Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 441326 |
|---|---|
| ensemblid | ENSG00000285913.1 |
| hgncid | 32266 |
| symbol | FAM90A18 |
| name | family with sequence similarity 90 member A18 |
| refseq_nuc | NM_001164451.1 |
| refseq_prot | NP_001157923.1 |
| ensembl_nuc | ENST00000647769.1 |
| ensembl_prot | ENSP00000497429.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 7723091 |
| end | 7726101 |
| strand | + |
| ver | v1.2 |
| region | chr8:7723091-7726101 |
| region5000 | chr8:7718091-7731101 |
| regionname0 | FAM90A18_chr8_7723091_7726101 |
| regionname5000 | FAM90A18_chr8_7718091_7731101 |
| 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 | 0/0 | 464 | 4 | 2 | 0 | 0 | 1 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0002 | 0/0 | 464 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0003 | 0/0 | 464 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0004 | 0/0 | 464 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0005 | 0/0 | 464 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0006 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0007 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0008 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0009 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0010 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0011 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0012 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0013 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0014 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0015 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0016 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0017 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0018 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0019 | 0/0 | 465 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0020 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0021 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0022 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0023 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0024 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0025 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0026 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0027 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0028 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0029 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0030 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0031 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1395 | 3 | 1 | 1 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0002 | 0/0 | 1395 | 3 | 1 | 0 | 0 | 1 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0003 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0004 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0005 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0006 | 0/0 | 1395 | 2 | 0 | 1 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0007 | 0/0 | 1395 | 2 | 0 | 0 | 0 | 1 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0008 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0009 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0010 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0011 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0012 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0013 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0014 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0015 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0016 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0017 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0018 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0019 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0020 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0021 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0022 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0023 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0024 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0025 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0026 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0027 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0028 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0029 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0030 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0031 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0032 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| c0033 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| 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 |
|---|
| 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 | 4 | 4 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0002 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0004 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1395 | 3 | 1 | 0 | 0 | 1 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0001c0017 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0002c0003 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0002c0031 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0003c0001 | 0/0 | 1395 | 3 | 1 | 1 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0004c0007 | 0/0 | 1395 | 2 | 0 | 0 | 0 | 1 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0005c0006 | 0/0 | 1395 | 2 | 0 | 1 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0006c0005 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0007c0008 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0008c0004 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0009c0010 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0010c0009 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0011c0015 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0012c0026 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0013c0018 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0014c0024 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0015c0025 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0016c0023 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0017c0022 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0018c0020 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0019c0019 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0020c0021 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0021c0016 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0022c0027 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0023c0028 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0024c0030 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0025c0029 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0026c0032 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0027c0014 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0028c0013 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0029c0033 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0030c0012 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0031c0011 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0000 | 0/0 | 1395 | 3 | 1 | 0 | 0 | 1 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0001c0017t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0002c0003t0000 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0002c0031t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0003c0001t0000 | 0/0 | 1395 | 3 | 1 | 1 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0004c0007t0000 | 0/0 | 1395 | 2 | 0 | 0 | 0 | 1 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0005c0006t0000 | 0/0 | 1395 | 2 | 0 | 1 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0006c0005t0000 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0007c0008t0000 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0008c0004t0000 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0009c0010t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0010c0009t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0011c0015t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0012c0026t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0013c0018t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0014c0024t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0015c0025t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0016c0023t0000 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0017c0022t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0018c0020t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0019c0019t0000 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0020c0021t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0021c0016t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0022c0027t0000 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0023c0028t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0024c0030t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0025c0029t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0026c0032t0000 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0027c0014t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0028c0013t0000 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0029c0033t0000 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0030c0012t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| a0031c0011t0000 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | copy fasta | chr8 | 7718091 | 7731101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0000g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0001c0002t0000g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0001c0017t0000g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0002c0003t0000g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0002c0031t0000g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0003c0001t0000g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0003c0001t0000g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0004c0007t0000g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0004c0007t0000g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0005c0006t0000g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0005c0006t0000g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0006c0005t0000g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0006c0005t0000g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0007c0008t0000g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0007c0008t0000g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0008c0004t0000g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0008c0004t0000g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0009c0010t0000g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0010c0009t0000g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0011c0015t0000g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0012c0026t0000g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0013c0018t0000g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0014c0024t0000g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0015c0025t0000g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0016c0023t0000g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0017c0022t0000g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0018c0020t0000g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0019c0019t0000g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0020c0021t0000g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0021c0016t0000g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0022c0027t0000g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0023c0028t0000g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0024c0030t0000g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0025c0029t0000g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0026c0032t0000g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0027c0014t0000g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0028c0013t0000g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0029c0033t0000g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0030c0012t0000g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| a0031c0011t0000g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0000 | g0005 | EUR | GBR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG00099 | hp2 | a0004 | c0007 | t0000 | g0021 | EUR | GBR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG00558 | hp1 | a0022 | c0027 | t0000 | g0002 | EAS | CHS | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG00558 | hp2 | a0028 | c0013 | t0000 | g0028 | EAS | CHS | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG00738 | hp1 | a0009 | c0010 | t0000 | g0003 | AMR | PUR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG00738 | hp2 | a0017 | c0022 | t0000 | g0003 | AMR | PUR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01071 | hp1 | a0010 | c0009 | t0000 | g0025 | AMR | PUR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01071 | hp2 | a0012 | c0026 | t0000 | g0004 | AMR | PUR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01243 | hp1 | a0023 | c0028 | t0000 | g0006 | AMR | PUR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01243 | hp2 | a0027 | c0014 | t0000 | g0011 | AMR | PUR | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01258 | hp1 | a0029 | c0033 | t0000 | g0009 | AMR | CLM | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01258 | hp2 | a0003 | c0001 | t0000 | g0003 | AMR | CLM | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01934 | hp1 | a0005 | c0006 | t0000 | g0027 | AMR | PEL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG01934 | hp2 | a0021 | c0016 | t0000 | g0022 | AMR | PEL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02132 | hp1 | a0016 | c0023 | t0000 | g0007 | EAS | KHV | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02132 | hp2 | a0005 | c0006 | t0000 | g0024 | EAS | KHV | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02145 | hp1 | a0018 | c0020 | t0000 | g0002 | AFR | ACB | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02145 | hp2 | a0003 | c0001 | t0000 | g0023 | AFR | ACB | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02622 | hp1 | a0008 | c0004 | t0000 | g0014 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02622 | hp2 | a0031 | c0011 | t0000 | g0012 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02630 | hp1 | a0024 | c0030 | t0000 | g0001 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02630 | hp2 | a0020 | c0021 | t0000 | g0002 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02647 | hp1 | a0011 | c0015 | t0000 | g0020 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02647 | hp2 | a0001 | c0017 | t0000 | g0030 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02895 | hp1 | a0002 | c0003 | t0000 | g0001 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02895 | hp2 | a0025 | c0029 | t0000 | g0017 | AFR | GWD | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03209 | hp1 | a0006 | c0005 | t0000 | g0002 | AFR | MSL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03209 | hp2 | a0002 | c0031 | t0000 | g0006 | AFR | MSL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03453 | hp1 | a0030 | c0012 | t0000 | g0010 | AFR | MSL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03453 | hp2 | a0013 | c0018 | t0000 | g0004 | AFR | MSL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03486 | hp1 | a0015 | c0025 | t0000 | g0026 | AFR | MSL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03486 | hp2 | a0019 | c0019 | t0000 | g0008 | AFR | MSL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03704 | hp1 | a0026 | c0032 | t0000 | g0019 | SAS | PJL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03704 | hp2 | a0001 | c0002 | t0000 | g0004 | SAS | PJL | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03831 | hp1 | a0004 | c0007 | t0000 | g0007 | SAS | BEB | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG03831 | hp2 | a0003 | c0001 | t0000 | g0003 | SAS | BEB | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| NA18522 | hp1 | a0006 | c0005 | t0000 | g0018 | AFR | YRI | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| NA18522 | hp2 | a0008 | c0004 | t0000 | g0013 | AFR | YRI | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| NA19030 | hp1 | a0002 | c0003 | t0000 | g0001 | AFR | LWK | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| NA19030 | hp2 | a0007 | c0008 | t0000 | g0016 | AFR | LWK | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| NA19043 | hp1 | a0007 | c0008 | t0000 | g0015 | AFR | LWK | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| NA19043 | hp2 | a0014 | c0024 | t0000 | g0029 | AFR | LWK | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02486 | hp1 | a0002 | c0003 | t0000 | g0001 | AFR | ACB | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| HG02486 | hp2 | a0001 | c0002 | t0000 | g0005 | AFR | ACB | FAM90A18_chr8_7718091_7731101 | FAM90A18 | chr8 | 7718091 | 7731101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7723161
|
G | A | 3 | a0003a0009a0010 | 5 | HG00738.hp1 HG01071.hp1 HG01258.hp2 others(2): Show |
missense_variant | MODERATE | c.71G>A | p.Arg24Gln | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/4 | 71/1395 | 71/1395 | 24/464 | chr8 | 7723161 | ||
| chr8:7723179
|
C | G | 3 | a0003a0009a0010 | 5 | HG00738.hp1 HG01071.hp1 HG01258.hp2 others(2): Show |
missense_variant | MODERATE | c.89C>G | p.Pro30Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/4 | 89/1395 | 89/1395 | 30/464 | chr8 | 7723179 | ||
| chr8:7723183
|
G | C | 3 | a0008a0030a0031 | 4 | HG02622.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.93G>C | p.Arg31Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/4 | 93/1395 | 93/1395 | 31/464 | chr8 | 7723183 | ||
| chr8:7723184
|
G | T | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.94G>T | p.Ala32Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/4 | 94/1395 | 94/1395 | 32/464 | chr8 | 7723184 | ||
| chr8:7723191
|
C | T | 1 | a0008 | 2 | HG02622.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.101C>T | p.Pro34Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/4 | 101/1395 | 101/1395 | 34/464 | chr8 | 7723191 | ||
| chr8:7723732
|
T | C | 1 | a0028 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.148T>C | p.Phe50Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/4 | 148/1395 | 148/1395 | 50/464 | chr8 | 7723732 | ||
| chr8:7723757
|
G | C | 1 | a0027 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.173G>C | p.Arg58Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/4 | 173/1395 | 173/1395 | 58/464 | chr8 | 7723757 | ||
| chr8:7723795
|
G | T | 1 | a0026 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.211G>T | p.Ala71Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/4 | 211/1395 | 211/1395 | 71/464 | chr8 | 7723795 | ||
| chr8:7723850
|
T | C | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.266T>C | p.Val89Ala | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/4 | 266/1395 | 266/1395 | 89/464 | chr8 | 7723850 | ||
| chr8:7723850
|
T | G | 21 | a0001a0003a0004others(18): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(26): Show |
missense_variant | MODERATE | c.266T>G | p.Val89Gly | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/4 | 266/1395 | 266/1395 | 89/464 | chr8 | 7723850 | ||
| chr8:7723856
|
C | G | 2 | a0008a0031 | 3 | HG02622.hp1 HG02622.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.272C>G | p.Ala91Gly | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/4 | 272/1395 | 272/1395 | 91/464 | chr8 | 7723856 | ||
| chr8:7724457
|
T | C | 1 | a0022 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.415T>C | p.Ser139Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/4 | 415/1395 | 415/1395 | 139/464 | chr8 | 7724457 | ||
| chr8:7724465
|
T | G | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.423T>G | p.Asp141Glu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/4 | 423/1395 | 423/1395 | 141/464 | chr8 | 7724465 | ||
| chr8:7724466
|
C | T | 21 | a0001a0003a0004others(18): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(26): Show |
missense_variant | MODERATE | c.424C>T | p.His142Tyr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/4 | 424/1395 | 424/1395 | 142/464 | chr8 | 7724466 | ||
| chr8:7725170
|
C | G | 2 | a0012a0027 | 2 | HG01071.hp2 HG01243.hp2 |
missense_variant | MODERATE | c.464C>G | p.Thr155Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 464/1395 | 464/1395 | 155/464 | chr8 | 7725170 | ||
| chr8:7725187
|
G | T | 20 | a0001a0003a0004others(17): Show | 28 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(25): Show |
missense_variant | MODERATE | c.481G>T | p.Val161Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 481/1395 | 481/1395 | 161/464 | chr8 | 7725187 | ||
| chr8:7725196
|
G | A | 4 | a0001a0012a0013others(1): Show | 7 | HG00099.hp1 HG01071.hp2 HG01243.hp2 others(4): Show |
missense_variant | MODERATE | c.490G>A | p.Val164Ile | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 490/1395 | 490/1395 | 164/464 | chr8 | 7725196 | ||
| chr8:7725202
|
G | A | 5 | a0006a0018a0019others(2): Show | 6 | HG00558.hp1 HG02145.hp1 HG02630.hp2 others(3): Show |
missense_variant | MODERATE | c.496G>A | p.Ala166Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 496/1395 | 496/1395 | 166/464 | chr8 | 7725202 | ||
| chr8:7725206
|
A | T | 1 | a0026 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.500A>T | p.Asp167Val | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 500/1395 | 500/1395 | 167/464 | chr8 | 7725206 | ||
| chr8:7725217
|
G | A | 21 | a0001a0003a0004others(18): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(26): Show |
missense_variant | MODERATE | c.511G>A | p.Ala171Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 511/1395 | 511/1395 | 171/464 | chr8 | 7725217 | ||
| chr8:7725221
|
A | C | 20 | a0001a0003a0004others(17): Show | 28 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(25): Show |
missense_variant | MODERATE | c.515A>C | p.Glu172Ala | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 515/1395 | 515/1395 | 172/464 | chr8 | 7725221 | ||
| chr8:7725238
|
T | A | 2 | a0003a0010 | 4 | HG01071.hp1 HG01258.hp2 HG02145.hp2 others(1): Show |
missense_variant | MODERATE | c.532T>A | p.Ser178Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 532/1395 | 532/1395 | 178/464 | chr8 | 7725238 | ||
| chr8:7725336
|
G | C | 4 | a0008a0021a0023others(1): Show | 5 | HG01243.hp1 HG01258.hp1 HG01934.hp2 others(2): Show |
missense_variant | MODERATE | c.630G>C | p.Met210Ile | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 630/1395 | 630/1395 | 210/464 | chr8 | 7725336 | ||
| chr8:7725349
|
G | T | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.643G>T | p.Val215Phe | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 643/1395 | 643/1395 | 215/464 | chr8 | 7725349 | ||
| chr8:7725365
|
G | C | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.659G>C | p.Arg220Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 659/1395 | 659/1395 | 220/464 | chr8 | 7725365 | ||
| chr8:7725398
|
G | T | 1 | a0028 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.692G>T | p.Ser231Ile | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 692/1395 | 692/1395 | 231/464 | chr8 | 7725398 | ||
| chr8:7725400
|
A | C | 24 | a0001a0003a0004others(21): Show | 34 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(31): Show |
missense_variant | MODERATE | c.694A>C | p.Ser232Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 694/1395 | 694/1395 | 232/464 | chr8 | 7725400 | ||
| chr8:7725458
|
T | C | 4 | a0001a0012a0013others(1): Show | 7 | HG00099.hp1 HG01071.hp2 HG01243.hp2 others(4): Show |
missense_variant | MODERATE | c.752T>C | p.Leu251Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 752/1395 | 752/1395 | 251/464 | chr8 | 7725458 | ||
| chr8:7725467
|
C | T | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.761C>T | p.Ala254Val | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 761/1395 | 761/1395 | 254/464 | chr8 | 7725467 | ||
| chr8:7725478
|
G | A | 3 | a0016a0017a0021 | 3 | HG00738.hp2 HG01934.hp2 HG02132.hp1 |
missense_variant | MODERATE | c.772G>A | p.Ala258Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 772/1395 | 772/1395 | 258/464 | chr8 | 7725478 | ||
| chr8:7725502
|
A | T | 6 | a0006a0018a0019others(3): Show | 7 | HG00558.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
missense_variant | MODERATE | c.796A>T | p.Thr266Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 796/1395 | 796/1395 | 266/464 | chr8 | 7725502 | ||
| chr8:7725509
|
A | T | 4 | a0001a0012a0013others(1): Show | 7 | HG00099.hp1 HG01071.hp2 HG01243.hp2 others(4): Show |
missense_variant | MODERATE | c.803A>T | p.Gln268Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 803/1395 | 803/1395 | 268/464 | chr8 | 7725509 | ||
| chr8:7725520
|
C | A | 2 | a0025a0030 | 2 | HG02895.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.814C>A | p.Pro272Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 814/1395 | 814/1395 | 272/464 | chr8 | 7725520 | ||
| chr8:7725615
|
A | C | 30 | a0001a0002a0003others(27): Show | 43 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(40): Show |
missense_variant | MODERATE | c.909A>C | p.Lys303Asn | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 909/1395 | 909/1395 | 303/464 | chr8 | 7725615 | ||
| chr8:7725629
|
C | T | 1 | a0013 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.923C>T | p.Pro308Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 923/1395 | 923/1395 | 308/464 | chr8 | 7725629 | ||
| chr8:7725682
|
G | C | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.976G>C | p.Gly326Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 976/1395 | 976/1395 | 326/464 | chr8 | 7725682 | ||
| chr8:7725689
|
C | T | 1 | a0011 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.983C>T | p.Pro328Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 983/1395 | 983/1395 | 328/464 | chr8 | 7725689 | ||
| chr8:7725692
|
G | A | 30 | a0001a0002a0003others(27): Show | 43 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(40): Show |
missense_variant | MODERATE | c.986G>A | p.Gly329Glu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 986/1395 | 986/1395 | 329/464 | chr8 | 7725692 | ||
| chr8:7725730
|
C | A | 1 | a0011 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1024C>A | p.Pro342Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1024/1395 | 1024/1395 | 342/464 | chr8 | 7725730 | ||
| chr8:7725787
|
T | C | 30 | a0001a0002a0003others(27): Show | 43 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(40): Show |
missense_variant | MODERATE | c.1081T>C | p.Trp361Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1081/1395 | 1081/1395 | 361/464 | chr8 | 7725787 | ||
| chr8:7725797
|
C | G | 1 | a0020 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1091C>G | p.Pro364Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1091/1395 | 1091/1395 | 364/464 | chr8 | 7725797 | ||
| chr8:7725806
|
C | G | 7 | a0003a0004a0005others(4): Show | 11 | HG00099.hp2 HG01071.hp1 HG01258.hp2 others(8): Show |
missense_variant | MODERATE | c.1100C>G | p.Thr367Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1100/1395 | 1100/1395 | 367/464 | chr8 | 7725806 | ||
| chr8:7725830
|
C | A | 1 | a0012 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1124C>A | p.Ala375Asp | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1124/1395 | 1124/1395 | 375/464 | chr8 | 7725830 | ||
| chr8:7725850
|
T | C | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.1144T>C | p.Ser382Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1144/1395 | 1144/1395 | 382/464 | chr8 | 7725850 | ||
| chr8:7725853
|
G | A | 2 | a0016a0017 | 2 | HG00738.hp2 HG02132.hp1 |
missense_variant | MODERATE | c.1147G>A | p.Ala383Thr | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1147/1395 | 1147/1395 | 383/464 | chr8 | 7725853 | ||
| chr8:7725859
|
A | G | 1 | a0029 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.1153A>G | p.Ser385Gly | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1153/1395 | 1153/1395 | 385/464 | chr8 | 7725859 | ||
| chr8:7725971
|
C | T | 2 | a0018a0019 | 2 | HG02145.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.1265C>T | p.Ala422Val | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1265/1395 | 1265/1395 | 422/464 | chr8 | 7725971 | ||
| chr8:7725989
|
C | G | 1 | a0015 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1283C>G | p.Pro428Arg | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1283/1395 | 1283/1395 | 428/464 | chr8 | 7725989 | ||
| chr8:7726052
|
A | G | 1 | a0014 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1346A>G | p.Asp449Gly | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1346/1395 | 1346/1395 | 449/464 | chr8 | 7726052 | ||
| chr8:7726079
|
A | ACAGCGAT others(6): Show |
1 | a0019 | 1 | HG03486.hp2 | frameshift_variant&stop_gained | HIGH | c.1375_1387dupAGCGAT others(7): Show |
p.Leu463fs | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1388/1395 | 1388/1395 | 463/464 | INFO_REALIGN_3_PRIME | chr8 | 7726079 | |
| chr8:7726088
|
C | T | 2 | a0003a0004 | 5 | HG00099.hp2 HG01258.hp2 HG02145.hp2 others(2): Show |
missense_variant | MODERATE | c.1382C>T | p.Ser461Phe | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1382/1395 | 1382/1395 | 461/464 | chr8 | 7726088 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7723168
|
C | A | 1 | a0031c0011 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.78C>A | p.Ala26Ala | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/4 | 78/1395 | 78/1395 | 26/464 | chr8 | 7723168 | ||
| chr8:7724456
|
G | A | 24 | a0001c0002a0001c0017a0003c0001others(21): Show | 31 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(28): Show |
synonymous_variant | LOW | c.414G>A | p.Glu138Glu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/4 | 414/1395 | 414/1395 | 138/464 | chr8 | 7724456 | ||
| chr8:7725213
|
A | G | 1 | a0021c0016 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.507A>G | p.Ser169Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 507/1395 | 507/1395 | 169/464 | chr8 | 7725213 | ||
| chr8:7725213
|
A | T | 1 | a0026c0032 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.507A>T | p.Ser169Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 507/1395 | 507/1395 | 169/464 | chr8 | 7725213 | ||
| chr8:7725390
|
G | A | 1 | a0026c0032 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.684G>A | p.Pro228Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 684/1395 | 684/1395 | 228/464 | chr8 | 7725390 | ||
| chr8:7725405
|
C | T | 2 | a0011c0015a0029c0033 | 2 | HG01258.hp1 HG02647.hp1 |
synonymous_variant | LOW | c.699C>T | p.Pro233Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 699/1395 | 699/1395 | 233/464 | chr8 | 7725405 | ||
| chr8:7725453
|
C | A | 5 | a0001c0002a0001c0017a0012c0026others(2): Show | 7 | HG00099.hp1 HG01071.hp2 HG01243.hp2 others(4): Show |
synonymous_variant | LOW | c.747C>A | p.Gly249Gly | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 747/1395 | 747/1395 | 249/464 | chr8 | 7725453 | ||
| chr8:7725453
|
C | T | 6 | a0006c0005a0018c0020a0019c0019others(3): Show | 7 | HG00558.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.747C>T | p.Gly249Gly | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 747/1395 | 747/1395 | 249/464 | chr8 | 7725453 | ||
| chr8:7725498
|
G | T | 6 | a0006c0005a0018c0020a0019c0019others(3): Show | 7 | HG00558.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.792G>T | p.Ala264Ala | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 792/1395 | 792/1395 | 264/464 | chr8 | 7725498 | ||
| chr8:7725507
|
G | A | 17 | a0001c0002a0001c0017a0003c0001others(14): Show | 23 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(20): Show |
synonymous_variant | LOW | c.801G>A | p.Ser267Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 801/1395 | 801/1395 | 267/464 | chr8 | 7725507 | ||
| chr8:7725507
|
G | T | 6 | a0006c0005a0018c0020a0019c0019others(3): Show | 7 | HG00558.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.801G>T | p.Ser267Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 801/1395 | 801/1395 | 267/464 | chr8 | 7725507 | ||
| chr8:7725546
|
A | C | 1 | a0002c0031 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.840A>C | p.Leu280Leu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 840/1395 | 840/1395 | 280/464 | chr8 | 7725546 | ||
| chr8:7725798
|
G | A | 1 | a0014c0024 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1092G>A | p.Pro364Pro | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1092/1395 | 1092/1395 | 364/464 | chr8 | 7725798 | ||
| chr8:7725909
|
C | T | 1 | a0013c0018 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1203C>T | p.Asn401Asn | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1203/1395 | 1203/1395 | 401/464 | chr8 | 7725909 | ||
| chr8:7725936
|
G | C | 1 | a0029c0033 | 1 | HG01258.hp1 | synonymous_variant | LOW | c.1230G>C | p.Ala410Ala | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1230/1395 | 1230/1395 | 410/464 | chr8 | 7725936 | ||
| chr8:7725987
|
C | T | 4 | a0001c0002a0012c0026a0018c0020others(1): Show | 6 | HG00099.hp1 HG01071.hp2 HG02145.hp1 others(3): Show |
synonymous_variant | LOW | c.1281C>T | p.Ser427Ser | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1281/1395 | 1281/1395 | 427/464 | chr8 | 7725987 | ||
| chr8:7726011
|
G | A | 1 | a0021c0016 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.1305G>A | p.Glu435Glu | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 4/4 | 1305/1395 | 1305/1395 | 435/464 | chr8 | 7726011 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7723220
|
C | G | 15 | a0001c0017t0000g0030a0003c0001t0000g0003a0003c0001t0000g0023others(12): Show | 16 | HG00099.hp2 HG00558.hp2 HG00738.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.123+7C>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723220 | ||||||
| chr8:7723244
|
G | T | 1 | a0001c0017t0000g0030 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.123+31G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723244 | ||||||
| chr8:7723248
|
T | G | 1 | a0019c0019t0000g0008 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+35T>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723248 | ||||||
| chr8:7723270
|
G | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.123+57G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723270 | ||||||
| chr8:7723272
|
G | C | 2 | a0001c0017t0000g0030a0004c0007t0000g0021 | 2 | HG00099.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.123+59G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723272 | ||||||
| chr8:7723369
|
C | T | 1 | a0014c0024t0000g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+156C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723369 | ||||||
| chr8:7723378
|
G | A | 1 | a0021c0016t0000g0022 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.123+165G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723378 | ||||||
| chr8:7723406
|
G | T | 1 | a0011c0015t0000g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.123+193G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723406 | ||||||
| chr8:7723429
|
A | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.123+216A>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723429 | ||||||
| chr8:7723448
|
T | A | 1 | a0003c0001t0000g0023 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.123+235T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723448 | ||||||
| chr8:7723526
|
C | A | 21 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(18): Show | 23 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-182C>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723526 | ||||||
| chr8:7723529
|
T | A | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.124-179T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723529 | ||||||
| chr8:7723529
|
T | C | 1 | a0030c0012t0000g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124-179T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723529 | ||||||
| chr8:7723551
|
T | C | 10 | a0001c0002t0000g0004a0001c0017t0000g0030a0003c0001t0000g0003others(7): Show | 11 | HG00738.hp1 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-157T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723551 | ||||||
| chr8:7723553
|
C | T | 27 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(24): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.124-155C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723553 | ||||||
| chr8:7723556
|
G | A | 2 | a0001c0002t0000g0005a0031c0011t0000g0012 | 3 | HG00099.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.124-152G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723556 | ||||||
| chr8:7723559
|
C | G | 8 | a0001c0017t0000g0030a0004c0007t0000g0007a0005c0006t0000g0027others(5): Show | 8 | HG00558.hp2 HG01243.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-149C>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723559 | ||||||
| chr8:7723566
|
G | A | 26 | a0001c0002t0000g0004a0001c0017t0000g0030a0003c0001t0000g0003others(23): Show | 27 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.124-142G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723566 | ||||||
| chr8:7723601
|
T | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.124-107T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723601 | ||||||
| chr8:7723604
|
A | T | 1 | a0028c0013t0000g0028 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.124-104A>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723604 | ||||||
| chr8:7723631
|
T | A | 2 | a0008c0004t0000g0013a0008c0004t0000g0014 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124-77T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723631 | ||||||
| chr8:7723704
|
A | G | 15 | a0001c0017t0000g0030a0003c0001t0000g0003a0003c0001t0000g0023others(12): Show | 16 | HG00099.hp2 HG00558.hp2 HG00738.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.124-4A>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 1/3 | chr8 | 7723704 | ||||||
| chr8:7723938
|
T | A | 4 | a0001c0002t0000g0004a0012c0026t0000g0004a0013c0018t0000g0004others(1): Show | 4 | HG01071.hp2 HG03453.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+31T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723938 | ||||||
| chr8:7723939
|
A | G | 6 | a0001c0002t0000g0004a0001c0002t0000g0005a0011c0015t0000g0020others(3): Show | 7 | HG00099.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+32A>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723939 | ||||||
| chr8:7723942
|
A | G | 29 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(26): Show | 31 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.323+35A>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723942 | ||||||
| chr8:7723944
|
G | A | 28 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(25): Show | 30 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.323+37G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723944 | ||||||
| chr8:7723946
|
T | G | 16 | a0001c0017t0000g0030a0003c0001t0000g0003a0003c0001t0000g0023others(13): Show | 17 | HG00099.hp2 HG00558.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.323+39T>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723946 | ||||||
| chr8:7723953
|
T | C | 15 | a0001c0017t0000g0030a0003c0001t0000g0003a0003c0001t0000g0023others(12): Show | 16 | HG00099.hp2 HG00558.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.323+46T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723953 | ||||||
| chr8:7723959
|
C | G | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.323+52C>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7723959 | ||||||
| chr8:7724016
|
G | A | 28 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(25): Show | 30 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.323+109G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724016 | ||||||
| chr8:7724055
|
G | A | 1 | a0028c0013t0000g0028 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.323+148G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724055 | ||||||
| chr8:7724109
|
C | T | 1 | a0010c0009t0000g0025 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.323+202C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724109 | ||||||
| chr8:7724134
|
A | G | 1 | a0011c0015t0000g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.323+227A>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724134 | ||||||
| chr8:7724141
|
G | C | 27 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(24): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.324-225G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724141 | ||||||
| chr8:7724178
|
T | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.324-188T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724178 | ||||||
| chr8:7724179
|
C | G | 29 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(26): Show | 31 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.324-187C>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724179 | ||||||
| chr8:7724216
|
G | C | 2 | a0005c0006t0000g0024a0015c0025t0000g0026 | 2 | HG02132.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324-150G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724216 | ||||||
| chr8:7724288
|
G | T | 1 | a0025c0029t0000g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.324-78G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724288 | ||||||
| chr8:7724307
|
C | G | 1 | a0030c0012t0000g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324-59C>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724307 | ||||||
| chr8:7724307
|
C | T | 32 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(29): Show | 34 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.324-59C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724307 | ||||||
| chr8:7724341
|
G | C | 9 | a0006c0005t0000g0002a0006c0005t0000g0018a0011c0015t0000g0020others(6): Show | 9 | HG00558.hp1 HG01258.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.324-25G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724341 | ||||||
| chr8:7724352
|
T | C | 29 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(26): Show | 31 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.324-14T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 2/3 | chr8 | 7724352 | ||||||
| chr8:7724476
|
T | C | 27 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(24): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(26): Show |
splice_donor_variant&intron_variant | HIGH | c.432+2T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724476 | ||||||
| chr8:7724501
|
C | T | 27 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(24): Show | 29 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.432+27C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724501 | ||||||
| chr8:7724551
|
C | T | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.432+77C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724551 | ||||||
| chr8:7724606
|
G | A | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.432+132G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724606 | ||||||
| chr8:7724634
|
C | T | 1 | a0027c0014t0000g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.432+160C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724634 | ||||||
| chr8:7724648
|
G | C | 26 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(23): Show | 28 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.432+174G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724648 | ||||||
| chr8:7724655
|
T | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+181T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724655 | ||||||
| chr8:7724658
|
T | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+184T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724658 | ||||||
| chr8:7724659
|
T | C | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+185T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724659 | ||||||
| chr8:7724665
|
G | T | 24 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(21): Show | 26 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.432+191G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724665 | ||||||
| chr8:7724666
|
G | C | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+192G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724666 | ||||||
| chr8:7724668
|
T | G | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+194T>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724668 | ||||||
| chr8:7724685
|
A | C | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+211A>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724685 | ||||||
| chr8:7724741
|
G | T | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+267G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724741 | ||||||
| chr8:7724754
|
G | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+280G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724754 | ||||||
| chr8:7724755
|
A | T | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+281A>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724755 | ||||||
| chr8:7724756
|
G | T | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+282G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724756 | ||||||
| chr8:7724760
|
G | T | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+286G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724760 | ||||||
| chr8:7724762
|
G | T | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.432+288G>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724762 | ||||||
| chr8:7724769
|
A | C | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+295A>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724769 | ||||||
| chr8:7724771
|
G | A | 7 | a0001c0002t0000g0004a0001c0002t0000g0005a0004c0007t0000g0021others(4): Show | 8 | HG00099.hp1 HG00099.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+297G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724771 | ||||||
| chr8:7724775
|
A | T | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+301A>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724775 | ||||||
| chr8:7724780
|
T | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+306T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724780 | ||||||
| chr8:7724782
|
T | G | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+308T>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724782 | ||||||
| chr8:7724783
|
G | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+309G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724783 | ||||||
| chr8:7724784
|
T | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+310T>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724784 | ||||||
| chr8:7724785
|
T | G | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+311T>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724785 | ||||||
| chr8:7724786
|
C | A | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+312C>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724786 | ||||||
| chr8:7724788
|
G | C | 1 | a0004c0007t0000g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.432+314G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724788 | ||||||
| chr8:7724817
|
G | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.433-322G>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724817 | ||||||
| chr8:7724828
|
C | T | 22 | a0001c0002t0000g0004a0001c0002t0000g0005a0001c0017t0000g0030others(19): Show | 24 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.433-311C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724828 | ||||||
| chr8:7724922
|
G | A | 1 | a0021c0016t0000g0022 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.433-217G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724922 | ||||||
| chr8:7724932
|
C | G | 1 | a0006c0005t0000g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.433-207C>G | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724932 | ||||||
| chr8:7724953
|
C | T | 1 | a0030c0012t0000g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.433-186C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724953 | ||||||
| chr8:7724957
|
T | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.433-182T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724957 | ||||||
| chr8:7724965
|
G | A | 1 | a0030c0012t0000g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.433-174G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7724965 | ||||||
| chr8:7725058
|
A | C | 8 | a0006c0005t0000g0002a0006c0005t0000g0018a0007c0008t0000g0016others(5): Show | 8 | HG00558.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-81A>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7725058 | ||||||
| chr8:7725073
|
G | A | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.433-66G>A | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7725073 | ||||||
| chr8:7725076
|
C | T | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.433-63C>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7725076 | ||||||
| chr8:7725101
|
T | C | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.433-38T>C | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7725101 | ||||||
| chr8:7725103
|
A | T | 1 | a0029c0033t0000g0009 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.433-36A>T | FAM90A18 | ENSG00000285913.1 | transcript | ENST00000647769.1 | protein_coding | 3/3 | chr8 | 7725103 |