| geneid | 222584 |
|---|---|
| ensemblid | ENSG00000168143.9 |
| hgncid | 21357 |
| symbol | FAM83B |
| name | family with sequence similarity 83 member B |
| refseq_nuc | NM_001010872.3 |
| refseq_prot | NP_001010872.1 |
| ensembl_nuc | ENST00000306858.8 |
| ensembl_prot | ENSP00000304078.7 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 54846771 |
| end | 54945099 |
| strand | + |
| ver | v1.2 |
| region | chr6:54846771-54945099 |
| region5000 | chr6:54841771-54950099 |
| regionname0 | FAM83B_chr6_54846771_54945099 |
| regionname5000 | FAM83B_chr6_54841771_54950099 |
| 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 | 1011 | 174 | 19 | 43 | 78 | 3 | 29 | 58 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002 | 0/0 | 1011 | 60 | 37 | 11 | 5 | 3 | 4 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003 | 0/0 | 1011 | 22 | 22 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004 | 0/0 | 1011 | 10 | 8 | 1 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0005 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0006 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0007 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0008 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0009 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3036 | 92 | 10 | 23 | 41 | 2 | 15 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0002 | 0/1 | 3036 | 66 | 6 | 20 | 26 | 1 | 12 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0003 | 0/0 | 3036 | 23 | 13 | 6 | 0 | 1 | 3 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0004 | 0/0 | 3036 | 13 | 8 | 0 | 4 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0005 | 0/0 | 3036 | 10 | 9 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0006 | 0/0 | 3036 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0007 | 0/0 | 3036 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0008 | 0/0 | 3036 | 8 | 0 | 0 | 7 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0009 | 0/0 | 3036 | 6 | 3 | 3 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0010 | 0/0 | 3036 | 5 | 2 | 2 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0011 | 0/0 | 3036 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0012 | 0/0 | 3036 | 3 | 2 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0013 | 0/0 | 3036 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0014 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0015 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0016 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0017 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0018 | 0/0 | 3036 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0019 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0020 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0021 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0022 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0023 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0024 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0025 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0026 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0027 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| c0028 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| 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 | 0/0 | 3209 | 69 | 1 | 12 | 41 | 2 | 13 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0002 | 1/1 | 3209 | 69 | 12 | 21 | 21 | 1 | 12 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0003 | 0/0 | 3210 | 29 | 17 | 6 | 1 | 1 | 4 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0004 | 0/0 | 3210 | 12 | 2 | 10 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0005 | 0/0 | 3209 | 11 | 1 | 0 | 9 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0006 | 0/0 | 3209 | 10 | 10 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0007 | 0/0 | 3209 | 10 | 10 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0008 | 0/0 | 3209 | 8 | 6 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0009 | 0/0 | 3209 | 6 | 2 | 2 | 0 | 2 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0010 | 0/0 | 3209 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0011 | 0/0 | 3344 | 5 | 2 | 3 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0012 | 0/0 | 3210 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0013 | 0/0 | 3370 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0014 | 0/0 | 3209 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0015 | 0/0 | 3209 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0016 | 0/0 | 3209 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0017 | 0/0 | 3209 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0018 | 0/0 | 3371 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0019 | 0/0 | 3376 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0020 | 0/0 | 3383 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0021 | 0/0 | 3209 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0022 | 0/0 | 3209 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0023 | 0/0 | 3209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0024 | 0/0 | 3209 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0025 | 0/0 | 3209 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0026 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0027 | 0/0 | 3209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0028 | 0/0 | 3209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0029 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0030 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0031 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0032 | 0/0 | 3380 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0033 | 0/0 | 3209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0034 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| t0035 | 0/0 | 3209 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3036 | 92 | 10 | 23 | 41 | 2 | 15 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0002 | 0/1 | 3036 | 66 | 6 | 20 | 26 | 1 | 12 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0008 | 0/0 | 3036 | 8 | 0 | 0 | 7 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0012 | 0/0 | 3036 | 3 | 2 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0013 | 0/0 | 3036 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0021 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0022 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0003 | 0/0 | 3036 | 23 | 13 | 6 | 0 | 1 | 3 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004 | 0/0 | 3036 | 13 | 8 | 0 | 4 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0005 | 0/0 | 3036 | 10 | 9 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0009 | 0/0 | 3036 | 6 | 3 | 3 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0010 | 0/0 | 3036 | 5 | 2 | 2 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0023 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0026 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0028 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0006 | 0/0 | 3036 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0007 | 0/0 | 3036 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0016 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0017 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0011 | 0/0 | 3036 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0014 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0018 | 0/0 | 3036 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0024 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0005c0015 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0006c0020 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0007c0025 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0008c0027 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0009c0019 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6244 | 65 | 1 | 12 | 38 | 2 | 12 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0002 | 1/0 | 6244 | 6 | 1 | 0 | 2 | 0 | 2 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0004 | 0/0 | 6245 | 12 | 2 | 10 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0010 | 0/0 | 6244 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0023 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0024 | 0/0 | 6244 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0034 | 0/0 | 6245 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0001t0035 | 0/0 | 6244 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0002t0001 | 0/0 | 6244 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0002t0002 | 0/1 | 6244 | 57 | 6 | 20 | 19 | 1 | 10 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0002t0014 | 0/0 | 6244 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0002t0015 | 0/0 | 6244 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0002t0021 | 0/0 | 6244 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0008t0005 | 0/0 | 6244 | 7 | 0 | 0 | 6 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0008t0025 | 0/0 | 6244 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0012t0001 | 0/0 | 6244 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0012t0002 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0012t0008 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0013t0005 | 0/0 | 6244 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0021t0005 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0001c0022t0001 | 0/0 | 6244 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0003t0003 | 0/0 | 6245 | 21 | 11 | 6 | 0 | 1 | 3 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0003t0016 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0003t0026 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004t0003 | 0/0 | 6245 | 4 | 3 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004t0012 | 0/0 | 6245 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004t0020 | 0/0 | 6418 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004t0030 | 0/0 | 6393 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004t0032 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0004t0033 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0005t0003 | 0/0 | 6245 | 3 | 2 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0005t0013 | 0/0 | 6405 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0005t0018 | 0/0 | 6406 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0005t0019 | 0/0 | 6411 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0009t0011 | 0/0 | 6379 | 5 | 2 | 3 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0009t0029 | 0/0 | 6380 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0010t0009 | 0/0 | 6244 | 5 | 2 | 2 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0023t0031 | 0/0 | 6401 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0026t0016 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0002c0028t0009 | 0/0 | 6244 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0006t0007 | 0/0 | 6244 | 9 | 9 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0007t0006 | 0/0 | 6244 | 8 | 8 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0007t0028 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0016t0007 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0016t0027 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0003c0017t0006 | 0/0 | 6244 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0011t0008 | 0/0 | 6244 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0014t0002 | 0/0 | 6244 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0018t0008 | 0/0 | 6244 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0004c0024t0008 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0005c0015t0017 | 0/0 | 6244 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0006c0020t0002 | 0/0 | 6244 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0007c0025t0003 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0008c0027t0002 | 0/0 | 6244 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| a0009c0019t0022 | 0/0 | 6244 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | copy fasta | chr6 | 54841771 | 54950099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0023g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0024g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0034g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0001t0035g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0014g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0014g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0014g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0015g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0015g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0021g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0002t0021g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0008t0025g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0012t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0012t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0012t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0013t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0013t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0013t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0021t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0001c0022t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0016g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0003t0026g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0030g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0032g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0004t0033g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0013g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0018g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0018g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0019g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0005t0019g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0011g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0009t0029g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0010t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0023t0031g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0026t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0002c0028t0009g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0006t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0007t0028g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0016t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0016t0027g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0017t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0003c0017t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0011t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0014t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0014t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0014t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0018t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0018t0008g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0004c0024t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0005c0015t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0005c0015t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0006c0020t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0007c0025t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0008c0027t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| a0009c0019t0022g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0010 | t0009 | g0006 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0213 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00323 | hp1 | a0002 | c0028 | t0009 | g0189 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00438 | hp2 | a0002 | c0004 | t0012 | g0177 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00544 | hp1 | a0001 | c0008 | t0005 | g0015 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | CHS | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00642 | hp2 | a0002 | c0010 | t0009 | g0007 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00735 | hp1 | a0001 | c0001 | t0035 | g0103 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0117 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG00741 | hp2 | a0002 | c0009 | t0011 | g0164 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0136 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0161 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01167 | hp2 | a0002 | c0009 | t0011 | g0250 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0123 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01169 | hp1 | a0002 | c0009 | t0011 | g0248 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01169 | hp2 | a0002 | c0003 | t0003 | g0108 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01175 | hp2 | a0004 | c0018 | t0008 | g0141 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01192 | hp2 | a0002 | c0003 | t0003 | g0135 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0102 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0203 | AMR | PUR | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0227 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01361 | hp1 | a0002 | c0010 | t0009 | g0025 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0111 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01884 | hp1 | a0002 | c0010 | t0009 | g0150 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01884 | hp2 | a0002 | c0005 | t0013 | g0202 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01891 | hp1 | a0002 | c0005 | t0013 | g0226 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01891 | hp2 | a0002 | c0009 | t0029 | g0244 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01934 | hp1 | a0002 | c0003 | t0003 | g0124 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0151 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01978 | hp1 | a0008 | c0027 | t0002 | g0182 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02027 | hp1 | a0002 | c0004 | t0012 | g0180 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02132 | hp2 | a0002 | c0004 | t0012 | g0219 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02145 | hp1 | a0004 | c0011 | t0008 | g0263 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02165 | hp2 | a0001 | c0002 | t0021 | g0198 | EAS | CDX | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0201 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02257 | hp2 | a0004 | c0011 | t0008 | g0257 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02258 | hp1 | a0002 | c0005 | t0003 | g0016 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02258 | hp2 | a0002 | c0005 | t0003 | g0121 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02280 | hp1 | a0003 | c0006 | t0007 | g0167 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02280 | hp2 | a0002 | c0003 | t0003 | g0125 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0072 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0146 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02451 | hp2 | a0003 | c0007 | t0006 | g0261 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0256 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02572 | hp2 | a0002 | c0023 | t0031 | g0236 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02602 | hp1 | a0001 | c0012 | t0001 | g0004 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02615 | hp1 | a0003 | c0007 | t0028 | g0235 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02615 | hp2 | a0001 | c0012 | t0008 | g0170 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02622 | hp1 | a0002 | c0004 | t0030 | g0245 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02630 | hp1 | a0002 | c0004 | t0020 | g0107 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02630 | hp2 | a0002 | c0003 | t0003 | g0129 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0131 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02683 | hp2 | a0004 | c0018 | t0008 | g0156 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02717 | hp1 | a0003 | c0006 | t0007 | g0252 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02717 | hp2 | a0003 | c0006 | t0007 | g0175 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02723 | hp1 | a0003 | c0007 | t0006 | g0240 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02809 | hp1 | a0004 | c0024 | t0008 | g0092 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0140 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02818 | hp1 | a0002 | c0003 | t0003 | g0128 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02818 | hp2 | a0006 | c0020 | t0002 | g0031 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02895 | hp1 | a0002 | c0005 | t0013 | g0147 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02895 | hp2 | a0003 | c0007 | t0006 | g0262 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02896 | hp1 | a0002 | c0005 | t0019 | g0242 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02896 | hp2 | a0004 | c0014 | t0002 | g0143 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02897 | hp1 | a0003 | c0007 | t0006 | g0169 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02897 | hp2 | a0004 | c0014 | t0002 | g0144 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02922 | hp1 | a0005 | c0015 | t0017 | g0148 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02922 | hp2 | a0004 | c0014 | t0002 | g0260 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02965 | hp1 | a0003 | c0007 | t0006 | g0255 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02965 | hp2 | a0002 | c0010 | t0009 | g0149 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02970 | hp1 | a0003 | c0006 | t0007 | g0171 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02976 | hp1 | a0003 | c0006 | t0007 | g0246 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02976 | hp2 | a0004 | c0011 | t0008 | g0258 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03041 | hp1 | a0003 | c0007 | t0006 | g0237 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03041 | hp2 | a0002 | c0003 | t0003 | g0137 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03098 | hp1 | a0002 | c0005 | t0019 | g0241 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03098 | hp2 | a0003 | c0006 | t0007 | g0166 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03130 | hp1 | a0002 | c0004 | t0003 | g0154 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03139 | hp1 | a0003 | c0017 | t0006 | g0200 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03139 | hp2 | a0002 | c0003 | t0026 | g0168 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03195 | hp1 | a0001 | c0021 | t0005 | g0118 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03195 | hp2 | a0003 | c0007 | t0006 | g0239 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03225 | hp1 | a0002 | c0004 | t0033 | g0152 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03225 | hp2 | a0002 | c0003 | t0003 | g0120 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03453 | hp1 | a0002 | c0003 | t0003 | g0001 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03453 | hp2 | a0003 | c0006 | t0007 | g0174 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03486 | hp1 | a0002 | c0009 | t0011 | g0247 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03486 | hp2 | a0002 | c0003 | t0016 | g0254 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03490 | hp1 | a0001 | c0001 | t0024 | g0075 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0209 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03491 | hp2 | a0001 | c0008 | t0005 | g0017 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03516 | hp1 | a0003 | c0016 | t0027 | g0003 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03516 | hp2 | a0001 | c0001 | t0023 | g0087 | AFR | ESN | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03540 | hp1 | a0002 | c0003 | t0003 | g0109 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03540 | hp2 | a0002 | c0026 | t0016 | g0264 | AFR | GWD | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03579 | hp2 | a0001 | c0012 | t0002 | g0127 | AFR | MSL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03654 | hp1 | a0001 | c0002 | t0015 | g0008 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03669 | hp1 | a0002 | c0004 | t0003 | g0142 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0132 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0190 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG03927 | hp2 | a0002 | c0003 | t0003 | g0133 | SAS | BEB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04204 | hp1 | a0001 | c0002 | t0015 | g0005 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0176 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18522 | hp1 | a0003 | c0016 | t0007 | g0002 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18522 | hp2 | a0002 | c0004 | t0020 | g0134 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18747 | hp1 | a0002 | c0004 | t0012 | g0220 | EAS | CHB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18906 | hp1 | a0002 | c0005 | t0018 | g0225 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18906 | hp2 | a0002 | c0004 | t0003 | g0155 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18943 | hp1 | a0001 | c0008 | t0005 | g0122 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18963 | hp2 | a0001 | c0008 | t0005 | g0014 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18964 | hp1 | a0001 | c0008 | t0005 | g0012 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18965 | hp2 | a0001 | c0013 | t0005 | g0270 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18966 | hp1 | a0001 | c0008 | t0005 | g0013 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18968 | hp2 | a0001 | c0022 | t0001 | g0055 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18980 | hp2 | a0001 | c0013 | t0005 | g0079 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18981 | hp2 | a0001 | c0002 | t0021 | g0159 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18983 | hp2 | a0009 | c0019 | t0022 | g0053 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18985 | hp2 | a0001 | c0013 | t0005 | g0267 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19010 | hp1 | a0001 | c0002 | t0014 | g0269 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19012 | hp1 | a0001 | c0002 | t0014 | g0266 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19043 | hp1 | a0002 | c0009 | t0011 | g0249 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19043 | hp2 | a0004 | c0011 | t0008 | g0259 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19055 | hp1 | a0001 | c0001 | t0034 | g0157 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19056 | hp2 | a0001 | c0008 | t0005 | g0011 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19070 | hp1 | a0002 | c0005 | t0003 | g0224 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19080 | hp2 | a0001 | c0002 | t0014 | g0268 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19089 | hp2 | a0001 | c0008 | t0025 | g0018 | EAS | JPT | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19240 | hp1 | a0005 | c0015 | t0017 | g0019 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0165 | AFR | YRI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20129 | hp1 | a0002 | c0004 | t0032 | g0138 | AFR | ASW | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | ASW | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0126 | EUR | TSI | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0207 | SAS | GIH | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | CLM | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02109 | hp1 | a0003 | c0006 | t0007 | g0173 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02109 | hp2 | a0002 | c0004 | t0003 | g0243 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02486 | hp1 | a0007 | c0025 | t0003 | g0105 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02559 | hp1 | a0003 | c0017 | t0006 | g0153 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG02559 | hp2 | a0002 | c0005 | t0018 | g0130 | AFR | ACB | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG06807 | hp1 | a0003 | c0006 | t0007 | g0172 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| HG06807 | hp2 | a0002 | c0003 | t0003 | g0251 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | USA | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA21309 | hp1 | a0003 | c0007 | t0006 | g0238 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| NA21309 | hp2 | a0002 | c0003 | t0003 | g0253 | AFR | LWK | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0113 | REF | REF | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0026 | REF | REF | FAM83B_chr6_54841771_54950099 | FAM83B | chr6 | 54841771 | 54950099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54870280
|
G | A | 1 | a0009 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.34G>A | p.Asp12Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 150/6244 | 34/3036 | 12/1011 | chr6 | 54870280 | ||
| chr6:54870665
|
G | A | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.419G>A | p.Arg140Gln | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 535/6244 | 419/3036 | 140/1011 | chr6 | 54870665 | ||
| chr6:54927521
|
G | A | 1 | a0005 | 2 | HG02922.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.623G>A | p.Arg208Gln | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/5 | 739/6244 | 623/3036 | 208/1011 | chr6 | 54927521 | ||
| chr6:54927622
|
G | A | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.724G>A | p.Gly242Ser | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/5 | 840/6244 | 724/3036 | 242/1011 | chr6 | 54927622 | ||
| chr6:54940200
|
A | G | 1 | a0004 | 10 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
missense_variant | MODERATE | c.1229A>G | p.Asn410Ser | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1345/6244 | 1229/3036 | 410/1011 | chr6 | 54940200 | ||
| chr6:54940276
|
C | G | 2 | a0003a0005 | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
missense_variant | MODERATE | c.1305C>G | p.Ser435Arg | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1421/6244 | 1305/3036 | 435/1011 | chr6 | 54940276 | ||
| chr6:54940839
|
C | G | 1 | a0007 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1868C>G | p.Ala623Gly | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1984/6244 | 1868/3036 | 623/1011 | chr6 | 54940839 | ||
| chr6:54940890
|
A | C | 4 | a0002a0003a0005others(1): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
missense_variant | MODERATE | c.1919A>C | p.Lys640Thr | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2035/6244 | 1919/3036 | 640/1011 | chr6 | 54940890 | ||
| chr6:54941691
|
C | A | 4 | a0002a0003a0005others(1): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
missense_variant | MODERATE | c.2720C>A | p.Thr907Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2836/6244 | 2720/3036 | 907/1011 | chr6 | 54941691 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54870324
|
A | G | 8 | a0001c0002a0001c0013a0002c0005others(5): Show | 97 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(94): Show |
synonymous_variant | LOW | c.78A>G | p.Glu26Glu | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 194/6244 | 78/3036 | 26/1011 | chr6 | 54870324 | ||
| chr6:54870546
|
A | G | 4 | a0001c0012a0002c0003a0002c0026others(1): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
synonymous_variant | LOW | c.300A>G | p.Glu100Glu | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 416/6244 | 300/3036 | 100/1011 | chr6 | 54870546 | ||
| chr6:54870585
|
C | T | 2 | a0002c0009a0003c0006 | 15 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
synonymous_variant | LOW | c.339C>T | p.Pro113Pro | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/5 | 455/6244 | 339/3036 | 113/1011 | chr6 | 54870585 | ||
| chr6:54926424
|
C | T | 1 | a0002c0026 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.498C>T | p.Ile166Ile | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/5 | 614/6244 | 498/3036 | 166/1011 | chr6 | 54926424 | ||
| chr6:54940000
|
T | C | 3 | a0001c0008a0001c0013a0001c0021 | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
synonymous_variant | LOW | c.1029T>C | p.Tyr343Tyr | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1145/6244 | 1029/3036 | 343/1011 | chr6 | 54940000 | ||
| chr6:54940081
|
C | T | 3 | a0004c0011a0004c0018a0004c0024 | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
synonymous_variant | LOW | c.1110C>T | p.Asn370Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1226/6244 | 1110/3036 | 370/1011 | chr6 | 54940081 | ||
| chr6:54940144
|
G | A | 2 | a0004c0011a0004c0024 | 5 | HG02145.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1173G>A | p.Gly391Gly | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1289/6244 | 1173/3036 | 391/1011 | chr6 | 54940144 | ||
| chr6:54940468
|
C | T | 1 | a0002c0023 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1497C>T | p.Ser499Ser | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1613/6244 | 1497/3036 | 499/1011 | chr6 | 54940468 | ||
| chr6:54941041
|
G | A | 1 | a0001c0022 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.2070G>A | p.Arg690Arg | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2186/6244 | 2070/3036 | 690/1011 | chr6 | 54941041 | ||
| chr6:54941581
|
A | G | 2 | a0002c0010a0002c0028 | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
synonymous_variant | LOW | c.2610A>G | p.Pro870Pro | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2726/6244 | 2610/3036 | 870/1011 | chr6 | 54941581 | ||
| chr6:54941788
|
G | A | 1 | a0001c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2817G>A | p.Pro939Pro | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2933/6244 | 2817/3036 | 939/1011 | chr6 | 54941788 | ||
| chr6:54941827
|
C | T | 2 | a0003c0007a0003c0017 | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
synonymous_variant | LOW | c.2856C>T | p.Asn952Asn | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2972/6244 | 2856/3036 | 952/1011 | chr6 | 54941827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54942208
|
T | G | 47 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(44): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*201T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 201 | chr6 | 54942208 | |||||
| chr6:54942367
|
C | T | 1 | a0001c0001t0035 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 360 | chr6 | 54942367 | |||||
| chr6:54942565
|
A | AT | 2 | a0001c0001t0004a0001c0001t0034 | 13 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*567dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 568 | INFO_REALIGN_3_PRIME | chr6 | 54942565 | ||||
| chr6:54942644
|
A | C | 1 | a0002c0004t0033 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*637A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 637 | chr6 | 54942644 | |||||
| chr6:54942715
|
A | AGGCTGCT others(128): Show |
1 | a0002c0009t0011 | 5 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(129): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(129): Show |
1 | a0002c0009t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(130): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(142): Show |
1 | a0002c0004t0030 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(143): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(150): Show |
1 | a0002c0023t0031 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(151): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(154): Show |
1 | a0002c0005t0013 | 3 | HG01884.hp2 HG01891.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(155): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(155): Show |
1 | a0002c0005t0018 | 2 | HG02559.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(156): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(160): Show |
1 | a0002c0005t0019 | 2 | HG02896.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(161): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(164): Show |
1 | a0002c0004t0032 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(165): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942715
|
A | AGGCTGCT others(167): Show |
1 | a0002c0004t0020 | 2 | HG02630.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*723_*724insTTTTTT others(168): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 724 | INFO_REALIGN_3_PRIME | chr6 | 54942715 | ||||
| chr6:54942783
|
C | T | 7 | a0003c0006t0007a0003c0007t0006a0003c0007t0028others(4): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*776C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 776 | chr6 | 54942783 | |||||
| chr6:54942824
|
T | A | 11 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(8): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*817T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 817 | chr6 | 54942824 | |||||
| chr6:54942856
|
A | T | 1 | a0001c0001t0024 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 849 | chr6 | 54942856 | |||||
| chr6:54942890
|
C | T | 9 | a0002c0004t0020a0002c0004t0030a0002c0004t0032others(6): Show | 18 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*883C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 883 | chr6 | 54942890 | |||||
| chr6:54942904
|
C | CT | 6 | a0002c0003t0003a0002c0003t0026a0002c0004t0003others(3): Show | 34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*908dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 909 | INFO_REALIGN_3_PRIME | chr6 | 54942904 | ||||
| chr6:54942944
|
C | T | 1 | a0003c0007t0028 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 937 | chr6 | 54942944 | |||||
| chr6:54942948
|
G | C | 1 | a0009c0019t0022 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*941G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 941 | chr6 | 54942948 | |||||
| chr6:54943153
|
G | A | 1 | a0001c0002t0015 | 2 | HG03654.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1146G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1146 | chr6 | 54943153 | |||||
| chr6:54943190
|
C | A | 1 | a0001c0001t0010 | 5 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1183C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1183 | chr6 | 54943190 | |||||
| chr6:54943231
|
T | C | 47 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(44): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1224T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1224 | chr6 | 54943231 | |||||
| chr6:54943232
|
G | A | 1 | a0005c0015t0017 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1225G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1225 | chr6 | 54943232 | |||||
| chr6:54943244
|
T | C | 1 | a0001c0002t0021 | 2 | HG02165.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1237T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1237 | chr6 | 54943244 | |||||
| chr6:54943268
|
G | T | 1 | a0001c0001t0034 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1261 | chr6 | 54943268 | |||||
| chr6:54943540
|
T | C | 1 | a0001c0002t0014 | 3 | NA19010.hp1 NA19012.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1533T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1533 | chr6 | 54943540 | |||||
| chr6:54943544
|
G | A | 27 | a0002c0003t0003a0002c0003t0016a0002c0003t0026others(24): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1537G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1537 | chr6 | 54943544 | |||||
| chr6:54943742
|
A | G | 27 | a0002c0003t0003a0002c0003t0016a0002c0003t0026others(24): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1735A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1735 | chr6 | 54943742 | |||||
| chr6:54943763
|
A | G | 1 | a0003c0016t0027 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1756 | chr6 | 54943763 | |||||
| chr6:54943870
|
C | G | 3 | a0003c0006t0007a0003c0016t0007a0003c0016t0027 | 11 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1863C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1863 | chr6 | 54943870 | |||||
| chr6:54943918
|
T | C | 1 | a0001c0008t0025 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1911T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 1911 | chr6 | 54943918 | |||||
| chr6:54944053
|
G | A | 4 | a0001c0008t0005a0001c0008t0025a0001c0013t0005others(1): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2046G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2046 | chr6 | 54944053 | |||||
| chr6:54944090
|
C | T | 1 | a0002c0003t0026 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2083C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2083 | chr6 | 54944090 | |||||
| chr6:54944101
|
A | G | 3 | a0003c0007t0006a0003c0007t0028a0003c0017t0006 | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2094A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2094 | chr6 | 54944101 | |||||
| chr6:54944163
|
T | A | 2 | a0002c0010t0009a0002c0028t0009 | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2156T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2156 | chr6 | 54944163 | |||||
| chr6:54944166
|
G | T | 4 | a0003c0006t0007a0003c0016t0007a0003c0016t0027others(1): Show | 13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2159G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2159 | chr6 | 54944166 | |||||
| chr6:54944304
|
C | A | 20 | a0002c0003t0003a0002c0003t0016a0002c0003t0026others(17): Show | 61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2297C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2297 | chr6 | 54944304 | |||||
| chr6:54944486
|
A | G | 1 | a0002c0004t0012 | 4 | HG00438.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2479A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2479 | chr6 | 54944486 | |||||
| chr6:54944656
|
C | T | 2 | a0002c0010t0009a0002c0028t0009 | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2649C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2649 | chr6 | 54944656 | |||||
| chr6:54944695
|
C | T | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(17): Show | 113 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2688C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2688 | chr6 | 54944695 | |||||
| chr6:54944789
|
C | T | 6 | a0002c0003t0003a0002c0003t0026a0002c0004t0003others(3): Show | 34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2782 | chr6 | 54944789 | |||||
| chr6:54944791
|
T | A | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(17): Show | 113 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2784T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2784 | chr6 | 54944791 | |||||
| chr6:54944966
|
C | T | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2959C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 5/5 | 2959 | chr6 | 54944966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:54846875
|
C | T | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+49C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846875 | ||||||
| chr6:54846906
|
A | G | 107 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(104): Show | 107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-61+80A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846906 | ||||||
| chr6:54846908
|
T | TG | 69 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0194others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-61+89dupG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54846908 | |||||
| chr6:54846908
|
T | TGGG | 21 | a0001c0002t0002g0256a0002c0003t0003g0251a0002c0003t0003g0253others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-61+87_-61+89dupGG others(1): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54846908 | |||||
| chr6:54846909
|
G | C | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+83G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846909 | ||||||
| chr6:54846916
|
C | G | 107 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(104): Show | 107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-61+90C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846916 | ||||||
| chr6:54846988
|
C | A | 6 | a0001c0001t0001g0009a0001c0002t0015g0005a0001c0002t0015g0008others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61+162C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54846988 | ||||||
| chr6:54847040
|
C | T | 5 | a0003c0006t0007g0171a0003c0006t0007g0172a0003c0006t0007g0173others(2): Show | 5 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61+214C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847040 | ||||||
| chr6:54847061
|
G | A | 16 | a0001c0001t0001g0010a0001c0002t0002g0265a0001c0002t0002g0271others(13): Show | 16 | HG00544.hp1 HG02015.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-61+235G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847061 | ||||||
| chr6:54847100
|
C | T | 9 | a0001c0001t0001g0010a0001c0008t0005g0011a0001c0008t0005g0012others(6): Show | 9 | HG00544.hp1 HG02258.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61+274C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847100 | ||||||
| chr6:54847193
|
C | T | 13 | a0001c0002t0002g0256a0001c0012t0008g0170a0002c0003t0016g0254others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-61+367C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847193 | ||||||
| chr6:54847214
|
GAGACCGC others(22): Show |
G | 9 | a0002c0004t0003g0243a0002c0005t0019g0241a0002c0005t0019g0242others(6): Show | 9 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-61+391_-61+419del others(29): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54847214 | |||||
| chr6:54847342
|
G | T | 1 | a0004c0018t0008g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-61+516G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847342 | ||||||
| chr6:54847391
|
G | T | 3 | a0002c0004t0003g0154a0002c0004t0003g0155a0003c0017t0006g0153 | 3 | HG02559.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-61+565G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847391 | ||||||
| chr6:54847429
|
CTG | C | 108 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(105): Show | 108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-61+607_-61+608del others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54847429 | |||||
| chr6:54847527
|
C | G | 2 | a0002c0003t0003g0253a0002c0003t0026g0168 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-61+701C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847527 | ||||||
| chr6:54847623
|
TG | T | 61 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(58): Show | 62 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.-61+798delG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847623 | ||||||
| chr6:54847624
|
G | C | 1 | a0005c0015t0017g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-61+798G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847624 | ||||||
| chr6:54847626
|
G | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(59): Show | 63 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-61+800G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847626 | ||||||
| chr6:54847731
|
A | G | 6 | a0001c0001t0001g0009a0001c0002t0015g0005a0001c0002t0015g0008others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61+905A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847731 | ||||||
| chr6:54847760
|
G | A | 107 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(104): Show | 107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-61+934G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847760 | ||||||
| chr6:54847873
|
A | G | 1 | a0002c0004t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-61+1047A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54847873 | ||||||
| chr6:54848092
|
T | G | 40 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0035g0103others(37): Show | 41 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-61+1266T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848092 | ||||||
| chr6:54848103
|
A | AG | 3 | a0001c0002t0002g0178a0001c0012t0001g0004a0002c0004t0012g0177 | 3 | HG00438.hp2 HG01109.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-61+1278dupG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54848103 | |||||
| chr6:54848105
|
T | G | 184 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0104others(181): Show | 185 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-61+1279T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848105 | ||||||
| chr6:54848106
|
G | C | 40 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0035g0103others(37): Show | 41 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.-61+1280G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848106 | ||||||
| chr6:54848111
|
T | G | 1 | a0001c0002t0001g0158 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-61+1285T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848111 | ||||||
| chr6:54848111
|
T | TG | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0010g0140others(6): Show | 9 | HG01243.hp1 HG02027.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61+1290dupG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54848111 | |||||
| chr6:54848172
|
T | G | 1 | a0008c0027t0002g0182 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-61+1346T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848172 | ||||||
| chr6:54848225
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-61+1399T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848225 | ||||||
| chr6:54848259
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+1433C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848259 | ||||||
| chr6:54848290
|
G | T | 10 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0255others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-61+1464G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848290 | ||||||
| chr6:54848699
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-61+1873A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848699 | ||||||
| chr6:54848902
|
T | A | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+2076T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54848902 | ||||||
| chr6:54849030
|
A | G | 62 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(59): Show | 63 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-61+2204A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849030 | ||||||
| chr6:54849104
|
C | T | 76 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(73): Show | 77 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-61+2278C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849104 | ||||||
| chr6:54849253
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-61+2427C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849253 | ||||||
| chr6:54849254
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-61+2428A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849254 | ||||||
| chr6:54849463
|
C | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(48): Show | 52 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-61+2637C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849463 | ||||||
| chr6:54849464
|
T | C | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-61+2638T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849464 | ||||||
| chr6:54849573
|
G | A | 2 | a0004c0018t0008g0141a0004c0018t0008g0156 | 2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-61+2747G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849573 | ||||||
| chr6:54849632
|
T | C | 8 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(5): Show | 8 | HG00544.hp1 HG02258.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+2806T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849632 | ||||||
| chr6:54849739
|
T | TAAGAGTG others(317): Show |
2 | a0002c0003t0003g0136a0002c0003t0003g0137 | 2 | HG01069.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(326): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849739
|
T | TAAGAGTG others(318): Show |
30 | a0001c0002t0002g0110a0001c0002t0002g0111a0001c0002t0002g0112others(27): Show | 31 | HG00735.hp2 HG01167.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(327): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849739
|
T | TAAGAGTG others(319): Show |
5 | a0001c0001t0001g0104a0001c0001t0001g0106a0002c0003t0003g0102others(2): Show | 5 | HG00741.hp1 HG01243.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(328): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849739
|
T | TAAGAGTG others(320): Show |
1 | a0001c0001t0035g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-61+2927_-61+2928i others(329): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849739
|
T | TAAGAGTG others(315): Show |
2 | a0002c0010t0009g0149a0002c0010t0009g0150 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-61+2927_-61+2928i others(324): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849739
|
T | TAAGAGTG others(318): Show |
1 | a0002c0004t0032g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-61+2927_-61+2928i others(327): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849739
|
T | TAAGAGTG others(320): Show |
1 | a0001c0002t0002g0139 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-61+2927_-61+2928i others(329): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54849739 | |||||
| chr6:54849837
|
T | G | 115 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-61+3011T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849837 | ||||||
| chr6:54849962
|
C | G | 42 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0035g0103others(39): Show | 43 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-61+3136C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849962 | ||||||
| chr6:54849975
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-61+3149C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54849975 | ||||||
| chr6:54850249
|
T | A | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+3423T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850249 | ||||||
| chr6:54850249
|
T | C | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+3423T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850249 | ||||||
| chr6:54850320
|
A | C | 1 | a0002c0003t0003g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-61+3494A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850320 | ||||||
| chr6:54850328
|
A | C | 119 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-61+3502A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850328 | ||||||
| chr6:54850389
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+3563C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850389 | ||||||
| chr6:54850402
|
T | C | 13 | a0001c0002t0002g0256a0001c0012t0008g0170a0002c0003t0016g0254others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-61+3576T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850402 | ||||||
| chr6:54850409
|
G | T | 1 | a0002c0004t0032g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-61+3583G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850409 | ||||||
| chr6:54850476
|
G | T | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+3650G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850476 | ||||||
| chr6:54850879
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-61+4053C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850879 | ||||||
| chr6:54850879
|
C | T | 1 | a0002c0004t0020g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-61+4053C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850879 | ||||||
| chr6:54850946
|
A | C | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+4120A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850946 | ||||||
| chr6:54850959
|
A | G | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-61+4133A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850959 | ||||||
| chr6:54850972
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-61+4146C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850972 | ||||||
| chr6:54850974
|
C | T | 2 | a0001c0001t0010g0145a0001c0001t0010g0146 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-61+4148C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850974 | ||||||
| chr6:54850989
|
G | T | 1 | a0001c0001t0010g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-61+4163G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54850989 | ||||||
| chr6:54851016
|
CA | C | 146 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0022others(143): Show | 147 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.-61+4212delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851016 | |||||
| chr6:54851016
|
CAA | C | 90 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(87): Show | 90 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-61+4211_-61+4212d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851016 | |||||
| chr6:54851016
|
CAAA | C | 19 | a0001c0002t0002g0256a0002c0003t0003g0165a0002c0003t0016g0254others(16): Show | 19 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-61+4210_-61+4212d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851016 | |||||
| chr6:54851038
|
A | C | 103 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-61+4212A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851038 | ||||||
| chr6:54851146
|
A | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-61+4320A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851146 | ||||||
| chr6:54851288
|
C | A | 2 | a0001c0002t0002g0184a0002c0028t0009g0189 | 2 | HG00323.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-61+4462C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851288 | ||||||
| chr6:54851386
|
C | T | 187 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(184): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-61+4560C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851386 | ||||||
| chr6:54851493
|
G | A | 2 | a0002c0010t0009g0149a0002c0010t0009g0150 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-61+4667G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851493 | ||||||
| chr6:54851647
|
G | GT | 93 | a0001c0001t0001g0021a0001c0001t0001g0094a0001c0001t0001g0096others(90): Show | 93 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-61+4839dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851647 | |||||
| chr6:54851647
|
G | GTT | 38 | a0001c0001t0001g0162a0001c0002t0001g0158a0001c0002t0001g0231others(35): Show | 38 | HG00741.hp2 HG01109.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.-61+4838_-61+4839d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851647 | |||||
| chr6:54851647
|
G | GTTT | 6 | a0001c0001t0010g0020a0001c0002t0002g0271a0001c0002t0014g0269others(3): Show | 6 | HG02015.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61+4837_-61+4839d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851647 | |||||
| chr6:54851710
|
A | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-61+4884A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851710 | ||||||
| chr6:54851714
|
C | G | 1 | a0001c0001t0004g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-61+4888C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851714 | ||||||
| chr6:54851737
|
T | C | 1 | a0002c0005t0013g0147 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-61+4911T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851737 | ||||||
| chr6:54851738
|
C | T | 1 | a0002c0005t0013g0147 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-61+4912C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851738 | ||||||
| chr6:54851748
|
T | C | 187 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(184): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-61+4922T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851748 | ||||||
| chr6:54851796
|
C | T | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+4970C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851796 | ||||||
| chr6:54851802
|
T | C | 9 | a0001c0002t0002g0110a0001c0002t0002g0111a0001c0002t0002g0112others(6): Show | 9 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61+4976T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851802 | ||||||
| chr6:54851809
|
G | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-61+4983G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851809 | ||||||
| chr6:54851839
|
G | A | 8 | a0001c0002t0002g0178a0001c0002t0002g0184a0001c0002t0002g0185others(5): Show | 8 | HG00323.hp1 HG01109.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+5013G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851839 | ||||||
| chr6:54851875
|
T | C | 112 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-61+5049T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851875 | ||||||
| chr6:54851886
|
A | G | 1 | a0001c0002t0002g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-61+5060A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851886 | ||||||
| chr6:54851927
|
G | A | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-61+5101G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851927 | ||||||
| chr6:54851942
|
C | T | 2 | a0001c0012t0008g0170a0002c0026t0016g0264 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-61+5116C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851942 | ||||||
| chr6:54851945
|
CCTAATTT others(134): Show |
C | 9 | a0001c0002t0002g0110a0001c0002t0002g0111a0001c0002t0002g0112others(6): Show | 9 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61+5121_-61+5261d others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54851945 | |||||
| chr6:54851975
|
G | A | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+5149G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54851975 | ||||||
| chr6:54852015
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-61+5189T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852015 | ||||||
| chr6:54852073
|
G | A | 8 | a0001c0002t0002g0119a0001c0021t0005g0118a0002c0003t0003g0102others(5): Show | 8 | HG01069.hp2 HG01243.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61+5247G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852073 | ||||||
| chr6:54852288
|
G | A | 23 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0035g0103others(20): Show | 24 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.-61+5462G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852288 | ||||||
| chr6:54852333
|
A | G | 112 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-61+5507A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852333 | ||||||
| chr6:54852336
|
A | G | 1 | a0004c0024t0008g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-61+5510A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852336 | ||||||
| chr6:54852409
|
T | G | 64 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+5583T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852409 | ||||||
| chr6:54852431
|
C | T | 66 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(63): Show | 67 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-61+5605C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852431 | ||||||
| chr6:54852586
|
G | A | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61+5760G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852586 | ||||||
| chr6:54852691
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | NA18943.hp2 NA18950.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-61+5865T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852691 | ||||||
| chr6:54852754
|
C | G | 14 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(11): Show | 14 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-61+5928C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852754 | ||||||
| chr6:54852899
|
T | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(55): Show | 59 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-61+6073T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852899 | ||||||
| chr6:54852938
|
A | AT | 167 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(164): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-61+6121dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54852938 | |||||
| chr6:54852938
|
A | ATT | 20 | a0001c0001t0010g0020a0001c0012t0008g0170a0002c0004t0003g0142others(17): Show | 20 | HG01175.hp2 HG02109.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.-61+6120_-61+6121d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54852938 | |||||
| chr6:54852969
|
ATTG | A | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+6149_-61+6151d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54852969 | |||||
| chr6:54852974
|
T | C | 113 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-61+6148T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852974 | ||||||
| chr6:54852991
|
C | T | 1 | a0001c0001t0035g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-61+6165C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54852991 | ||||||
| chr6:54853101
|
C | A | 1 | a0001c0012t0001g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-61+6275C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853101 | ||||||
| chr6:54853118
|
C | T | 29 | a0001c0002t0002g0256a0002c0003t0003g0165a0002c0003t0003g0251others(26): Show | 29 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.-61+6292C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853118 | ||||||
| chr6:54853195
|
A | G | 269 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(266): Show | 270 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-61+6369A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853195 | ||||||
| chr6:54853338
|
C | A | 178 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(175): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-61+6512C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853338 | ||||||
| chr6:54853380
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-61+6554G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853380 | ||||||
| chr6:54853508
|
A | C | 1 | a0001c0002t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-61+6682A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853508 | ||||||
| chr6:54853771
|
G | T | 2 | a0003c0007t0006g0169a0003c0007t0006g0262 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-61+6945G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853771 | ||||||
| chr6:54853795
|
T | C | 64 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+6969T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853795 | ||||||
| chr6:54853805
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-61+6979A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853805 | ||||||
| chr6:54853891
|
A | T | 178 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0106others(175): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-61+7065A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853891 | ||||||
| chr6:54853894
|
A | G | 3 | a0002c0003t0003g0165a0003c0006t0007g0166a0003c0006t0007g0167 | 3 | HG02280.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-61+7068A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54853894 | ||||||
| chr6:54854006
|
G | T | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+7180G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854006 | ||||||
| chr6:54854027
|
A | T | 11 | a0001c0002t0002g0256a0002c0003t0016g0254a0003c0007t0006g0169others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-61+7201A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854027 | ||||||
| chr6:54854047
|
G | A | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-61+7221G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854047 | ||||||
| chr6:54854238
|
A | C | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-61+7412A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854238 | ||||||
| chr6:54854336
|
G | A | 1 | a0001c0002t0002g0139 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-61+7510G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854336 | ||||||
| chr6:54854573
|
T | C | 1 | a0001c0002t0002g0196 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-61+7747T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854573 | ||||||
| chr6:54854687
|
T | C | 64 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+7861T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854687 | ||||||
| chr6:54854872
|
A | G | 23 | a0001c0002t0002g0256a0002c0003t0016g0254a0002c0004t0003g0154others(20): Show | 23 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-61+8046A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854872 | ||||||
| chr6:54854893
|
G | A | 64 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+8067G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54854893 | ||||||
| chr6:54855001
|
T | C | 1 | a0001c0002t0001g0158 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-61+8175T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855001 | ||||||
| chr6:54855122
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-61+8296G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855122 | ||||||
| chr6:54855194
|
T | C | 2 | a0002c0010t0009g0149a0002c0010t0009g0150 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-61+8368T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855194 | ||||||
| chr6:54855281
|
G | C | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+8455G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855281 | ||||||
| chr6:54855332
|
A | G | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+8506A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855332 | ||||||
| chr6:54855477
|
G | C | 83 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(80): Show | 83 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-61+8651G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855477 | ||||||
| chr6:54855481
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-61+8655A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855481 | ||||||
| chr6:54855645
|
G | A | 64 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+8819G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855645 | ||||||
| chr6:54855687
|
C | T | 64 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-61+8861C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855687 | ||||||
| chr6:54855776
|
C | T | 2 | a0003c0006t0007g0166a0003c0006t0007g0167 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-61+8950C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855776 | ||||||
| chr6:54855880
|
A | C | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+9054A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54855880 | ||||||
| chr6:54856236
|
C | T | 1 | a0001c0002t0002g0233 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-61+9410C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856236 | ||||||
| chr6:54856238
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-61+9412A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856238 | ||||||
| chr6:54856286
|
C | T | 33 | a0001c0012t0008g0170a0002c0003t0003g0165a0002c0003t0003g0251others(30): Show | 33 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.-61+9460C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856286 | ||||||
| chr6:54856461
|
T | A | 6 | a0001c0001t0001g0009a0001c0002t0015g0005a0001c0002t0015g0008others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61+9635T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856461 | ||||||
| chr6:54856579
|
ATTTC | A | 17 | a0002c0003t0003g0165a0002c0003t0003g0251a0002c0004t0030g0245others(14): Show | 17 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-61+9757_-61+9760d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54856579 | |||||
| chr6:54856683
|
G | A | 12 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(9): Show | 12 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-61+9857G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856683 | ||||||
| chr6:54856819
|
G | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0162a0001c0001t0001g0183others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-61+9993G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856819 | ||||||
| chr6:54856937
|
A | C | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-61+10111A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54856937 | ||||||
| chr6:54857022
|
C | T | 24 | a0001c0001t0001g0009a0001c0002t0015g0005a0001c0002t0015g0008others(21): Show | 24 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-61+10196C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857022 | ||||||
| chr6:54857141
|
G | A | 10 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(7): Show | 10 | HG00544.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-61+10315G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857141 | ||||||
| chr6:54857164
|
A | C | 2 | a0001c0001t0010g0145a0001c0001t0010g0146 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-61+10338A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857164 | ||||||
| chr6:54857215
|
A | G | 78 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0010g0020others(75): Show | 79 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.-61+10389A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857215 | ||||||
| chr6:54857309
|
G | A | 1 | a0001c0002t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-61+10483G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857309 | ||||||
| chr6:54857394
|
G | C | 1 | a0001c0002t0002g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-61+10568G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857394 | ||||||
| chr6:54857408
|
A | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+10582A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857408 | ||||||
| chr6:54857527
|
C | T | 10 | a0002c0003t0016g0254a0003c0007t0006g0169a0003c0007t0006g0255others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-61+10701C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857527 | ||||||
| chr6:54857726
|
T | C | 21 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(18): Show | 21 | HG02015.hp1 HG02109.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.-61+10900T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857726 | ||||||
| chr6:54857773
|
A | G | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61+10947A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857773 | ||||||
| chr6:54857813
|
C | T | 3 | a0001c0002t0002g0184a0001c0002t0002g0185a0002c0028t0009g0189 | 3 | HG00323.hp1 HG02293.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-61+10987C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857813 | ||||||
| chr6:54857838
|
T | C | 1 | a0001c0001t0010g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-61+11012T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857838 | ||||||
| chr6:54857959
|
G | A | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-61+11133G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54857959 | ||||||
| chr6:54858036
|
A | C | 1 | a0001c0002t0015g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-61+11210A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858036 | ||||||
| chr6:54858261
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18943.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-61+11435A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858261 | ||||||
| chr6:54858345
|
A | G | 1 | a0001c0001t0023g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-61+11519A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858345 | ||||||
| chr6:54858550
|
T | C | 2 | a0002c0004t0032g0138a0002c0005t0013g0147 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-60-11637T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858550 | ||||||
| chr6:54858556
|
TA | T | 14 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(11): Show | 14 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-60-11628delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54858556 | |||||
| chr6:54858577
|
C | T | 1 | a0002c0005t0003g0121 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-60-11610C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858577 | ||||||
| chr6:54858809
|
A | G | 7 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(4): Show | 7 | HG02015.hp1 NA18960.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-11378A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54858809 | ||||||
| chr6:54859012
|
G | A | 178 | a0001c0001t0001g0035a0001c0001t0001g0162a0001c0001t0001g0183others(175): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-60-11175G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859012 | ||||||
| chr6:54859047
|
G | A | 1 | a0001c0001t0010g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-60-11140G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859047 | ||||||
| chr6:54859047
|
G | C | 177 | a0001c0001t0001g0035a0001c0001t0001g0162a0001c0001t0001g0183others(174): Show | 178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-60-11140G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859047 | ||||||
| chr6:54859060
|
C | T | 1 | a0002c0005t0003g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-60-11127C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859060 | ||||||
| chr6:54859093
|
C | G | 1 | a0002c0003t0003g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-60-11094C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859093 | ||||||
| chr6:54859098
|
T | C | 16 | a0002c0004t0003g0142a0002c0010t0009g0006a0002c0010t0009g0007others(13): Show | 16 | HG00280.hp1 HG00642.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-60-11089T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859098 | ||||||
| chr6:54859154
|
G | A | 18 | a0002c0003t0003g0165a0002c0003t0003g0251a0002c0004t0030g0245others(15): Show | 18 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-60-11033G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859154 | ||||||
| chr6:54859176
|
C | T | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-60-11011C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859176 | ||||||
| chr6:54859189
|
G | A | 14 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(11): Show | 14 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-60-10998G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859189 | ||||||
| chr6:54859282
|
C | T | 12 | a0002c0004t0003g0142a0003c0007t0006g0169a0003c0007t0006g0255others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-10905C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859282 | ||||||
| chr6:54859376
|
T | C | 4 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0149others(1): Show | 4 | HG00280.hp1 HG00642.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-60-10811T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859376 | ||||||
| chr6:54859481
|
G | A | 1 | a0001c0002t0002g0223 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-60-10706G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859481 | ||||||
| chr6:54859607
|
A | G | 188 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(185): Show | 189 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-60-10580A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859607 | ||||||
| chr6:54859743
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01258.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-60-10444G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54859743 | ||||||
| chr6:54860043
|
T | TTG | 5 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0201others(2): Show | 5 | HG00280.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-10118_-60-1011 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | |||||
| chr6:54860043
|
TTG | T | 89 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(86): Show | 89 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-60-10118_-60-1011 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | |||||
| chr6:54860043
|
TTGTG | T | 135 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(132): Show | 136 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-60-10120_-60-1011 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | |||||
| chr6:54860043
|
TTGTGTG | T | 12 | a0003c0007t0006g0169a0003c0007t0006g0240a0003c0007t0006g0255others(9): Show | 12 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-10122_-60-1011 others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54860043 | |||||
| chr6:54860075
|
C | A | 10 | a0003c0007t0006g0169a0003c0007t0006g0240a0003c0007t0006g0255others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-60-10112C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860075 | ||||||
| chr6:54860446
|
G | A | 13 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(10): Show | 13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-60-9741G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860446 | ||||||
| chr6:54860872
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-60-9315C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860872 | ||||||
| chr6:54860882
|
T | C | 10 | a0003c0007t0006g0169a0003c0007t0006g0240a0003c0007t0006g0255others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-60-9305T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860882 | ||||||
| chr6:54860883
|
G | C | 1 | a0003c0007t0006g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-60-9304G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860883 | ||||||
| chr6:54860916
|
C | T | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-9271C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54860916 | ||||||
| chr6:54861131
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-60-9056A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861131 | ||||||
| chr6:54861380
|
C | G | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-8807C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861380 | ||||||
| chr6:54861503
|
GC | G | 3 | a0002c0005t0013g0147a0004c0014t0002g0143a0004c0014t0002g0144 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-8682delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54861503 | |||||
| chr6:54861505
|
C | G | 3 | a0002c0005t0013g0147a0004c0014t0002g0143a0004c0014t0002g0144 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-8682C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861505 | ||||||
| chr6:54861527
|
G | A | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-8660G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861527 | ||||||
| chr6:54861529
|
G | A | 50 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0131others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.-60-8658G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861529 | ||||||
| chr6:54861650
|
A | G | 7 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-8537A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861650 | ||||||
| chr6:54861687
|
C | T | 8 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(5): Show | 8 | HG00544.hp1 HG03491.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-60-8500C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861687 | ||||||
| chr6:54861745
|
G | A | 119 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(116): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-60-8442G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861745 | ||||||
| chr6:54861795
|
C | T | 2 | a0001c0012t0008g0170a0002c0026t0016g0264 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-60-8392C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861795 | ||||||
| chr6:54861869
|
C | T | 1 | a0002c0023t0031g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-60-8318C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54861869 | ||||||
| chr6:54862053
|
A | G | 121 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0035g0103others(118): Show | 122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-60-8134A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862053 | ||||||
| chr6:54862062
|
T | C | 1 | a0003c0006t0007g0173 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-60-8125T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862062 | ||||||
| chr6:54862071
|
C | T | 91 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(88): Show | 91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-60-8116C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862071 | ||||||
| chr6:54862110
|
C | T | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-8077C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862110 | ||||||
| chr6:54862111
|
G | A | 3 | a0001c0001t0001g0038a0002c0005t0019g0241a0002c0005t0019g0242 | 3 | HG02165.hp1 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-60-8076G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862111 | ||||||
| chr6:54862131
|
T | C | 1 | a0002c0004t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-60-8056T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862131 | ||||||
| chr6:54862181
|
G | A | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-8006G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862181 | ||||||
| chr6:54862261
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-60-7926G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862261 | ||||||
| chr6:54862277
|
A | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-60-7910A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862277 | ||||||
| chr6:54862387
|
C | T | 2 | a0001c0002t0002g0184a0002c0028t0009g0189 | 2 | HG00323.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-60-7800C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862387 | ||||||
| chr6:54862430
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-60-7757A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862430 | ||||||
| chr6:54862635
|
G | T | 8 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(5): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-60-7552G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862635 | ||||||
| chr6:54862756
|
T | C | 150 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(147): Show | 151 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.-60-7431T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862756 | ||||||
| chr6:54862798
|
C | A | 8 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(5): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-60-7389C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862798 | ||||||
| chr6:54862864
|
CA | C | 26 | a0001c0001t0001g0039a0001c0012t0001g0004a0001c0012t0002g0127others(23): Show | 27 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-60-7318delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54862864 | |||||
| chr6:54862869
|
A | C | 103 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(100): Show | 103 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-60-7318A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862869 | ||||||
| chr6:54862878
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-60-7309C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862878 | ||||||
| chr6:54862890
|
GA | G | 11 | a0001c0001t0001g0078a0001c0002t0002g0232a0001c0008t0005g0011others(8): Show | 11 | HG00544.hp1 HG01928.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.-60-7287delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54862890 | |||||
| chr6:54862933
|
A | T | 71 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-60-7254A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54862933 | ||||||
| chr6:54863017
|
C | T | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-7170C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863017 | ||||||
| chr6:54863053
|
C | T | 1 | a0001c0002t0002g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-60-7134C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863053 | ||||||
| chr6:54863206
|
C | A | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-6981C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863206 | ||||||
| chr6:54863219
|
G | T | 3 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0023t0031g0236 | 3 | HG02572.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-60-6968G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863219 | ||||||
| chr6:54863252
|
A | C | 1 | a0001c0002t0002g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-60-6935A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863252 | ||||||
| chr6:54863331
|
G | T | 92 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(89): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-60-6856G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863331 | ||||||
| chr6:54863388
|
A | C | 15 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(12): Show | 15 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-60-6799A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863388 | ||||||
| chr6:54863546
|
C | CCAA | 16 | a0001c0002t0002g0256a0002c0005t0013g0147a0002c0005t0013g0202others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-60-6639_-60-6637d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54863546 | |||||
| chr6:54863555
|
G | GACTTTTG others(19): Show |
124 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(121): Show | 125 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-60-6628_-60-6627i others(28): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54863555 | |||||
| chr6:54863991
|
C | T | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-6196C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54863991 | ||||||
| chr6:54864047
|
T | G | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-6140T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864047 | ||||||
| chr6:54864156
|
AT | A | 3 | a0002c0003t0003g0108a0002c0003t0003g0123a0002c0003t0003g0124 | 3 | HG01168.hp2 HG01169.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-60-6024delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54864156 | |||||
| chr6:54864169
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(247): Show | 251 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-60-6018A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864169 | ||||||
| chr6:54864443
|
C | G | 1 | a0002c0003t0003g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-60-5744C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864443 | ||||||
| chr6:54864457
|
C | T | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-5730C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864457 | ||||||
| chr6:54864570
|
T | C | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.-60-5617T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864570 | ||||||
| chr6:54864587
|
T | C | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-60-5600T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864587 | ||||||
| chr6:54864727
|
G | A | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-60-5460G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864727 | ||||||
| chr6:54864793
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-60-5394A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864793 | ||||||
| chr6:54864813
|
A | G | 1 | a0002c0003t0003g0124 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-60-5374A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864813 | ||||||
| chr6:54864984
|
T | A | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(243): Show | 247 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.-60-5203T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54864984 | ||||||
| chr6:54865001
|
A | G | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-60-5186A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865001 | ||||||
| chr6:54865056
|
A | C | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-5131A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865056 | ||||||
| chr6:54865151
|
C | A | 92 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(89): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-60-5036C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865151 | ||||||
| chr6:54865196
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-60-4991A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865196 | ||||||
| chr6:54865363
|
C | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0085 | 2 | NA18953.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-60-4824C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865363 | ||||||
| chr6:54865379
|
A | T | 1 | a0002c0004t0012g0220 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-60-4808A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865379 | ||||||
| chr6:54865382
|
T | C | 62 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-60-4805T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865382 | ||||||
| chr6:54865414
|
A | C | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-4773A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865414 | ||||||
| chr6:54865546
|
A | G | 219 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(216): Show | 219 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.-60-4641A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865546 | ||||||
| chr6:54865585
|
T | C | 127 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(124): Show | 127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-60-4602T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865585 | ||||||
| chr6:54865706
|
C | T | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(243): Show | 247 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.-60-4481C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865706 | ||||||
| chr6:54865781
|
G | C | 1 | a0001c0002t0002g0139 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-60-4406G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865781 | ||||||
| chr6:54865914
|
A | G | 2 | a0001c0012t0008g0170a0002c0026t0016g0264 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-60-4273A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865914 | ||||||
| chr6:54865931
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-60-4256A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54865931 | ||||||
| chr6:54865967
|
CATA | C | 19 | a0001c0002t0002g0271a0001c0002t0014g0266a0001c0002t0014g0268others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.-60-4188_-60-4186d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | |||||
| chr6:54865967
|
CATAATA | C | 193 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(190): Show | 193 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.-60-4191_-60-4186d others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | |||||
| chr6:54865967
|
CATAATAA others(2): Show |
C | 43 | a0001c0002t0002g0265a0001c0012t0001g0004a0001c0012t0002g0127others(40): Show | 44 | HG00741.hp2 HG01069.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.-60-4194_-60-4186d others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | |||||
| chr6:54865967
|
CATAATAA others(8): Show |
C | 1 | a0001c0002t0002g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-60-4200_-60-4186d others(17): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54865967 | |||||
| chr6:54866013
|
A | G | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(211): Show | 214 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-60-4174A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866013 | ||||||
| chr6:54866071
|
C | G | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-4116C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866071 | ||||||
| chr6:54866153
|
A | C | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-4034A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866153 | ||||||
| chr6:54866171
|
A | G | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-4016A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866171 | ||||||
| chr6:54866201
|
G | GT | 9 | a0001c0002t0001g0231a0002c0003t0003g0102a0002c0003t0003g0109others(6): Show | 9 | HG01069.hp2 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-60-3974dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54866201 | |||||
| chr6:54866201
|
GT | G | 17 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(14): Show | 17 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-60-3974delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 54866201 | |||||
| chr6:54866218
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-60-3969C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866218 | ||||||
| chr6:54866435
|
A | G | 1 | a0003c0006t0007g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-60-3752A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866435 | ||||||
| chr6:54866481
|
C | A | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-3706C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866481 | ||||||
| chr6:54866521
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-60-3666G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866521 | ||||||
| chr6:54866734
|
A | C | 4 | a0001c0002t0002g0184a0001c0002t0002g0185a0001c0002t0002g0192others(1): Show | 4 | HG00323.hp1 HG02293.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-60-3453A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866734 | ||||||
| chr6:54866872
|
A | C | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-3315A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866872 | ||||||
| chr6:54866899
|
C | T | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-60-3288C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866899 | ||||||
| chr6:54866937
|
A | C | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.-60-3250A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54866937 | ||||||
| chr6:54867070
|
T | A | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-3117T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867070 | ||||||
| chr6:54867241
|
A | G | 27 | a0001c0012t0001g0004a0001c0012t0002g0127a0001c0012t0008g0170others(24): Show | 28 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-60-2946A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867241 | ||||||
| chr6:54867274
|
T | C | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-2913T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867274 | ||||||
| chr6:54867333
|
T | C | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-2854T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867333 | ||||||
| chr6:54867425
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-60-2762G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867425 | ||||||
| chr6:54867830
|
A | G | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-60-2357A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867830 | ||||||
| chr6:54867832
|
C | T | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-2355C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54867832 | ||||||
| chr6:54868121
|
G | A | 81 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-60-2066G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868121 | ||||||
| chr6:54868123
|
G | A | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-60-2064G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868123 | ||||||
| chr6:54868167
|
C | T | 127 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(124): Show | 127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-60-2020C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868167 | ||||||
| chr6:54868243
|
A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-60-1944A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868243 | ||||||
| chr6:54868334
|
T | G | 8 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(5): Show | 8 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-60-1853T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868334 | ||||||
| chr6:54868499
|
G | A | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-1688G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868499 | ||||||
| chr6:54868568
|
G | A | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-60-1619G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868568 | ||||||
| chr6:54868582
|
C | G | 1 | a0002c0005t0003g0121 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-60-1605C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868582 | ||||||
| chr6:54868677
|
C | G | 16 | a0001c0002t0002g0256a0002c0005t0013g0147a0002c0005t0013g0202others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-60-1510C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868677 | ||||||
| chr6:54868789
|
A | G | 1 | a0001c0002t0002g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-60-1398A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54868789 | ||||||
| chr6:54869072
|
G | A | 15 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(12): Show | 15 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-60-1115G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869072 | ||||||
| chr6:54869325
|
C | T | 97 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-60-862C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869325 | ||||||
| chr6:54869388
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-60-799G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869388 | ||||||
| chr6:54869394
|
G | T | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.-60-793G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869394 | ||||||
| chr6:54869526
|
T | A | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-661T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869526 | ||||||
| chr6:54869622
|
C | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-565C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869622 | ||||||
| chr6:54869679
|
A | G | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-60-508A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869679 | ||||||
| chr6:54869772
|
G | C | 257 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(254): Show | 258 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.-60-415G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869772 | ||||||
| chr6:54869782
|
T | G | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.-60-405T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869782 | ||||||
| chr6:54869804
|
A | T | 127 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(124): Show | 127 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-60-383A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869804 | ||||||
| chr6:54869849
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-60-338A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869849 | ||||||
| chr6:54869987
|
A | G | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-60-200A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54869987 | ||||||
| chr6:54870053
|
A | T | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-60-134A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54870053 | ||||||
| chr6:54870116
|
T | G | 1 | a0001c0002t0002g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-60-71T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54870116 | ||||||
| chr6:54870143
|
C | A | 63 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-60-44C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 1/4 | chr6 | 54870143 | ||||||
| chr6:54870739
|
G | C | 1 | a0001c0001t0004g0040 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.444+49G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870739 | ||||||
| chr6:54870796
|
G | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.444+106G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870796 | ||||||
| chr6:54870808
|
G | A | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.444+118G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870808 | ||||||
| chr6:54870814
|
A | G | 3 | a0001c0001t0010g0020a0005c0015t0017g0019a0005c0015t0017g0148 | 3 | HG02922.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.444+124A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54870814 | ||||||
| chr6:54871170
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.444+480T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871170 | ||||||
| chr6:54871233
|
GC | G | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+544delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871233 | ||||||
| chr6:54871334
|
A | T | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+644A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871334 | ||||||
| chr6:54871389
|
CA | C | 4 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+706delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871389 | |||||
| chr6:54871555
|
C | CAAT | 75 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0110others(72): Show | 75 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.444+904_444+906dup others(3): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | |||||
| chr6:54871555
|
C | CAATAAT | 11 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0002t0002g0217others(8): Show | 11 | HG00438.hp1 HG00639.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+901_444+906dup others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | |||||
| chr6:54871555
|
CAAT | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.444+904_444+906del others(3): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | |||||
| chr6:54871555
|
CAATAATA others(5): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.444+895_444+906del others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871555 | |||||
| chr6:54871634
|
T | C | 1 | a0001c0002t0002g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.444+944T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871634 | ||||||
| chr6:54871648
|
C | T | 1 | a0003c0006t0007g0246 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+958C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871648 | ||||||
| chr6:54871729
|
C | T | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+1039C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871729 | ||||||
| chr6:54871745
|
C | CA | 101 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0037others(98): Show | 101 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.444+1081dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | |||||
| chr6:54871745
|
C | CAA | 35 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0160others(32): Show | 36 | HG01069.hp2 HG01167.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.444+1080_444+1081d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | |||||
| chr6:54871745
|
C | CAAAAAAA others(3): Show |
1 | a0001c0008t0025g0018 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.444+1072_444+1081d others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | |||||
| chr6:54871745
|
CA | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(8): Show | 11 | HG01074.hp2 HG01256.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+1081delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54871745 | |||||
| chr6:54871801
|
A | G | 8 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(5): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+1111A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871801 | ||||||
| chr6:54871803
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.444+1113A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871803 | ||||||
| chr6:54871919
|
C | G | 63 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.444+1229C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871919 | ||||||
| chr6:54871929
|
T | C | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.444+1239T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54871929 | ||||||
| chr6:54872446
|
G | C | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.444+1756G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872446 | ||||||
| chr6:54872633
|
C | T | 260 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(257): Show | 261 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.444+1943C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872633 | ||||||
| chr6:54872844
|
C | T | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+2154C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872844 | ||||||
| chr6:54872992
|
G | GT | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(243): Show | 247 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.444+2307dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54872992 | |||||
| chr6:54872998
|
G | T | 260 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(257): Show | 261 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.444+2308G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54872998 | ||||||
| chr6:54873023
|
T | A | 92 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(89): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.444+2333T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873023 | ||||||
| chr6:54873155
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.444+2465A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873155 | ||||||
| chr6:54873229
|
T | C | 4 | a0001c0012t0008g0170a0002c0026t0016g0264a0003c0016t0007g0002others(1): Show | 4 | HG02615.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+2539T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873229 | ||||||
| chr6:54873249
|
T | C | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+2559T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873249 | ||||||
| chr6:54873267
|
TTTG | T | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+2578_444+2580d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873267 | ||||||
| chr6:54873332
|
G | A | 267 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(264): Show | 268 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.444+2642G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873332 | ||||||
| chr6:54873348
|
C | T | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+2658C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873348 | ||||||
| chr6:54873376
|
G | T | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+2686G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873376 | ||||||
| chr6:54873448
|
A | G | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(95): Show | 98 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.444+2758A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873448 | ||||||
| chr6:54873533
|
G | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+2843G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873533 | ||||||
| chr6:54873642
|
CT | C | 5 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0113others(2): Show | 5 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+2961delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54873642 | |||||
| chr6:54873683
|
G | C | 1 | a0004c0024t0008g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.444+2993G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873683 | ||||||
| chr6:54873690
|
G | GT | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(114): Show | 117 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.444+3015dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54873690 | |||||
| chr6:54873690
|
G | GTT | 8 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0096others(5): Show | 8 | HG00438.hp1 HG00741.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+3014_444+3015d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54873690 | |||||
| chr6:54873747
|
T | C | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+3057T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873747 | ||||||
| chr6:54873794
|
C | T | 6 | a0002c0005t0019g0241a0002c0005t0019g0242a0003c0007t0006g0237others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+3104C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873794 | ||||||
| chr6:54873910
|
T | C | 1 | a0001c0002t0002g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.444+3220T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54873910 | ||||||
| chr6:54874061
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+3371A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874061 | ||||||
| chr6:54874159
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.444+3469C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874159 | ||||||
| chr6:54874275
|
A | C | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+3585A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874275 | ||||||
| chr6:54874570
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.444+3880T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874570 | ||||||
| chr6:54874645
|
G | A | 4 | a0001c0012t0008g0170a0002c0026t0016g0264a0003c0016t0007g0002others(1): Show | 4 | HG02615.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+3955G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874645 | ||||||
| chr6:54874741
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.444+4051T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874741 | ||||||
| chr6:54874834
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0002g0095 | 3 | HG02698.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.444+4144C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874834 | ||||||
| chr6:54874982
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.444+4292G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54874982 | ||||||
| chr6:54875099
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00558.hp1 NA18960.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.444+4409C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875099 | ||||||
| chr6:54875273
|
G | A | 4 | a0001c0012t0008g0170a0002c0026t0016g0264a0003c0016t0007g0002others(1): Show | 4 | HG02615.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+4583G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875273 | ||||||
| chr6:54875363
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+4673A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875363 | ||||||
| chr6:54875418
|
T | C | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+4728T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875418 | ||||||
| chr6:54875542
|
G | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.444+4852G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875542 | ||||||
| chr6:54875624
|
A | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG00323.hp2 NA18963.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+4934A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875624 | ||||||
| chr6:54875639
|
C | T | 4 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+4949C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875639 | ||||||
| chr6:54875640
|
G | A | 12 | a0001c0001t0001g0101a0001c0002t0002g0256a0003c0007t0006g0169others(9): Show | 12 | HG00544.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+4950G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875640 | ||||||
| chr6:54875663
|
CGGAGGGG others(51): Show |
C | 1 | a0001c0001t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.444+5021_444+5078d others(60): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54875663 | |||||
| chr6:54875664
|
G | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+4974G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875664 | ||||||
| chr6:54875672
|
A | G | 1 | a0002c0004t0003g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.444+4982A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875672 | ||||||
| chr6:54875702
|
G | A | 4 | a0001c0002t0002g0265a0001c0002t0014g0266a0001c0002t0014g0268others(1): Show | 4 | NA18960.hp2 NA19010.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+5012G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875702 | ||||||
| chr6:54875706
|
G | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+5016G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875706 | ||||||
| chr6:54875711
|
GAAGAAGA others(51): Show |
G | 6 | a0001c0012t0001g0004a0002c0003t0003g0108a0002c0003t0003g0123others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+5026_444+5083d others(60): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54875711 | |||||
| chr6:54875725
|
G | GGGAAAGA others(2): Show |
115 | a0001c0002t0001g0158a0001c0002t0001g0231a0001c0002t0002g0088others(112): Show | 116 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.444+5037_444+5038i others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54875725 | |||||
| chr6:54875743
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+5053A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875743 | ||||||
| chr6:54875856
|
C | A | 2 | a0002c0010t0009g0149a0002c0010t0009g0150 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.444+5166C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875856 | ||||||
| chr6:54875930
|
T | C | 6 | a0002c0005t0019g0241a0002c0005t0019g0242a0003c0007t0006g0237others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+5240T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54875930 | ||||||
| chr6:54876225
|
C | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(94): Show | 97 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.444+5535C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876225 | ||||||
| chr6:54876278
|
C | CAT | 19 | a0001c0001t0010g0020a0001c0001t0010g0146a0001c0002t0002g0113others(16): Show | 19 | HG00423.hp2 HG01928.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.444+5629_444+5630d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
C | CATATATA others(1): Show |
4 | a0001c0001t0010g0140a0001c0008t0005g0012a0002c0004t0003g0155others(1): Show | 4 | HG02809.hp2 NA18906.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+5623_444+5630d others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CAT | C | 22 | a0001c0002t0001g0231a0001c0002t0002g0111a0001c0002t0002g0117others(19): Show | 22 | HG00558.hp2 HG00735.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.444+5629_444+5630d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATAT | C | 14 | a0001c0001t0010g0145a0001c0001t0010g0201a0001c0002t0002g0110others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.444+5627_444+5630d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATAT | C | 5 | a0001c0002t0002g0161a0001c0002t0002g0188a0001c0002t0002g0204others(2): Show | 5 | HG01074.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+5625_444+5630d others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(1): Show |
C | 11 | a0001c0002t0002g0186a0001c0002t0014g0269a0001c0013t0005g0079others(8): Show | 11 | HG00738.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+5623_444+5630d others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(3): Show |
C | 19 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(16): Show | 19 | HG00741.hp2 HG01167.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.444+5621_444+5630d others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(7): Show |
C | 4 | a0002c0005t0019g0241a0002c0005t0019g0242a0004c0014t0002g0143others(1): Show | 4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+5617_444+5630d others(16): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(11): Show |
C | 2 | a0001c0012t0008g0170a0002c0026t0016g0264 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+5613_444+5630d others(20): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(13): Show |
C | 5 | a0001c0002t0002g0199a0001c0002t0002g0233a0001c0002t0021g0159others(2): Show | 5 | HG02165.hp2 NA18946.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+5611_444+5630d others(22): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(15): Show |
C | 2 | a0001c0002t0002g0191a0001c0002t0002g0222 | 2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.444+5609_444+5630d others(24): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(17): Show |
C | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(97): Show | 100 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.444+5607_444+5630d others(26): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(19): Show |
C | 1 | a0001c0002t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.444+5605_444+5630d others(28): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876278
|
CATATATA others(21): Show |
C | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+5603_444+5630d others(30): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876278 | |||||
| chr6:54876327
|
G | GC | 6 | a0002c0005t0019g0241a0002c0005t0019g0242a0003c0007t0006g0237others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+5637_444+5638i others(3): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876327 | ||||||
| chr6:54876327
|
G | GT | 17 | a0001c0001t0001g0078a0001c0001t0001g0096a0001c0001t0001g0193others(14): Show | 17 | HG00438.hp1 HG00544.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.444+5651dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54876327 | |||||
| chr6:54876451
|
A | T | 8 | a0002c0005t0019g0241a0002c0005t0019g0242a0003c0007t0006g0237others(5): Show | 8 | HG02615.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+5761A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876451 | ||||||
| chr6:54876522
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.444+5832G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876522 | ||||||
| chr6:54876540
|
G | T | 1 | a0001c0001t0010g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+5850G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876540 | ||||||
| chr6:54876660
|
G | T | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+5970G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876660 | ||||||
| chr6:54876664
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0064 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.444+5974A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876664 | ||||||
| chr6:54876803
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.444+6113G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876803 | ||||||
| chr6:54876808
|
G | C | 62 | a0001c0002t0001g0231a0001c0002t0002g0088a0001c0002t0002g0110others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.444+6118G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876808 | ||||||
| chr6:54876990
|
G | C | 10 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(7): Show | 10 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.444+6300G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54876990 | ||||||
| chr6:54877055
|
A | G | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(127): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+6365A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877055 | ||||||
| chr6:54877315
|
AGG | A | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+6628_444+6629d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54877315 | |||||
| chr6:54877381
|
G | A | 49 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(46): Show | 49 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.444+6691G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877381 | ||||||
| chr6:54877446
|
G | T | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.444+6756G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877446 | ||||||
| chr6:54877447
|
C | T | 3 | a0002c0004t0003g0142a0004c0018t0008g0141a0004c0018t0008g0156 | 3 | HG01175.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.444+6757C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877447 | ||||||
| chr6:54877470
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.444+6780G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877470 | ||||||
| chr6:54877512
|
A | G | 1 | a0001c0002t0002g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.444+6822A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877512 | ||||||
| chr6:54877518
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.444+6828C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877518 | ||||||
| chr6:54877591
|
T | C | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+6901T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877591 | ||||||
| chr6:54877692
|
T | C | 1 | a0001c0002t0002g0265 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.444+7002T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877692 | ||||||
| chr6:54877871
|
C | A | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+7181C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54877871 | ||||||
| chr6:54878323
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.444+7633C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878323 | ||||||
| chr6:54878449
|
T | A | 2 | a0004c0018t0008g0141a0004c0018t0008g0156 | 2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.444+7759T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878449 | ||||||
| chr6:54878707
|
C | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+8017C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878707 | ||||||
| chr6:54878846
|
GC | G | 62 | a0001c0002t0001g0231a0001c0002t0002g0088a0001c0002t0002g0110others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.444+8157delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54878846 | ||||||
| chr6:54879015
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444+8325T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879015 | ||||||
| chr6:54879114
|
G | A | 12 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(9): Show | 12 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+8424G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879114 | ||||||
| chr6:54879153
|
A | T | 10 | a0001c0002t0002g0265a0001c0002t0002g0271a0001c0002t0014g0266others(7): Show | 10 | HG02015.hp1 HG03654.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+8463A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879153 | ||||||
| chr6:54879200
|
G | A | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(127): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+8510G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879200 | ||||||
| chr6:54879221
|
A | C | 1 | a0002c0004t0012g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.444+8531A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879221 | ||||||
| chr6:54879251
|
A | G | 1 | a0001c0002t0002g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+8561A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879251 | ||||||
| chr6:54879538
|
A | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+8848A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879538 | ||||||
| chr6:54879563
|
T | C | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+8873T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879563 | ||||||
| chr6:54879599
|
C | T | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+8909C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879599 | ||||||
| chr6:54879652
|
G | T | 13 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(10): Show | 13 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+8962G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879652 | ||||||
| chr6:54879682
|
T | C | 1 | a0003c0006t0007g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+8992T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879682 | ||||||
| chr6:54879830
|
G | A | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.444+9140G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879830 | ||||||
| chr6:54879840
|
T | A | 1 | a0004c0011t0008g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.444+9150T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879840 | ||||||
| chr6:54879866
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.444+9176T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879866 | ||||||
| chr6:54879902
|
C | G | 4 | a0002c0004t0003g0154a0002c0004t0003g0155a0002c0004t0003g0243others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+9212C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879902 | ||||||
| chr6:54879947
|
A | C | 1 | a0002c0005t0018g0225 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.444+9257A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879947 | ||||||
| chr6:54879966
|
A | T | 260 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(257): Show | 261 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.444+9276A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54879966 | ||||||
| chr6:54880039
|
A | C | 1 | a0001c0002t0002g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.444+9349A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880039 | ||||||
| chr6:54880109
|
C | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+9419C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880109 | ||||||
| chr6:54880128
|
C | G | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.444+9438C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880128 | ||||||
| chr6:54880148
|
G | A | 62 | a0001c0002t0001g0231a0001c0002t0002g0088a0001c0002t0002g0110others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.444+9458G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880148 | ||||||
| chr6:54880171
|
G | T | 62 | a0001c0002t0001g0231a0001c0002t0002g0088a0001c0002t0002g0110others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.444+9481G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880171 | ||||||
| chr6:54880300
|
G | A | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(127): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+9610G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880300 | ||||||
| chr6:54880375
|
A | G | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+9685A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880375 | ||||||
| chr6:54880399
|
A | T | 1 | a0001c0002t0002g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.444+9709A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880399 | ||||||
| chr6:54880413
|
G | A | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 252 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.444+9723G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880413 | ||||||
| chr6:54880441
|
C | CT | 48 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0099others(45): Show | 49 | HG00642.hp1 HG01069.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.444+9772dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | |||||
| chr6:54880441
|
C | CTT | 5 | a0001c0001t0001g0021a0001c0002t0002g0115a0001c0002t0002g0221others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+9771_444+9772d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | |||||
| chr6:54880441
|
C | CTTT | 63 | a0001c0002t0001g0231a0001c0002t0002g0088a0001c0002t0002g0110others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.444+9770_444+9772d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | |||||
| chr6:54880441
|
C | CTTTT | 6 | a0001c0002t0002g0178a0001c0002t0002g0179a0001c0002t0002g0181others(3): Show | 6 | HG01109.hp2 HG02027.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+9769_444+9772d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | |||||
| chr6:54880441
|
CT | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0010g0146others(2): Show | 5 | HG00323.hp2 HG01256.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+9772delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880441 | |||||
| chr6:54880519
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.444+9829A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880519 | ||||||
| chr6:54880692
|
C | T | 1 | a0002c0010t0009g0025 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.444+10002C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880692 | ||||||
| chr6:54880883
|
TTAAA | T | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0240others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+10200_444+1020 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54880883 | |||||
| chr6:54880994
|
T | A | 12 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(9): Show | 12 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+10304T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54880994 | ||||||
| chr6:54881021
|
T | G | 7 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+10331T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881021 | ||||||
| chr6:54881047
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.444+10357T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881047 | ||||||
| chr6:54881111
|
A | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+10421A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881111 | ||||||
| chr6:54881142
|
A | G | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+10452A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881142 | ||||||
| chr6:54881157
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.444+10467A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881157 | ||||||
| chr6:54881357
|
A | G | 256 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(253): Show | 257 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.444+10667A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881357 | ||||||
| chr6:54881521
|
T | C | 16 | a0001c0002t0002g0256a0002c0005t0013g0147a0002c0005t0013g0202others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+10831T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881521 | ||||||
| chr6:54881524
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.444+10834C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881524 | ||||||
| chr6:54881625
|
A | G | 1 | a0002c0003t0003g0165 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.444+10935A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881625 | ||||||
| chr6:54881862
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.444+11172C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881862 | ||||||
| chr6:54881927
|
C | T | 1 | a0003c0006t0007g0246 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+11237C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54881927 | ||||||
| chr6:54882087
|
A | ATG | 61 | a0001c0002t0001g0231a0001c0002t0002g0088a0001c0002t0002g0110others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.444+11398_444+1139 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54882087 | |||||
| chr6:54882214
|
C | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+11524C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882214 | ||||||
| chr6:54882339
|
T | A | 2 | a0001c0001t0004g0028a0001c0001t0004g0046 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.444+11649T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882339 | ||||||
| chr6:54882544
|
G | T | 25 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(22): Show | 26 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.444+11854G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882544 | ||||||
| chr6:54882580
|
T | C | 1 | a0002c0003t0003g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+11890T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882580 | ||||||
| chr6:54882716
|
C | T | 1 | a0004c0018t0008g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.444+12026C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882716 | ||||||
| chr6:54882721
|
C | G | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444+12031C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882721 | ||||||
| chr6:54882803
|
A | G | 26 | a0001c0012t0001g0004a0001c0012t0002g0127a0002c0003t0003g0001others(23): Show | 27 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.444+12113A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882803 | ||||||
| chr6:54882894
|
C | T | 6 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(3): Show | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+12204C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882894 | ||||||
| chr6:54882910
|
C | T | 8 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(5): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+12220C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882910 | ||||||
| chr6:54882975
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.444+12285G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882975 | ||||||
| chr6:54882992
|
G | A | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+12302G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54882992 | ||||||
| chr6:54883006
|
C | T | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.444+12316C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883006 | ||||||
| chr6:54883045
|
C | T | 2 | a0003c0006t0007g0174a0003c0006t0007g0175 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.444+12355C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883045 | ||||||
| chr6:54883144
|
C | T | 2 | a0001c0012t0008g0170a0002c0026t0016g0264 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+12454C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883144 | ||||||
| chr6:54883185
|
C | T | 9 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(6): Show | 9 | HG01167.hp1 HG01361.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+12495C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883185 | ||||||
| chr6:54883196
|
G | GC | 4 | a0001c0002t0015g0005a0001c0013t0005g0079a0001c0013t0005g0267others(1): Show | 4 | HG04204.hp1 NA18965.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+12508dupC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883196 | |||||
| chr6:54883204
|
A | C | 45 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0063others(42): Show | 46 | HG00323.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.444+12514A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883204 | ||||||
| chr6:54883223
|
G | A | 1 | a0001c0002t0002g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+12533G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883223 | ||||||
| chr6:54883225
|
G | A | 1 | a0001c0002t0002g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+12535G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883225 | ||||||
| chr6:54883253
|
T | C | 261 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(258): Show | 262 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.444+12563T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883253 | ||||||
| chr6:54883320
|
AT | A | 8 | a0002c0004t0033g0152a0003c0006t0007g0166a0003c0006t0007g0167others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+12639delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883320 | |||||
| chr6:54883332
|
G | GT | 18 | a0001c0001t0002g0077a0001c0001t0010g0145a0001c0002t0002g0160others(15): Show | 18 | HG01243.hp2 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+12661dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883332 | |||||
| chr6:54883332
|
GT | G | 172 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(169): Show | 173 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.444+12661delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883332 | |||||
| chr6:54883332
|
GTT | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0010g0020others(15): Show | 18 | HG01175.hp2 HG01978.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+12660_444+1266 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883332 | |||||
| chr6:54883420
|
C | T | 136 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(133): Show | 137 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.444+12730C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883420 | ||||||
| chr6:54883421
|
G | A | 55 | a0001c0001t0002g0077a0001c0001t0002g0095a0001c0002t0002g0115others(52): Show | 55 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.444+12731G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883421 | ||||||
| chr6:54883459
|
C | A | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+12769C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883459 | ||||||
| chr6:54883497
|
G | T | 9 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(6): Show | 9 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+12807G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883497 | ||||||
| chr6:54883503
|
T | G | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+12813T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883503 | ||||||
| chr6:54883524
|
C | T | 1 | a0001c0002t0002g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.444+12834C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883524 | ||||||
| chr6:54883626
|
G | A | 57 | a0001c0001t0002g0030a0001c0001t0002g0077a0001c0001t0002g0095others(54): Show | 57 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.444+12936G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883626 | ||||||
| chr6:54883699
|
A | T | 1 | a0001c0001t0001g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.444+13009A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883699 | ||||||
| chr6:54883763
|
G | GT | 6 | a0001c0001t0001g0094a0001c0008t0005g0011a0001c0008t0005g0013others(3): Show | 6 | HG00544.hp1 NA18963.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+13073_444+1307 others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883763 | ||||||
| chr6:54883764
|
G | GT | 20 | a0001c0002t0014g0266a0002c0003t0003g0128a0002c0004t0020g0107others(17): Show | 20 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.444+13085dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54883764 | |||||
| chr6:54883764
|
G | T | 157 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(154): Show | 158 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.444+13074G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883764 | ||||||
| chr6:54883838
|
C | G | 1 | a0002c0004t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.444+13148C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883838 | ||||||
| chr6:54883883
|
C | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+13193C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883883 | ||||||
| chr6:54883902
|
G | A | 2 | a0003c0006t0007g0246a0003c0006t0007g0252 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.444+13212G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883902 | ||||||
| chr6:54883935
|
C | T | 39 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(36): Show | 40 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+13245C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54883935 | ||||||
| chr6:54884026
|
A | G | 35 | a0001c0002t0002g0256a0001c0002t0015g0005a0001c0002t0015g0008others(32): Show | 35 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.444+13336A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884026 | ||||||
| chr6:54884041
|
C | T | 6 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+13351C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884041 | ||||||
| chr6:54884099
|
C | T | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(153): Show | 157 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.444+13409C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884099 | ||||||
| chr6:54884177
|
C | CT | 4 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0201others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+13488dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884177 | |||||
| chr6:54884217
|
G | C | 1 | a0001c0001t0024g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.444+13527G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884217 | ||||||
| chr6:54884234
|
G | A | 213 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(210): Show | 214 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.444+13544G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884234 | ||||||
| chr6:54884257
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.444+13567G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884257 | ||||||
| chr6:54884259
|
G | A | 1 | a0004c0011t0008g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.444+13569G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884259 | ||||||
| chr6:54884299
|
T | TA | 7 | a0001c0002t0002g0181a0002c0003t0003g0128a0002c0009t0011g0164others(4): Show | 7 | HG00741.hp2 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+13628dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | |||||
| chr6:54884299
|
T | TAA | 12 | a0001c0002t0015g0005a0001c0013t0005g0079a0001c0013t0005g0267others(9): Show | 12 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+13627_444+1362 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | |||||
| chr6:54884299
|
T | TAAA | 11 | a0001c0002t0002g0256a0001c0002t0015g0008a0001c0008t0005g0017others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+13626_444+1362 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | |||||
| chr6:54884299
|
T | TAAAA | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0022others(127): Show | 131 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.444+13625_444+1362 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | |||||
| chr6:54884299
|
T | TAAAAA | 36 | a0001c0001t0001g0021a0001c0001t0001g0089a0001c0001t0001g0099others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.444+13624_444+1362 others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884299 | |||||
| chr6:54884318
|
AG | A | 10 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0112others(7): Show | 10 | HG00735.hp2 HG01167.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+13629delG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884318 | ||||||
| chr6:54884319
|
G | A | 2 | a0001c0002t0002g0111a0001c0002t0002g0119 | 2 | HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.444+13629G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884319 | ||||||
| chr6:54884350
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.444+13660C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884350 | ||||||
| chr6:54884351
|
G | A | 11 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+13661G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884351 | ||||||
| chr6:54884443
|
T | C | 1 | a0001c0002t0002g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.444+13753T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884443 | ||||||
| chr6:54884481
|
C | CA | 8 | a0001c0001t0001g0045a0001c0002t0001g0158a0001c0002t0002g0199others(5): Show | 8 | HG02258.hp1 HG02615.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+13809dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | |||||
| chr6:54884481
|
C | CAA | 16 | a0001c0001t0001g0078a0002c0004t0003g0142a0002c0004t0033g0152others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.444+13808_444+1380 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | |||||
| chr6:54884481
|
CA | C | 21 | a0001c0001t0010g0020a0001c0001t0010g0145a0001c0001t0010g0146others(18): Show | 21 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.444+13809delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | |||||
| chr6:54884481
|
CAA | C | 14 | a0002c0003t0003g0128a0002c0004t0020g0107a0002c0004t0020g0134others(11): Show | 14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+13808_444+1380 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884481 | |||||
| chr6:54884578
|
A | G | 1 | a0002c0005t0003g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.444+13888A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884578 | ||||||
| chr6:54884693
|
A | T | 3 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0023t0031g0236 | 3 | HG02572.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.444+14003A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884693 | ||||||
| chr6:54884698
|
C | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+14008C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884698 | ||||||
| chr6:54884775
|
A | AT | 32 | a0001c0002t0002g0256a0001c0008t0005g0122a0002c0004t0003g0142others(29): Show | 32 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.444+14100dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884775 | |||||
| chr6:54884775
|
AT | A | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(130): Show | 134 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.444+14100delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54884775 | |||||
| chr6:54884817
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.444+14127T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884817 | ||||||
| chr6:54884858
|
C | T | 1 | a0002c0010t0009g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.444+14168C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884858 | ||||||
| chr6:54884865
|
C | T | 3 | a0002c0005t0003g0016a0005c0015t0017g0019a0005c0015t0017g0148 | 3 | HG02258.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.444+14175C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884865 | ||||||
| chr6:54884889
|
C | CT | 3 | a0001c0001t0002g0095a0001c0002t0002g0186a0001c0002t0002g0232 | 3 | HG00738.hp2 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.444+14199_444+1420 others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884889 | ||||||
| chr6:54884897
|
C | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+14207C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884897 | ||||||
| chr6:54884973
|
T | C | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+14283T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54884973 | ||||||
| chr6:54885038
|
C | T | 5 | a0001c0002t0015g0005a0001c0002t0015g0008a0001c0013t0005g0079others(2): Show | 5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+14348C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885038 | ||||||
| chr6:54885051
|
C | T | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.444+14361C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885051 | ||||||
| chr6:54885052
|
G | A | 2 | a0002c0010t0009g0149a0002c0010t0009g0150 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.444+14362G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885052 | ||||||
| chr6:54885348
|
GTTTGA | G | 3 | a0002c0005t0003g0016a0005c0015t0017g0019a0005c0015t0017g0148 | 3 | HG02258.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.444+14662_444+1466 others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54885348 | |||||
| chr6:54885395
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+14705A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885395 | ||||||
| chr6:54885402
|
T | C | 1 | a0004c0024t0008g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.444+14712T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885402 | ||||||
| chr6:54885584
|
A | G | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.444+14894A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885584 | ||||||
| chr6:54885690
|
C | T | 135 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(132): Show | 136 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.444+15000C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885690 | ||||||
| chr6:54885733
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.444+15043C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885733 | ||||||
| chr6:54885737
|
C | T | 8 | a0002c0004t0003g0142a0002c0004t0033g0152a0002c0010t0009g0006others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+15047C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885737 | ||||||
| chr6:54885738
|
G | A | 9 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+15048G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885738 | ||||||
| chr6:54885929
|
G | A | 1 | a0001c0002t0002g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.444+15239G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885929 | ||||||
| chr6:54885962
|
TATA | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+15295_444+1529 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54885962 | |||||
| chr6:54885985
|
T | G | 1 | a0002c0005t0003g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.444+15295T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54885985 | ||||||
| chr6:54886303
|
A | AT | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+15622dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886303 | |||||
| chr6:54886303
|
AT | A | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(87): Show | 90 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.444+15622delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886303 | |||||
| chr6:54886383
|
G | C | 3 | a0001c0002t0002g0187a0001c0002t0002g0196a0001c0002t0002g0230 | 3 | NA18964.hp2 NA18965.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.444+15693G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886383 | ||||||
| chr6:54886529
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.444+15839T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886529 | ||||||
| chr6:54886698
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.444+16008G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886698 | ||||||
| chr6:54886841
|
A | G | 1 | a0001c0001t0004g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.444+16151A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886841 | ||||||
| chr6:54886846
|
AT | A | 5 | a0001c0002t0015g0005a0001c0002t0015g0008a0001c0013t0005g0079others(2): Show | 5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+16162delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886846 | |||||
| chr6:54886899
|
T | G | 6 | a0002c0003t0003g0102a0002c0003t0003g0109a0002c0003t0003g0120others(3): Show | 6 | HG01069.hp2 HG01243.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+16209T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886899 | ||||||
| chr6:54886904
|
CTTA | C | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+16223_444+1622 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54886904 | |||||
| chr6:54886925
|
A | G | 1 | a0002c0003t0003g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+16235A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54886925 | ||||||
| chr6:54887023
|
A | G | 12 | a0002c0003t0003g0128a0002c0005t0013g0147a0002c0005t0013g0202others(9): Show | 12 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+16333A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887023 | ||||||
| chr6:54887182
|
TA | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+16493delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887182 | ||||||
| chr6:54887391
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+16701C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887391 | ||||||
| chr6:54887442
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+16752A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887442 | ||||||
| chr6:54887715
|
ATAAC | A | 13 | a0002c0004t0003g0142a0002c0004t0033g0152a0002c0005t0013g0147others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+17028_444+1703 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54887715 | |||||
| chr6:54887783
|
T | G | 30 | a0001c0002t0002g0256a0001c0002t0015g0005a0001c0002t0015g0008others(27): Show | 30 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.444+17093T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887783 | ||||||
| chr6:54887845
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0085 | 2 | NA18953.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.444+17155T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887845 | ||||||
| chr6:54887895
|
C | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+17205C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54887895 | ||||||
| chr6:54888009
|
CT | C | 18 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0116others(15): Show | 18 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+17326delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54888009 | |||||
| chr6:54888018
|
T | G | 4 | a0003c0007t0006g0237a0003c0007t0006g0238a0003c0007t0006g0239others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+17328T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888018 | ||||||
| chr6:54888187
|
T | C | 1 | a0003c0006t0007g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.444+17497T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888187 | ||||||
| chr6:54888193
|
A | G | 13 | a0002c0004t0003g0142a0002c0004t0033g0152a0002c0005t0013g0147others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+17503A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888193 | ||||||
| chr6:54888209
|
T | C | 39 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(36): Show | 40 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+17519T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888209 | ||||||
| chr6:54888256
|
A | T | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(153): Show | 157 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.444+17566A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888256 | ||||||
| chr6:54888274
|
T | TTATTGTT others(30): Show |
9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+17595_444+1759 others(41): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54888274 | |||||
| chr6:54888526
|
T | C | 4 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0116others(1): Show | 4 | NA18953.hp2 NA18977.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+17836T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888526 | ||||||
| chr6:54888542
|
G | T | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(153): Show | 157 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.444+17852G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888542 | ||||||
| chr6:54888661
|
C | A | 5 | a0001c0001t0004g0048a0001c0001t0004g0052a0001c0001t0004g0054others(2): Show | 5 | HG01109.hp1 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+17971C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888661 | ||||||
| chr6:54888743
|
T | C | 129 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(126): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.444+18053T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888743 | ||||||
| chr6:54888828
|
A | C | 135 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(132): Show | 136 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.444+18138A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54888828 | ||||||
| chr6:54889056
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.444+18366T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889056 | ||||||
| chr6:54889087
|
T | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+18397T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889087 | ||||||
| chr6:54889112
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG00558.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.444+18422A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889112 | ||||||
| chr6:54889177
|
G | A | 1 | a0002c0026t0016g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.444+18487G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889177 | ||||||
| chr6:54889442
|
A | G | 201 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(198): Show | 202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.444+18752A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889442 | ||||||
| chr6:54889447
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.444+18757C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889447 | ||||||
| chr6:54889467
|
A | G | 13 | a0002c0004t0003g0142a0002c0004t0033g0152a0002c0005t0013g0147others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+18777A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889467 | ||||||
| chr6:54889468
|
C | T | 7 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0106others(4): Show | 7 | HG00735.hp1 HG00741.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+18778C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889468 | ||||||
| chr6:54889469
|
G | A | 4 | a0003c0007t0006g0237a0003c0007t0006g0238a0003c0007t0006g0239others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+18779G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889469 | ||||||
| chr6:54889494
|
C | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+18804C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54889494 | ||||||
| chr6:54890147
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.444+19457A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890147 | ||||||
| chr6:54890240
|
AC | A | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+19552delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54890240 | |||||
| chr6:54890349
|
C | G | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+19659C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890349 | ||||||
| chr6:54890539
|
C | T | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+19849C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890539 | ||||||
| chr6:54890541
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0076a0001c0001t0001g0083others(6): Show | 9 | HG00438.hp1 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+19851A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890541 | ||||||
| chr6:54890590
|
C | G | 9 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+19900C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890590 | ||||||
| chr6:54890953
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.444+20263A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890953 | ||||||
| chr6:54890954
|
GA | G | 25 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(22): Show | 25 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.444+20275delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54890954 | |||||
| chr6:54890992
|
G | A | 25 | a0001c0002t0002g0256a0002c0003t0003g0128a0002c0004t0020g0107others(22): Show | 25 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.444+20302G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54890992 | ||||||
| chr6:54891073
|
G | A | 161 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(158): Show | 162 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.444+20383G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891073 | ||||||
| chr6:54891156
|
A | G | 1 | a0002c0003t0003g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.444+20466A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891156 | ||||||
| chr6:54891342
|
C | CT | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(130): Show | 133 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.444+20654dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54891342 | |||||
| chr6:54891451
|
A | G | 1 | a0001c0002t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444+20761A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891451 | ||||||
| chr6:54891510
|
C | T | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(130): Show | 133 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.444+20820C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891510 | ||||||
| chr6:54891697
|
C | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(117): Show | 120 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.444+21007C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891697 | ||||||
| chr6:54891731
|
G | A | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(87): Show | 90 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.444+21041G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891731 | ||||||
| chr6:54891735
|
A | G | 5 | a0001c0002t0015g0005a0001c0002t0015g0008a0001c0013t0005g0079others(2): Show | 5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+21045A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891735 | ||||||
| chr6:54891853
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.444+21163C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891853 | ||||||
| chr6:54891949
|
A | C | 5 | a0001c0002t0015g0005a0001c0002t0015g0008a0001c0013t0005g0079others(2): Show | 5 | HG03654.hp1 HG04204.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+21259A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54891949 | ||||||
| chr6:54892157
|
A | G | 1 | a0001c0021t0005g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.444+21467A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892157 | ||||||
| chr6:54892159
|
A | C | 40 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.444+21469A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892159 | ||||||
| chr6:54892268
|
T | A | 1 | a0003c0007t0028g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.444+21578T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892268 | ||||||
| chr6:54892722
|
A | G | 143 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(140): Show | 143 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.444+22032A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892722 | ||||||
| chr6:54892733
|
A | G | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+22043A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892733 | ||||||
| chr6:54892755
|
A | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+22065A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892755 | ||||||
| chr6:54892828
|
T | A | 4 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+22138T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892828 | ||||||
| chr6:54892838
|
G | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+22148G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892838 | ||||||
| chr6:54892867
|
A | C | 1 | a0001c0002t0002g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.444+22177A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892867 | ||||||
| chr6:54892940
|
G | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+22250G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892940 | ||||||
| chr6:54892993
|
G | C | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+22303G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54892993 | ||||||
| chr6:54893271
|
A | G | 11 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+22581A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893271 | ||||||
| chr6:54893352
|
A | C | 2 | a0002c0003t0003g0253a0002c0003t0026g0168 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.444+22662A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893352 | ||||||
| chr6:54893830
|
G | A | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+23140G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893830 | ||||||
| chr6:54893881
|
A | G | 3 | a0002c0004t0003g0154a0002c0004t0003g0155a0003c0017t0006g0153 | 3 | HG02559.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.444+23191A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893881 | ||||||
| chr6:54893961
|
A | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+23271A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54893961 | ||||||
| chr6:54894216
|
A | G | 57 | a0001c0012t0002g0127a0001c0012t0008g0170a0002c0003t0003g0001others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.444+23526A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894216 | ||||||
| chr6:54894428
|
A | G | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+23738A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894428 | ||||||
| chr6:54894587
|
G | A | 1 | a0001c0021t0005g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.444+23897G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894587 | ||||||
| chr6:54894595
|
G | C | 1 | a0001c0002t0002g0114 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.444+23905G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894595 | ||||||
| chr6:54894685
|
A | G | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(114): Show | 117 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.444+23995A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894685 | ||||||
| chr6:54894697
|
G | T | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(114): Show | 117 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.444+24007G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894697 | ||||||
| chr6:54894778
|
CTT | C | 32 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(29): Show | 33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.444+24089_444+2409 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54894778 | ||||||
| chr6:54895131
|
A | G | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(114): Show | 117 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.444+24441A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895131 | ||||||
| chr6:54895222
|
A | G | 1 | a0002c0005t0019g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.444+24532A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895222 | ||||||
| chr6:54895379
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.444+24689C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895379 | ||||||
| chr6:54895403
|
A | G | 14 | a0002c0003t0003g0128a0002c0004t0020g0107a0002c0004t0020g0134others(11): Show | 14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+24713A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895403 | ||||||
| chr6:54895469
|
T | C | 73 | a0001c0012t0002g0127a0001c0012t0008g0170a0002c0003t0003g0001others(70): Show | 74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.444+24779T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895469 | ||||||
| chr6:54895882
|
C | CT | 6 | a0003c0016t0007g0002a0003c0016t0027g0003a0004c0011t0008g0257others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+25197dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54895882 | |||||
| chr6:54895888
|
G | T | 114 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(111): Show | 114 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.444+25198G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54895888 | ||||||
| chr6:54896000
|
T | C | 57 | a0001c0012t0002g0127a0001c0012t0008g0170a0002c0003t0003g0001others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.444+25310T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896000 | ||||||
| chr6:54896125
|
C | T | 2 | a0003c0016t0007g0002a0003c0016t0027g0003 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444+25435C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896125 | ||||||
| chr6:54896378
|
A | G | 4 | a0003c0007t0006g0237a0003c0007t0006g0238a0003c0007t0006g0239others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+25688A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896378 | ||||||
| chr6:54896484
|
C | G | 190 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.444+25794C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896484 | ||||||
| chr6:54896558
|
C | A | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+25868C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896558 | ||||||
| chr6:54896609
|
A | T | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444+25919A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896609 | ||||||
| chr6:54896724
|
T | C | 9 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(6): Show | 9 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+26034T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896724 | ||||||
| chr6:54896978
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0193 | 2 | NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.444+26288G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54896978 | ||||||
| chr6:54897006
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+26316A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897006 | ||||||
| chr6:54897019
|
C | T | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+26329C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897019 | ||||||
| chr6:54897038
|
G | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+26348G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897038 | ||||||
| chr6:54897227
|
T | TAAAA | 73 | a0001c0012t0002g0127a0001c0012t0008g0170a0002c0003t0003g0001others(70): Show | 74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.444+26546_444+2654 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54897227 | |||||
| chr6:54897413
|
G | T | 1 | a0003c0006t0007g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.444+26723G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897413 | ||||||
| chr6:54897512
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.444+26822G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897512 | ||||||
| chr6:54897524
|
A | C | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.444+26834A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897524 | ||||||
| chr6:54897642
|
T | G | 1 | a0002c0003t0003g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+26952T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897642 | ||||||
| chr6:54897681
|
A | T | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444+26991A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897681 | ||||||
| chr6:54897827
|
T | G | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.444+27137T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897827 | ||||||
| chr6:54897935
|
G | A | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.444+27245G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897935 | ||||||
| chr6:54897992
|
T | C | 2 | a0001c0008t0005g0012a0001c0008t0005g0122 | 2 | NA18943.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.444+27302T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54897992 | ||||||
| chr6:54898106
|
G | T | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+27416G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898106 | ||||||
| chr6:54898166
|
T | C | 21 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(18): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.444+27476T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898166 | ||||||
| chr6:54898220
|
G | T | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(137): Show | 140 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.444+27530G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898220 | ||||||
| chr6:54898375
|
T | C | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.444+27685T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898375 | ||||||
| chr6:54898603
|
G | C | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-27768G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898603 | ||||||
| chr6:54898664
|
C | T | 9 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-27707C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898664 | ||||||
| chr6:54898697
|
C | G | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-27674C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898697 | ||||||
| chr6:54898697
|
C | T | 11 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(8): Show | 11 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.445-27674C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898697 | ||||||
| chr6:54898720
|
A | G | 5 | a0001c0001t0002g0095a0001c0002t0002g0186a0001c0002t0002g0197others(2): Show | 5 | HG00738.hp2 HG01928.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-27651A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898720 | ||||||
| chr6:54898778
|
G | A | 5 | a0002c0003t0003g0108a0002c0003t0003g0123a0002c0003t0003g0124others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-27593G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898778 | ||||||
| chr6:54898796
|
G | A | 5 | a0001c0012t0008g0170a0002c0005t0003g0016a0002c0026t0016g0264others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-27575G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898796 | ||||||
| chr6:54898998
|
C | T | 1 | a0001c0001t0023g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-27373C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54898998 | ||||||
| chr6:54899148
|
T | C | 5 | a0001c0012t0008g0170a0002c0005t0003g0016a0002c0026t0016g0264others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-27223T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899148 | ||||||
| chr6:54899223
|
C | A | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-27148C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899223 | ||||||
| chr6:54899240
|
G | A | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-27131G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899240 | ||||||
| chr6:54899250
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.445-27121A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899250 | ||||||
| chr6:54899385
|
C | T | 1 | a0001c0002t0002g0114 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.445-26986C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899385 | ||||||
| chr6:54899509
|
G | A | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-26862G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899509 | ||||||
| chr6:54899522
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0027others(34): Show | 37 | HG00423.hp1 HG00558.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.445-26849A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899522 | ||||||
| chr6:54899559
|
A | G | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-26812A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899559 | ||||||
| chr6:54899592
|
C | G | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-26779C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899592 | ||||||
| chr6:54899627
|
G | A | 1 | a0001c0002t0002g0196 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.445-26744G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899627 | ||||||
| chr6:54899751
|
G | A | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-26620G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899751 | ||||||
| chr6:54899768
|
A | G | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-26603A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899768 | ||||||
| chr6:54899852
|
T | C | 1 | a0001c0002t0002g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.445-26519T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899852 | ||||||
| chr6:54899862
|
A | G | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-26509A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54899862 | ||||||
| chr6:54900300
|
C | T | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-26071C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900300 | ||||||
| chr6:54900657
|
A | C | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-25714A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900657 | ||||||
| chr6:54900678
|
G | A | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-25693G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900678 | ||||||
| chr6:54900685
|
A | G | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-25686A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900685 | ||||||
| chr6:54900685
|
A | T | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-25686A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900685 | ||||||
| chr6:54900711
|
C | A | 14 | a0002c0003t0003g0128a0002c0004t0020g0107a0002c0004t0020g0134others(11): Show | 14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.445-25660C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900711 | ||||||
| chr6:54900968
|
T | C | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.445-25403T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54900968 | ||||||
| chr6:54901087
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.445-25284G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901087 | ||||||
| chr6:54901245
|
GTGTTCTT others(4): Show |
G | 1 | a0001c0001t0001g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.445-25122_445-2511 others(15): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54901245 | |||||
| chr6:54901357
|
A | T | 1 | a0001c0002t0002g0185 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.445-25014A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901357 | ||||||
| chr6:54901420
|
G | GATAA | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24948_445-2494 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54901420 | |||||
| chr6:54901424
|
G | C | 6 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-24947G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901424 | ||||||
| chr6:54901438
|
A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-24933A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901438 | ||||||
| chr6:54901591
|
C | T | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24780C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901591 | ||||||
| chr6:54901636
|
A | G | 5 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-24735A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901636 | ||||||
| chr6:54901678
|
G | T | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24693G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901678 | ||||||
| chr6:54901742
|
A | C | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24629A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901742 | ||||||
| chr6:54901933
|
G | A | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-24438G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54901933 | ||||||
| chr6:54902127
|
T | G | 59 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-24244T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902127 | ||||||
| chr6:54902189
|
G | A | 1 | a0004c0018t0008g0141 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.445-24182G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902189 | ||||||
| chr6:54902293
|
A | G | 1 | a0001c0002t0002g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445-24078A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902293 | ||||||
| chr6:54902316
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-24055G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902316 | ||||||
| chr6:54902577
|
C | T | 1 | a0002c0003t0003g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.445-23794C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902577 | ||||||
| chr6:54902598
|
G | GACATTTC others(3): Show |
1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-23767_445-2376 others(14): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54902598 | |||||
| chr6:54902608
|
T | C | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-23763T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902608 | ||||||
| chr6:54902664
|
G | GGCTCCCC others(22): Show |
6 | a0003c0007t0006g0169a0003c0007t0006g0240a0003c0007t0006g0255others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-23705_445-2370 others(33): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54902664 | |||||
| chr6:54902917
|
T | G | 3 | a0003c0007t0006g0169a0003c0007t0006g0255a0003c0007t0006g0262 | 3 | HG02895.hp2 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.445-23454T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54902917 | ||||||
| chr6:54903071
|
T | G | 5 | a0001c0012t0008g0170a0002c0005t0003g0016a0002c0026t0016g0264others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-23300T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903071 | ||||||
| chr6:54903361
|
C | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(196): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.445-23010C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903361 | ||||||
| chr6:54903416
|
C | T | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-22955C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903416 | ||||||
| chr6:54903515
|
G | A | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-22856G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903515 | ||||||
| chr6:54903805
|
T | A | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-22566T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903805 | ||||||
| chr6:54903841
|
T | C | 21 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(18): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-22530T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903841 | ||||||
| chr6:54903958
|
A | G | 2 | a0003c0006t0007g0246a0003c0006t0007g0252 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.445-22413A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903958 | ||||||
| chr6:54903972
|
A | T | 1 | a0001c0002t0002g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.445-22399A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54903972 | ||||||
| chr6:54904085
|
G | A | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-22286G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904085 | ||||||
| chr6:54904154
|
T | G | 1 | a0001c0021t0005g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.445-22217T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904154 | ||||||
| chr6:54904363
|
A | G | 1 | a0001c0002t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.445-22008A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904363 | ||||||
| chr6:54904538
|
G | C | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-21833G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904538 | ||||||
| chr6:54904555
|
A | G | 59 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-21816A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904555 | ||||||
| chr6:54904602
|
A | G | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-21769A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904602 | ||||||
| chr6:54904762
|
C | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-21609C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54904762 | ||||||
| chr6:54905072
|
GGGCACCT others(34): Show |
G | 4 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0001g0194others(1): Show | 4 | HG03831.hp2 NA19000.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-21297_445-2125 others(45): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54905072 | |||||
| chr6:54905116
|
GCA | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0001g0194others(1): Show | 4 | HG03831.hp2 NA19000.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-21254_445-2125 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905116 | ||||||
| chr6:54905177
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-21194A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905177 | ||||||
| chr6:54905446
|
T | C | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-20925T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905446 | ||||||
| chr6:54905531
|
G | A | 39 | a0001c0002t0002g0203a0001c0012t0002g0127a0002c0003t0003g0001others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.445-20840G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905531 | ||||||
| chr6:54905544
|
A | T | 1 | a0002c0003t0003g0165 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445-20827A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905544 | ||||||
| chr6:54905577
|
G | A | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-20794G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905577 | ||||||
| chr6:54905630
|
A | T | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-20741A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905630 | ||||||
| chr6:54905786
|
G | A | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-20585G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905786 | ||||||
| chr6:54905812
|
CATA | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(83): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.445-20555_445-2055 others(7): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54905812 | |||||
| chr6:54905871
|
A | T | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-20500A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54905871 | ||||||
| chr6:54906004
|
T | A | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-20367T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906004 | ||||||
| chr6:54906053
|
G | GA | 10 | a0001c0001t0001g0078a0001c0001t0010g0020a0001c0001t0010g0140others(7): Show | 10 | HG02056.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-20303dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54906053 | |||||
| chr6:54906053
|
GA | G | 22 | a0001c0001t0023g0087a0002c0003t0016g0254a0002c0004t0020g0107others(19): Show | 22 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.445-20303delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54906053 | |||||
| chr6:54906053
|
GAA | G | 39 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.445-20304_445-2030 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54906053 | |||||
| chr6:54906071
|
A | G | 7 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(4): Show | 7 | HG00544.hp1 NA18943.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-20300A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906071 | ||||||
| chr6:54906138
|
A | G | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-20233A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906138 | ||||||
| chr6:54906221
|
G | A | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(138): Show | 141 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.445-20150G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906221 | ||||||
| chr6:54906232
|
C | A | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-20139C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906232 | ||||||
| chr6:54906339
|
A | C | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(208): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.445-20032A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906339 | ||||||
| chr6:54906487
|
C | T | 1 | a0001c0012t0002g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445-19884C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906487 | ||||||
| chr6:54906499
|
C | A | 19 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(16): Show | 19 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.445-19872C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906499 | ||||||
| chr6:54906683
|
C | T | 1 | a0002c0005t0003g0224 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.445-19688C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906683 | ||||||
| chr6:54906684
|
G | A | 1 | a0002c0003t0026g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.445-19687G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906684 | ||||||
| chr6:54906716
|
A | G | 2 | a0004c0014t0002g0143a0004c0014t0002g0144 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-19655A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906716 | ||||||
| chr6:54906749
|
A | G | 1 | a0002c0003t0003g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445-19622A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906749 | ||||||
| chr6:54906760
|
A | G | 5 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-19611A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906760 | ||||||
| chr6:54906793
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-19578A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906793 | ||||||
| chr6:54906833
|
A | C | 7 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-19538A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906833 | ||||||
| chr6:54906861
|
A | T | 1 | a0002c0005t0013g0147 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.445-19510A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54906861 | ||||||
| chr6:54907140
|
C | T | 40 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0012t0002g0127others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.445-19231C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907140 | ||||||
| chr6:54907300
|
G | A | 13 | a0001c0012t0002g0127a0002c0003t0003g0108a0002c0003t0003g0123others(10): Show | 13 | HG00438.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.445-19071G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907300 | ||||||
| chr6:54907362
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.445-19009A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907362 | ||||||
| chr6:54907412
|
G | GTA | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(208): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.445-18958_445-1895 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907412 | |||||
| chr6:54907484
|
C | T | 2 | a0002c0003t0003g0251a0002c0005t0003g0121 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.445-18887C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907484 | ||||||
| chr6:54907604
|
T | TTTTTTTT others(298): Show |
10 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(7): Show | 10 | HG03195.hp1 HG03491.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-18764_445-1876 others(309): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907604 | |||||
| chr6:54907604
|
T | TTTTTTTT others(299): Show |
2 | a0001c0008t0005g0015a0001c0013t0005g0270 | 2 | HG00544.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.445-18764_445-1876 others(310): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907604 | |||||
| chr6:54907629
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.445-18742A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907629 | ||||||
| chr6:54907629
|
AT | A | 57 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.445-18733delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54907629 | |||||
| chr6:54907638
|
T | A | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-18733T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907638 | ||||||
| chr6:54907744
|
G | A | 38 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.445-18627G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907744 | ||||||
| chr6:54907978
|
A | C | 5 | a0001c0001t0010g0140a0001c0001t0010g0145a0001c0001t0010g0146others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-18393A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54907978 | ||||||
| chr6:54908016
|
G | T | 140 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(137): Show | 140 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.445-18355G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908016 | ||||||
| chr6:54908131
|
GAA | G | 202 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(199): Show | 203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.445-18223_445-1822 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54908131 | |||||
| chr6:54908276
|
T | C | 57 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.445-18095T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908276 | ||||||
| chr6:54908295
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-18076A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908295 | ||||||
| chr6:54908402
|
G | C | 1 | a0002c0010t0009g0007 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.445-17969G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908402 | ||||||
| chr6:54908495
|
ATTAG | A | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-17872_445-1786 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54908495 | |||||
| chr6:54908841
|
C | T | 32 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(29): Show | 33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-17530C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908841 | ||||||
| chr6:54908850
|
A | G | 2 | a0002c0003t0016g0254a0002c0004t0033g0152 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.445-17521A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908850 | ||||||
| chr6:54908956
|
G | A | 5 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-17415G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908956 | ||||||
| chr6:54908988
|
T | C | 21 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(18): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-17383T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54908988 | ||||||
| chr6:54909019
|
G | A | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-17352G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909019 | ||||||
| chr6:54909146
|
G | GT | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(90): Show | 93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-17219dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54909146 | |||||
| chr6:54909214
|
G | A | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-17157G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909214 | ||||||
| chr6:54909373
|
G | A | 1 | a0006c0020t0002g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.445-16998G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909373 | ||||||
| chr6:54909412
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-16959G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909412 | ||||||
| chr6:54909414
|
T | C | 5 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-16957T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909414 | ||||||
| chr6:54909449
|
A | C | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-16922A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909449 | ||||||
| chr6:54909480
|
G | T | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-16891G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909480 | ||||||
| chr6:54909624
|
A | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-16747A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909624 | ||||||
| chr6:54909647
|
G | A | 43 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.445-16724G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909647 | ||||||
| chr6:54909648
|
C | A | 16 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-16723C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909648 | ||||||
| chr6:54909659
|
G | A | 4 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-16712G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909659 | ||||||
| chr6:54909667
|
C | T | 1 | a0002c0003t0003g0165 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445-16704C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909667 | ||||||
| chr6:54909797
|
C | T | 1 | a0004c0011t0008g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445-16574C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54909797 | ||||||
| chr6:54910187
|
G | T | 2 | a0003c0006t0007g0171a0003c0006t0007g0172 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.445-16184G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910187 | ||||||
| chr6:54910286
|
T | G | 1 | a0001c0002t0002g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.445-16085T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910286 | ||||||
| chr6:54910388
|
G | A | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-15983G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910388 | ||||||
| chr6:54910402
|
T | TC | 5 | a0001c0001t0001g0106a0001c0001t0001g0195a0001c0001t0004g0028others(2): Show | 5 | HG00741.hp1 HG01175.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-15966dupC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54910402 | |||||
| chr6:54910587
|
T | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-15784T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910587 | ||||||
| chr6:54910682
|
T | G | 7 | a0002c0003t0003g0128a0002c0009t0011g0164a0002c0009t0011g0247others(4): Show | 7 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-15689T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910682 | ||||||
| chr6:54910683
|
C | G | 32 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(29): Show | 33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-15688C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910683 | ||||||
| chr6:54910775
|
C | T | 6 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-15596C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910775 | ||||||
| chr6:54910877
|
G | GT | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(89): Show | 92 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.445-15486dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54910877 | |||||
| chr6:54910882
|
T | C | 5 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-15489T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910882 | ||||||
| chr6:54910897
|
G | C | 6 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-15474G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910897 | ||||||
| chr6:54910996
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.445-15375C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910996 | ||||||
| chr6:54910997
|
A | G | 2 | a0002c0003t0016g0254a0002c0004t0033g0152 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.445-15374A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54910997 | ||||||
| chr6:54911079
|
C | A | 11 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-15292C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911079 | ||||||
| chr6:54911140
|
C | CGT | 8 | a0001c0001t0002g0095a0001c0001t0010g0201a0001c0002t0002g0115others(5): Show | 8 | HG01243.hp2 HG02257.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-15206_445-1520 others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGT | 28 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(25): Show | 28 | HG00735.hp2 HG00741.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.445-15208_445-1520 others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGTGT | 39 | a0001c0001t0001g0078a0001c0001t0010g0145a0001c0001t0010g0146others(36): Show | 39 | HG00544.hp1 HG01175.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.445-15210_445-1520 others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGTGTG others(1): Show |
22 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0004g0052others(19): Show | 22 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.445-15212_445-1520 others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGTGTG others(3): Show |
93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(90): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-15214_445-1520 others(14): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGTGTG others(5): Show |
6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0076others(3): Show | 6 | HG02280.hp2 HG03669.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-15216_445-1520 others(16): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGTGTG others(7): Show |
11 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(8): Show | 11 | HG01069.hp2 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-15218_445-1520 others(18): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | CGTGTGTG others(9): Show |
4 | a0002c0003t0003g0120a0002c0005t0013g0147a0005c0015t0017g0019others(1): Show | 4 | HG02895.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-15220_445-1520 others(20): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54911140 | |||||
| chr6:54911140
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-15231C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911140 | ||||||
| chr6:54911190
|
T | C | 1 | a0001c0001t0010g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-15181T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911190 | ||||||
| chr6:54911465
|
T | C | 32 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(29): Show | 33 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-14906T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911465 | ||||||
| chr6:54911484
|
C | T | 2 | a0002c0003t0003g0001a0002c0003t0003g0125 | 3 | HG02280.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445-14887C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54911484 | ||||||
| chr6:54912097
|
C | G | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-14274C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912097 | ||||||
| chr6:54912204
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.445-14167A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912204 | ||||||
| chr6:54912420
|
CA | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0097others(3): Show | 6 | HG00423.hp1 HG01074.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-13939delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54912420 | |||||
| chr6:54912509
|
A | C | 1 | a0001c0012t0001g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.445-13862A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912509 | ||||||
| chr6:54912690
|
C | T | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-13681C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912690 | ||||||
| chr6:54912875
|
A | G | 1 | a0002c0003t0003g0165 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445-13496A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54912875 | ||||||
| chr6:54913035
|
G | A | 138 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(135): Show | 138 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.445-13336G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913035 | ||||||
| chr6:54913143
|
TA | T | 3 | a0001c0012t0008g0170a0002c0005t0003g0016a0002c0026t0016g0264 | 3 | HG02258.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-13224delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54913143 | |||||
| chr6:54913303
|
A | T | 1 | a0006c0020t0002g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.445-13068A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913303 | ||||||
| chr6:54913334
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.445-13037G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913334 | ||||||
| chr6:54913513
|
C | T | 1 | a0001c0001t0010g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.445-12858C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913513 | ||||||
| chr6:54913578
|
T | C | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-12793T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913578 | ||||||
| chr6:54913630
|
A | T | 1 | a0002c0003t0003g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.445-12741A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913630 | ||||||
| chr6:54913664
|
C | A | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-12707C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913664 | ||||||
| chr6:54913805
|
G | A | 19 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(16): Show | 19 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.445-12566G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913805 | ||||||
| chr6:54913854
|
A | G | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-12517A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913854 | ||||||
| chr6:54913893
|
CT | C | 21 | a0001c0001t0001g0074a0001c0002t0002g0088a0001c0002t0002g0110others(18): Show | 21 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.445-12468delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54913893 | |||||
| chr6:54913902
|
T | A | 125 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(122): Show | 126 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.445-12469T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913902 | ||||||
| chr6:54913902
|
T | TA | 16 | a0002c0003t0003g0128a0002c0005t0013g0147a0002c0005t0013g0202others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-12469_445-1246 others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913902 | ||||||
| chr6:54913903
|
T | A | 264 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(261): Show | 265 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.445-12468T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913903 | ||||||
| chr6:54913918
|
G | T | 1 | a0001c0013t0005g0267 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.445-12453G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54913918 | ||||||
| chr6:54914047
|
A | G | 19 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(16): Show | 19 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.445-12324A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914047 | ||||||
| chr6:54914056
|
A | C | 11 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-12315A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914056 | ||||||
| chr6:54914127
|
C | T | 3 | a0001c0012t0008g0170a0002c0005t0003g0016a0002c0026t0016g0264 | 3 | HG02258.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-12244C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914127 | ||||||
| chr6:54914136
|
G | A | 1 | a0002c0010t0009g0025 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.445-12235G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914136 | ||||||
| chr6:54914721
|
C | A | 59 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-11650C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914721 | ||||||
| chr6:54914838
|
G | T | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-11533G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914838 | ||||||
| chr6:54914905
|
C | A | 59 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-11466C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914905 | ||||||
| chr6:54914984
|
T | C | 2 | a0005c0015t0017g0019a0005c0015t0017g0148 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.445-11387T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54914984 | ||||||
| chr6:54915365
|
C | A | 1 | a0002c0003t0003g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.445-11006C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915365 | ||||||
| chr6:54915367
|
G | A | 3 | a0004c0014t0002g0143a0004c0014t0002g0144a0004c0014t0002g0260 | 3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.445-11004G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915367 | ||||||
| chr6:54915387
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.445-10984G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915387 | ||||||
| chr6:54915488
|
C | G | 21 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(18): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-10883C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915488 | ||||||
| chr6:54915508
|
TAGAAACT others(321): Show |
T | 59 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-10846_445-1051 others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915508 | |||||
| chr6:54915581
|
T | C | 1 | a0001c0021t0005g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.445-10790T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915581 | ||||||
| chr6:54915589
|
G | T | 1 | a0004c0014t0002g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.445-10782G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915589 | ||||||
| chr6:54915667
|
G | A | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-10704G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915667 | ||||||
| chr6:54915735
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.445-10636A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915735 | ||||||
| chr6:54915755
|
G | C | 9 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-10616G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915755 | ||||||
| chr6:54915812
|
C | CA | 16 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0076others(13): Show | 16 | HG00423.hp1 HG00735.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.445-10534dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
C | CAAAAA | 9 | a0001c0008t0025g0018a0003c0007t0006g0169a0003c0007t0006g0237others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-10538_445-1053 others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
C | CAAAAAA | 20 | a0001c0002t0002g0256a0001c0008t0005g0011a0001c0008t0005g0013others(17): Show | 20 | HG00544.hp1 HG02109.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-10539_445-1053 others(10): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
C | CAAAAAAA | 11 | a0001c0008t0005g0012a0003c0006t0007g0166a0003c0006t0007g0171others(8): Show | 11 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.445-10540_445-1053 others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
C | CAAAAAAA others(3): Show |
3 | a0001c0002t0002g0088a0001c0002t0002g0116a0001c0002t0002g0139 | 3 | NA18953.hp2 NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.445-10543_445-1053 others(14): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
C | CAAAAAAA others(4): Show |
2 | a0001c0002t0002g0110a0001c0002t0002g0113 | 2 | NA18977.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.445-10544_445-1053 others(15): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
C | CAAAAAAA others(5): Show |
5 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0114others(2): Show | 5 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-10545_445-1053 others(16): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915812
|
CA | C | 16 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0082others(13): Show | 16 | HG01069.hp1 HG01256.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-10534delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54915812 | |||||
| chr6:54915845
|
A | G | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-10526A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915845 | ||||||
| chr6:54915982
|
C | G | 59 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-10389C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54915982 | ||||||
| chr6:54916013
|
A | G | 10 | a0001c0002t0002g0256a0003c0007t0006g0169a0003c0007t0006g0237others(7): Show | 10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-10358A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916013 | ||||||
| chr6:54916036
|
G | A | 5 | a0001c0001t0010g0140a0001c0001t0010g0145a0001c0001t0010g0146others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-10335G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916036 | ||||||
| chr6:54916217
|
G | A | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445-10154G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916217 | ||||||
| chr6:54916379
|
AT | A | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-9983delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54916379 | |||||
| chr6:54916558
|
A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-9813A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916558 | ||||||
| chr6:54916590
|
A | G | 44 | a0001c0012t0002g0127a0002c0003t0003g0001a0002c0003t0003g0102others(41): Show | 45 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.445-9781A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916590 | ||||||
| chr6:54916743
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445-9628C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916743 | ||||||
| chr6:54916788
|
T | C | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-9583T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916788 | ||||||
| chr6:54916802
|
A | T | 1 | a0001c0002t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.445-9569A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916802 | ||||||
| chr6:54916810
|
C | T | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-9561C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916810 | ||||||
| chr6:54916940
|
T | C | 34 | a0002c0003t0003g0128a0002c0003t0016g0254a0002c0004t0020g0107others(31): Show | 34 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.445-9431T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916940 | ||||||
| chr6:54916964
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-9407G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54916964 | ||||||
| chr6:54917476
|
T | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-8895T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917476 | ||||||
| chr6:54917491
|
A | G | 13 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-8880A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917491 | ||||||
| chr6:54917495
|
A | C | 2 | a0005c0015t0017g0019a0005c0015t0017g0148 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.445-8876A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917495 | ||||||
| chr6:54917846
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | NA18963.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.445-8525C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917846 | ||||||
| chr6:54917854
|
A | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-8517A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917854 | ||||||
| chr6:54917861
|
C | G | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-8510C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54917861 | ||||||
| chr6:54918095
|
A | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.445-8276A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918095 | ||||||
| chr6:54918416
|
G | A | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-7955G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918416 | ||||||
| chr6:54918468
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(90): Show | 93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-7903C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918468 | ||||||
| chr6:54918492
|
A | G | 21 | a0002c0003t0016g0254a0002c0004t0020g0107a0002c0004t0020g0134others(18): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.445-7879A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918492 | ||||||
| chr6:54918539
|
G | A | 1 | a0004c0024t0008g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.445-7832G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918539 | ||||||
| chr6:54918572
|
T | A | 19 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(16): Show | 19 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.445-7799T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918572 | ||||||
| chr6:54918613
|
C | G | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-7758C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918613 | ||||||
| chr6:54918859
|
C | G | 1 | a0001c0002t0002g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.445-7512C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54918859 | ||||||
| chr6:54919141
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.445-7230A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919141 | ||||||
| chr6:54919254
|
T | G | 1 | a0002c0004t0012g0219 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445-7117T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919254 | ||||||
| chr6:54919388
|
C | A | 1 | a0001c0001t0002g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.445-6983C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919388 | ||||||
| chr6:54919425
|
T | C | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-6946T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919425 | ||||||
| chr6:54919579
|
A | G | 4 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0174others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-6792A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919579 | ||||||
| chr6:54919654
|
C | T | 1 | a0002c0003t0003g0136 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.445-6717C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919654 | ||||||
| chr6:54919733
|
A | G | 1 | a0002c0003t0003g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-6638A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919733 | ||||||
| chr6:54919854
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.445-6517C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919854 | ||||||
| chr6:54919862
|
T | C | 1 | a0002c0005t0013g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445-6509T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54919862 | ||||||
| chr6:54920004
|
T | C | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-6367T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920004 | ||||||
| chr6:54920039
|
G | C | 2 | a0004c0018t0008g0141a0004c0018t0008g0156 | 2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.445-6332G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920039 | ||||||
| chr6:54920238
|
C | T | 1 | a0002c0004t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445-6133C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920238 | ||||||
| chr6:54920749
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.445-5622A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920749 | ||||||
| chr6:54920827
|
G | A | 16 | a0002c0003t0016g0254a0002c0004t0020g0107a0002c0004t0020g0134others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-5544G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920827 | ||||||
| chr6:54920983
|
G | A | 60 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.445-5388G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54920983 | ||||||
| chr6:54921158
|
C | T | 1 | a0002c0003t0016g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445-5213C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921158 | ||||||
| chr6:54921242
|
T | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039 | 3 | HG01258.hp1 HG02055.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.445-5129T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921242 | ||||||
| chr6:54921244
|
C | T | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-5127C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921244 | ||||||
| chr6:54921251
|
A | G | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-5120A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921251 | ||||||
| chr6:54921358
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0195 | 2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5013G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921358 | ||||||
| chr6:54921362
|
T | TACAGTCT others(3): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0195 | 2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5009_445-5008i others(12): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921362 | ||||||
| chr6:54921363
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0195 | 2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5008C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921363 | ||||||
| chr6:54921365
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0195 | 2 | NA18943.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.445-5006G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921365 | ||||||
| chr6:54921492
|
G | T | 1 | a0005c0015t0017g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445-4879G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921492 | ||||||
| chr6:54921579
|
G | A | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-4792G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921579 | ||||||
| chr6:54921608
|
A | G | 3 | a0004c0014t0002g0143a0004c0014t0002g0144a0004c0014t0002g0260 | 3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.445-4763A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921608 | ||||||
| chr6:54921698
|
A | G | 1 | a0001c0002t0002g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.445-4673A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921698 | ||||||
| chr6:54921768
|
T | C | 1 | a0001c0002t0002g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.445-4603T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921768 | ||||||
| chr6:54921797
|
T | C | 2 | a0001c0012t0002g0127a0006c0020t0002g0031 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.445-4574T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921797 | ||||||
| chr6:54921800
|
A | G | 7 | a0003c0007t0006g0169a0003c0007t0006g0240a0003c0007t0006g0255others(4): Show | 7 | HG02451.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-4571A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921800 | ||||||
| chr6:54921967
|
C | T | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445-4404C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54921967 | ||||||
| chr6:54922060
|
C | A | 16 | a0002c0003t0016g0254a0002c0004t0020g0107a0002c0004t0020g0134others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-4311C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922060 | ||||||
| chr6:54922161
|
A | G | 13 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-4210A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922161 | ||||||
| chr6:54922348
|
T | C | 1 | a0001c0002t0002g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.445-4023T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922348 | ||||||
| chr6:54922465
|
G | A | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-3906G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922465 | ||||||
| chr6:54922473
|
AT | A | 13 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(10): Show | 13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-3896delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54922473 | |||||
| chr6:54922717
|
T | C | 1 | a0001c0001t0023g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-3654T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922717 | ||||||
| chr6:54922718
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.445-3653C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922718 | ||||||
| chr6:54922934
|
C | T | 7 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0173others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-3437C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922934 | ||||||
| chr6:54922958
|
A | G | 2 | a0004c0018t0008g0141a0004c0018t0008g0156 | 2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.445-3413A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54922958 | ||||||
| chr6:54923069
|
G | A | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-3302G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923069 | ||||||
| chr6:54923090
|
G | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.445-3281G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923090 | ||||||
| chr6:54923095
|
A | G | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-3276A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923095 | ||||||
| chr6:54923110
|
C | T | 2 | a0002c0004t0003g0154a0002c0004t0003g0155 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.445-3261C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923110 | ||||||
| chr6:54923115
|
A | G | 1 | a0001c0008t0005g0014 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.445-3256A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923115 | ||||||
| chr6:54923254
|
G | T | 1 | a0008c0027t0002g0182 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-3117G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923254 | ||||||
| chr6:54923340
|
T | A | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-3031T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923340 | ||||||
| chr6:54923435
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.445-2936C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923435 | ||||||
| chr6:54923442
|
A | G | 1 | a0001c0002t0002g0256 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-2929A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923442 | ||||||
| chr6:54923454
|
G | A | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(194): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.445-2917G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923454 | ||||||
| chr6:54923657
|
G | A | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-2714G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923657 | ||||||
| chr6:54923790
|
T | TA | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-2580dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923790 | |||||
| chr6:54923818
|
C | A | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-2553C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923818 | ||||||
| chr6:54923822
|
T | C | 1 | a0001c0008t0005g0015 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.445-2549T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923822 | ||||||
| chr6:54923866
|
C | CT | 8 | a0001c0002t0015g0005a0001c0002t0015g0008a0004c0011t0008g0257others(5): Show | 8 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-2492dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923866 | |||||
| chr6:54923866
|
CT | C | 13 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0083others(10): Show | 13 | HG01243.hp2 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.445-2492delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923866 | |||||
| chr6:54923927
|
T | C | 20 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(17): Show | 20 | HG01175.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-2444T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54923927 | ||||||
| chr6:54923979
|
T | TA | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2390dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54923979 | |||||
| chr6:54924024
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(90): Show | 93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-2347C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924024 | ||||||
| chr6:54924095
|
G | T | 1 | a0001c0001t0004g0051 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.445-2276G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924095 | ||||||
| chr6:54924129
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.445-2242C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924129 | ||||||
| chr6:54924188
|
T | C | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445-2183T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924188 | ||||||
| chr6:54924188
|
TAC | T | 86 | a0001c0001t0010g0020a0001c0001t0010g0140a0001c0001t0010g0145others(83): Show | 87 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.445-2156_445-2155d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54924188 | |||||
| chr6:54924188
|
TACAC | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(94): Show | 97 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.445-2158_445-2155d others(6): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54924188 | |||||
| chr6:54924188
|
TACACAC | T | 6 | a0002c0009t0011g0164a0002c0009t0011g0247a0002c0009t0011g0248others(3): Show | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-2160_445-2155d others(8): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54924188 | |||||
| chr6:54924211
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.445-2160A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924211 | ||||||
| chr6:54924226
|
AC | A | 3 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0010g0201 | 3 | HG02257.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.445-2144delC | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924226 | ||||||
| chr6:54924274
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(90): Show | 93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.445-2097C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924274 | ||||||
| chr6:54924362
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-2009C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924362 | ||||||
| chr6:54924460
|
T | C | 1 | a0002c0026t0016g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.445-1911T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924460 | ||||||
| chr6:54924511
|
C | T | 3 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0125 | 4 | HG01243.hp1 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-1860C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924511 | ||||||
| chr6:54924722
|
A | T | 1 | a0001c0002t0002g0228 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.445-1649A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924722 | ||||||
| chr6:54924956
|
C | T | 2 | a0001c0002t0002g0115a0001c0002t0002g0221 | 2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.445-1415C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924956 | ||||||
| chr6:54924998
|
G | A | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-1373G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54924998 | ||||||
| chr6:54925023
|
A | G | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-1348A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925023 | ||||||
| chr6:54925122
|
A | G | 1 | a0001c0002t0002g0215 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.445-1249A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925122 | ||||||
| chr6:54925143
|
A | G | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.445-1228A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925143 | ||||||
| chr6:54925186
|
T | G | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-1185T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925186 | ||||||
| chr6:54925327
|
A | T | 2 | a0003c0006t0007g0246a0003c0006t0007g0252 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.445-1044A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925327 | ||||||
| chr6:54925685
|
A | G | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-686A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925685 | ||||||
| chr6:54925688
|
T | G | 84 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-683T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925688 | ||||||
| chr6:54925773
|
CTG | C | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-595_445-594del others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 54925773 | |||||
| chr6:54925800
|
G | T | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-571G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925800 | ||||||
| chr6:54925852
|
A | G | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.445-519A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925852 | ||||||
| chr6:54925883
|
A | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0090a0001c0001t0001g0162others(1): Show | 4 | HG01256.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-488A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925883 | ||||||
| chr6:54925930
|
T | G | 1 | a0001c0002t0002g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.445-441T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925930 | ||||||
| chr6:54925959
|
C | T | 1 | a0001c0002t0002g0214 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.445-412C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925959 | ||||||
| chr6:54925992
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-379A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54925992 | ||||||
| chr6:54926002
|
T | C | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.445-369T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54926002 | ||||||
| chr6:54926171
|
G | T | 9 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-200G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 2/4 | chr6 | 54926171 | ||||||
| chr6:54926591
|
T | C | 5 | a0001c0002t0002g0161a0001c0002t0002g0163a0001c0002t0002g0210others(2): Show | 5 | HG00280.hp2 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+56T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926591 | ||||||
| chr6:54926606
|
C | T | 13 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.609+71C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926606 | ||||||
| chr6:54926692
|
T | C | 2 | a0005c0015t0017g0019a0005c0015t0017g0148 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609+157T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926692 | ||||||
| chr6:54926783
|
A | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.609+248A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926783 | ||||||
| chr6:54926812
|
T | C | 2 | a0001c0001t0004g0028a0001c0001t0004g0046 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.609+277T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926812 | ||||||
| chr6:54926887
|
A | G | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.609+352A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926887 | ||||||
| chr6:54926922
|
A | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.609+387A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926922 | ||||||
| chr6:54926925
|
G | A | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(95): Show | 98 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.609+390G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926925 | ||||||
| chr6:54926975
|
C | A | 6 | a0002c0010t0009g0006a0002c0010t0009g0007a0002c0010t0009g0025others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+440C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54926975 | ||||||
| chr6:54927040
|
G | A | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.610-468G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927040 | ||||||
| chr6:54927079
|
A | C | 1 | a0002c0010t0009g0025 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.610-429A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927079 | ||||||
| chr6:54927163
|
G | A | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.610-345G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927163 | ||||||
| chr6:54927201
|
G | A | 60 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.610-307G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927201 | ||||||
| chr6:54927252
|
G | GT | 10 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(7): Show | 10 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-250dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 54927252 | |||||
| chr6:54927263
|
T | A | 2 | a0001c0001t0001g0194a0001c0002t0001g0158 | 2 | NA19000.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.610-245T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927263 | ||||||
| chr6:54927328
|
A | G | 2 | a0001c0002t0002g0161a0001c0002t0002g0210 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.610-180A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927328 | ||||||
| chr6:54927383
|
GT | G | 33 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(30): Show | 34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.610-115delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 54927383 | |||||
| chr6:54927410
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.610-98T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927410 | ||||||
| chr6:54927438
|
A | G | 60 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.610-70A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 3/4 | chr6 | 54927438 | ||||||
| chr6:54927728
|
T | TA | 94 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0022others(91): Show | 94 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.734+122dupA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54927728 | |||||
| chr6:54927728
|
T | TAA | 30 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0073others(27): Show | 30 | HG01175.hp1 HG01175.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.734+121_734+122dup others(2): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54927728 | |||||
| chr6:54927728
|
TA | T | 23 | a0001c0001t0001g0034a0001c0001t0002g0077a0001c0001t0002g0095others(20): Show | 23 | HG00735.hp2 HG01069.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.734+122delA | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54927728 | |||||
| chr6:54927794
|
C | T | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+162C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54927794 | ||||||
| chr6:54928349
|
G | A | 1 | a0001c0002t0002g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.734+717G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928349 | ||||||
| chr6:54928358
|
G | C | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+726G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928358 | ||||||
| chr6:54928641
|
C | A | 84 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.734+1009C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928641 | ||||||
| chr6:54928641
|
C | T | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.734+1009C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928641 | ||||||
| chr6:54928844
|
G | T | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+1212G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54928844 | ||||||
| chr6:54929059
|
T | C | 84 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.734+1427T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929059 | ||||||
| chr6:54929062
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.734+1430C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929062 | ||||||
| chr6:54929635
|
T | C | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+2003T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929635 | ||||||
| chr6:54929649
|
G | A | 1 | a0002c0003t0003g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.734+2017G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929649 | ||||||
| chr6:54929724
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.734+2092A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929724 | ||||||
| chr6:54929743
|
C | T | 1 | a0002c0005t0003g0224 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.734+2111C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929743 | ||||||
| chr6:54929860
|
T | A | 1 | a0002c0026t0016g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.734+2228T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54929860 | ||||||
| chr6:54930084
|
A | C | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(194): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.734+2452A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930084 | ||||||
| chr6:54930222
|
G | C | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.734+2590G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930222 | ||||||
| chr6:54930240
|
G | A | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.734+2608G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930240 | ||||||
| chr6:54930249
|
T | A | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+2617T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930249 | ||||||
| chr6:54930470
|
T | C | 2 | a0002c0004t0003g0154a0002c0004t0003g0155 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.734+2838T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930470 | ||||||
| chr6:54930563
|
T | G | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+2931T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930563 | ||||||
| chr6:54930595
|
C | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.734+2963C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930595 | ||||||
| chr6:54930786
|
G | C | 1 | a0001c0001t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.734+3154G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930786 | ||||||
| chr6:54930817
|
A | T | 2 | a0003c0006t0007g0246a0003c0006t0007g0252 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.734+3185A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930817 | ||||||
| chr6:54930937
|
C | G | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(211): Show | 215 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.734+3305C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54930937 | ||||||
| chr6:54931004
|
A | G | 45 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.734+3372A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931004 | ||||||
| chr6:54931111
|
A | G | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.734+3479A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931111 | ||||||
| chr6:54931164
|
T | C | 7 | a0002c0003t0003g0109a0002c0003t0003g0120a0002c0003t0003g0129others(4): Show | 7 | HG01069.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.734+3532T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931164 | ||||||
| chr6:54931484
|
CTTATAAT others(2): Show |
C | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+3867_734+3875d others(11): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54931484 | |||||
| chr6:54931513
|
T | A | 5 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+3881T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931513 | ||||||
| chr6:54931627
|
C | T | 1 | a0001c0002t0002g0215 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.734+3995C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931627 | ||||||
| chr6:54931803
|
C | T | 5 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.734+4171C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931803 | ||||||
| chr6:54931847
|
A | G | 1 | a0001c0008t0005g0017 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.734+4215A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54931847 | ||||||
| chr6:54932007
|
C | CT | 109 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(106): Show | 109 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.734+4395dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | |||||
| chr6:54932007
|
C | CTT | 25 | a0002c0003t0003g0108a0002c0003t0003g0136a0002c0004t0020g0134others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.734+4394_734+4395d others(4): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | |||||
| chr6:54932007
|
C | CTTT | 54 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0109others(51): Show | 55 | HG00438.hp2 HG01168.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.734+4393_734+4395d others(5): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | |||||
| chr6:54932007
|
CT | C | 13 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(10): Show | 13 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.734+4395delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932007 | |||||
| chr6:54932032
|
C | T | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+4400C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932032 | ||||||
| chr6:54932067
|
A | G | 2 | a0005c0015t0017g0019a0005c0015t0017g0148 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.734+4435A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932067 | ||||||
| chr6:54932086
|
T | C | 84 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.734+4454T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932086 | ||||||
| chr6:54932165
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.734+4533C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932165 | ||||||
| chr6:54932294
|
A | G | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+4662A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932294 | ||||||
| chr6:54932571
|
A | T | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.734+4939A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932571 | ||||||
| chr6:54932676
|
C | CTCAGATT | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(194): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.734+5047_734+5048i others(9): Show |
FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54932676 | |||||
| chr6:54932815
|
G | A | 1 | a0002c0003t0003g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.734+5183G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932815 | ||||||
| chr6:54932831
|
C | G | 2 | a0001c0002t0015g0005a0001c0002t0015g0008 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.734+5199C>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54932831 | ||||||
| chr6:54933057
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.734+5425C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933057 | ||||||
| chr6:54933142
|
C | CT | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.734+5520dupT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54933142 | |||||
| chr6:54933508
|
T | C | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.734+5876T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933508 | ||||||
| chr6:54933561
|
TG | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.734+5930delG | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933561 | ||||||
| chr6:54933711
|
T | C | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-5995T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933711 | ||||||
| chr6:54933735
|
A | T | 11 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-5971A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933735 | ||||||
| chr6:54933919
|
A | T | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-5787A>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933919 | ||||||
| chr6:54933984
|
A | G | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-5722A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54933984 | ||||||
| chr6:54934049
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.735-5657G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934049 | ||||||
| chr6:54934058
|
C | A | 1 | a0001c0002t0002g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.735-5648C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934058 | ||||||
| chr6:54934070
|
G | T | 1 | a0002c0004t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.735-5636G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934070 | ||||||
| chr6:54934089
|
G | A | 44 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(41): Show | 45 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.735-5617G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934089 | ||||||
| chr6:54934112
|
G | T | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-5594G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934112 | ||||||
| chr6:54934134
|
C | T | 12 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(9): Show | 12 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-5572C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934134 | ||||||
| chr6:54934171
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.735-5535C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934171 | ||||||
| chr6:54934191
|
G | A | 11 | a0003c0007t0006g0169a0003c0007t0006g0237a0003c0007t0006g0238others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.735-5515G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934191 | ||||||
| chr6:54934323
|
T | C | 33 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(30): Show | 34 | HG00438.hp2 HG01069.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.735-5383T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934323 | ||||||
| chr6:54934355
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.735-5351A>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934355 | ||||||
| chr6:54934467
|
G | T | 14 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(11): Show | 14 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.735-5239G>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934467 | ||||||
| chr6:54934538
|
C | T | 3 | a0004c0014t0002g0143a0004c0014t0002g0144a0004c0014t0002g0260 | 3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.735-5168C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934538 | ||||||
| chr6:54934683
|
T | C | 2 | a0005c0015t0017g0019a0005c0015t0017g0148 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.735-5023T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934683 | ||||||
| chr6:54934716
|
G | C | 2 | a0003c0007t0006g0238a0003c0007t0028g0235 | 2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.735-4990G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934716 | ||||||
| chr6:54934810
|
C | A | 2 | a0001c0001t0001g0009a0001c0012t0001g0004 | 2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.735-4896C>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54934810 | ||||||
| chr6:54935022
|
T | A | 45 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.735-4684T>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935022 | ||||||
| chr6:54935218
|
G | A | 60 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.735-4488G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935218 | ||||||
| chr6:54935346
|
G | A | 1 | a0001c0002t0002g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.735-4360G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935346 | ||||||
| chr6:54935477
|
A | G | 17 | a0001c0001t0002g0234a0001c0002t0002g0131a0001c0002t0002g0161others(14): Show | 17 | HG00280.hp2 HG00639.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.735-4229A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935477 | ||||||
| chr6:54935521
|
T | G | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-4185T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935521 | ||||||
| chr6:54935864
|
T | C | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-3842T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935864 | ||||||
| chr6:54935934
|
C | T | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-3772C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935934 | ||||||
| chr6:54935972
|
T | C | 2 | a0005c0015t0017g0019a0005c0015t0017g0148 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.735-3734T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935972 | ||||||
| chr6:54935991
|
G | A | 1 | a0001c0002t0002g0214 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.735-3715G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54935991 | ||||||
| chr6:54936015
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.735-3691T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936015 | ||||||
| chr6:54936016
|
T | C | 13 | a0002c0003t0003g0108a0002c0003t0003g0123a0002c0003t0003g0124others(10): Show | 13 | HG00438.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.735-3690T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936016 | ||||||
| chr6:54936076
|
A | G | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(194): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.735-3630A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936076 | ||||||
| chr6:54936209
|
C | T | 1 | a0001c0002t0002g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.735-3497C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936209 | ||||||
| chr6:54936247
|
G | C | 1 | a0002c0004t0033g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735-3459G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936247 | ||||||
| chr6:54936284
|
A | G | 1 | a0002c0004t0003g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.735-3422A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936284 | ||||||
| chr6:54936378
|
T | C | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-3328T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936378 | ||||||
| chr6:54936551
|
G | A | 84 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.735-3155G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54936551 | ||||||
| chr6:54937079
|
T | G | 12 | a0001c0008t0005g0011a0001c0008t0005g0012a0001c0008t0005g0013others(9): Show | 12 | HG00544.hp1 HG03195.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.735-2627T>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937079 | ||||||
| chr6:54937125
|
A | G | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.735-2581A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937125 | ||||||
| chr6:54937130
|
G | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.735-2576G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937130 | ||||||
| chr6:54937246
|
C | T | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(194): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.735-2460C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937246 | ||||||
| chr6:54937307
|
A | G | 3 | a0004c0014t0002g0143a0004c0014t0002g0144a0004c0014t0002g0260 | 3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.735-2399A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937307 | ||||||
| chr6:54937323
|
A | G | 1 | a0001c0012t0008g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.735-2383A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937323 | ||||||
| chr6:54937431
|
A | G | 84 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.735-2275A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937431 | ||||||
| chr6:54937538
|
A | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.735-2168A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937538 | ||||||
| chr6:54937577
|
T | C | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(211): Show | 215 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.735-2129T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937577 | ||||||
| chr6:54937700
|
G | A | 13 | a0002c0004t0020g0107a0002c0004t0020g0134a0002c0004t0030g0245others(10): Show | 13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.735-2006G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937700 | ||||||
| chr6:54937711
|
T | C | 11 | a0002c0005t0013g0147a0002c0005t0013g0202a0002c0005t0013g0226others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.735-1995T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937711 | ||||||
| chr6:54937795
|
A | G | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(194): Show | 198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.735-1911A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54937795 | ||||||
| chr6:54938004
|
G | C | 24 | a0003c0006t0007g0166a0003c0006t0007g0167a0003c0006t0007g0171others(21): Show | 24 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.735-1702G>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938004 | ||||||
| chr6:54938051
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0194others(1): Show | 4 | HG03831.hp2 NA19000.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-1655C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938051 | ||||||
| chr6:54938182
|
GT | G | 4 | a0002c0004t0012g0177a0002c0004t0012g0180a0002c0004t0012g0219others(1): Show | 4 | HG00438.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.735-1522delT | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 54938182 | |||||
| chr6:54938208
|
T | C | 60 | a0002c0003t0003g0001a0002c0003t0003g0102a0002c0003t0003g0108others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.735-1498T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938208 | ||||||
| chr6:54938304
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.735-1402A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938304 | ||||||
| chr6:54938512
|
C | T | 1 | a0001c0001t0010g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.735-1194C>T | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938512 | ||||||
| chr6:54938524
|
T | C | 7 | a0004c0011t0008g0257a0004c0011t0008g0258a0004c0011t0008g0259others(4): Show | 7 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.735-1182T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938524 | ||||||
| chr6:54938997
|
T | C | 2 | a0001c0002t0002g0191a0001c0002t0002g0222 | 2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.735-709T>C | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54938997 | ||||||
| chr6:54939260
|
G | A | 14 | a0001c0002t0002g0088a0001c0002t0002g0110a0001c0002t0002g0111others(11): Show | 14 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.735-446G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54939260 | ||||||
| chr6:54939644
|
G | A | 2 | a0002c0005t0019g0241a0002c0005t0019g0242 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.735-62G>A | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54939644 | ||||||
| chr6:54939681
|
A | G | 1 | a0002c0026t0016g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.735-25A>G | FAM83B | ENSG00000168143.9 | transcript | ENST00000306858.8 | protein_coding | 4/4 | chr6 | 54939681 |