0002g0098a0003c0003t0001g0015others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.1434+2270T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14717679 | ||||||
| chr3:14717696
|
C | T | 1 | a0003c0003t0001g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1434+2287C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14717696 | ||||||
| chr3:14717706
|
A | T | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1434+2297A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14717706 | ||||||
| chr3:14717862
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1434+2453T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14717862 | ||||||
| chr3:14718084
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1434+2675A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718084 | ||||||
| chr3:14718161
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1434+2752A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718161 | ||||||
| chr3:14718164
|
A | G | 1 | a0003c0003t0001g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1434+2755A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718164 | ||||||
| chr3:14718217
|
T | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1434+2808T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718217 | ||||||
| chr3:14718316
|
TCTA | T | 39 | a0001c0001t0001g0112a0001c0001t0001g0316a0001c0001t0002g0042others(36): Show | 40 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1434+2911_1434+291 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14718316 | |||||
| chr3:14718383
|
C | A | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1434+2974C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718383 | ||||||
| chr3:14718436
|
A | C | 2 | a0003c0003t0001g0015a0025c0020t0001g0016 | 2 | NA18944.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1434+3027A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718436 | ||||||
| chr3:14718466
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1434+3057C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718466 | ||||||
| chr3:14718560
|
G | A | 32 | a0001c0001t0001g0320a0001c0001t0002g0033a0001c0001t0002g0069others(29): Show | 32 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1435-3093G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718560 | ||||||
| chr3:14718687
|
G | T | 5 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0344others(2): Show | 5 | NA18612.hp1 NA18954.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-2966G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718687 | ||||||
| chr3:14718741
|
G | A | 1 | a0001c0001t0001g0313 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1435-2912G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718741 | ||||||
| chr3:14718750
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435-2903G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718750 | ||||||
| chr3:14718939
|
A | G | 282 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0111others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1435-2714A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718939 | ||||||
| chr3:14718957
|
A | G | 283 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0111others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1435-2696A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14718957 | ||||||
| chr3:14719004
|
C | T | 1 | a0002c0002t0001g0368 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1435-2649C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719004 | ||||||
| chr3:14719104
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1435-2549C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719104 | ||||||
| chr3:14719125
|
G | GT | 36 | a0001c0001t0001g0027a0001c0001t0001g0316a0001c0001t0001g0364others(33): Show | 37 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1435-2511dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14719125 | |||||
| chr3:14719125
|
GT | G | 104 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0113others(101): Show | 105 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1435-2511delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14719125 | |||||
| chr3:14719242
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1435-2411G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719242 | ||||||
| chr3:14719274
|
G | T | 145 | a0002c0002t0001g0141a0002c0002t0001g0237a0002c0002t0001g0238others(142): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1435-2379G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719274 | ||||||
| chr3:14719356
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1435-2297G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719356 | ||||||
| chr3:14719466
|
A | G | 1 | a0002c0002t0002g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1435-2187A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719466 | ||||||
| chr3:14719510
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1435-2143T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719510 | ||||||
| chr3:14719620
|
G | C | 2 | a0001c0001t0001g0053a0019c0029t0001g0054 | 2 | HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1435-2033G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719620 | ||||||
| chr3:14719835
|
T | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435-1818T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719835 | ||||||
| chr3:14719985
|
G | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0030a0024c0019t0001g0211 | 5 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-1668G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14719985 | ||||||
| chr3:14720006
|
T | TTTTTG | 67 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0244others(64): Show | 68 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1435-1627_1435-162 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720006 | |||||
| chr3:14720006
|
TTTTTG | T | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1435-1627_1435-162 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720006 | |||||
| chr3:14720021
|
G | GTTTTGTT | 4 | a0002c0002t0001g0245a0002c0002t0001g0341a0002c0002t0001g0345others(1): Show | 4 | NA18953.hp1 NA18970.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435-1613_1435-160 others(11): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720021 | |||||
| chr3:14720054
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(81): Show | 85 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1435-1599G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720054 | ||||||
| chr3:14720091
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1435-1562G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720091 | ||||||
| chr3:14720092
|
T | C | 260 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(257): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1435-1561T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720092 | ||||||
| chr3:14720155
|
G | A | 1 | a0005c0004t0001g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1435-1498G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720155 | ||||||
| chr3:14720220
|
C | T | 8 | a0002c0002t0001g0239a0002c0002t0001g0332a0002c0002t0001g0333others(5): Show | 8 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1435-1433C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720220 | ||||||
| chr3:14720221
|
G | A | 1 | a0002c0002t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1435-1432G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720221 | ||||||
| chr3:14720223
|
G | T | 29 | a0001c0001t0001g0027a0001c0001t0001g0316a0001c0001t0002g0042others(26): Show | 30 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1435-1430G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720223 | ||||||
| chr3:14720319
|
C | T | 1 | a0005c0004t0001g0214 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1435-1334C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720319 | ||||||
| chr3:14720325
|
C | T | 28 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1435-1328C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720325 | ||||||
| chr3:14720533
|
G | GGTT | 3 | a0003c0003t0001g0200a0004c0005t0002g0086a0009c0011t0002g0041 | 3 | HG03195.hp1 HG03516.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1435-1071_1435-106 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720533
|
GGTT | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(64): Show | 69 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1435-1071_1435-106 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720533
|
GGTTGTT | G | 62 | a0001c0001t0001g0111a0001c0001t0002g0104a0001c0001t0003g0009others(59): Show | 64 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1435-1074_1435-106 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720533
|
GGTTGTTG others(2): Show |
G | 41 | a0001c0001t0001g0027a0001c0001t0001g0231a0001c0001t0001g0232others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1435-1077_1435-106 others(13): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720533
|
GGTTGTTG others(5): Show |
G | 91 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0240others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1435-1080_1435-106 others(16): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720533
|
GGTTGTTG others(8): Show |
G | 21 | a0001c0001t0001g0244a0001c0001t0001g0298a0001c0001t0001g0300others(18): Show | 22 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1435-1083_1435-106 others(19): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720533
|
GGTTGTTG others(14): Show |
G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1435-1089_1435-106 others(25): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 14720533 | |||||
| chr3:14720545
|
T | G | 1 | a0003c0003t0001g0015 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1435-1108T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720545 | ||||||
| chr3:14720582
|
G | T | 1 | a0001c0001t0002g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1435-1071G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720582 | ||||||
| chr3:14720608
|
G | A | 1 | a0026c0016t0001g0135 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1435-1045G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720608 | ||||||
| chr3:14720647
|
G | C | 5 | a0001c0001t0001g0357a0001c0009t0001g0233a0001c0009t0001g0234others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1435-1006G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720647 | ||||||
| chr3:14720707
|
C | T | 13 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1435-946C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720707 | ||||||
| chr3:14720903
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1435-750C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720903 | ||||||
| chr3:14720975
|
G | A | 9 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0297others(6): Show | 9 | HG02071.hp1 NA18944.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1435-678G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14720975 | ||||||
| chr3:14721210
|
C | T | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1435-443C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721210 | ||||||
| chr3:14721228
|
C | T | 2 | a0005c0004t0001g0185a0005c0004t0001g0226 | 2 | NA18945.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1435-425C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721228 | ||||||
| chr3:14721242
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1435-411T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721242 | ||||||
| chr3:14721580
|
C | T | 5 | a0003c0003t0001g0128a0003c0003t0001g0167a0003c0003t0001g0168others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-73C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721580 | ||||||
| chr3:14721584
|
G | C | 1 | a0006c0006t0001g0149 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1435-69G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721584 | ||||||
| chr3:14721587
|
G | A | 6 | a0003c0003t0001g0128a0003c0003t0001g0166a0003c0003t0001g0167others(3): Show | 6 | HG01069.hp1 HG01243.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1435-66G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721587 | ||||||
| chr3:14721598
|
G | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1435-55G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721598 | ||||||
| chr3:14721611
|
G | A | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1435-42G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721611 | ||||||
| chr3:14721633
|
T | C | 3 | a0001c0001t0001g0357a0001c0009t0001g0235a0001c0009t0001g0236 | 3 | HG01884.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1435-20T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 9/16 | chr3 | 14721633 | ||||||
| chr3:14721834
|
C | T | 1 | a0004c0005t0002g0080 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1566+50C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14721834 | ||||||
| chr3:14721874
|
T | A | 23 | a0002c0002t0001g0243a0002c0002t0001g0253a0002c0002t0001g0259others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1566+90T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14721874 | ||||||
| chr3:14721963
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1566+179A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14721963 | ||||||
| chr3:14721984
|
G | T | 1 | a0006c0006t0001g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1566+200G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14721984 | ||||||
| chr3:14722022
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1566+238A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722022 | ||||||
| chr3:14722178
|
C | T | 10 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(7): Show | 10 | HG01109.hp2 HG01934.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1566+394C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722178 | ||||||
| chr3:14722380
|
G | A | 1 | a0002c0002t0001g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1566+596G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722380 | ||||||
| chr3:14722447
|
G | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(78): Show | 82 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1566+663G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722447 | ||||||
| chr3:14722489
|
A | T | 2 | a0001c0001t0001g0242a0004c0005t0001g0241 | 2 | HG02071.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1566+705A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722489 | ||||||
| chr3:14722543
|
C | T | 2 | a0001c0001t0002g0042a0005c0004t0001g0216 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1566+759C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722543 | ||||||
| chr3:14722600
|
CT | C | 8 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1566+817delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722600 | ||||||
| chr3:14722602
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1566+818G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722602 | ||||||
| chr3:14722606
|
G | A | 1 | a0004c0005t0002g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1566+822G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722606 | ||||||
| chr3:14722614
|
G | A | 1 | a0017c0027t0001g0366 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1566+830G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722614 | ||||||
| chr3:14722714
|
G | A | 1 | a0002c0002t0001g0330 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1566+930G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722714 | ||||||
| chr3:14722724
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1566+940A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722724 | ||||||
| chr3:14722738
|
C | G | 13 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1566+954C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722738 | ||||||
| chr3:14722952
|
C | T | 1 | a0003c0003t0001g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1566+1168C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722952 | ||||||
| chr3:14722980
|
C | A | 1 | a0002c0002t0001g0330 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1566+1196C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14722980 | ||||||
| chr3:14723099
|
A | C | 24 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(21): Show | 24 | HG01109.hp2 HG01891.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.1566+1315A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723099 | ||||||
| chr3:14723153
|
G | T | 1 | a0001c0001t0005g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1566+1369G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723153 | ||||||
| chr3:14723324
|
T | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG01168.hp1 HG01175.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566+1540T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723324 | ||||||
| chr3:14723518
|
G | A | 2 | a0003c0003t0001g0132a0003c0003t0001g0133 | 2 | HG00642.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1566+1734G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723518 | ||||||
| chr3:14723615
|
C | T | 28 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1566+1831C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723615 | ||||||
| chr3:14723676
|
C | T | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1566+1892C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723676 | ||||||
| chr3:14723755
|
C | T | 258 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1566+1971C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723755 | ||||||
| chr3:14723777
|
GTTTTA | G | 49 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0320others(46): Show | 49 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1566+2056_1566+206 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14723777 | |||||
| chr3:14723777
|
GTTTTATT others(3): Show |
G | 26 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0028others(23): Show | 28 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.1566+2051_1566+206 others(14): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14723777 | |||||
| chr3:14723777
|
GTTTTATT others(8): Show |
G | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(20): Show | 23 | HG00099.hp1 HG01106.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1566+2046_1566+206 others(19): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14723777 | |||||
| chr3:14723777
|
GTTTTATT others(13): Show |
G | 84 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0113others(81): Show | 85 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1566+2041_1566+206 others(24): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14723777 | |||||
| chr3:14723777
|
GTTTTATT others(18): Show |
G | 63 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0001g0232others(60): Show | 64 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1566+2036_1566+206 others(29): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14723777 | |||||
| chr3:14723777
|
GTTTTATT others(23): Show |
G | 118 | a0002c0002t0001g0141a0002c0002t0001g0237a0002c0002t0001g0238others(115): Show | 120 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1566+2031_1566+206 others(34): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14723777 | |||||
| chr3:14723978
|
C | A | 9 | a0001c0001t0001g0321a0002c0002t0001g0245a0002c0002t0001g0339others(6): Show | 9 | NA18939.hp1 NA18953.hp1 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1566+2194C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14723978 | ||||||
| chr3:14724063
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566+2279C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724063 | ||||||
| chr3:14724066
|
G | A | 1 | a0003c0003t0001g0171 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1566+2282G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724066 | ||||||
| chr3:14724101
|
G | A | 1 | a0001c0001t0001g0364 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1566+2317G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724101 | ||||||
| chr3:14724109
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566+2325G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724109 | ||||||
| chr3:14724125
|
A | T | 1 | a0001c0022t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1566+2341A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724125 | ||||||
| chr3:14724417
|
C | T | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1567-2484C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724417 | ||||||
| chr3:14724932
|
G | A | 28 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(25): Show | 29 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1567-1969G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14724932 | ||||||
| chr3:14725042
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1567-1859C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725042 | ||||||
| chr3:14725056
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1567-1845C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725056 | ||||||
| chr3:14725091
|
A | G | 10 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(7): Show | 10 | HG01109.hp2 HG01934.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1567-1810A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725091 | ||||||
| chr3:14725195
|
G | GCATCTCA others(10): Show |
1 | a0002c0002t0001g0245 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1567-1702_1567-168 others(21): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14725195 | |||||
| chr3:14725244
|
A | G | 5 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0344others(2): Show | 5 | NA18612.hp1 NA18954.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567-1657A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725244 | ||||||
| chr3:14725257
|
G | T | 2 | a0005c0004t0001g0185a0005c0004t0001g0226 | 2 | NA18945.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1567-1644G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725257 | ||||||
| chr3:14725292
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567-1609G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725292 | ||||||
| chr3:14725319
|
A | G | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567-1582A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725319 | ||||||
| chr3:14725382
|
C | T | 149 | a0001c0001t0001g0310a0001c0001t0001g0321a0001c0001t0001g0356others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1567-1519C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725382 | ||||||
| chr3:14725542
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1567-1359G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725542 | ||||||
| chr3:14725658
|
A | G | 2 | a0001c0001t0001g0344a0001c0001t0001g0348 | 2 | NA18980.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1567-1243A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725658 | ||||||
| chr3:14725697
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1567-1204C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14725697 | ||||||
| chr3:14725869
|
G | GA | 8 | a0001c0001t0001g0111a0001c0001t0001g0371a0001c0001t0003g0010others(5): Show | 8 | HG02273.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567-1016dupA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14725869 | |||||
| chr3:14725869
|
GA | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(90): Show | 94 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1567-1016delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr3 | 14725869 | |||||
| chr3:14726162
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567-739C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726162 | ||||||
| chr3:14726282
|
C | T | 1 | a0003c0003t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1567-619C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726282 | ||||||
| chr3:14726412
|
C | T | 132 | a0001c0001t0001g0027a0001c0001t0001g0321a0002c0002t0001g0141others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1567-489C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726412 | ||||||
| chr3:14726430
|
G | C | 2 | a0001c0009t0001g0233a0001c0009t0001g0234 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1567-471G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726430 | ||||||
| chr3:14726487
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1567-414G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726487 | ||||||
| chr3:14726488
|
C | A | 2 | a0001c0001t0001g0252a0008c0008t0001g0225 | 2 | HG03017.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1567-413C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726488 | ||||||
| chr3:14726543
|
G | A | 132 | a0001c0001t0001g0027a0001c0001t0001g0321a0002c0002t0001g0141others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1567-358G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726543 | ||||||
| chr3:14726681
|
C | T | 1 | a0002c0002t0001g0330 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1567-220C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726681 | ||||||
| chr3:14726701
|
G | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG02280.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-200G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726701 | ||||||
| chr3:14726787
|
G | T | 2 | a0001c0001t0004g0121a0001c0001t0004g0122 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1567-114G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726787 | ||||||
| chr3:14726878
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1567-23C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 10/16 | chr3 | 14726878 | ||||||
| chr3:14727027
|
A | G | 132 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(131): Show |
splice_region_variant&intron_variant | LOW | c.1690+3A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727027 | ||||||
| chr3:14727047
|
G | A | 132 | a0001c0001t0001g0027a0001c0001t0001g0321a0002c0002t0001g0141others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1690+23G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727047 | ||||||
| chr3:14727059
|
G | T | 1 | a0001c0001t0002g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+35G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727059 | ||||||
| chr3:14727093
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1690+69A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727093 | ||||||
| chr3:14727120
|
C | T | 1 | a0005c0004t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1690+96C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727120 | ||||||
| chr3:14727135
|
C | A | 1 | a0001c0001t0001g0364 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1690+111C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727135 | ||||||
| chr3:14727296
|
G | A | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0254others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690+272G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727296 | ||||||
| chr3:14727318
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1690+294G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727318 | ||||||
| chr3:14727348
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(91): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1690+324C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727348 | ||||||
| chr3:14727433
|
A | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(91): Show | 95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1690+409A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727433 | ||||||
| chr3:14727584
|
T | C | 271 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0111others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1690+560T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727584 | ||||||
| chr3:14727585
|
C | T | 3 | a0003c0003t0001g0175a0003c0003t0001g0207a0003c0003t0001g0208 | 3 | HG01192.hp2 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1690+561C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727585 | ||||||
| chr3:14727833
|
C | T | 80 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0244others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1691-606C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727833 | ||||||
| chr3:14727905
|
T | G | 4 | a0001c0001t0001g0350a0002c0002t0002g0043a0002c0002t0002g0048others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-534T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14727905 | ||||||
| chr3:14728020
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1691-419A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728020 | ||||||
| chr3:14728021
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1691-418T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728021 | ||||||
| chr3:14728032
|
A | C | 1 | a0003c0003t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1691-407A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728032 | ||||||
| chr3:14728091
|
C | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0113others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1691-348C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728091 | ||||||
| chr3:14728121
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1691-318G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728121 | ||||||
| chr3:14728156
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1691-283G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728156 | ||||||
| chr3:14728180
|
G | A | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 21 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1691-259G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728180 | ||||||
| chr3:14728226
|
C | T | 1 | a0003c0003t0001g0171 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1691-213C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728226 | ||||||
| chr3:14728234
|
A | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0111a0001c0001t0001g0112others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1691-205A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728234 | ||||||
| chr3:14728260
|
G | C | 1 | a0005c0004t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1691-179G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728260 | ||||||
| chr3:14728388
|
G | A | 4 | a0001c0001t0001g0350a0002c0002t0002g0043a0002c0002t0002g0048others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-51G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 11/16 | chr3 | 14728388 | ||||||
| chr3:14728764
|
A | G | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 29 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1940+76A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14728764 | ||||||
| chr3:14728772
|
C | T | 1 | a0003c0003t0001g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1940+84C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14728772 | ||||||
| chr3:14728793
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1940+105A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14728793 | ||||||
| chr3:14728988
|
A | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(311): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1940+300A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14728988 | ||||||
| chr3:14728990
|
A | G | 1 | a0002c0002t0001g0243 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1940+302A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14728990 | ||||||
| chr3:14729279
|
C | T | 297 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1940+591C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729279 | ||||||
| chr3:14729285
|
C | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1940+597C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729285 | ||||||
| chr3:14729349
|
G | A | 1 | a0002c0002t0001g0308 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1940+661G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729349 | ||||||
| chr3:14729517
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1940+829C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729517 | ||||||
| chr3:14729545
|
A | G | 1 | a0002c0002t0001g0308 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1940+857A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729545 | ||||||
| chr3:14729557
|
T | C | 3 | a0001c0001t0001g0310a0001c0001t0001g0356a0001c0001t0001g0371 | 3 | HG01516.hp2 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1940+869T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729557 | ||||||
| chr3:14729777
|
C | T | 97 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1940+1089C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729777 | ||||||
| chr3:14729834
|
T | C | 1 | a0001c0001t0001g0289 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1940+1146T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729834 | ||||||
| chr3:14729872
|
T | A | 297 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1940+1184T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729872 | ||||||
| chr3:14729966
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1940+1278A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14729966 | ||||||
| chr3:14730161
|
G | C | 1 | a0005c0004t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1940+1473G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730161 | ||||||
| chr3:14730275
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1940+1587C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730275 | ||||||
| chr3:14730370
|
A | G | 97 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1940+1682A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730370 | ||||||
| chr3:14730426
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940+1738G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730426 | ||||||
| chr3:14730460
|
TG | T | 7 | a0001c0001t0001g0295a0001c0001t0001g0325a0001c0001t0001g0326others(4): Show | 7 | NA18612.hp1 NA18941.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1940+1774delG | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14730460 | |||||
| chr3:14730525
|
T | C | 297 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1940+1837T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730525 | ||||||
| chr3:14730533
|
C | T | 4 | a0002c0002t0001g0237a0002c0002t0001g0238a0002c0002t0001g0346others(1): Show | 4 | HG01106.hp2 HG01515.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940+1845C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730533 | ||||||
| chr3:14730549
|
A | AAAT | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 29 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1940+1880_1940+188 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14730549 | |||||
| chr3:14730833
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1940+2145A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730833 | ||||||
| chr3:14730850
|
G | T | 27 | a0001c0001t0001g0316a0001c0001t0002g0042a0001c0001t0003g0008others(24): Show | 28 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1940+2162G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730850 | ||||||
| chr3:14730905
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1940+2217A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730905 | ||||||
| chr3:14730943
|
T | A | 1 | a0003c0003t0001g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1940+2255T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730943 | ||||||
| chr3:14730973
|
G | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1940+2285G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14730973 | ||||||
| chr3:14731002
|
T | C | 1 | a0002c0002t0001g0308 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1940+2314T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731002 | ||||||
| chr3:14731159
|
A | G | 135 | a0001c0001t0001g0027a0001c0001t0001g0321a0002c0002t0001g0141others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1940+2471A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731159 | ||||||
| chr3:14731360
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1940+2672G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731360 | ||||||
| chr3:14731428
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1940+2740C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731428 | ||||||
| chr3:14731432
|
T | G | 2 | a0006c0006t0001g0153a0006c0006t0001g0164 | 2 | HG01074.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1940+2744T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731432 | ||||||
| chr3:14731455
|
C | T | 297 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1940+2767C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731455 | ||||||
| chr3:14731760
|
A | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1940+3072A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731760 | ||||||
| chr3:14731776
|
C | A | 3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0021t0005g0120 | 3 | HG01934.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1940+3088C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731776 | ||||||
| chr3:14731839
|
T | A | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1940+3151T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731839 | ||||||
| chr3:14731951
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 8 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1940+3263T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14731951 | ||||||
| chr3:14732189
|
T | A | 1 | a0006c0006t0001g0176 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1940+3501T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732189 | ||||||
| chr3:14732209
|
A | G | 4 | a0001c0001t0001g0350a0002c0002t0002g0043a0002c0002t0002g0048others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940+3521A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732209 | ||||||
| chr3:14732515
|
G | A | 2 | a0001c0001t0001g0053a0019c0029t0001g0054 | 2 | HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1940+3827G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732515 | ||||||
| chr3:14732561
|
CTCAACCA others(12): Show |
C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940+3874_1940+389 others(23): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732561 | ||||||
| chr3:14732639
|
G | T | 1 | a0002c0002t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1940+3951G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732639 | ||||||
| chr3:14732793
|
T | A | 1 | a0001c0001t0004g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1940+4105T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732793 | ||||||
| chr3:14732871
|
T | TTATATTA others(11): Show |
1 | a0006c0006t0001g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1940+4188_1940+418 others(22): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14732871 | |||||
| chr3:14732871
|
T | TTATATTA others(15): Show |
132 | a0001c0001t0001g0027a0001c0001t0001g0321a0002c0002t0001g0141others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1940+4188_1940+418 others(26): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14732871 | |||||
| chr3:14732873
|
A | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0367a0017c0027t0001g0366 | 3 | NA18612.hp2 NA18990.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1940+4185A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732873 | ||||||
| chr3:14732950
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940+4262T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14732950 | ||||||
| chr3:14733098
|
A | G | 5 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940+4410A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733098 | ||||||
| chr3:14733101
|
CTTTTTCT others(32): Show |
C | 1 | a0002c0002t0001g0243 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1940+4415_1940+445 others(43): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14733101 | |||||
| chr3:14733136
|
T | C | 296 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(293): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1940+4448T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733136 | ||||||
| chr3:14733154
|
A | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 29 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1940+4466A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733154 | ||||||
| chr3:14733331
|
T | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0356 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1940+4643T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733331 | ||||||
| chr3:14733435
|
A | G | 2 | a0002c0002t0001g0340a0002c0002t0001g0372 | 2 | NA18945.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1940+4747A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733435 | ||||||
| chr3:14733514
|
A | G | 1 | a0003c0003t0001g0161 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1940+4826A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733514 | ||||||
| chr3:14733673
|
T | C | 1 | a0003c0003t0001g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1940+4985T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733673 | ||||||
| chr3:14733694
|
G | GT | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(29): Show | 32 | HG01109.hp1 HG01358.hp2 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.1940+5019dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14733694 | |||||
| chr3:14733712
|
C | T | 1 | a0002c0002t0001g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1940+5024C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733712 | ||||||
| chr3:14733769
|
A | G | 5 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940+5081A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733769 | ||||||
| chr3:14733838
|
A | G | 295 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1940+5150A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14733838 | ||||||
| chr3:14734265
|
T | C | 1 | a0006c0006t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1940+5577T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734265 | ||||||
| chr3:14734378
|
G | A | 139 | a0001c0001t0001g0027a0001c0001t0001g0255a0001c0001t0001g0321others(136): Show | 141 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1940+5690G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734378 | ||||||
| chr3:14734494
|
G | A | 5 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940+5806G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734494 | ||||||
| chr3:14734496
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940+5808G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734496 | ||||||
| chr3:14734543
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1940+5855G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734543 | ||||||
| chr3:14734572
|
C | G | 1 | a0003c0003t0001g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1940+5884C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734572 | ||||||
| chr3:14734679
|
G | A | 1 | a0011c0025t0001g0343 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1940+5991G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734679 | ||||||
| chr3:14734805
|
C | T | 133 | a0001c0001t0001g0027a0001c0001t0001g0321a0002c0002t0001g0141others(130): Show | 135 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1940+6117C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734805 | ||||||
| chr3:14734825
|
A | G | 97 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1940+6137A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14734825 | ||||||
| chr3:14735074
|
CTTTAT | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1940+6391_1940+639 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14735074 | |||||
| chr3:14735507
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1940+6819T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14735507 | ||||||
| chr3:14735568
|
A | G | 3 | a0001c0001t0001g0350a0002c0002t0002g0043a0002c0002t0002g0048 | 3 | HG02717.hp1 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1940+6880A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14735568 | ||||||
| chr3:14735597
|
A | AT | 7 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1940+6923dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14735597 | |||||
| chr3:14735616
|
C | T | 5 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940+6928C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14735616 | ||||||
| chr3:14735928
|
A | G | 1 | a0001c0001t0001g0365 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1940+7240A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14735928 | ||||||
| chr3:14736296
|
C | CT | 31 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(28): Show | 31 | HG01109.hp1 HG01516.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.1940+7620dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14736296 | |||||
| chr3:14736296
|
C | CTT | 266 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0111others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1940+7619_1940+762 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14736296 | |||||
| chr3:14736296
|
CT | C | 24 | a0001c0001t0001g0320a0001c0001t0002g0069a0001c0001t0002g0070others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1940+7620delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14736296 | |||||
| chr3:14736333
|
C | A | 1 | a0002c0002t0002g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1940+7645C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14736333 | ||||||
| chr3:14736590
|
C | CT | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(111): Show | 115 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1940+7914dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14736590 | |||||
| chr3:14736755
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(212): Show | 218 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1940+8067T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14736755 | ||||||
| chr3:14736769
|
G | A | 80 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0244others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1940+8081G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14736769 | ||||||
| chr3:14737099
|
TA | T | 2 | a0006c0006t0001g0002a0006c0006t0001g0176 | 3 | HG01934.hp2 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1940+8414delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14737099 | |||||
| chr3:14737233
|
T | C | 4 | a0001c0001t0001g0350a0002c0002t0002g0043a0002c0002t0002g0048others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940+8545T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14737233 | ||||||
| chr3:14737412
|
A | T | 7 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(4): Show | 7 | HG01192.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1940+8724A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14737412 | ||||||
| chr3:14738053
|
C | G | 85 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0247others(82): Show | 86 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1940+9365C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738053 | ||||||
| chr3:14738072
|
C | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(28): Show | 31 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.1940+9384C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738072 | ||||||
| chr3:14738147
|
A | G | 6 | a0001c0001t0001g0254a0001c0001t0001g0358a0001c0001t0001g0360others(3): Show | 6 | HG02486.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1940+9459A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738147 | ||||||
| chr3:14738164
|
C | CT | 161 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0028others(158): Show | 165 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.1940+9497dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738164 | |||||
| chr3:14738164
|
C | CTT | 18 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0113others(15): Show | 18 | HG00738.hp1 HG01070.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1940+9496_1940+949 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738164 | |||||
| chr3:14738164
|
C | CTTT | 7 | a0001c0001t0001g0242a0001c0001t0003g0009a0001c0009t0001g0236others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1940+9495_1940+949 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738164 | |||||
| chr3:14738164
|
CT | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 26 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1940+9497delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738164 | |||||
| chr3:14738234
|
C | A | 1 | a0001c0001t0002g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1940+9546C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738234 | ||||||
| chr3:14738263
|
G | C | 1 | a0002c0002t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1940+9575G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738263 | ||||||
| chr3:14738307
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 27 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.1940+9619A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738307 | ||||||
| chr3:14738316
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(212): Show | 219 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.1940+9628T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738316 | ||||||
| chr3:14738334
|
A | AT | 6 | a0001c0001t0001g0320a0001c0001t0002g0105a0001c0001t0003g0011others(3): Show | 6 | HG01192.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1940+9659dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738334 | |||||
| chr3:14738524
|
G | A | 4 | a0001c0001t0001g0282a0001c0001t0001g0286a0001c0001t0001g0305others(1): Show | 4 | HG01106.hp1 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940+9836G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738524 | ||||||
| chr3:14738533
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(212): Show | 219 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.1940+9845A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738533 | ||||||
| chr3:14738611
|
A | G | 6 | a0001c0001t0001g0323a0001c0001t0002g0072a0001c0001t0002g0073others(3): Show | 6 | NA18612.hp2 NA18970.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.1940+9923A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738611 | ||||||
| chr3:14738630
|
C | CT | 40 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0112others(37): Show | 40 | HG00639.hp2 HG01081.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1940+9964dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738630 | |||||
| chr3:14738630
|
C | CTT | 44 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0247others(41): Show | 45 | HG00408.hp1 HG00673.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1940+9963_1940+996 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738630 | |||||
| chr3:14738630
|
C | CTTT | 7 | a0001c0001t0001g0249a0001c0001t0001g0301a0002c0002t0001g0290others(4): Show | 7 | HG00423.hp2 HG01978.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1940+9962_1940+996 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738630 | |||||
| chr3:14738630
|
CT | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0114others(64): Show | 68 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1940+9964delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738630 | |||||
| chr3:14738630
|
CTT | C | 38 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 38 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.1940+9963_1940+996 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738630 | |||||
| chr3:14738667
|
C | G | 1 | a0003c0003t0001g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1940+9979C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738667 | ||||||
| chr3:14738721
|
A | C | 1 | a0019c0029t0001g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1940+10033A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738721 | ||||||
| chr3:14738738
|
T | TCAAGCGA others(12): Show |
64 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(61): Show | 65 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1940+10051_1940+10 others(25): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738738 | |||||
| chr3:14738744
|
G | GACTCTCC others(12): Show |
3 | a0001c0001t0005g0118a0001c0001t0005g0119a0001c0021t0005g0120 | 3 | HG01934.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1940+10069_1940+10 others(25): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738744 | |||||
| chr3:14738782
|
A | C | 2 | a0001c0001t0001g0027a0003c0003t0001g0200 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1940+10094A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738782 | ||||||
| chr3:14738802
|
G | A | 1 | a0006c0006t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1940+10114G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738802 | ||||||
| chr3:14738815
|
G | GT | 15 | a0001c0001t0001g0112a0001c0001t0002g0058a0001c0001t0003g0014others(12): Show | 15 | HG00639.hp2 HG01255.hp1 HG03471.hp2 others(12): Show |
intron_variant | MODIFIER | c.1940+10147dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738815 | |||||
| chr3:14738815
|
G | GTT | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0355others(3): Show | 6 | HG01891.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940+10146_1940+10 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738815 | |||||
| chr3:14738815
|
G | GTTT | 61 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0240others(58): Show | 62 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1940+10145_1940+10 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738815 | |||||
| chr3:14738815
|
G | GTTTT | 6 | a0001c0001t0001g0281a0001c0001t0001g0302a0001c0001t0001g0367others(3): Show | 6 | HG00609.hp2 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1940+10144_1940+10 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738815 | |||||
| chr3:14738815
|
G | T | 10 | a0002c0002t0001g0239a0002c0002t0001g0243a0002c0002t0001g0333others(7): Show | 10 | HG00140.hp1 HG00408.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1940+10127G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738815 | ||||||
| chr3:14738815
|
GTT | G | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1940+10146_1940+10 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14738815 | |||||
| chr3:14738818
|
T | A | 4 | a0001c0001t0001g0350a0002c0002t0002g0043a0002c0002t0002g0048others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940+10130T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738818 | ||||||
| chr3:14738819
|
T | A | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1940+10131T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14738819 | ||||||
| chr3:14739044
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0356 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1940+10356G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739044 | ||||||
| chr3:14739076
|
CCACTGTG others(7): Show |
C | 5 | a0002c0002t0002g0046a0003c0003t0001g0003a0003c0003t0001g0203others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1940+10392_1940+10 others(20): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14739076 | |||||
| chr3:14739093
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1940+10405C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739093 | ||||||
| chr3:14739259
|
A | G | 1 | a0002c0002t0001g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1940+10571A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739259 | ||||||
| chr3:14739531
|
A | G | 4 | a0002c0002t0001g0253a0002c0002t0001g0267a0002c0002t0001g0268others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940+10843A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739531 | ||||||
| chr3:14739618
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG02280.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940+10930C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739618 | ||||||
| chr3:14739640
|
A | C | 34 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 34 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.1940+10952A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739640 | ||||||
| chr3:14739857
|
G | A | 39 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(36): Show | 39 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1940+11169G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14739857 | ||||||
| chr3:14740078
|
C | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0240a0001c0001t0001g0242others(65): Show | 69 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1940+11390C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14740078 | ||||||
| chr3:14740201
|
C | T | 1 | a0003c0003t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1940+11513C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14740201 | ||||||
| chr3:14740504
|
A | G | 1 | a0003c0003t0001g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1940+11816A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14740504 | ||||||
| chr3:14741231
|
T | C | 2 | a0005c0004t0001g0006a0023c0018t0001g0116 | 3 | HG01167.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1940+12543T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741231 | ||||||
| chr3:14741287
|
G | A | 38 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 38 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.1940+12599G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741287 | ||||||
| chr3:14741340
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0004g0123a0001c0001t0004g0124others(2): Show | 5 | HG01168.hp1 HG01175.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940+12652G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741340 | ||||||
| chr3:14741399
|
T | G | 4 | a0001c0001t0001g0282a0001c0001t0001g0286a0001c0001t0001g0305others(1): Show | 4 | HG01106.hp1 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940+12711T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741399 | ||||||
| chr3:14741443
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940+12755T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741443 | ||||||
| chr3:14741487
|
T | A | 1 | a0001c0001t0003g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1940+12799T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741487 | ||||||
| chr3:14741525
|
A | G | 5 | a0006c0006t0001g0002a0006c0006t0001g0176a0006c0006t0001g0179others(2): Show | 6 | HG01934.hp2 HG01952.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1940+12837A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741525 | ||||||
| chr3:14741690
|
G | A | 1 | a0004c0005t0002g0080 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1940+13002G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741690 | ||||||
| chr3:14741717
|
T | C | 42 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(39): Show | 42 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1940+13029T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741717 | ||||||
| chr3:14741864
|
C | T | 1 | a0001c0022t0001g0110 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1940+13176C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741864 | ||||||
| chr3:14741886
|
G | A | 35 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.1940+13198G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741886 | ||||||
| chr3:14741926
|
G | T | 3 | a0001c0001t0002g0042a0001c0001t0003g0008a0005c0004t0001g0216 | 3 | HG02559.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1940+13238G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741926 | ||||||
| chr3:14741975
|
G | A | 2 | a0001c0001t0001g0053a0019c0029t0001g0054 | 2 | HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1940+13287G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741975 | ||||||
| chr3:14741980
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1940+13292T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14741980 | ||||||
| chr3:14742102
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1940+13414T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742102 | ||||||
| chr3:14742163
|
C | T | 3 | a0001c0001t0002g0042a0001c0001t0003g0008a0005c0004t0001g0216 | 3 | HG02559.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1940+13475C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742163 | ||||||
| chr3:14742167
|
A | G | 3 | a0001c0001t0002g0042a0001c0001t0003g0008a0005c0004t0001g0216 | 3 | HG02559.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1940+13479A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742167 | ||||||
| chr3:14742233
|
A | G | 1 | a0001c0001t0001g0360 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1940+13545A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742233 | ||||||
| chr3:14742294
|
G | A | 10 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0057others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1940+13606G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742294 | ||||||
| chr3:14742359
|
G | A | 1 | a0001c0001t0005g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1940+13671G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742359 | ||||||
| chr3:14742530
|
C | T | 1 | a0002c0002t0001g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1940+13842C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742530 | ||||||
| chr3:14742661
|
T | C | 1 | a0001c0001t0001g0367 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1940+13973T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742661 | ||||||
| chr3:14742692
|
G | A | 1 | a0002c0002t0001g0368 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1940+14004G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742692 | ||||||
| chr3:14742703
|
C | G | 1 | a0001c0001t0002g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1940+14015C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742703 | ||||||
| chr3:14742709
|
A | G | 1 | a0011c0025t0001g0343 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1940+14021A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742709 | ||||||
| chr3:14742712
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1940+14024G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742712 | ||||||
| chr3:14742741
|
T | C | 32 | a0001c0001t0001g0028a0001c0001t0001g0306a0001c0001t0001g0328others(29): Show | 33 | HG00408.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1940+14053T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742741 | ||||||
| chr3:14742744
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1940+14056G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742744 | ||||||
| chr3:14742754
|
G | A | 1 | a0002c0002t0002g0098 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1940+14066G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742754 | ||||||
| chr3:14742771
|
T | A | 7 | a0001c0001t0001g0288a0001c0001t0001g0370a0002c0002t0001g0333others(4): Show | 7 | HG01074.hp2 HG01496.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1940+14083T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742771 | ||||||
| chr3:14742807
|
C | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0009t0001g0233others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1940+14119C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742807 | ||||||
| chr3:14742823
|
G | A | 63 | a0001c0001t0001g0056a0001c0001t0001g0231a0001c0001t0001g0232others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1940+14135G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742823 | ||||||
| chr3:14742833
|
C | T | 94 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0244others(91): Show | 95 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1940+14145C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742833 | ||||||
| chr3:14742838
|
A | G | 1 | a0001c0001t0005g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1940+14150A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742838 | ||||||
| chr3:14742841
|
C | G | 27 | a0001c0001t0001g0251a0001c0001t0001g0364a0001c0001t0002g0042others(24): Show | 29 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1940+14153C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742841 | ||||||
| chr3:14742874
|
GGAGAATA others(1908): Show |
G | 4 | a0001c0001t0003g0011a0003c0003t0001g0175a0003c0003t0001g0207others(1): Show | 4 | HG01192.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940+14254_1941-12 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14742874 | |||||
| chr3:14742960
|
T | G | 1 | a0002c0002t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1940+14272T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742960 | ||||||
| chr3:14742976
|
A | T | 32 | a0001c0001t0001g0114a0001c0001t0001g0350a0001c0001t0001g0357others(29): Show | 33 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1940+14288A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742976 | ||||||
| chr3:14742998
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1940+14310A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14742998 | ||||||
| chr3:14743157
|
T | C | 1 | a0002c0002t0002g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1941-14214T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743157 | ||||||
| chr3:14743168
|
A | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0012 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1941-14203A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743168 | ||||||
| chr3:14743229
|
C | T | 1 | a0003c0003t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1941-14142C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743229 | ||||||
| chr3:14743300
|
G | A | 13 | a0001c0001t0002g0042a0003c0003t0001g0163a0004c0005t0001g0004others(10): Show | 13 | HG00140.hp2 HG02071.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1941-14071G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743300 | ||||||
| chr3:14743399
|
T | C | 5 | a0001c0001t0001g0350a0001c0009t0001g0236a0002c0002t0002g0043others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1941-13972T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743399 | ||||||
| chr3:14743677
|
G | A | 2 | a0001c0001t0001g0278a0002c0002t0001g0266 | 2 | NA18939.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1941-13694G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743677 | ||||||
| chr3:14743684
|
T | C | 110 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 110 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1941-13687T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743684 | ||||||
| chr3:14743759
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0002g0059 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1941-13612G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743759 | ||||||
| chr3:14743801
|
G | A | 103 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0275others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1941-13570G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743801 | ||||||
| chr3:14743808
|
C | T | 81 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 81 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.1941-13563C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743808 | ||||||
| chr3:14743851
|
A | G | 1 | a0018c0028t0002g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1941-13520A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743851 | ||||||
| chr3:14743927
|
G | A | 3 | a0001c0001t0005g0119a0002c0002t0002g0047a0003c0003t0001g0171 | 3 | HG02922.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1941-13444G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14743927 | ||||||
| chr3:14744035
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-13336A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744035 | ||||||
| chr3:14744073
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0012 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1941-13298G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744073 | ||||||
| chr3:14744256
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1941-13115A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744256 | ||||||
| chr3:14744451
|
GTCT | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0302a0001c0001t0002g0055 | 3 | HG01109.hp1 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1941-12913_1941-12 others(9): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14744451 | |||||
| chr3:14744608
|
G | A | 1 | a0010c0010t0001g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1941-12763G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744608 | ||||||
| chr3:14744707
|
G | A | 3 | a0001c0001t0001g0294a0003c0003t0001g0150a0003c0003t0001g0220 | 3 | HG02056.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1941-12664G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744707 | ||||||
| chr3:14744857
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(258): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1941-12514T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744857 | ||||||
| chr3:14744900
|
G | C | 1 | a0002c0002t0001g0291 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1941-12471G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744900 | ||||||
| chr3:14744980
|
G | A | 6 | a0001c0001t0001g0369a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG01255.hp2 HG01346.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941-12391G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14744980 | ||||||
| chr3:14745038
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1941-12333A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14745038 | ||||||
| chr3:14745144
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1941-12227T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14745144 | ||||||
| chr3:14745182
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-12189A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14745182 | ||||||
| chr3:14745198
|
A | G | 1 | a0001c0001t0003g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1941-12173A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14745198 | ||||||
| chr3:14745338
|
C | T | 4 | a0001c0001t0002g0042a0001c0009t0001g0234a0003c0003t0001g0163others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1941-12033C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14745338 | ||||||
| chr3:14745853
|
C | A | 108 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 108 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.1941-11518C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14745853 | ||||||
| chr3:14746335
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(6): Show | 11 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1941-11036C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14746335 | ||||||
| chr3:14746528
|
C | T | 108 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 108 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.1941-10843C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14746528 | ||||||
| chr3:14746600
|
T | C | 41 | a0001c0001t0001g0321a0002c0002t0001g0245a0002c0002t0001g0339others(38): Show | 41 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1941-10771T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14746600 | ||||||
| chr3:14746618
|
G | T | 1 | a0001c0001t0004g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1941-10753G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14746618 | ||||||
| chr3:14746720
|
A | G | 2 | a0001c0001t0002g0099a0001c0024t0002g0037 | 2 | HG02083.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1941-10651A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14746720 | ||||||
| chr3:14747205
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1941-10166C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747205 | ||||||
| chr3:14747206
|
G | A | 17 | a0001c0001t0001g0027a0001c0001t0001g0112a0001c0001t0002g0042others(14): Show | 17 | HG01168.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1941-10165G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747206 | ||||||
| chr3:14747264
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(6): Show | 11 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1941-10107T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747264 | ||||||
| chr3:14747330
|
A | T | 4 | a0001c0001t0001g0367a0002c0002t0001g0368a0006c0006t0001g0179others(1): Show | 4 | NA18978.hp1 NA18982.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1941-10041A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747330 | ||||||
| chr3:14747536
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(1): Show | 6 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941-9835A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747536 | ||||||
| chr3:14747589
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(256): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1941-9782G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747589 | ||||||
| chr3:14747961
|
T | G | 4 | a0001c0001t0002g0042a0001c0009t0001g0234a0003c0003t0001g0163others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1941-9410T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747961 | ||||||
| chr3:14747968
|
T | A | 1 | a0002c0002t0001g0342 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1941-9403T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14747968 | ||||||
| chr3:14748314
|
C | T | 1 | a0004c0005t0002g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1941-9057C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14748314 | ||||||
| chr3:14748407
|
C | G | 89 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(86): Show | 89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1941-8964C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14748407 | ||||||
| chr3:14748903
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-8468A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14748903 | ||||||
| chr3:14748926
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0351 | 2 | NA18961.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1941-8445G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14748926 | ||||||
| chr3:14749143
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0004g0123a0001c0001t0004g0126others(1): Show | 4 | HG01168.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1941-8228A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14749143 | ||||||
| chr3:14749304
|
A | C | 1 | a0002c0002t0002g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1941-8067A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14749304 | ||||||
| chr3:14749327
|
A | G | 4 | a0001c0001t0002g0042a0001c0009t0001g0234a0003c0003t0001g0163others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1941-8044A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14749327 | ||||||
| chr3:14749543
|
G | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(12): Show | 17 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1941-7828G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14749543 | ||||||
| chr3:14749697
|
A | AT | 257 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(254): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1941-7662dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14749697 | |||||
| chr3:14749697
|
A | ATT | 6 | a0001c0001t0001g0350a0001c0001t0004g0121a0001c0009t0001g0236others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1941-7663_1941-766 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14749697 | |||||
| chr3:14749868
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(12): Show | 17 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1941-7503C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14749868 | ||||||
| chr3:14749921
|
C | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(12): Show | 17 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1941-7450C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14749921 | ||||||
| chr3:14749996
|
G | GAA | 110 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 110 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1941-7366_1941-736 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14749996 | |||||
| chr3:14749996
|
GA | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(12): Show | 17 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1941-7365delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14749996 | |||||
| chr3:14750285
|
C | T | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(114): Show | 117 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.1941-7086C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14750285 | ||||||
| chr3:14750304
|
C | T | 1 | a0002c0002t0007g0261 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1941-7067C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14750304 | ||||||
| chr3:14750532
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(12): Show | 17 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1941-6839G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14750532 | ||||||
| chr3:14750554
|
T | TA | 7 | a0001c0001t0001g0112a0001c0001t0004g0121a0001c0001t0004g0124others(4): Show | 7 | HG01175.hp2 HG02896.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1941-6799dupA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14750554 | |||||
| chr3:14750554
|
T | TAA | 6 | a0010c0010t0001g0213a0010c0010t0001g0224a0012c0012t0002g0039others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1941-6800_1941-679 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14750554 | |||||
| chr3:14750554
|
TA | T | 200 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1941-6799delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14750554 | |||||
| chr3:14750554
|
TAA | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(13): Show | 18 | HG01081.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1941-6800_1941-679 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14750554 | |||||
| chr3:14750616
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1941-6755C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14750616 | ||||||
| chr3:14750779
|
TCTCTTTG others(9): Show |
T | 6 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01192.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941-6590_1941-657 others(20): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14750779 | |||||
| chr3:14750965
|
T | A | 1 | a0002c0002t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1941-6406T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14750965 | ||||||
| chr3:14750973
|
T | C | 1 | a0024c0019t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1941-6398T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14750973 | ||||||
| chr3:14751074
|
T | G | 50 | a0001c0001t0001g0027a0001c0001t0001g0112a0001c0001t0002g0042others(47): Show | 50 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1941-6297T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14751074 | ||||||
| chr3:14751204
|
T | C | 50 | a0001c0001t0001g0027a0001c0001t0001g0112a0001c0001t0002g0042others(47): Show | 50 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1941-6167T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14751204 | ||||||
| chr3:14751235
|
T | C | 33 | a0004c0005t0001g0004a0004c0005t0001g0241a0004c0005t0001g0296others(30): Show | 33 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1941-6136T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14751235 | ||||||
| chr3:14751443
|
C | T | 8 | a0001c0001t0001g0112a0010c0010t0001g0213a0010c0010t0001g0221others(5): Show | 8 | HG02615.hp2 HG02896.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1941-5928C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14751443 | ||||||
| chr3:14751911
|
A | G | 4 | a0001c0001t0001g0282a0001c0001t0001g0286a0001c0001t0001g0305others(1): Show | 4 | HG01106.hp1 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1941-5460A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14751911 | ||||||
| chr3:14752420
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(1): Show | 6 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941-4951G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752420 | ||||||
| chr3:14752583
|
ATC | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(1): Show | 6 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941-4787_1941-478 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752583 | ||||||
| chr3:14752670
|
G | A | 2 | a0002c0002t0001g0260a0002c0002t0001g0269 | 2 | NA19066.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1941-4701G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752670 | ||||||
| chr3:14752672
|
G | A | 1 | a0002c0002t0001g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1941-4699G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752672 | ||||||
| chr3:14752727
|
A | G | 1 | a0002c0002t0001g0291 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1941-4644A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752727 | ||||||
| chr3:14752778
|
C | T | 1 | a0001c0001t0004g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1941-4593C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752778 | ||||||
| chr3:14752783
|
A | G | 4 | a0001c0001t0006g0005a0001c0001t0006g0280a0001c0001t0006g0354others(1): Show | 5 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1941-4588A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14752783 | ||||||
| chr3:14753463
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(4): Show | 9 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1941-3908T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14753463 | ||||||
| chr3:14753817
|
A | G | 1 | a0006c0006t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1941-3554A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14753817 | ||||||
| chr3:14753889
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0004g0123a0001c0001t0004g0126others(1): Show | 4 | HG01168.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1941-3482A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14753889 | ||||||
| chr3:14753999
|
C | G | 2 | a0001c0001t0001g0365a0001c0001t0002g0089 | 2 | HG00597.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1941-3372C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14753999 | ||||||
| chr3:14754070
|
A | C | 1 | a0024c0019t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1941-3301A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14754070 | ||||||
| chr3:14754244
|
C | T | 4 | a0001c0001t0005g0119a0002c0002t0002g0047a0002c0002t0002g0049others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1941-3127C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14754244 | ||||||
| chr3:14754262
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(1): Show | 6 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941-3109G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14754262 | ||||||
| chr3:14754637
|
C | T | 55 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0247others(52): Show | 56 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1941-2734C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14754637 | ||||||
| chr3:14754933
|
C | T | 3 | a0001c0001t0002g0042a0001c0009t0001g0234a0005c0004t0001g0216 | 3 | HG02559.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1941-2438C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14754933 | ||||||
| chr3:14754978
|
G | A | 1 | a0005c0004t0001g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1941-2393G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14754978 | ||||||
| chr3:14755202
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-2169A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755202 | ||||||
| chr3:14755207
|
T | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-2164T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755207 | ||||||
| chr3:14755213
|
A | G | 65 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0258others(62): Show | 65 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1941-2158A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755213 | ||||||
| chr3:14755267
|
G | A | 5 | a0001c0001t0001g0350a0001c0009t0001g0236a0002c0002t0002g0043others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1941-2104G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755267 | ||||||
| chr3:14755284
|
G | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(255): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1941-2087G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755284 | ||||||
| chr3:14755288
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-2083T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755288 | ||||||
| chr3:14755317
|
T | C | 1 | a0002c0002t0001g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1941-2054T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755317 | ||||||
| chr3:14755368
|
G | C | 2 | a0001c0001t0004g0122a0001c0009t0001g0233 | 2 | HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1941-2003G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755368 | ||||||
| chr3:14755548
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(4): Show | 9 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1941-1823C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755548 | ||||||
| chr3:14755768
|
G | A | 1 | a0006c0006t0001g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1941-1603G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755768 | ||||||
| chr3:14755825
|
C | T | 5 | a0001c0001t0001g0279a0001c0001t0001g0303a0001c0001t0001g0324others(2): Show | 5 | HG01109.hp2 HG03490.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1941-1546C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755825 | ||||||
| chr3:14755924
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1941-1447G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755924 | ||||||
| chr3:14755970
|
A | C | 1 | a0002c0002t0001g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1941-1401A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755970 | ||||||
| chr3:14755978
|
G | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.1941-1393G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14755978 | ||||||
| chr3:14756028
|
CA | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(214): Show | 219 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.1941-1324delA | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 14756028 | |||||
| chr3:14756042
|
A | G | 7 | a0001c0001t0001g0364a0001c0001t0002g0058a0001c0001t0002g0059others(4): Show | 8 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1941-1329A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756042 | ||||||
| chr3:14756077
|
T | G | 33 | a0004c0005t0001g0004a0004c0005t0001g0241a0004c0005t0001g0296others(30): Show | 33 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1941-1294T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756077 | ||||||
| chr3:14756219
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1941-1152G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756219 | ||||||
| chr3:14756238
|
C | T | 1 | a0003c0003t0001g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1941-1133C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756238 | ||||||
| chr3:14756270
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1941-1101G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756270 | ||||||
| chr3:14756300
|
G | A | 2 | a0012c0012t0002g0039a0012c0012t0002g0040 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1941-1071G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756300 | ||||||
| chr3:14756300
|
G | T | 9 | a0001c0001t0001g0282a0001c0001t0001g0285a0001c0001t0001g0286others(6): Show | 9 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1941-1071G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756300 | ||||||
| chr3:14756511
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1941-860C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756511 | ||||||
| chr3:14756572
|
T | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0112a0001c0001t0002g0042others(14): Show | 17 | HG01168.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1941-799T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756572 | ||||||
| chr3:14756606
|
G | A | 2 | a0001c0001t0004g0122a0001c0009t0001g0233 | 2 | HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1941-765G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756606 | ||||||
| chr3:14756638
|
G | A | 1 | a0002c0002t0001g0332 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1941-733G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756638 | ||||||
| chr3:14756835
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1941-536A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756835 | ||||||
| chr3:14756873
|
C | T | 79 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1941-498C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14756873 | ||||||
| chr3:14757005
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(3): Show | 8 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1941-366G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14757005 | ||||||
| chr3:14757099
|
G | A | 1 | a0005c0004t0001g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1941-272G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14757099 | ||||||
| chr3:14757306
|
G | A | 1 | a0001c0001t0004g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1941-65G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 12/16 | chr3 | 14757306 | ||||||
| chr3:14757849
|
C | G | 3 | a0001c0001t0001g0294a0003c0003t0001g0150a0003c0003t0001g0220 | 3 | HG02056.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2244+175C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14757849 | ||||||
| chr3:14757998
|
G | C | 83 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2244+324G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14757998 | ||||||
| chr3:14758179
|
T | C | 2 | a0001c0001t0002g0099a0001c0024t0002g0037 | 2 | HG02083.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.2244+505T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758179 | ||||||
| chr3:14758230
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2244+556A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758230 | ||||||
| chr3:14758273
|
C | CAGGTGAT others(1): Show |
6 | a0001c0001t0001g0350a0001c0009t0001g0236a0002c0002t0002g0043others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244+601_2244+608d others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 14758273 | |||||
| chr3:14758388
|
A | G | 1 | a0002c0002t0001g0262 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2244+714A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758388 | ||||||
| chr3:14758426
|
T | C | 1 | a0001c0001t0002g0095 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2244+752T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758426 | ||||||
| chr3:14758508
|
C | A | 33 | a0004c0005t0001g0004a0004c0005t0001g0241a0004c0005t0001g0296others(30): Show | 33 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.2244+834C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758508 | ||||||
| chr3:14758597
|
C | G | 2 | a0004c0005t0002g0079a0004c0005t0002g0091 | 2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2244+923C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758597 | ||||||
| chr3:14758741
|
C | T | 99 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 99 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.2244+1067C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758741 | ||||||
| chr3:14758884
|
G | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2245-1007G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758884 | ||||||
| chr3:14758912
|
A | C | 252 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(249): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.2245-979A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14758912 | ||||||
| chr3:14759243
|
T | G | 3 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097 | 3 | NA18942.hp1 NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2245-648T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759243 | ||||||
| chr3:14759326
|
T | G | 2 | a0001c0001t0001g0344a0001c0001t0001g0348 | 2 | NA18980.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2245-565T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759326 | ||||||
| chr3:14759354
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2245-537G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759354 | ||||||
| chr3:14759401
|
G | A | 1 | a0002c0002t0001g0333 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2245-490G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759401 | ||||||
| chr3:14759525
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(4): Show | 9 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2245-366A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759525 | ||||||
| chr3:14759611
|
C | T | 6 | a0001c0001t0001g0350a0001c0009t0001g0236a0002c0002t0002g0043others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-280C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759611 | ||||||
| chr3:14759680
|
G | A | 1 | a0002c0002t0001g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2245-211G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759680 | ||||||
| chr3:14759848
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0004g0126a0003c0003t0001g0200others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-43A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 13/16 | chr3 | 14759848 | ||||||
| chr3:14760043
|
G | A | 72 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0250others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2352+45G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760043 | ||||||
| chr3:14760051
|
C | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030 | 5 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2352+53C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760051 | ||||||
| chr3:14760235
|
C | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0028others(12): Show | 17 | HG01081.hp2 HG01168.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2352+237C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760235 | ||||||
| chr3:14760248
|
C | T | 5 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0329others(2): Show | 5 | NA18940.hp1 NA18979.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352+250C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760248 | ||||||
| chr3:14760429
|
A | T | 1 | a0002c0002t0001g0259 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2352+431A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760429 | ||||||
| chr3:14760490
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2352+492T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760490 | ||||||
| chr3:14760502
|
T | C | 1 | a0016c0031t0001g0361 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2352+504T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760502 | ||||||
| chr3:14760559
|
T | A | 127 | a0001c0001t0001g0027a0001c0001t0001g0056a0001c0001t0001g0057others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2352+561T>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760559 | ||||||
| chr3:14760601
|
GTCT | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0031a0002c0002t0001g0317others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2352+608_2352+610d others(5): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14760601 | |||||
| chr3:14760606
|
C | CT | 69 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0250others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.2352+629dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14760606 | |||||
| chr3:14760606
|
C | CTT | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359others(5): Show | 8 | HG00642.hp1 HG00642.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2352+628_2352+629d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14760606 | |||||
| chr3:14760606
|
CT | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(149): Show | 158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.2352+629delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14760606 | |||||
| chr3:14760606
|
CTT | C | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(111): Show | 114 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.2352+628_2352+629d others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14760606 | |||||
| chr3:14760606
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0255 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2352+617_2352+629d others(15): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14760606 | |||||
| chr3:14760644
|
C | G | 2 | a0004c0005t0001g0296a0004c0005t0002g0075 | 2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2352+646C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760644 | ||||||
| chr3:14760679
|
G | A | 3 | a0001c0001t0002g0100a0001c0001t0002g0101a0006c0006t0001g0223 | 3 | HG02056.hp2 HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2352+681G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760679 | ||||||
| chr3:14760717
|
A | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2352+719A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760717 | ||||||
| chr3:14760724
|
C | T | 1 | a0002c0002t0001g0340 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2352+726C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760724 | ||||||
| chr3:14760745
|
G | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359others(1): Show | 4 | HG02145.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353-728G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760745 | ||||||
| chr3:14760862
|
C | T | 2 | a0002c0002t0001g0363a0018c0028t0002g0102 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2353-611C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14760862 | ||||||
| chr3:14761034
|
C | G | 28 | a0004c0005t0001g0004a0004c0005t0001g0241a0004c0005t0001g0296others(25): Show | 28 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.2353-439C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14761034 | ||||||
| chr3:14761132
|
G | A | 85 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0114others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2353-341G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14761132 | ||||||
| chr3:14761202
|
A | G | 153 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2353-271A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14761202 | ||||||
| chr3:14761227
|
AG | A | 28 | a0001c0001t0001g0053a0001c0001t0001g0113a0001c0001t0001g0231others(25): Show | 28 | HG01106.hp2 HG01515.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.2353-244delG | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 14761227 | |||||
| chr3:14761351
|
G | A | 3 | a0001c0001t0003g0014a0001c0001t0004g0122a0001c0009t0001g0233 | 3 | HG02258.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2353-122G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14761351 | ||||||
| chr3:14761423
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2353-50T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 14/16 | chr3 | 14761423 | ||||||
| chr3:14761641
|
G | A | 2 | a0003c0003t0001g0168a0003c0003t0001g0169 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2495+26G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14761641 | ||||||
| chr3:14761849
|
G | A | 17 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0249others(14): Show | 18 | HG00621.hp2 HG00673.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.2495+234G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14761849 | ||||||
| chr3:14761942
|
C | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(8): Show | 11 | HG01168.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2495+327C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14761942 | ||||||
| chr3:14761958
|
G | GT | 3 | a0001c0001t0003g0014a0001c0001t0004g0122a0001c0009t0001g0233 | 3 | HG02258.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2495+345dupT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14761958 | |||||
| chr3:14762328
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2495+713G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762328 | ||||||
| chr3:14762549
|
T | G | 1 | a0003c0003t0001g0138 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2495+934T>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762549 | ||||||
| chr3:14762585
|
C | T | 2 | a0003c0003t0001g0203a0003c0003t0001g0204 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2495+970C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762585 | ||||||
| chr3:14762617
|
C | T | 5 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(2): Show | 5 | NA18970.hp1 NA19003.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495+1002C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762617 | ||||||
| chr3:14762652
|
C | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030 | 5 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495+1037C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762652 | ||||||
| chr3:14762760
|
A | C | 1 | a0006c0006t0001g0209 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2495+1145A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762760 | ||||||
| chr3:14762815
|
T | TC | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0027others(63): Show | 68 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.2495+1201dupC | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14762815 | |||||
| chr3:14762898
|
A | C | 12 | a0001c0001t0001g0309a0002c0002t0001g0253a0002c0002t0001g0267others(9): Show | 12 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495+1283A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762898 | ||||||
| chr3:14762930
|
A | G | 40 | a0001c0001t0001g0320a0002c0002t0001g0245a0002c0002t0001g0341others(37): Show | 40 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2495+1315A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762930 | ||||||
| chr3:14762947
|
C | A | 39 | a0001c0001t0001g0320a0001c0001t0004g0121a0002c0002t0001g0245others(36): Show | 39 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2495+1332C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762947 | ||||||
| chr3:14762998
|
A | AAGAAAAG others(8): Show |
1 | a0006c0006t0001g0209 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2495+1383_2495+138 others(19): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14762998 | ||||||
| chr3:14763127
|
G | A | 2 | a0002c0002t0001g0341a0002c0002t0001g0345 | 2 | NA18953.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2495+1512G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763127 | ||||||
| chr3:14763317
|
C | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0027others(11): Show | 16 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2495+1702C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763317 | ||||||
| chr3:14763320
|
T | C | 3 | a0001c0001t0003g0014a0001c0001t0004g0122a0001c0009t0001g0233 | 3 | HG02258.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2495+1705T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763320 | ||||||
| chr3:14763501
|
A | T | 1 | a0003c0003t0001g0137 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2495+1886A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763501 | ||||||
| chr3:14763538
|
A | G | 1 | a0002c0002t0001g0332 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2495+1923A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763538 | ||||||
| chr3:14763726
|
C | T | 1 | a0002c0002t0001g0373 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2495+2111C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763726 | ||||||
| chr3:14763767
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2495+2152T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763767 | ||||||
| chr3:14763781
|
G | T | 1 | a0005c0004t0001g0188 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2495+2166G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763781 | ||||||
| chr3:14763977
|
C | G | 7 | a0001c0001t0001g0350a0001c0009t0001g0236a0002c0002t0002g0043others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2495+2362C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14763977 | ||||||
| chr3:14764029
|
A | G | 369 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(366): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.2495+2414A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764029 | ||||||
| chr3:14764065
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359 | 3 | HG02145.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2495+2450A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764065 | ||||||
| chr3:14764090
|
G | T | 1 | a0002c0002t0001g0245 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2495+2475G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764090 | ||||||
| chr3:14764209
|
G | A | 2 | a0006c0006t0001g0179a0013c0014t0001g0194 | 2 | NA18978.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2495+2594G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764209 | ||||||
| chr3:14764217
|
CAT | C | 3 | a0001c0001t0003g0014a0001c0001t0004g0122a0001c0009t0001g0233 | 3 | HG02258.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2495+2604_2495+260 others(6): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764217 | |||||
| chr3:14764415
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2495+2800T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764415 | ||||||
| chr3:14764480
|
T | TTTA | 17 | a0001c0001t0001g0113a0001c0001t0001g0275a0001c0001t0001g0277others(14): Show | 17 | HG01069.hp1 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2495+2892_2495+289 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764480
|
T | TTTATTA | 31 | a0001c0001t0001g0323a0001c0001t0002g0101a0001c0001t0003g0011others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.2495+2889_2495+289 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764480
|
T | TTTATTAT others(2): Show |
36 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0270others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.2495+2886_2495+289 others(13): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764480
|
T | TTTATTAT others(5): Show |
3 | a0001c0001t0002g0061a0002c0002t0001g0308a0006c0006t0001g0174 | 3 | HG01081.hp1 HG01361.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2495+2883_2495+289 others(16): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764480
|
T | TTTATTAT others(8): Show |
1 | a0001c0009t0001g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495+2880_2495+289 others(19): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764480
|
T | TTTTTTA | 6 | a0002c0002t0001g0253a0002c0002t0001g0267a0002c0002t0001g0268others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495+2867_2495+286 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764480
|
TTTA | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(11): Show | 14 | HG01168.hp1 HG01192.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495+2892_2495+289 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764480 | |||||
| chr3:14764504
|
A | ATTGTTG | 5 | a0001c0009t0001g0236a0002c0002t0002g0043a0002c0002t0002g0048others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495+2891_2495+289 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764504 | |||||
| chr3:14764504
|
A | G | 2 | a0001c0001t0001g0350a0002c0002t0002g0107 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2495+2889A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764504 | ||||||
| chr3:14764504
|
ATTATTG | A | 26 | a0001c0001t0001g0320a0004c0005t0001g0004a0004c0005t0001g0296others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2495+2892_2495+289 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764504 | |||||
| chr3:14764507
|
A | ATTATTAT others(5): Show |
1 | a0007c0007t0001g0198 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2495+2894_2495+289 others(16): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764507 | |||||
| chr3:14764507
|
A | ATTG | 4 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(1): Show | 6 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495+2919_2495+292 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764507 | |||||
| chr3:14764507
|
A | ATTGTTG | 3 | a0001c0001t0001g0027a0001c0001t0001g0302a0003c0003t0001g0200 | 3 | HG02145.hp1 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2495+2916_2495+292 others(10): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764507 | |||||
| chr3:14764507
|
A | G | 15 | a0001c0001t0001g0306a0001c0001t0001g0328a0001c0001t0001g0350others(12): Show | 15 | HG01891.hp2 HG01943.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2495+2892A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764507 | ||||||
| chr3:14764507
|
ATTG | A | 10 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0359others(7): Show | 10 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495+2919_2495+292 others(7): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14764507 | |||||
| chr3:14764510
|
G | A | 4 | a0001c0001t0003g0014a0001c0001t0004g0122a0001c0009t0001g0233others(1): Show | 4 | HG02258.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495+2895G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764510 | ||||||
| chr3:14764513
|
G | A | 3 | a0001c0001t0003g0014a0001c0001t0004g0122a0001c0009t0001g0233 | 3 | HG02258.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2495+2898G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764513 | ||||||
| chr3:14764794
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0027others(58): Show | 63 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495+3179G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764794 | ||||||
| chr3:14764826
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2495+3211C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764826 | ||||||
| chr3:14764892
|
C | T | 6 | a0010c0010t0001g0224a0012c0012t0002g0039a0012c0012t0002g0040others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495+3277C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764892 | ||||||
| chr3:14764961
|
C | T | 1 | a0001c0001t0004g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2495+3346C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14764961 | ||||||
| chr3:14765122
|
G | A | 1 | a0005c0004t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2495+3507G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765122 | ||||||
| chr3:14765317
|
G | A | 10 | a0001c0001t0001g0350a0001c0001t0002g0032a0001c0001t0002g0050others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2495+3702G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765317 | ||||||
| chr3:14765354
|
A | C | 6 | a0001c0001t0001g0279a0001c0001t0001g0303a0001c0001t0001g0324others(3): Show | 6 | HG01109.hp2 HG03490.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495+3739A>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765354 | ||||||
| chr3:14765380
|
C | T | 6 | a0001c0001t0001g0279a0001c0001t0001g0303a0001c0001t0001g0324others(3): Show | 6 | HG01109.hp2 HG03490.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495+3765C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765380 | ||||||
| chr3:14765549
|
T | C | 1 | a0001c0001t0001g0360 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2495+3934T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765549 | ||||||
| chr3:14765611
|
G | A | 1 | a0020c0030t0001g0349 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2495+3996G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765611 | ||||||
| chr3:14765868
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2495+4253T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765868 | ||||||
| chr3:14765896
|
G | T | 2 | a0001c0001t0001g0302a0001c0001t0002g0055 | 2 | HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2495+4281G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765896 | ||||||
| chr3:14765903
|
C | T | 5 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0329others(2): Show | 5 | NA18940.hp1 NA18979.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495+4288C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14765903 | ||||||
| chr3:14766049
|
C | G | 1 | a0003c0003t0001g0138 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2495+4434C>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766049 | ||||||
| chr3:14766092
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2495+4477G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766092 | ||||||
| chr3:14766239
|
G | A | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2495+4624G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766239 | ||||||
| chr3:14766455
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2495+4840C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766455 | ||||||
| chr3:14766518
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0004g0123others(1): Show | 4 | HG01168.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495+4903G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766518 | ||||||
| chr3:14766572
|
G | A | 1 | a0023c0018t0001g0116 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2495+4957G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766572 | ||||||
| chr3:14766577
|
A | G | 1 | a0002c0002t0001g0372 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2495+4962A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766577 | ||||||
| chr3:14766898
|
AGGCTTTG others(16): Show |
A | 146 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(143): Show | 149 | HG00423.hp2 HG00544.hp2 HG01070.hp2 others(146): Show |
intron_variant | MODIFIER | c.2496-5145_2496-512 others(27): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14766898 | |||||
| chr3:14766968
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2496-5099G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14766968 | ||||||
| chr3:14767246
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2496-4821G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767246 | ||||||
| chr3:14767258
|
G | A | 86 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0270others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.2496-4809G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767258 | ||||||
| chr3:14767305
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2496-4762A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767305 | ||||||
| chr3:14767324
|
G | A | 1 | a0002c0002t0001g0291 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2496-4743G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767324 | ||||||
| chr3:14767513
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0002g0105 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2496-4554A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767513 | ||||||
| chr3:14767590
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2496-4477C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767590 | ||||||
| chr3:14767666
|
C | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0358a0001c0001t0001g0360others(2): Show | 5 | HG02486.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2496-4401C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767666 | ||||||
| chr3:14767776
|
T | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0030others(17): Show | 22 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2496-4291T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767776 | ||||||
| chr3:14767797
|
G | A | 1 | a0019c0029t0001g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2496-4270G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767797 | ||||||
| chr3:14767802
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0030 | 4 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496-4265T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767802 | ||||||
| chr3:14767823
|
A | G | 7 | a0001c0001t0001g0350a0001c0009t0001g0236a0002c0002t0002g0043others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2496-4244A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14767823 | ||||||
| chr3:14768046
|
CCTGTAAC others(1383): Show |
C | 1 | a0001c0001t0004g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2496-3842_2496-245 others(4): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14768046 | |||||
| chr3:14768249
|
G | A | 1 | a0024c0019t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2496-3818G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768249 | ||||||
| chr3:14768254
|
A | G | 1 | a0004c0005t0002g0060 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2496-3813A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768254 | ||||||
| chr3:14768324
|
G | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0357a0001c0009t0001g0235 | 3 | HG01884.hp2 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2496-3743G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768324 | ||||||
| chr3:14768549
|
G | A | 1 | a0001c0009t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2496-3518G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768549 | ||||||
| chr3:14768690
|
T | C | 4 | a0003c0003t0001g0183a0003c0003t0001g0184a0006c0006t0001g0153others(1): Show | 4 | HG01074.hp1 HG01123.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496-3377T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768690 | ||||||
| chr3:14768783
|
G | A | 112 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0270others(109): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.2496-3284G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768783 | ||||||
| chr3:14768984
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0364 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2496-3083C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14768984 | ||||||
| chr3:14769124
|
A | T | 5 | a0010c0010t0001g0224a0012c0012t0002g0039a0012c0012t0002g0040others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2496-2943A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769124 | ||||||
| chr3:14769187
|
G | A | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2496-2880G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769187 | ||||||
| chr3:14769347
|
G | A | 220 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(217): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2496-2720G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769347 | ||||||
| chr3:14769653
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(212): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2496-2414G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769653 | ||||||
| chr3:14769751
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(96): Show | 102 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(99): Show |
intron_variant | MODIFIER | c.2496-2316G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769751 | ||||||
| chr3:14769870
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(219): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2496-2197A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769870 | ||||||
| chr3:14769936
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2496-2131A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769936 | ||||||
| chr3:14769937
|
A | AGAAT | 3 | a0001c0001t0001g0027a0001c0001t0004g0126a0003c0003t0001g0200 | 3 | HG03209.hp2 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496-2127_2496-212 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14769937 | |||||
| chr3:14769941
|
A | AGAAT | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(16): Show | 19 | HG01168.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2496-2122_2496-211 others(8): Show |
C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 14769941 | |||||
| chr3:14769941
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0004g0126a0003c0003t0001g0200 | 3 | HG03209.hp2 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496-2126A>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769941 | ||||||
| chr3:14769955
|
A | G | 16 | a0001c0001t0001g0027a0001c0001t0001g0113a0001c0001t0001g0114others(13): Show | 16 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2496-2112A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769955 | ||||||
| chr3:14769980
|
C | T | 1 | a0004c0005t0001g0296 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2496-2087C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14769980 | ||||||
| chr3:14770007
|
C | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(3): Show | 6 | HG01168.hp1 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2496-2060C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770007 | ||||||
| chr3:14770038
|
C | T | 38 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0057others(35): Show | 38 | HG01106.hp2 HG01192.hp2 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.2496-2029C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770038 | ||||||
| chr3:14770121
|
T | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0113others(14): Show | 17 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2496-1946T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770121 | ||||||
| chr3:14770219
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2496-1848T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770219 | ||||||
| chr3:14770275
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2496-1792G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770275 | ||||||
| chr3:14770290
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2496-1777C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770290 | ||||||
| chr3:14770347
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2496-1720G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770347 | ||||||
| chr3:14770389
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(198): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.2496-1678C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770389 | ||||||
| chr3:14770494
|
C | T | 10 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2496-1573C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770494 | ||||||
| chr3:14770499
|
A | G | 17 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0113others(14): Show | 17 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2496-1568A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770499 | ||||||
| chr3:14770534
|
C | T | 36 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0270others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.2496-1533C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770534 | ||||||
| chr3:14770611
|
G | A | 78 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0270others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2496-1456G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770611 | ||||||
| chr3:14770661
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0351others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2496-1406A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770661 | ||||||
| chr3:14770953
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(197): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.2496-1114G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14770953 | ||||||
| chr3:14771151
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0004g0123others(1): Show | 4 | HG01168.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2496-916G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771151 | ||||||
| chr3:14771155
|
C | A | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2496-912C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771155 | ||||||
| chr3:14771159
|
G | A | 78 | a0001c0001t0001g0250a0001c0001t0001g0255a0001c0001t0001g0270others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2496-908G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771159 | ||||||
| chr3:14771210
|
G | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0113others(14): Show | 17 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2496-857G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771210 | ||||||
| chr3:14771221
|
G | T | 1 | a0013c0014t0001g0194 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2496-846G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771221 | ||||||
| chr3:14771250
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2496-817G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771250 | ||||||
| chr3:14771330
|
C | T | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2496-737C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771330 | ||||||
| chr3:14771331
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2496-736G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771331 | ||||||
| chr3:14771425
|
G | T | 1 | a0013c0014t0001g0194 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2496-642G>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771425 | ||||||
| chr3:14771495
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0030 | 4 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496-572T>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771495 | ||||||
| chr3:14771643
|
C | A | 1 | a0001c0001t0004g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2496-424C>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771643 | ||||||
| chr3:14771653
|
A | G | 1 | a0006c0006t0001g0173 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2496-414A>G | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771653 | ||||||
| chr3:14771669
|
C | T | 38 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0056others(35): Show | 38 | HG01106.hp2 HG01192.hp2 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.2496-398C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771669 | ||||||
| chr3:14771762
|
CT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(27): Show | 32 | HG01081.hp2 HG01168.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.2496-304delT | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 15/16 | chr3 | 14771762 | ||||||
| chr3:14772318
|
G | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.2630+117G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/16 | chr3 | 14772318 | ||||||
| chr3:14772522
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0030 | 4 | HG01081.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2631-269C>T | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/16 | chr3 | 14772522 | ||||||
| chr3:14772636
|
G | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(22): Show | 25 | HG01168.hp1 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2631-155G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/16 | chr3 | 14772636 | ||||||
| chr3:14772649
|
G | A | 48 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0258others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.2631-142G>A | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/16 | chr3 | 14772649 | ||||||
| chr3:14772701
|
G | C | 1 | a0013c0014t0001g0194 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2631-90G>C | C3orf20 | ENSG00000131379.10 | transcript | ENST00000253697.8 | protein_coding | 16/16 | chr3 | 14772701 |