| geneid | 57579 |
|---|---|
| ensemblid | ENSG00000082269.17 |
| hgncid | 21084 |
| symbol | FAM135A |
| name | family with sequence similarity 135 member A |
| refseq_nuc | NM_001162529.3 |
| refseq_prot | NP_001156001.1 |
| ensembl_nuc | ENST00000418814.7 |
| ensembl_prot | ENSP00000410768.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 70413508 |
| end | 70561174 |
| strand | + |
| ver | v1.2 |
| region | chr6:70413508-70561174 |
| region5000 | chr6:70408508-70566174 |
| regionname0 | FAM135A_chr6_70413508_70561174 |
| regionname5000 | FAM135A_chr6_70408508_70566174 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1515 | 191 | 70 | 49 | 48 | 7 | 16 | 40 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002 | 0/1 | 1515 | 57 | 3 | 8 | 32 | 5 | 8 | 25 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0003 | 0/0 | 1515 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0004 | 0/0 | 1515 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0005 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0006 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0007 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0008 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0009 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0010 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0011 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0012 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| 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 | 4548 | 91 | 29 | 29 | 16 | 5 | 11 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0002 | 0/0 | 4548 | 65 | 10 | 16 | 32 | 2 | 5 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0003 | 0/1 | 4548 | 51 | 3 | 7 | 27 | 5 | 8 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0004 | 0/0 | 4548 | 31 | 28 | 3 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0005 | 0/0 | 4548 | 8 | 7 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0006 | 0/0 | 4548 | 5 | 0 | 0 | 5 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0007 | 0/0 | 4548 | 2 | 0 | 0 | 2 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0008 | 0/0 | 4548 | 2 | 0 | 2 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0009 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0010 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0011 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0012 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0013 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0014 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0015 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0016 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0017 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0018 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| c0019 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1668 | 166 | 46 | 39 | 50 | 10 | 19 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0002 | 0/0 | 1668 | 67 | 10 | 17 | 33 | 2 | 5 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0003 | 0/0 | 1668 | 27 | 26 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0004 | 0/0 | 1668 | 3 | 1 | 2 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0005 | 0/0 | 1668 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0006 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0007 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| t0008 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| 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 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| 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 | 4548 | 91 | 29 | 29 | 16 | 5 | 11 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0002 | 0/0 | 4548 | 65 | 10 | 16 | 32 | 2 | 5 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0004 | 0/0 | 4548 | 31 | 28 | 3 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0009 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0012 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0013 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0003 | 0/1 | 4548 | 51 | 3 | 7 | 27 | 5 | 8 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0006 | 0/0 | 4548 | 5 | 0 | 0 | 5 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0016 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0003c0005 | 0/0 | 4548 | 8 | 7 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0004c0007 | 0/0 | 4548 | 2 | 0 | 0 | 2 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0005c0008 | 0/0 | 4548 | 2 | 0 | 2 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0006c0010 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0007c0019 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0008c0011 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0009c0014 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0010c0015 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0011c0017 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0012c0018 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6215 | 91 | 29 | 29 | 16 | 5 | 11 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0002t0002 | 0/0 | 6215 | 65 | 10 | 16 | 32 | 2 | 5 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0004t0001 | 0/0 | 6215 | 4 | 3 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0004t0003 | 0/0 | 6215 | 24 | 23 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0004t0004 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0004t0006 | 0/0 | 6215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0004t0007 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0009t0001 | 0/0 | 6215 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0012t0001 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0001c0013t0001 | 0/0 | 6215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0003t0001 | 0/1 | 6215 | 50 | 3 | 7 | 26 | 5 | 8 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0003t0008 | 0/0 | 6215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0006t0001 | 0/0 | 6215 | 5 | 0 | 0 | 5 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0002c0016t0002 | 0/0 | 6215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0003c0005t0001 | 0/0 | 6215 | 8 | 7 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0004c0007t0001 | 0/0 | 6215 | 2 | 0 | 0 | 2 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0005c0008t0004 | 0/0 | 6215 | 2 | 0 | 2 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0006c0010t0003 | 0/0 | 6215 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0007c0019t0001 | 0/0 | 6215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0008c0011t0002 | 0/0 | 6215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0009c0014t0003 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0010c0015t0005 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0011c0017t0001 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| a0012c0018t0005 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | copy fasta | chr6 | 70408508 | 70566174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0009t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0009t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0012t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0013t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0016t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0004c0007t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0004c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0005c0008t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0005c0008t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0006c0010t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0006c0010t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0007c0019t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0008c0011t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0009c0014t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0010c0015t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0011c0017t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0012c0018t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0216 | EUR | GBR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0253 | EUR | FIN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0121 | EUR | FIN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00597 | hp2 | a0002 | c0006 | t0001 | g0034 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0125 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00621 | hp2 | a0002 | c0006 | t0001 | g0131 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0257 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01069 | hp1 | a0001 | c0004 | t0003 | g0234 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01074 | hp2 | a0005 | c0008 | t0004 | g0003 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0160 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0134 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01192 | hp2 | a0001 | c0004 | t0006 | g0019 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0114 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0263 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01346 | hp1 | a0005 | c0008 | t0004 | g0004 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0051 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0137 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0261 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0139 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0138 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01975 | hp1 | a0002 | c0016 | t0002 | g0185 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0193 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01981 | hp2 | a0001 | c0013 | t0001 | g0085 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0044 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02027 | hp1 | a0002 | c0006 | t0001 | g0130 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0122 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02083 | hp2 | a0007 | c0019 | t0001 | g0083 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0136 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0232 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02293 | hp1 | a0003 | c0005 | t0001 | g0243 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0042 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02451 | hp2 | a0011 | c0017 | t0001 | g0018 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0252 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02572 | hp2 | a0003 | c0005 | t0001 | g0245 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0156 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0239 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0162 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02622 | hp2 | a0001 | c0004 | t0003 | g0233 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02647 | hp1 | a0003 | c0005 | t0001 | g0242 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0119 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0260 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0236 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02717 | hp2 | a0001 | c0004 | t0003 | g0013 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0127 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02809 | hp1 | a0009 | c0014 | t0003 | g0001 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02886 | hp1 | a0012 | c0018 | t0005 | g0006 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02895 | hp2 | a0003 | c0005 | t0001 | g0247 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0238 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0259 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02897 | hp1 | a0001 | c0004 | t0003 | g0235 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02965 | hp1 | a0001 | c0004 | t0003 | g0231 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02970 | hp2 | a0001 | c0012 | t0001 | g0029 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03041 | hp1 | a0001 | c0004 | t0003 | g0230 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03041 | hp2 | a0003 | c0005 | t0001 | g0248 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03130 | hp2 | a0006 | c0010 | t0003 | g0007 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03195 | hp1 | a0006 | c0010 | t0003 | g0008 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0251 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0264 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0014 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03453 | hp1 | a0001 | c0004 | t0003 | g0017 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03453 | hp2 | a0001 | c0009 | t0001 | g0211 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0135 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0161 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03579 | hp2 | a0003 | c0005 | t0001 | g0246 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0110 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0213 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0038 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0266 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0001 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0240 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0205 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18939 | hp1 | a0008 | c0011 | t0002 | g0170 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18950 | hp1 | a0004 | c0007 | t0001 | g0152 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18956 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18959 | hp2 | a0004 | c0007 | t0001 | g0123 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0128 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18980 | hp1 | a0002 | c0006 | t0001 | g0129 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19006 | hp1 | a0002 | c0006 | t0001 | g0149 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0118 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0241 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19043 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19043 | hp2 | a0001 | c0004 | t0003 | g0237 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19081 | hp2 | a0002 | c0003 | t0008 | g0113 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19083 | hp1 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0108 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0204 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19240 | hp2 | a0001 | c0004 | t0003 | g0016 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20129 | hp1 | a0010 | c0015 | t0005 | g0005 | AFR | ASW | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0217 | EUR | TSI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0037 | SAS | GIH | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0255 | SAS | GIH | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02109 | hp1 | a0003 | c0005 | t0001 | g0244 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02109 | hp2 | a0001 | c0004 | t0007 | g0265 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0150 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02486 | hp2 | a0003 | c0005 | t0001 | g0249 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02559 | hp1 | a0001 | c0004 | t0003 | g0010 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02559 | hp2 | a0001 | c0009 | t0001 | g0212 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0250 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0015 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0132 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA21309 | hp2 | a0001 | c0004 | t0003 | g0009 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0035 | REF | REF | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0032 | REF | REF | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70452506
|
G | A | 1 | a0004 | 2 | NA18950.hp1 NA18959.hp2 |
missense_variant | MODERATE | c.92G>A | p.Arg31His | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/22 | 506/6215 | 92/4548 | 31/1515 | chr6 | 70452506 | ||
| chr6:70475446
|
C | G | 1 | a0007 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.194C>G | p.Ser65Cys | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 6/22 | 608/6215 | 194/4548 | 65/1515 | chr6 | 70475446 | ||
| chr6:70477227
|
G | A | 1 | a0008 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.437G>A | p.Arg146Lys | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/22 | 851/6215 | 437/4548 | 146/1515 | chr6 | 70477227 | ||
| chr6:70480984
|
G | A | 1 | a0005 | 2 | HG01074.hp2 HG01346.hp1 |
missense_variant | MODERATE | c.626G>A | p.Ser209Asn | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/22 | 1040/6215 | 626/4548 | 209/1515 | chr6 | 70480984 | ||
| chr6:70522577
|
A | G | 1 | a0012 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1094A>G | p.Gln365Arg | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/22 | 1508/6215 | 1094/4548 | 365/1515 | chr6 | 70522577 | ||
| chr6:70524846
|
C | T | 1 | a0011 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1762C>T | p.Pro588Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2176/6215 | 1762/4548 | 588/1515 | chr6 | 70524846 | ||
| chr6:70525257
|
A | G | 1 | a0003 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
missense_variant | MODERATE | c.2173A>G | p.Ile725Val | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2587/6215 | 2173/4548 | 725/1515 | chr6 | 70525257 | ||
| chr6:70525282
|
G | A | 1 | a0009 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2198G>A | p.Arg733Gln | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2612/6215 | 2198/4548 | 733/1515 | chr6 | 70525282 | ||
| chr6:70525660
|
T | C | 2 | a0010a0012 | 2 | HG02886.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.2576T>C | p.Val859Ala | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2990/6215 | 2576/4548 | 859/1515 | chr6 | 70525660 | ||
| chr6:70525711
|
C | T | 1 | a0006 | 2 | HG03130.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2627C>T | p.Thr876Met | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 3041/6215 | 2627/4548 | 876/1515 | chr6 | 70525711 | ||
| chr6:70525944
|
C | T | 1 | a0003 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
missense_variant | MODERATE | c.2860C>T | p.Pro954Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 3274/6215 | 2860/4548 | 954/1515 | chr6 | 70525944 | ||
| chr6:70528402
|
A | G | 2 | a0002a0004 | 59 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(56): Show |
missense_variant | MODERATE | c.3725A>G | p.Asp1242Gly | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/22 | 4139/6215 | 3725/4548 | 1242/1515 | chr6 | 70528402 | ||
| chr6:70559767
|
G | A | 2 | a0010a0012 | 2 | HG02886.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.4394G>A | p.Ser1465Asn | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 4808/6215 | 4394/4548 | 1465/1515 | chr6 | 70559767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70502686
|
G | A | 1 | a0001c0012 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.924G>A | p.Ala308Ala | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/22 | 1338/6215 | 924/4548 | 308/1515 | chr6 | 70502686 | ||
| chr6:70502740
|
G | A | 1 | a0001c0013 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.978G>A | p.Thr326Thr | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/22 | 1392/6215 | 978/4548 | 326/1515 | chr6 | 70502740 | ||
| chr6:70524545
|
A | G | 1 | a0002c0006 | 5 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(2): Show |
synonymous_variant | LOW | c.1461A>G | p.Ser487Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 1875/6215 | 1461/4548 | 487/1515 | chr6 | 70524545 | ||
| chr6:70525514
|
A | G | 1 | a0003c0005 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
synonymous_variant | LOW | c.2430A>G | p.Lys810Lys | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2844/6215 | 2430/4548 | 810/1515 | chr6 | 70525514 | ||
| chr6:70526513
|
C | T | 10 | a0001c0002a0001c0004a0001c0009others(7): Show | 107 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(104): Show |
synonymous_variant | LOW | c.3429C>T | p.Asn1143Asn | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 3843/6215 | 3429/4548 | 1143/1515 | chr6 | 70526513 | ||
| chr6:70536275
|
G | A | 2 | a0001c0009a0003c0005 | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.3981G>A | p.Ser1327Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/22 | 4395/6215 | 3981/4548 | 1327/1515 | chr6 | 70536275 | ||
| chr6:70538343
|
A | G | 1 | a0003c0005 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
synonymous_variant | LOW | c.4170A>G | p.Thr1390Thr | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/22 | 4584/6215 | 4170/4548 | 1390/1515 | chr6 | 70538343 | ||
| chr6:70559756
|
C | T | 3 | a0001c0002a0002c0016a0008c0011 | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
synonymous_variant | LOW | c.4383C>T | p.Pro1461Pro | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 4797/6215 | 4383/4548 | 1461/1515 | chr6 | 70559756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70413617
|
C | T | 1 | a0002c0003t0008 | 1 | NA19081.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-305C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/22 | chr6 | 70413617 | ||||||
| chr6:70413655
|
G | A | 1 | a0001c0004t0006 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/22 | 14688 | chr6 | 70413655 | |||||
| chr6:70559929
|
G | A | 4 | a0001c0002t0002a0001c0004t0007a0002c0016t0002others(1): Show | 68 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*8G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 8 | chr6 | 70559929 | |||||
| chr6:70560069
|
C | G | 2 | a0010c0015t0005a0012c0018t0005 | 2 | HG02886.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 148 | chr6 | 70560069 | |||||
| chr6:70560528
|
A | T | 7 | a0001c0004t0003a0001c0004t0004a0005c0008t0004others(4): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*607A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 607 | chr6 | 70560528 | |||||
| chr6:70560674
|
A | G | 2 | a0001c0004t0004a0005c0008t0004 | 3 | HG01074.hp2 HG01346.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*753A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 753 | chr6 | 70560674 | |||||
| chr6:70560840
|
A | C | 3 | a0001c0002t0002a0002c0016t0002a0008c0011t0002 | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*919A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 919 | chr6 | 70560840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70413763
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-220+61C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70413763 | ||||||
| chr6:70413963
|
G | T | 17 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(14): Show | 17 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.-220+261G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70413963 | ||||||
| chr6:70414044
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-220+342C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414044 | ||||||
| chr6:70414053
|
C | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-220+351C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414053 | ||||||
| chr6:70414267
|
C | T | 11 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(8): Show | 11 | HG00609.hp1 HG00621.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-220+565C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414267 | ||||||
| chr6:70414486
|
A | T | 5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0218others(2): Show | 5 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-220+784A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414486 | ||||||
| chr6:70414515
|
TC | T | 33 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(30): Show | 33 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.-219-767delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 70414515 | |||||
| chr6:70414522
|
C | G | 1 | a0002c0003t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-219-769C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414522 | ||||||
| chr6:70414638
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-219-653A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414638 | ||||||
| chr6:70414798
|
G | A | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-219-493G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414798 | ||||||
| chr6:70414826
|
A | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-219-465A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414826 | ||||||
| chr6:70414827
|
A | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-219-464A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414827 | ||||||
| chr6:70414856
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-219-435A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414856 | ||||||
| chr6:70414869
|
C | CAACAGAC others(5): Show |
1 | a0002c0003t0001g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-219-420_-219-419i others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 70414869 | |||||
| chr6:70414924
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-219-367C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414924 | ||||||
| chr6:70415023
|
C | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-219-268C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70415023 | ||||||
| chr6:70415139
|
T | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-219-152T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70415139 | ||||||
| chr6:70415417
|
T | A | 1 | a0001c0002t0002g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-134+41T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415417 | ||||||
| chr6:70415513
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-134+137A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415513 | ||||||
| chr6:70415757
|
T | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-134+381T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415757 | ||||||
| chr6:70415806
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+430A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415806 | ||||||
| chr6:70416002
|
TTGAC | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-134+629_-134+632d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70416002 | |||||
| chr6:70416092
|
G | T | 1 | a0002c0003t0001g0165 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-134+716G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416092 | ||||||
| chr6:70416229
|
T | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+853T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416229 | ||||||
| chr6:70416230
|
C | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+854C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416230 | ||||||
| chr6:70416231
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+855A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416231 | ||||||
| chr6:70416232
|
C | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+856C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416232 | ||||||
| chr6:70416350
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-134+974T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416350 | ||||||
| chr6:70416353
|
C | T | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-134+977C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416353 | ||||||
| chr6:70417191
|
A | G | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+1815A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417191 | ||||||
| chr6:70417201
|
A | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+1825A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417201 | ||||||
| chr6:70417259
|
CT | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG01074.hp2 HG01346.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-134+1898delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70417259 | |||||
| chr6:70417307
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-134+1931G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417307 | ||||||
| chr6:70417585
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-134+2209A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417585 | ||||||
| chr6:70417680
|
T | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-134+2304T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417680 | ||||||
| chr6:70417784
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-134+2408A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417784 | ||||||
| chr6:70417789
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-134+2413G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417789 | ||||||
| chr6:70417815
|
T | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-134+2439T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417815 | ||||||
| chr6:70418176
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-134+2800C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418176 | ||||||
| chr6:70418235
|
G | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+2859G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418235 | ||||||
| chr6:70418317
|
AATTT | A | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-134+2946_-134+294 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70418317 | |||||
| chr6:70418500
|
T | C | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-134+3124T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418500 | ||||||
| chr6:70418550
|
G | A | 1 | a0001c0002t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-134+3174G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418550 | ||||||
| chr6:70418656
|
T | C | 1 | a0001c0012t0001g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-134+3280T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418656 | ||||||
| chr6:70418952
|
T | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-134+3576T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418952 | ||||||
| chr6:70419054
|
G | A | 2 | a0002c0003t0001g0030a0002c0003t0001g0031 | 2 | NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-134+3678G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419054 | ||||||
| chr6:70419086
|
G | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+3710G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419086 | ||||||
| chr6:70419103
|
C | G | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+3727C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419103 | ||||||
| chr6:70419158
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-134+3782C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419158 | ||||||
| chr6:70419368
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-134+3992G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419368 | ||||||
| chr6:70419413
|
C | T | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-134+4037C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419413 | ||||||
| chr6:70419418
|
CA | C | 190 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(187): Show | 190 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(187): Show |
intron_variant | MODIFIER | c.-134+4057delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70419418 | |||||
| chr6:70419418
|
CAA | C | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-134+4056_-134+405 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70419418 | |||||
| chr6:70419426
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-134+4050A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419426 | ||||||
| chr6:70419431
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-134+4055A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419431 | ||||||
| chr6:70419576
|
T | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+4200T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419576 | ||||||
| chr6:70419587
|
T | G | 1 | a0002c0003t0001g0035 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-134+4211T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419587 | ||||||
| chr6:70419680
|
T | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-134+4304T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419680 | ||||||
| chr6:70419725
|
T | C | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-134+4349T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419725 | ||||||
| chr6:70419970
|
C | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+4594C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419970 | ||||||
| chr6:70420285
|
TG | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.-134+4910delG | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420285 | ||||||
| chr6:70420391
|
A | G | 2 | a0001c0002t0002g0168a0001c0002t0002g0209 | 2 | NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-134+5015A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420391 | ||||||
| chr6:70420627
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-134+5251G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420627 | ||||||
| chr6:70420680
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-134+5304T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420680 | ||||||
| chr6:70420698
|
T | A | 2 | a0002c0003t0001g0037a0002c0003t0001g0038 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-134+5322T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420698 | ||||||
| chr6:70420890
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-134+5514T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420890 | ||||||
| chr6:70421021
|
A | G | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-5418A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421021 | ||||||
| chr6:70421365
|
C | T | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-5074C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421365 | ||||||
| chr6:70421889
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-133-4550A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421889 | ||||||
| chr6:70421896
|
G | A | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-133-4543G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421896 | ||||||
| chr6:70421995
|
G | A | 1 | a0001c0009t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-133-4444G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421995 | ||||||
| chr6:70422119
|
A | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-4320A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422119 | ||||||
| chr6:70422211
|
G | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-133-4228G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422211 | ||||||
| chr6:70422321
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-133-4118A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422321 | ||||||
| chr6:70422469
|
G | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-3970G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422469 | ||||||
| chr6:70422491
|
A | C | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.-133-3948A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422491 | ||||||
| chr6:70422569
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-133-3870A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422569 | ||||||
| chr6:70422677
|
C | T | 11 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(8): Show | 11 | HG00609.hp1 HG00621.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-133-3762C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422677 | ||||||
| chr6:70422914
|
G | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-3525G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422914 | ||||||
| chr6:70422965
|
G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-3474G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422965 | ||||||
| chr6:70423014
|
G | T | 1 | a0001c0002t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-133-3425G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423014 | ||||||
| chr6:70423015
|
T | C | 4 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(1): Show | 4 | HG03540.hp1 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-133-3424T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423015 | ||||||
| chr6:70423197
|
G | A | 6 | a0002c0003t0001g0002a0002c0003t0001g0039a0002c0003t0001g0040others(3): Show | 6 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-133-3242G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423197 | ||||||
| chr6:70423675
|
T | C | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-2764T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423675 | ||||||
| chr6:70423957
|
T | G | 1 | a0008c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-133-2482T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423957 | ||||||
| chr6:70424023
|
A | G | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-133-2416A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424023 | ||||||
| chr6:70424048
|
T | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-133-2391T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424048 | ||||||
| chr6:70424060
|
G | A | 1 | a0002c0003t0001g0044 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-133-2379G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424060 | ||||||
| chr6:70424143
|
C | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-133-2296C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424143 | ||||||
| chr6:70424316
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-2123A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424316 | ||||||
| chr6:70424320
|
A | G | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-133-2119A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424320 | ||||||
| chr6:70424329
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-133-2110C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424329 | ||||||
| chr6:70424413
|
G | A | 3 | a0001c0004t0003g0250a0001c0004t0003g0251a0001c0004t0003g0252 | 3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-133-2026G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424413 | ||||||
| chr6:70424447
|
A | G | 1 | a0002c0003t0001g0044 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-133-1992A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424447 | ||||||
| chr6:70424555
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-1884A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424555 | ||||||
| chr6:70424557
|
C | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-133-1882C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424557 | ||||||
| chr6:70424644
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-133-1795G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424644 | ||||||
| chr6:70424736
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-133-1703G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424736 | ||||||
| chr6:70424791
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-1648A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424791 | ||||||
| chr6:70424841
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-133-1598A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424841 | ||||||
| chr6:70425140
|
G | A | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-133-1299G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425140 | ||||||
| chr6:70425153
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-1286T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425153 | ||||||
| chr6:70425557
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0004t0003g0016others(1): Show | 4 | HG03453.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-882C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425557 | ||||||
| chr6:70425671
|
A | G | 40 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0177others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-133-768A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425671 | ||||||
| chr6:70425744
|
C | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-695C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425744 | ||||||
| chr6:70425749
|
A | G | 46 | a0001c0002t0002g0167a0001c0002t0002g0169a0001c0002t0002g0176others(43): Show | 46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-133-690A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425749 | ||||||
| chr6:70425778
|
C | T | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-661C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425778 | ||||||
| chr6:70425875
|
G | A | 28 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.-133-564G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425875 | ||||||
| chr6:70425930
|
T | C | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.-133-509T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425930 | ||||||
| chr6:70425933
|
T | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-506T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425933 | ||||||
| chr6:70425960
|
G | A | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-133-479G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425960 | ||||||
| chr6:70425965
|
C | T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-133-474C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425965 | ||||||
| chr6:70426059
|
C | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-133-380C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426059 | ||||||
| chr6:70426072
|
C | T | 1 | a0004c0007t0001g0152 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-133-367C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426072 | ||||||
| chr6:70426109
|
C | CAAAA | 51 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(48): Show | 51 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-133-321_-133-318d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70426109 | |||||
| chr6:70426119
|
A | AAAAAC | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-133-318_-133-317i others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70426119 | |||||
| chr6:70426119
|
A | AAAC | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-311_-133-309d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70426119 | |||||
| chr6:70426119
|
A | C | 3 | a0001c0001t0001g0151a0010c0015t0005g0005a0012c0018t0005g0006 | 3 | HG02602.hp1 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-133-320A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426119 | ||||||
| chr6:70426131
|
A | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0004t0003g0241 | 3 | HG02818.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-133-308A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426131 | ||||||
| chr6:70426250
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-133-189A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426250 | ||||||
| chr6:70426613
|
T | G | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-40+81T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426613 | ||||||
| chr6:70426692
|
T | C | 1 | a0002c0003t0001g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-40+160T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426692 | ||||||
| chr6:70426792
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+260A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426792 | ||||||
| chr6:70426870
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-40+338C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426870 | ||||||
| chr6:70427228
|
A | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40+696A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427228 | ||||||
| chr6:70427253
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40+721C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427253 | ||||||
| chr6:70427463
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-39-841C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427463 | ||||||
| chr6:70427497
|
A | G | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-39-807A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427497 | ||||||
| chr6:70427533
|
C | CA | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(16): Show | 19 | HG01074.hp2 HG01346.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-39-753dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr6 | 70427533 | |||||
| chr6:70427533
|
CA | C | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-39-753delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr6 | 70427533 | |||||
| chr6:70427659
|
TA | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39-644delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427659 | ||||||
| chr6:70427707
|
A | C | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39-597A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427707 | ||||||
| chr6:70427742
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-39-562A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427742 | ||||||
| chr6:70427948
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-39-356C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427948 | ||||||
| chr6:70427988
|
C | A | 81 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(78): Show | 81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-39-316C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427988 | ||||||
| chr6:70428011
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-39-293A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428011 | ||||||
| chr6:70428139
|
C | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39-165C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428139 | ||||||
| chr6:70428140
|
A | G | 1 | a0001c0004t0003g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-39-164A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428140 | ||||||
| chr6:70428181
|
G | A | 142 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(139): Show | 142 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-39-123G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428181 | ||||||
| chr6:70428228
|
T | A | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-39-76T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428228 | ||||||
| chr6:70428289
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-15C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428289 | ||||||
| chr6:70428456
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.77+37A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428456 | ||||||
| chr6:70428472
|
A | G | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.77+53A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428472 | ||||||
| chr6:70428625
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+206C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428625 | ||||||
| chr6:70428680
|
G | C | 1 | a0001c0004t0003g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.77+261G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428680 | ||||||
| chr6:70428840
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.77+421A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428840 | ||||||
| chr6:70428886
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.77+467G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428886 | ||||||
| chr6:70429001
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+582A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429001 | ||||||
| chr6:70429078
|
G | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+659G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429078 | ||||||
| chr6:70429244
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.77+825G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429244 | ||||||
| chr6:70429464
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77+1045G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429464 | ||||||
| chr6:70429467
|
T | C | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77+1048T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429467 | ||||||
| chr6:70429470
|
G | A | 1 | a0001c0002t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.77+1051G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429470 | ||||||
| chr6:70429481
|
C | CT | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.77+1062_77+1063ins others(1): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429481 | ||||||
| chr6:70429539
|
A | T | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77+1120A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429539 | ||||||
| chr6:70429664
|
T | G | 1 | a0001c0004t0003g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+1245T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429664 | ||||||
| chr6:70429761
|
C | T | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.77+1342C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429761 | ||||||
| chr6:70429842
|
T | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.77+1423T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429842 | ||||||
| chr6:70430175
|
A | G | 1 | a0002c0003t0001g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.77+1756A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430175 | ||||||
| chr6:70430209
|
C | T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+1790C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430209 | ||||||
| chr6:70430213
|
T | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+1794T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430213 | ||||||
| chr6:70430316
|
A | G | 220 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(217): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.77+1897A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430316 | ||||||
| chr6:70430328
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+1909C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430328 | ||||||
| chr6:70430335
|
T | TA | 16 | a0001c0001t0001g0036a0001c0004t0003g0001a0001c0004t0003g0230others(13): Show | 16 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+1927dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70430335 | |||||
| chr6:70430351
|
AAAAG | A | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.77+1938_77+1941del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70430351 | |||||
| chr6:70430354
|
A | G | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77+1935A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430354 | ||||||
| chr6:70430355
|
G | A | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.77+1936G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430355 | ||||||
| chr6:70430528
|
C | G | 1 | a0002c0003t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77+2109C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430528 | ||||||
| chr6:70430664
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0256others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.77+2245A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430664 | ||||||
| chr6:70430811
|
A | C | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+2392A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430811 | ||||||
| chr6:70431157
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+2738A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431157 | ||||||
| chr6:70431275
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+2856G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431275 | ||||||
| chr6:70431285
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+2866A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431285 | ||||||
| chr6:70431312
|
G | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+2893G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431312 | ||||||
| chr6:70431366
|
G | A | 1 | a0001c0002t0002g0256 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.77+2947G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431366 | ||||||
| chr6:70431500
|
T | C | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+3081T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431500 | ||||||
| chr6:70431618
|
T | C | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+3199T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431618 | ||||||
| chr6:70431823
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.77+3404A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431823 | ||||||
| chr6:70431849
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+3430C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431849 | ||||||
| chr6:70431863
|
G | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+3444G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431863 | ||||||
| chr6:70431987
|
C | G | 15 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(12): Show | 15 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+3568C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431987 | ||||||
| chr6:70432065
|
C | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+3646C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432065 | ||||||
| chr6:70432163
|
T | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+3744T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432163 | ||||||
| chr6:70432171
|
C | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+3752C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432171 | ||||||
| chr6:70432197
|
C | T | 1 | a0002c0003t0001g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.77+3778C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432197 | ||||||
| chr6:70432405
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.77+3986T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432405 | ||||||
| chr6:70432428
|
T | G | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.77+4009T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432428 | ||||||
| chr6:70432510
|
C | CT | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.77+4093dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70432510 | |||||
| chr6:70432593
|
T | C | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.77+4174T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432593 | ||||||
| chr6:70432606
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.77+4187A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432606 | ||||||
| chr6:70432760
|
CT | C | 18 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(15): Show | 18 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+4351delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70432760 | |||||
| chr6:70432882
|
A | T | 161 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(158): Show | 161 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.77+4463A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432882 | ||||||
| chr6:70433009
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77+4590C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433009 | ||||||
| chr6:70433077
|
CT | C | 57 | a0001c0001t0001g0091a0001c0001t0001g0210a0001c0001t0001g0267others(54): Show | 57 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.77+4674delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433077 | |||||
| chr6:70433113
|
C | T | 25 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(22): Show | 25 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+4694C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433113 | ||||||
| chr6:70433370
|
G | A | 2 | a0001c0002t0002g0255a0001c0002t0002g0257 | 2 | HG00639.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.77+4951G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433370 | ||||||
| chr6:70433373
|
C | G | 9 | a0001c0002t0002g0253a0001c0002t0002g0255a0001c0002t0002g0256others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+4954C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433373 | ||||||
| chr6:70433388
|
T | C | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.77+4969T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433388 | ||||||
| chr6:70433436
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+5017C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433436 | ||||||
| chr6:70433465
|
A | T | 136 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(133): Show | 136 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.77+5046A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433465 | ||||||
| chr6:70433505
|
C | CT | 116 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(113): Show | 116 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.77+5099dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433505 | |||||
| chr6:70433559
|
T | TCTTTTTT others(212): Show |
2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.77+5144_77+5145ins others(219): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433559 | |||||
| chr6:70433591
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.77+5172A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433591 | ||||||
| chr6:70433602
|
G | A | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.77+5183G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433602 | ||||||
| chr6:70433658
|
C | T | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+5239C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433658 | ||||||
| chr6:70433717
|
T | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5298T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433717 | ||||||
| chr6:70433762
|
C | T | 81 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(78): Show | 81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+5343C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433762 | ||||||
| chr6:70433778
|
T | G | 81 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(78): Show | 81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+5359T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433778 | ||||||
| chr6:70433832
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.77+5413T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433832 | ||||||
| chr6:70433925
|
A | C | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77+5506A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433925 | ||||||
| chr6:70433930
|
AAAGAAAA others(3): Show |
A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+5513_77+5522del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433930 | |||||
| chr6:70434207
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+5788G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434207 | ||||||
| chr6:70434400
|
A | G | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77+5981A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434400 | ||||||
| chr6:70434501
|
C | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+6082C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434501 | ||||||
| chr6:70434507
|
A | ACC | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+6088_77+6089ins others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434507 | ||||||
| chr6:70434508
|
A | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+6089A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434508 | ||||||
| chr6:70434562
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.77+6143C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434562 | ||||||
| chr6:70434702
|
C | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+6283C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434702 | ||||||
| chr6:70434846
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.77+6427G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434846 | ||||||
| chr6:70434864
|
A | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.77+6445A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434864 | ||||||
| chr6:70434886
|
T | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+6467T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434886 | ||||||
| chr6:70434916
|
G | A | 1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.77+6497G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434916 | ||||||
| chr6:70435026
|
G | C | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+6607G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435026 | ||||||
| chr6:70435079
|
GTGTA | G | 12 | a0001c0002t0002g0176a0001c0002t0002g0178a0001c0002t0002g0179others(9): Show | 12 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+6662_77+6665del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | |||||
| chr6:70435079
|
GTGTATA | G | 51 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(48): Show | 51 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.77+6662_77+6667del others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | |||||
| chr6:70435079
|
GTGTATAT others(1): Show |
G | 21 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 21 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+6662_77+6669del others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | |||||
| chr6:70435079
|
GTGTATAT others(5): Show |
G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+6662_77+6673del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | |||||
| chr6:70435081
|
G | A | 23 | a0001c0002t0002g0172a0001c0002t0002g0177a0001c0002t0002g0198others(20): Show | 23 | HG00673.hp2 HG00733.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+6662G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435081 | ||||||
| chr6:70435081
|
G | GTA | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+6690_77+6691dup others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | |||||
| chr6:70435081
|
G | GTATA | 3 | a0001c0001t0001g0075a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01255.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.77+6688_77+6691dup others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | |||||
| chr6:70435081
|
GTATATA | G | 46 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0053others(43): Show | 46 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.77+6686_77+6691del others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | |||||
| chr6:70435081
|
GTATATAT others(3): Show |
G | 3 | a0001c0004t0003g0230a0010c0015t0005g0005a0012c0018t0005g0006 | 3 | HG02886.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.77+6682_77+6691del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | |||||
| chr6:70435083
|
A | G | 19 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(16): Show | 19 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.77+6664A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435083 | ||||||
| chr6:70435085
|
A | G | 4 | a0001c0004t0003g0016a0001c0004t0003g0017a0001c0009t0001g0211others(1): Show | 4 | HG02559.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6666A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435085 | ||||||
| chr6:70435088
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.77+6669T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435088 | ||||||
| chr6:70435098
|
TATATATA | T | 6 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+6680_77+6686del others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435098 | ||||||
| chr6:70435098
|
TATATATA others(4): Show |
T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+6680_77+6690del others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435098 | ||||||
| chr6:70435101
|
ATATATAT others(3): Show |
A | 12 | a0001c0004t0003g0001a0001c0004t0003g0231a0001c0004t0003g0233others(9): Show | 12 | HG01069.hp1 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+6684_77+6693del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435101 | |||||
| chr6:70435102
|
TATATATA | T | 3 | a0001c0002t0002g0172a0001c0002t0002g0198a0001c0002t0002g0199 | 3 | HG00673.hp2 HG00733.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.77+6684_77+6690del others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435102 | ||||||
| chr6:70435105
|
ATATATT | A | 41 | a0001c0001t0001g0109a0001c0001t0001g0157a0002c0003t0001g0002others(38): Show | 41 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.77+6688_77+6693del others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435105 | |||||
| chr6:70435107
|
A | T | 6 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+6688A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435107 | ||||||
| chr6:70435109
|
A | T | 21 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0103others(18): Show | 21 | HG01074.hp2 HG01346.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+6690A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435109 | ||||||
| chr6:70435110
|
T | TA | 7 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(4): Show | 7 | HG02109.hp1 HG02293.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+6691_77+6692ins others(1): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435110 | ||||||
| chr6:70435111
|
T | A | 11 | a0001c0001t0001g0075a0001c0001t0001g0140a0001c0001t0001g0158others(8): Show | 11 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.77+6692T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435111 | ||||||
| chr6:70435112
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.77+6693T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435112 | ||||||
| chr6:70435139
|
T | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+6720T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435139 | ||||||
| chr6:70435319
|
G | T | 1 | a0002c0003t0001g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.77+6900G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435319 | ||||||
| chr6:70435322
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+6903C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435322 | ||||||
| chr6:70435400
|
C | T | 6 | a0002c0003t0001g0128a0002c0006t0001g0034a0002c0006t0001g0129others(3): Show | 6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+6981C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435400 | ||||||
| chr6:70435573
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0158 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.77+7154G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435573 | ||||||
| chr6:70435701
|
A | G | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 19 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.77+7282A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435701 | ||||||
| chr6:70435775
|
G | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+7356G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435775 | ||||||
| chr6:70435844
|
A | G | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+7425A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435844 | ||||||
| chr6:70436011
|
C | T | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 19 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.77+7592C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436011 | ||||||
| chr6:70436316
|
A | G | 1 | a0001c0002t0002g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.77+7897A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436316 | ||||||
| chr6:70436331
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+7912A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436331 | ||||||
| chr6:70436345
|
G | A | 25 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(22): Show | 25 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+7926G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436345 | ||||||
| chr6:70436499
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.77+8080A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436499 | ||||||
| chr6:70436610
|
C | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+8191C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436610 | ||||||
| chr6:70436633
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+8214G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436633 | ||||||
| chr6:70436740
|
T | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.77+8321T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436740 | ||||||
| chr6:70436792
|
T | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+8373T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436792 | ||||||
| chr6:70437187
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0095others(1): Show | 4 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+8768G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437187 | ||||||
| chr6:70437509
|
ATTAC | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+9094_77+9097del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70437509 | |||||
| chr6:70437558
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.77+9139G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437558 | ||||||
| chr6:70437574
|
C | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+9155C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437574 | ||||||
| chr6:70437937
|
A | G | 28 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9518A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437937 | ||||||
| chr6:70438242
|
C | T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+9823C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438242 | ||||||
| chr6:70438593
|
C | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG00738.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+10174C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438593 | ||||||
| chr6:70438774
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+10355G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438774 | ||||||
| chr6:70438815
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+10396A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438815 | ||||||
| chr6:70438987
|
C | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+10568C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438987 | ||||||
| chr6:70439026
|
G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+10607G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439026 | ||||||
| chr6:70439208
|
A | G | 1 | a0001c0004t0003g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+10789A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439208 | ||||||
| chr6:70439659
|
C | T | 1 | a0002c0003t0001g0033 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.77+11240C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439659 | ||||||
| chr6:70439874
|
C | T | 9 | a0002c0003t0001g0051a0002c0003t0001g0107a0002c0003t0001g0108others(6): Show | 9 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+11455C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439874 | ||||||
| chr6:70439989
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+11570A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439989 | ||||||
| chr6:70440039
|
A | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.77+11620A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440039 | ||||||
| chr6:70440298
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0095others(3): Show | 6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+11879C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440298 | ||||||
| chr6:70440324
|
A | G | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.77+11905A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440324 | ||||||
| chr6:70440329
|
T | C | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+11910T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440329 | ||||||
| chr6:70440659
|
A | G | 1 | a0002c0003t0001g0124 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.78-11833A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440659 | ||||||
| chr6:70440715
|
T | G | 1 | a0002c0003t0001g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.78-11777T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440715 | ||||||
| chr6:70440983
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-11509C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440983 | ||||||
| chr6:70441061
|
T | A | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.78-11431T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441061 | ||||||
| chr6:70441113
|
G | T | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.78-11379G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441113 | ||||||
| chr6:70441136
|
G | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-11356G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441136 | ||||||
| chr6:70441311
|
C | G | 1 | a0002c0003t0008g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.78-11181C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441311 | ||||||
| chr6:70441399
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.78-11093A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441399 | ||||||
| chr6:70441667
|
A | G | 2 | a0001c0001t0001g0109a0002c0003t0001g0150 | 2 | HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.78-10825A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441667 | ||||||
| chr6:70441685
|
A | AT | 31 | a0001c0001t0001g0036a0001c0001t0001g0092a0001c0001t0001g0094others(28): Show | 31 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.78-10790dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70441685 | |||||
| chr6:70441685
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.78-10807A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441685 | ||||||
| chr6:70441830
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.78-10662G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441830 | ||||||
| chr6:70442071
|
A | G | 1 | a0002c0003t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.78-10421A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442071 | ||||||
| chr6:70442238
|
G | GT | 8 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0195others(5): Show | 8 | HG00280.hp1 HG01243.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-10254_78-10253i others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | ||||||
| chr6:70442238
|
G | GTT | 13 | a0001c0004t0006g0019a0001c0009t0001g0211a0001c0009t0001g0212others(10): Show | 13 | HG01192.hp2 HG02109.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.78-10254_78-10253i others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | ||||||
| chr6:70442238
|
G | GTTT | 27 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(24): Show | 27 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.78-10254_78-10253i others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | ||||||
| chr6:70442238
|
G | GTTTT | 3 | a0001c0004t0003g0240a0001c0004t0003g0241a0001c0004t0003g0252 | 3 | HG02572.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.78-10254_78-10253i others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | ||||||
| chr6:70442239
|
G | GT | 12 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0088others(9): Show | 12 | HG00735.hp1 HG01192.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-10235dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70442239 | |||||
| chr6:70442239
|
G | T | 111 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.78-10253G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442239 | ||||||
| chr6:70442260
|
C | T | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.78-10232C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442260 | ||||||
| chr6:70442273
|
G | A | 72 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(69): Show | 72 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.78-10219G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442273 | ||||||
| chr6:70442339
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-10153A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442339 | ||||||
| chr6:70442369
|
T | C | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-10123T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442369 | ||||||
| chr6:70442411
|
T | C | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.78-10081T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442411 | ||||||
| chr6:70442427
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-10065C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442427 | ||||||
| chr6:70442459
|
A | G | 31 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0177others(28): Show | 31 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.78-10033A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442459 | ||||||
| chr6:70442708
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.78-9784G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442708 | ||||||
| chr6:70442737
|
C | CA | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-9746dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70442737 | |||||
| chr6:70442759
|
T | A | 143 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(140): Show | 143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.78-9733T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442759 | ||||||
| chr6:70442772
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.78-9720T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442772 | ||||||
| chr6:70442826
|
A | G | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.78-9666A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442826 | ||||||
| chr6:70443005
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0095others(3): Show | 6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-9487A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443005 | ||||||
| chr6:70443101
|
G | T | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-9391G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443101 | ||||||
| chr6:70443308
|
ATGGTAGT others(5): Show |
A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.78-9178_78-9167del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70443308 | |||||
| chr6:70443469
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-9023C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443469 | ||||||
| chr6:70443516
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-8976G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443516 | ||||||
| chr6:70443535
|
C | T | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.78-8957C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443535 | ||||||
| chr6:70443656
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.78-8836T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443656 | ||||||
| chr6:70443715
|
C | T | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-8777C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443715 | ||||||
| chr6:70443857
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.78-8635A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443857 | ||||||
| chr6:70443990
|
A | C | 5 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-8502A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443990 | ||||||
| chr6:70444020
|
A | G | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-8472A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444020 | ||||||
| chr6:70444046
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.78-8446G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444046 | ||||||
| chr6:70444065
|
C | T | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.78-8427C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444065 | ||||||
| chr6:70444171
|
A | G | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.78-8321A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444171 | ||||||
| chr6:70444174
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-8318A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444174 | ||||||
| chr6:70444290
|
C | T | 2 | a0002c0003t0001g0138a0002c0003t0001g0139 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.78-8202C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444290 | ||||||
| chr6:70444335
|
A | G | 3 | a0001c0004t0004g0015a0005c0008t0004g0003a0005c0008t0004g0004 | 3 | HG01074.hp2 HG01346.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.78-8157A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444335 | ||||||
| chr6:70444345
|
T | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-8147T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444345 | ||||||
| chr6:70444406
|
AAAAT | A | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.78-8063_78-8060del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70444406 | |||||
| chr6:70444429
|
A | C | 47 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(44): Show | 47 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.78-8063A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444429 | ||||||
| chr6:70444732
|
C | T | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.78-7760C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444732 | ||||||
| chr6:70444760
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-7732A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444760 | ||||||
| chr6:70444791
|
A | G | 1 | a0001c0004t0003g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.78-7701A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444791 | ||||||
| chr6:70444851
|
A | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-7641A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444851 | ||||||
| chr6:70445021
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-7471A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445021 | ||||||
| chr6:70445102
|
T | C | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-7390T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445102 | ||||||
| chr6:70445138
|
CAG | C | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-7353_78-7352del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445138 | ||||||
| chr6:70445146
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78-7346G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445146 | ||||||
| chr6:70445361
|
G | GAGACCA | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.78-7131_78-7130ins others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445361 | ||||||
| chr6:70445362
|
T | C | 1 | a0008c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.78-7130T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445362 | ||||||
| chr6:70445362
|
T | G | 116 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(113): Show | 116 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.78-7130T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445362 | ||||||
| chr6:70445365
|
T | C | 220 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(217): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.78-7127T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445365 | ||||||
| chr6:70445392
|
G | A | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-7100G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445392 | ||||||
| chr6:70445472
|
A | G | 1 | a0002c0003t0001g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.78-7020A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445472 | ||||||
| chr6:70445734
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78-6758C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445734 | ||||||
| chr6:70445735
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78-6757G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445735 | ||||||
| chr6:70445852
|
G | C | 6 | a0002c0003t0001g0128a0002c0006t0001g0034a0002c0006t0001g0129others(3): Show | 6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-6640G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445852 | ||||||
| chr6:70445856
|
G | A | 18 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(15): Show | 18 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-6636G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445856 | ||||||
| chr6:70445856
|
G | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78-6636G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445856 | ||||||
| chr6:70446149
|
T | C | 8 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-6343T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446149 | ||||||
| chr6:70446155
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.78-6337A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446155 | ||||||
| chr6:70446159
|
C | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-6333C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446159 | ||||||
| chr6:70446186
|
C | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-6306C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446186 | ||||||
| chr6:70446236
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-6256A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446236 | ||||||
| chr6:70446312
|
C | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-6180C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446312 | ||||||
| chr6:70446408
|
A | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.78-6084A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446408 | ||||||
| chr6:70446442
|
C | G | 8 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-6050C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446442 | ||||||
| chr6:70446447
|
T | A | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.78-6045T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446447 | ||||||
| chr6:70446475
|
G | A | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-6017G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446475 | ||||||
| chr6:70446489
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-6003G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446489 | ||||||
| chr6:70446692
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.78-5800T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446692 | ||||||
| chr6:70446693
|
T | G | 1 | a0001c0002t0002g0168 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.78-5799T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446693 | ||||||
| chr6:70446882
|
T | C | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.78-5610T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446882 | ||||||
| chr6:70446924
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.78-5568G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446924 | ||||||
| chr6:70447004
|
C | T | 2 | a0001c0002t0002g0168a0001c0002t0002g0209 | 2 | NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.78-5488C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447004 | ||||||
| chr6:70447005
|
G | A | 1 | a0002c0003t0001g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.78-5487G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447005 | ||||||
| chr6:70447042
|
G | A | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.78-5450G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447042 | ||||||
| chr6:70447083
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-5409G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447083 | ||||||
| chr6:70447099
|
G | A | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5393G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447099 | ||||||
| chr6:70447359
|
A | G | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-5133A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447359 | ||||||
| chr6:70447471
|
C | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-5021C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447471 | ||||||
| chr6:70447530
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-4962A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447530 | ||||||
| chr6:70447565
|
G | A | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.78-4927G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447565 | ||||||
| chr6:70447759
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0151 | 2 | HG01109.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.78-4733T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447759 | ||||||
| chr6:70447791
|
C | T | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-4701C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447791 | ||||||
| chr6:70447849
|
C | T | 3 | a0001c0002t0002g0254a0001c0002t0002g0258a0001c0002t0002g0259 | 3 | HG00642.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.78-4643C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447849 | ||||||
| chr6:70447876
|
C | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-4616C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447876 | ||||||
| chr6:70447967
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.78-4525A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447967 | ||||||
| chr6:70448007
|
TATA | T | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.78-4481_78-4479del others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70448007 | |||||
| chr6:70448194
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-4298G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448194 | ||||||
| chr6:70448582
|
T | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-3910T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448582 | ||||||
| chr6:70448600
|
C | T | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.78-3892C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448600 | ||||||
| chr6:70448641
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.78-3851A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448641 | ||||||
| chr6:70448671
|
G | A | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.78-3821G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448671 | ||||||
| chr6:70448687
|
G | A | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-3805G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448687 | ||||||
| chr6:70448689
|
G | A | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78-3803G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448689 | ||||||
| chr6:70448748
|
A | C | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-3744A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448748 | ||||||
| chr6:70448778
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-3714G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448778 | ||||||
| chr6:70448850
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0105 | 3 | HG01074.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.78-3642C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448850 | ||||||
| chr6:70448983
|
A | G | 1 | a0001c0004t0003g0239 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-3509A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448983 | ||||||
| chr6:70449039
|
C | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-3453C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449039 | ||||||
| chr6:70449107
|
C | A | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-3385C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449107 | ||||||
| chr6:70449130
|
A | G | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.78-3362A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449130 | ||||||
| chr6:70449139
|
T | A | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-3353T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449139 | ||||||
| chr6:70449296
|
C | T | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-3196C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449296 | ||||||
| chr6:70449586
|
T | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-2906T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449586 | ||||||
| chr6:70449608
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.78-2884G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449608 | ||||||
| chr6:70449931
|
C | T | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-2561C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449931 | ||||||
| chr6:70449960
|
C | T | 1 | a0001c0002t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.78-2532C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449960 | ||||||
| chr6:70450072
|
A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78-2420A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450072 | ||||||
| chr6:70450215
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.78-2277G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450215 | ||||||
| chr6:70450481
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78-2011C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450481 | ||||||
| chr6:70450716
|
G | GT | 14 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0088others(11): Show | 14 | HG00673.hp1 HG01515.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-1734dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
G | GTT | 8 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0087others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-1735_78-1734dup others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78-1776G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450716 | ||||||
| chr6:70450716
|
GT | G | 45 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0053others(42): Show | 45 | HG00621.hp2 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.78-1734delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTT | G | 19 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0057others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.78-1735_78-1734del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTT | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0055others(10): Show | 13 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-1736_78-1734del others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(3): Show |
G | 11 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0232others(8): Show | 11 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.78-1743_78-1734del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(4): Show |
G | 5 | a0001c0001t0001g0154a0001c0004t0004g0015a0005c0008t0004g0003others(2): Show | 5 | HG01074.hp2 HG01346.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-1744_78-1734del others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(5): Show |
G | 4 | a0001c0001t0001g0153a0001c0004t0003g0009a0001c0004t0003g0251others(1): Show | 4 | HG03209.hp1 HG03491.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1745_78-1734del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(6): Show |
G | 10 | a0001c0001t0001g0104a0001c0004t0003g0010a0001c0004t0003g0011others(7): Show | 10 | HG01192.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-1746_78-1734del others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0001g0080a0001c0004t0003g0012a0001c0004t0003g0014 | 3 | HG03225.hp1 NA18979.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.78-1747_78-1734del others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(8): Show |
G | 11 | a0001c0001t0001g0063a0001c0009t0001g0211a0001c0009t0001g0212others(8): Show | 11 | HG01433.hp2 HG02109.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.78-1748_78-1734del others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(9): Show |
G | 3 | a0001c0002t0002g0168a0002c0003t0001g0116a0002c0003t0001g0117 | 3 | NA18962.hp1 NA19070.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.78-1749_78-1734del others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(10): Show |
G | 18 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0148others(15): Show | 18 | HG00673.hp2 HG01243.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.78-1750_78-1734del others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(11): Show |
G | 56 | a0001c0001t0001g0210a0001c0002t0002g0167a0001c0002t0002g0173others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-1751_78-1734del others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.78-1757_78-1734del others(24): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450716
|
GTTTTTTT others(19): Show |
G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1759_78-1734del others(26): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | |||||
| chr6:70450719
|
T | G | 1 | a0002c0003t0001g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.78-1773T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450719 | ||||||
| chr6:70450732
|
T | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-1760T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450732 | ||||||
| chr6:70450817
|
C | G | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-1675C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450817 | ||||||
| chr6:70451049
|
C | T | 161 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(158): Show | 161 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.78-1443C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451049 | ||||||
| chr6:70451118
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.78-1374T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451118 | ||||||
| chr6:70451413
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-1079G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451413 | ||||||
| chr6:70451416
|
T | C | 1 | a0002c0003t0001g0044 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.78-1076T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451416 | ||||||
| chr6:70451451
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.78-1041C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451451 | ||||||
| chr6:70451607
|
C | G | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78-885C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451607 | ||||||
| chr6:70451613
|
C | A | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.78-879C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451613 | ||||||
| chr6:70451677
|
C | A | 1 | a0002c0003t0008g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.78-815C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451677 | ||||||
| chr6:70451719
|
G | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-773G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451719 | ||||||
| chr6:70451826
|
T | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-666T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451826 | ||||||
| chr6:70451869
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-623A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451869 | ||||||
| chr6:70451966
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-526G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451966 | ||||||
| chr6:70452115
|
A | G | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78-377A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452115 | ||||||
| chr6:70452200
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG00639.hp2 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-292C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452200 | ||||||
| chr6:70452285
|
A | G | 1 | a0002c0003t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.78-207A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452285 | ||||||
| chr6:70452427
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-65G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452427 | ||||||
| chr6:70452584
|
A | C | 2 | a0001c0002t0002g0258a0001c0002t0002g0259 | 2 | HG00642.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.157+13A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70452584 | ||||||
| chr6:70452943
|
A | G | 2 | a0002c0003t0001g0030a0002c0003t0001g0031 | 2 | NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.157+372A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70452943 | ||||||
| chr6:70452989
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.157+418G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70452989 | ||||||
| chr6:70453007
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.157+436A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453007 | ||||||
| chr6:70453554
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.157+983T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453554 | ||||||
| chr6:70453576
|
C | A | 1 | a0002c0003t0001g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.157+1005C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453576 | ||||||
| chr6:70453618
|
A | G | 1 | a0001c0002t0002g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.157+1047A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453618 | ||||||
| chr6:70453628
|
C | T | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.157+1057C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453628 | ||||||
| chr6:70453764
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+1193A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453764 | ||||||
| chr6:70453773
|
C | T | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+1202C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453773 | ||||||
| chr6:70453865
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.157+1294C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453865 | ||||||
| chr6:70453922
|
A | G | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.157+1351A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453922 | ||||||
| chr6:70453952
|
G | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+1381G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453952 | ||||||
| chr6:70453969
|
A | T | 1 | a0008c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.157+1398A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453969 | ||||||
| chr6:70454074
|
T | G | 1 | a0002c0003t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.157+1503T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454074 | ||||||
| chr6:70454153
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+1582C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454153 | ||||||
| chr6:70454184
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+1613G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454184 | ||||||
| chr6:70454310
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+1739C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454310 | ||||||
| chr6:70454333
|
A | G | 1 | a0002c0003t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.157+1762A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454333 | ||||||
| chr6:70454461
|
T | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+1890T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454461 | ||||||
| chr6:70454588
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+2017G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454588 | ||||||
| chr6:70454602
|
G | A | 2 | a0001c0002t0002g0258a0001c0002t0002g0259 | 2 | HG00642.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.157+2031G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454602 | ||||||
| chr6:70454658
|
A | G | 1 | a0001c0002t0002g0192 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.157+2087A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454658 | ||||||
| chr6:70454812
|
A | G | 1 | a0002c0003t0001g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157+2241A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454812 | ||||||
| chr6:70454910
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+2339C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454910 | ||||||
| chr6:70454911
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+2340A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454911 | ||||||
| chr6:70454924
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.157+2353G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454924 | ||||||
| chr6:70454967
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+2396A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454967 | ||||||
| chr6:70454979
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+2408A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454979 | ||||||
| chr6:70454991
|
A | G | 1 | a0002c0003t0001g0135 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.157+2420A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454991 | ||||||
| chr6:70455020
|
C | T | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.157+2449C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455020 | ||||||
| chr6:70455165
|
C | A | 135 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.157+2594C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455165 | ||||||
| chr6:70455215
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.157+2644A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455215 | ||||||
| chr6:70455275
|
C | T | 9 | a0002c0003t0001g0051a0002c0003t0001g0107a0002c0003t0001g0108others(6): Show | 9 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+2704C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455275 | ||||||
| chr6:70455311
|
A | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+2740A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455311 | ||||||
| chr6:70455381
|
T | TAC | 15 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0087others(12): Show | 15 | HG00280.hp2 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+2841_157+2842d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | |||||
| chr6:70455381
|
T | TACAC | 9 | a0001c0001t0001g0094a0001c0004t0003g0010a0001c0004t0003g0011others(6): Show | 9 | HG00673.hp1 HG01074.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+2839_157+2842d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | |||||
| chr6:70455381
|
TAC | T | 71 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0053others(68): Show | 71 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.157+2841_157+2842d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | |||||
| chr6:70455381
|
TACAC | T | 33 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0168others(30): Show | 33 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.157+2839_157+2842d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | |||||
| chr6:70455381
|
TACACACA others(3): Show |
T | 1 | a0001c0002t0002g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157+2833_157+2842d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | |||||
| chr6:70455408
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.157+2837A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455408 | ||||||
| chr6:70455521
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+2950A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455521 | ||||||
| chr6:70455700
|
A | T | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.157+3129A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455700 | ||||||
| chr6:70455733
|
A | G | 1 | a0002c0003t0001g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.157+3162A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455733 | ||||||
| chr6:70455813
|
ATTAT | A | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.157+3244_157+3247d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455813 | |||||
| chr6:70455876
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.157+3305G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455876 | ||||||
| chr6:70455944
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+3373C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455944 | ||||||
| chr6:70455946
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+3375G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455946 | ||||||
| chr6:70455959
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+3388C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455959 | ||||||
| chr6:70456051
|
C | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+3480C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456051 | ||||||
| chr6:70456071
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+3500C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456071 | ||||||
| chr6:70456177
|
A | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+3606A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456177 | ||||||
| chr6:70456388
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+3817A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456388 | ||||||
| chr6:70456441
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.157+3870G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456441 | ||||||
| chr6:70456472
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.157+3901G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456472 | ||||||
| chr6:70456497
|
A | G | 1 | a0001c0013t0001g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.157+3926A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456497 | ||||||
| chr6:70456572
|
T | C | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.157+4001T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456572 | ||||||
| chr6:70456763
|
C | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+4192C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456763 | ||||||
| chr6:70456784
|
C | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+4213C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456784 | ||||||
| chr6:70456908
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.157+4337C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456908 | ||||||
| chr6:70456966
|
T | C | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.157+4395T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456966 | ||||||
| chr6:70457357
|
C | T | 8 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+4786C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457357 | ||||||
| chr6:70457382
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+4811C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457382 | ||||||
| chr6:70457404
|
A | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+4833A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457404 | ||||||
| chr6:70457597
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+5026A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457597 | ||||||
| chr6:70457679
|
T | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+5108T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457679 | ||||||
| chr6:70457993
|
T | G | 3 | a0001c0002t0002g0219a0001c0002t0002g0221a0001c0002t0002g0222 | 3 | HG00609.hp1 HG00621.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.157+5422T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457993 | ||||||
| chr6:70458125
|
A | G | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+5554A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458125 | ||||||
| chr6:70458128
|
A | ATC | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.157+5559_157+5560d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70458128 | |||||
| chr6:70458260
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.157+5689C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458260 | ||||||
| chr6:70458312
|
A | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+5741A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458312 | ||||||
| chr6:70458357
|
A | T | 1 | a0007c0019t0001g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.157+5786A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458357 | ||||||
| chr6:70458429
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+5858G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458429 | ||||||
| chr6:70458450
|
G | A | 1 | a0005c0008t0004g0003 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.157+5879G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458450 | ||||||
| chr6:70458697
|
T | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+6126T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458697 | ||||||
| chr6:70458728
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+6157A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458728 | ||||||
| chr6:70458809
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157+6238A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458809 | ||||||
| chr6:70458875
|
C | G | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+6304C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458875 | ||||||
| chr6:70458951
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+6380A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458951 | ||||||
| chr6:70458988
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.157+6417G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458988 | ||||||
| chr6:70459531
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+6960A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459531 | ||||||
| chr6:70459827
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+7256A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459827 | ||||||
| chr6:70459946
|
G | T | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.157+7375G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459946 | ||||||
| chr6:70459961
|
G | T | 1 | a0002c0003t0001g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157+7390G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459961 | ||||||
| chr6:70459977
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+7406G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459977 | ||||||
| chr6:70460088
|
T | C | 1 | a0001c0002t0002g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+7517T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460088 | ||||||
| chr6:70460114
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+7543G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460114 | ||||||
| chr6:70460144
|
G | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.157+7573G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460144 | ||||||
| chr6:70460598
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+8027G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460598 | ||||||
| chr6:70460635
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.157+8064G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460635 | ||||||
| chr6:70460788
|
GATCT | G | 9 | a0002c0003t0001g0051a0002c0003t0001g0107a0002c0003t0001g0108others(6): Show | 9 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+8235_157+8238d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70460788 | |||||
| chr6:70460810
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.157+8239G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460810 | ||||||
| chr6:70460852
|
T | TTTTTTTT others(1): Show |
56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+8288_157+8289i others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70460852 | |||||
| chr6:70461004
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+8433A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461004 | ||||||
| chr6:70461113
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+8542G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461113 | ||||||
| chr6:70461116
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+8545C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461116 | ||||||
| chr6:70461163
|
T | A | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.157+8592T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461163 | ||||||
| chr6:70461477
|
CAT | C | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+8908_157+8909d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70461477 | |||||
| chr6:70461548
|
G | A | 2 | a0001c0002t0002g0261a0001c0002t0002g0262 | 2 | HG01516.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.157+8977G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461548 | ||||||
| chr6:70461549
|
T | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+8978T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461549 | ||||||
| chr6:70461675
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+9104G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461675 | ||||||
| chr6:70461736
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+9165A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461736 | ||||||
| chr6:70462089
|
C | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+9518C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462089 | ||||||
| chr6:70462396
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.157+9825G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462396 | ||||||
| chr6:70462404
|
A | T | 40 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0177others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.157+9833A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462404 | ||||||
| chr6:70462604
|
C | G | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.157+10033C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462604 | ||||||
| chr6:70462609
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0157a0002c0003t0001g0022 | 3 | HG02027.hp2 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.157+10038A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462609 | ||||||
| chr6:70462686
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+10115G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462686 | ||||||
| chr6:70462887
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+10316G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462887 | ||||||
| chr6:70462930
|
T | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+10359T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462930 | ||||||
| chr6:70462944
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.157+10373A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462944 | ||||||
| chr6:70462948
|
G | GTTGTT | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+10381_157+1038 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70462948 | |||||
| chr6:70463250
|
G | C | 99 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(96): Show | 99 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.157+10679G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463250 | ||||||
| chr6:70463252
|
C | A | 1 | a0001c0002t0002g0223 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.157+10681C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463252 | ||||||
| chr6:70463419
|
T | TA | 96 | a0001c0001t0001g0028a0001c0001t0001g0081a0001c0001t0001g0158others(93): Show | 96 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.157+10864dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70463419 | |||||
| chr6:70463419
|
T | TAA | 14 | a0001c0002t0002g0171a0001c0002t0002g0253a0001c0002t0002g0254others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+10863_157+1086 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70463419 | |||||
| chr6:70463436
|
T | A | 1 | a0008c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.157+10865T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463436 | ||||||
| chr6:70463481
|
A | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+10910A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463481 | ||||||
| chr6:70463496
|
G | A | 1 | a0001c0004t0003g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.157+10925G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463496 | ||||||
| chr6:70463524
|
C | T | 81 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(78): Show | 81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.157+10953C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463524 | ||||||
| chr6:70463525
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.157+10954G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463525 | ||||||
| chr6:70463567
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.157+10996T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463567 | ||||||
| chr6:70463573
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+11002A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463573 | ||||||
| chr6:70463672
|
A | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+11101A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463672 | ||||||
| chr6:70463867
|
A | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+11296A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463867 | ||||||
| chr6:70463907
|
T | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+11336T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463907 | ||||||
| chr6:70464044
|
TCTTA | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-11361_158-1135 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464044 | |||||
| chr6:70464360
|
G | A | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.158-11050G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464360 | ||||||
| chr6:70464566
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10844C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464566 | ||||||
| chr6:70464608
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.158-10802G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464608 | ||||||
| chr6:70464638
|
ATTTC | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0002c0003t0001g0118 | 3 | HG00642.hp1 HG01515.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.158-10752_158-1074 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464638 | |||||
| chr6:70464654
|
CTTTCTTT others(2): Show |
C | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.158-10743_158-1073 others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464654 | |||||
| chr6:70464658
|
C | CT | 52 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(49): Show | 52 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.158-10744dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | |||||
| chr6:70464658
|
C | CTT | 9 | a0001c0001t0001g0210a0001c0002t0002g0182a0003c0005t0001g0242others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-10745_158-1074 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | |||||
| chr6:70464658
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0002g0173 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | |||||
| chr6:70464658
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0002g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | |||||
| chr6:70464658
|
C | CTTTTTTT others(10): Show |
1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(21): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | |||||
| chr6:70464658
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(25): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | |||||
| chr6:70464666
|
TC | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-10743delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464666 | ||||||
| chr6:70464667
|
C | CT | 9 | a0001c0001t0001g0133a0002c0003t0001g0035a0002c0003t0001g0044others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-10727dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464667 | |||||
| chr6:70464667
|
C | T | 85 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(82): Show | 85 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.158-10743C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464667 | ||||||
| chr6:70464770
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10640G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464770 | ||||||
| chr6:70464806
|
A | G | 12 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0140others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-10604A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464806 | ||||||
| chr6:70464833
|
A | AT | 22 | a0001c0001t0001g0020a0001c0001t0001g0087a0001c0001t0001g0089others(19): Show | 22 | HG00597.hp2 HG00735.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.158-10548dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
A | ATTTTT | 34 | a0001c0001t0001g0210a0001c0002t0002g0167a0001c0002t0002g0173others(31): Show | 34 | HG00597.hp1 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.158-10552_158-1054 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
A | ATTTTTT | 19 | a0001c0001t0001g0267a0001c0002t0002g0168a0001c0002t0002g0169others(16): Show | 19 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.158-10553_158-1054 others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
AT | A | 10 | a0001c0001t0001g0028a0001c0001t0001g0106a0002c0003t0001g0124others(7): Show | 10 | HG01168.hp1 HG02293.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-10548delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
ATT | A | 30 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.158-10549_158-1054 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
ATTTT | A | 17 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(14): Show | 17 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-10551_158-1054 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
ATTTTT | A | 22 | a0001c0002t0002g0256a0001c0004t0003g0001a0001c0004t0003g0010others(19): Show | 22 | HG01069.hp1 HG02280.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.158-10552_158-1054 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464833
|
ATTTTTTT others(12): Show |
A | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.158-10566_158-1054 others(23): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | |||||
| chr6:70464867
|
A | G | 8 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-10543A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464867 | ||||||
| chr6:70464890
|
G | A | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-10520G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464890 | ||||||
| chr6:70465024
|
T | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10386T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465024 | ||||||
| chr6:70465095
|
G | A | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.158-10315G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465095 | ||||||
| chr6:70465172
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-10238C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465172 | ||||||
| chr6:70465196
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.158-10214C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465196 | ||||||
| chr6:70465206
|
ATT | A | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-10201_158-1020 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70465206 | |||||
| chr6:70465305
|
A | G | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-10105A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465305 | ||||||
| chr6:70465375
|
G | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10035G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465375 | ||||||
| chr6:70465407
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158-10003A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465407 | ||||||
| chr6:70465448
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.158-9962G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465448 | ||||||
| chr6:70465631
|
C | T | 2 | a0002c0003t0001g0051a0002c0003t0001g0114 | 2 | HG01243.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.158-9779C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465631 | ||||||
| chr6:70465750
|
C | T | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-9660C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465750 | ||||||
| chr6:70465862
|
G | A | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.158-9548G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465862 | ||||||
| chr6:70465989
|
G | A | 43 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 43 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.158-9421G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465989 | ||||||
| chr6:70466360
|
G | T | 3 | a0001c0004t0004g0015a0005c0008t0004g0003a0005c0008t0004g0004 | 3 | HG01074.hp2 HG01346.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.158-9050G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466360 | ||||||
| chr6:70466403
|
A | G | 1 | a0008c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.158-9007A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466403 | ||||||
| chr6:70466515
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-8895G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466515 | ||||||
| chr6:70466586
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.158-8824G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466586 | ||||||
| chr6:70466739
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.158-8671G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466739 | ||||||
| chr6:70466956
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.158-8454G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466956 | ||||||
| chr6:70466992
|
C | T | 1 | a0002c0003t0001g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158-8418C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466992 | ||||||
| chr6:70467144
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.158-8266C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467144 | ||||||
| chr6:70467165
|
G | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-8245G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467165 | ||||||
| chr6:70467688
|
T | C | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-7722T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467688 | ||||||
| chr6:70467736
|
C | G | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-7674C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467736 | ||||||
| chr6:70467776
|
T | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-7634T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467776 | ||||||
| chr6:70468270
|
T | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-7140T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468270 | ||||||
| chr6:70468325
|
A | G | 1 | a0001c0002t0002g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.158-7085A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468325 | ||||||
| chr6:70468403
|
T | C | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-7007T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468403 | ||||||
| chr6:70468424
|
G | A | 5 | a0001c0002t0002g0168a0001c0002t0002g0171a0001c0002t0002g0172others(2): Show | 5 | HG00673.hp2 NA18939.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-6986G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468424 | ||||||
| chr6:70468617
|
A | G | 2 | a0005c0008t0004g0003a0005c0008t0004g0004 | 2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.158-6793A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468617 | ||||||
| chr6:70468618
|
T | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-6792T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468618 | ||||||
| chr6:70468813
|
T | C | 1 | a0002c0003t0008g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.158-6597T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468813 | ||||||
| chr6:70468862
|
C | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.158-6548C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468862 | ||||||
| chr6:70469078
|
G | A | 43 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 43 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.158-6332G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469078 | ||||||
| chr6:70469082
|
G | A | 143 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(140): Show | 143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.158-6328G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469082 | ||||||
| chr6:70469425
|
T | G | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.158-5985T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469425 | ||||||
| chr6:70469906
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.158-5504G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469906 | ||||||
| chr6:70469981
|
ACT | A | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.158-5426_158-5425d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70469981 | |||||
| chr6:70470009
|
A | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.158-5401A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470009 | ||||||
| chr6:70470011
|
AC | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0158 | 3 | HG02145.hp2 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.158-5398delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470011 | ||||||
| chr6:70470116
|
A | G | 28 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.158-5294A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470116 | ||||||
| chr6:70470362
|
C | CT | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-5039dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70470362 | |||||
| chr6:70470439
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-4971C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470439 | ||||||
| chr6:70470510
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.158-4900C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470510 | ||||||
| chr6:70470593
|
G | T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.158-4817G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470593 | ||||||
| chr6:70470679
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.158-4731A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470679 | ||||||
| chr6:70470802
|
C | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.158-4608C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470802 | ||||||
| chr6:70471168
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-4242G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471168 | ||||||
| chr6:70471177
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0104 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.158-4233G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471177 | ||||||
| chr6:70471257
|
G | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-4153G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471257 | ||||||
| chr6:70471282
|
G | A | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.158-4128G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471282 | ||||||
| chr6:70471422
|
C | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.158-3988C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471422 | ||||||
| chr6:70471588
|
GATCA | G | 99 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(96): Show | 99 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.158-3817_158-3814d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70471588 | |||||
| chr6:70471614
|
A | ATGCTG | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-3795_158-3791d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70471614 | |||||
| chr6:70471699
|
C | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-3711C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471699 | ||||||
| chr6:70471841
|
C | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0055others(18): Show | 21 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.158-3569C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471841 | ||||||
| chr6:70471972
|
C | A | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.158-3438C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471972 | ||||||
| chr6:70472101
|
G | A | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.158-3309G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472101 | ||||||
| chr6:70472221
|
C | T | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.158-3189C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472221 | ||||||
| chr6:70472310
|
C | T | 135 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.158-3100C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472310 | ||||||
| chr6:70472507
|
T | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-2903T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472507 | ||||||
| chr6:70472511
|
C | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-2899C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472511 | ||||||
| chr6:70472599
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.158-2811C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472599 | ||||||
| chr6:70472649
|
A | C | 1 | a0002c0003t0001g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.158-2761A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472649 | ||||||
| chr6:70472782
|
G | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.158-2628G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472782 | ||||||
| chr6:70472787
|
C | G | 8 | a0002c0003t0001g0002a0002c0003t0001g0039a0002c0003t0001g0040others(5): Show | 8 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-2623C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472787 | ||||||
| chr6:70472892
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-2518G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472892 | ||||||
| chr6:70472967
|
C | T | 1 | a0002c0003t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.158-2443C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472967 | ||||||
| chr6:70472968
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.158-2442G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472968 | ||||||
| chr6:70472978
|
T | G | 1 | a0002c0003t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.158-2432T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472978 | ||||||
| chr6:70473010
|
G | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-2400G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473010 | ||||||
| chr6:70473085
|
A | G | 2 | a0001c0002t0002g0258a0001c0002t0002g0259 | 2 | HG00642.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.158-2325A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473085 | ||||||
| chr6:70473173
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158-2237A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473173 | ||||||
| chr6:70473255
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.158-2155G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473255 | ||||||
| chr6:70473382
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.158-2028A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473382 | ||||||
| chr6:70473425
|
CTT | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-1983_158-1982d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70473425 | |||||
| chr6:70473473
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-1937A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473473 | ||||||
| chr6:70473512
|
G | A | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.158-1898G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473512 | ||||||
| chr6:70473706
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.158-1704T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473706 | ||||||
| chr6:70473810
|
G | A | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.158-1600G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473810 | ||||||
| chr6:70473880
|
C | T | 2 | a0001c0002t0002g0177a0001c0002t0002g0199 | 2 | NA18993.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.158-1530C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473880 | ||||||
| chr6:70473917
|
T | G | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.158-1493T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473917 | ||||||
| chr6:70473975
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0074 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.158-1435G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473975 | ||||||
| chr6:70474258
|
GTTTCTTT others(5): Show |
G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-1136_158-1125d others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70474258 | |||||
| chr6:70474365
|
A | G | 1 | a0001c0002t0002g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.158-1045A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474365 | ||||||
| chr6:70474410
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.158-1000C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474410 | ||||||
| chr6:70474613
|
A | G | 40 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0177others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.158-797A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474613 | ||||||
| chr6:70474699
|
G | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-711G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474699 | ||||||
| chr6:70474998
|
C | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.158-412C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474998 | ||||||
| chr6:70475008
|
A | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.158-402A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70475008 | ||||||
| chr6:70475163
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.158-247C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70475163 | ||||||
| chr6:70475190
|
T | G | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-220T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70475190 | ||||||
| chr6:70475583
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.297+34T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 6/21 | chr6 | 70475583 | ||||||
| chr6:70475648
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-15G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 6/21 | chr6 | 70475648 | ||||||
| chr6:70475933
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368+200C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70475933 | ||||||
| chr6:70476070
|
G | T | 40 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0177others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.368+337G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476070 | ||||||
| chr6:70476269
|
T | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.368+536T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476269 | ||||||
| chr6:70476315
|
G | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.368+582G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476315 | ||||||
| chr6:70476436
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.368+703C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476436 | ||||||
| chr6:70476578
|
T | A | 114 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(111): Show | 114 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.369-581T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476578 | ||||||
| chr6:70476653
|
G | A | 135 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.369-506G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476653 | ||||||
| chr6:70476692
|
A | T | 1 | a0004c0007t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.369-467A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476692 | ||||||
| chr6:70476725
|
G | T | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369-434G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476725 | ||||||
| chr6:70477112
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.369-47G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70477112 | ||||||
| chr6:70477399
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.542+67G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70477399 | ||||||
| chr6:70477468
|
G | A | 3 | a0002c0003t0001g0045a0002c0003t0001g0046a0002c0003t0001g0165 | 3 | HG02523.hp1 NA18953.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.542+136G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70477468 | ||||||
| chr6:70477618
|
C | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+286C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70477618 | ||||||
| chr6:70478110
|
C | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.542+778C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478110 | ||||||
| chr6:70478127
|
T | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.542+795T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478127 | ||||||
| chr6:70478144
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.542+812A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478144 | ||||||
| chr6:70478159
|
A | G | 1 | a0002c0003t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.542+827A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478159 | ||||||
| chr6:70478629
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+1297A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478629 | ||||||
| chr6:70478679
|
C | CA | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+1348dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 70478679 | |||||
| chr6:70478738
|
C | A | 1 | a0001c0002t0002g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542+1406C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478738 | ||||||
| chr6:70478825
|
G | A | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.542+1493G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478825 | ||||||
| chr6:70478869
|
T | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.542+1537T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478869 | ||||||
| chr6:70478895
|
ATG | A | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.542+1568_542+1569d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 70478895 | |||||
| chr6:70479371
|
G | A | 8 | a0002c0003t0001g0051a0002c0003t0001g0107a0002c0003t0001g0114others(5): Show | 8 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.543-1530G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479371 | ||||||
| chr6:70479702
|
T | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-1199T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479702 | ||||||
| chr6:70479710
|
A | G | 2 | a0001c0004t0003g0010a0001c0004t0003g0013 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.543-1191A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479710 | ||||||
| chr6:70479799
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.543-1102C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479799 | ||||||
| chr6:70479985
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.543-916C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479985 | ||||||
| chr6:70480064
|
C | T | 1 | a0002c0003t0001g0165 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.543-837C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480064 | ||||||
| chr6:70480094
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.543-807G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480094 | ||||||
| chr6:70480155
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-746A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480155 | ||||||
| chr6:70480339
|
A | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.543-562A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480339 | ||||||
| chr6:70480529
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-372A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480529 | ||||||
| chr6:70480742
|
A | T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.543-159A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480742 | ||||||
| chr6:70480874
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.543-27A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480874 | ||||||
| chr6:70481364
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.669+337G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | chr6 | 70481364 | ||||||
| chr6:70481539
|
A | G | 3 | a0001c0002t0002g0167a0001c0002t0002g0191a0001c0002t0002g0203 | 3 | HG01993.hp1 HG02004.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.670-462A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | chr6 | 70481539 | ||||||
| chr6:70481648
|
T | TA | 21 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.670-340dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 70481648 | |||||
| chr6:70481648
|
TA | T | 55 | a0001c0001t0001g0148a0001c0002t0002g0167a0001c0002t0002g0168others(52): Show | 55 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.670-340delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 70481648 | |||||
| chr6:70481873
|
AT | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.670-122delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 70481873 | |||||
| chr6:70481939
|
A | G | 1 | a0002c0003t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.670-62A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | chr6 | 70481939 | ||||||
| chr6:70482243
|
C | A | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.823+89C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482243 | ||||||
| chr6:70482388
|
TA | T | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.823+242delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70482388 | |||||
| chr6:70482683
|
C | G | 1 | a0002c0003t0008g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.823+529C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482683 | ||||||
| chr6:70482930
|
TAA | T | 46 | a0002c0003t0001g0002a0002c0003t0001g0022a0002c0003t0001g0030others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.823+777_823+778del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482930 | ||||||
| chr6:70482994
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0146 | 3 | HG02258.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823+840C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482994 | ||||||
| chr6:70483110
|
G | A | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.823+956G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483110 | ||||||
| chr6:70483394
|
A | G | 1 | a0002c0006t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.823+1240A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483394 | ||||||
| chr6:70483524
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+1370C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483524 | ||||||
| chr6:70483576
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+1422A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483576 | ||||||
| chr6:70483725
|
C | A | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.823+1571C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483725 | ||||||
| chr6:70483728
|
T | C | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.823+1574T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483728 | ||||||
| chr6:70483751
|
T | G | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.823+1597T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483751 | ||||||
| chr6:70483834
|
T | C | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.823+1680T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483834 | ||||||
| chr6:70483846
|
A | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.823+1692A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483846 | ||||||
| chr6:70484097
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.823+1943C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484097 | ||||||
| chr6:70484622
|
C | G | 4 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0084others(1): Show | 4 | NA18961.hp2 NA18962.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+2468C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484622 | ||||||
| chr6:70484653
|
C | T | 1 | a0002c0003t0001g0022 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.823+2499C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484653 | ||||||
| chr6:70484810
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823+2656A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484810 | ||||||
| chr6:70484968
|
T | C | 17 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0178others(14): Show | 17 | HG00597.hp1 HG01993.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2814T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484968 | ||||||
| chr6:70485426
|
G | A | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.823+3272G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70485426 | ||||||
| chr6:70485504
|
A | G | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.823+3350A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70485504 | ||||||
| chr6:70485739
|
C | T | 161 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(158): Show | 161 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.823+3585C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70485739 | ||||||
| chr6:70486215
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.823+4061A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486215 | ||||||
| chr6:70486484
|
G | A | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+4330G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486484 | ||||||
| chr6:70486573
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823+4419G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486573 | ||||||
| chr6:70486630
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0013t0001g0085 | 3 | HG01175.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.824-4404A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486630 | ||||||
| chr6:70486651
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.824-4383G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486651 | ||||||
| chr6:70486727
|
G | A | 1 | a0002c0003t0001g0135 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.824-4307G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486727 | ||||||
| chr6:70486796
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-4238C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486796 | ||||||
| chr6:70486839
|
A | G | 1 | a0002c0006t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.824-4195A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486839 | ||||||
| chr6:70486870
|
T | C | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-4164T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486870 | ||||||
| chr6:70487027
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.824-4007G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487027 | ||||||
| chr6:70487035
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-3999A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487035 | ||||||
| chr6:70487071
|
G | A | 262 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(259): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.824-3963G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487071 | ||||||
| chr6:70487083
|
C | CA | 87 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(84): Show | 87 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.824-3926dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | |||||
| chr6:70487083
|
C | CAA | 18 | a0001c0001t0001g0050a0001c0001t0001g0146a0001c0001t0001g0158others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.824-3927_824-3926d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | |||||
| chr6:70487083
|
CA | C | 33 | a0001c0001t0001g0155a0001c0001t0001g0210a0001c0001t0001g0267others(30): Show | 33 | HG01192.hp2 HG02109.hp1 HG02280.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-3926delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | |||||
| chr6:70487083
|
CAAA | C | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-3928_824-3926d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | |||||
| chr6:70487083
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.824-3936_824-3926d others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | |||||
| chr6:70487398
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.824-3636T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487398 | ||||||
| chr6:70487403
|
A | C | 69 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(66): Show | 69 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.824-3631A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487403 | ||||||
| chr6:70487403
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-3631A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487403 | ||||||
| chr6:70487404
|
T | C | 1 | a0001c0002t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-3630T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487404 | ||||||
| chr6:70487788
|
T | C | 1 | a0001c0004t0003g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.824-3246T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487788 | ||||||
| chr6:70488155
|
T | A | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2879T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488155 | ||||||
| chr6:70488276
|
T | G | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2758T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488276 | ||||||
| chr6:70488403
|
T | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-2631T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488403 | ||||||
| chr6:70488445
|
G | T | 55 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(52): Show | 55 | HG00597.hp1 HG00609.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.824-2589G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488445 | ||||||
| chr6:70488452
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.824-2582T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488452 | ||||||
| chr6:70488465
|
GC | G | 179 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(176): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.824-2558delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70488465 | |||||
| chr6:70488480
|
A | C | 1 | a0001c0002t0002g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.824-2554A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488480 | ||||||
| chr6:70488502
|
T | A | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2532T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488502 | ||||||
| chr6:70488503
|
A | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2531A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488503 | ||||||
| chr6:70488554
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.824-2480C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488554 | ||||||
| chr6:70488940
|
A | G | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.824-2094A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488940 | ||||||
| chr6:70489062
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-1972G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489062 | ||||||
| chr6:70489129
|
A | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-1905A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489129 | ||||||
| chr6:70489137
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.824-1897G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489137 | ||||||
| chr6:70489260
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.824-1774G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489260 | ||||||
| chr6:70489337
|
A | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-1697A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489337 | ||||||
| chr6:70489396
|
A | AT | 79 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(76): Show | 79 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.824-1635dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70489396 | |||||
| chr6:70489482
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.824-1552G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489482 | ||||||
| chr6:70489486
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.824-1548G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489486 | ||||||
| chr6:70489495
|
C | T | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1539C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489495 | ||||||
| chr6:70489497
|
T | G | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.824-1537T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489497 | ||||||
| chr6:70489499
|
C | T | 1 | a0001c0002t0002g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1535C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489499 | ||||||
| chr6:70489628
|
A | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-1406A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489628 | ||||||
| chr6:70489674
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.824-1360C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489674 | ||||||
| chr6:70489772
|
T | C | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.824-1262T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489772 | ||||||
| chr6:70489778
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-1256C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489778 | ||||||
| chr6:70489984
|
T | A | 1 | a0002c0003t0001g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.824-1050T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489984 | ||||||
| chr6:70490195
|
A | G | 1 | a0006c0010t0003g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.824-839A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490195 | ||||||
| chr6:70490215
|
G | C | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.824-819G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490215 | ||||||
| chr6:70490296
|
G | A | 1 | a0002c0003t0001g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.824-738G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490296 | ||||||
| chr6:70490521
|
C | T | 1 | a0001c0002t0002g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.824-513C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490521 | ||||||
| chr6:70491024
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.824-10C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70491024 | ||||||
| chr6:70491189
|
A | G | 5 | a0002c0003t0001g0045a0002c0003t0001g0046a0002c0003t0001g0120others(2): Show | 5 | HG02083.hp1 HG02523.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+106A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491189 | ||||||
| chr6:70491198
|
T | TA | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+119dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70491198 | |||||
| chr6:70491271
|
A | C | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+188A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491271 | ||||||
| chr6:70491271
|
AC | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+190delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70491271 | |||||
| chr6:70491287
|
A | G | 1 | a0001c0004t0003g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.873+204A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491287 | ||||||
| chr6:70491386
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+303A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491386 | ||||||
| chr6:70491417
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.873+334A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491417 | ||||||
| chr6:70491541
|
A | G | 3 | a0003c0005t0001g0243a0003c0005t0001g0245a0003c0005t0001g0246 | 3 | HG02293.hp1 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.873+458A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491541 | ||||||
| chr6:70491760
|
A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.873+677A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491760 | ||||||
| chr6:70491819
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.873+736A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491819 | ||||||
| chr6:70491930
|
C | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+847C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491930 | ||||||
| chr6:70492133
|
A | C | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.873+1050A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492133 | ||||||
| chr6:70492137
|
T | G | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.873+1054T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492137 | ||||||
| chr6:70492145
|
A | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.873+1062A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492145 | ||||||
| chr6:70492295
|
T | C | 1 | a0002c0006t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.873+1212T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492295 | ||||||
| chr6:70492312
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.873+1229C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492312 | ||||||
| chr6:70492351
|
G | A | 1 | a0001c0013t0001g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.873+1268G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492351 | ||||||
| chr6:70492385
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+1302A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492385 | ||||||
| chr6:70492478
|
C | A | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.873+1395C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492478 | ||||||
| chr6:70492489
|
A | G | 5 | a0001c0002t0002g0168a0001c0002t0002g0171a0001c0002t0002g0172others(2): Show | 5 | HG00673.hp2 NA18939.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+1406A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492489 | ||||||
| chr6:70492547
|
G | A | 21 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0055others(18): Show | 21 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.873+1464G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492547 | ||||||
| chr6:70492561
|
G | A | 1 | a0002c0003t0001g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.873+1478G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492561 | ||||||
| chr6:70492656
|
T | TA | 107 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0069others(104): Show | 107 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.873+1589dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70492656 | |||||
| chr6:70492656
|
TA | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0215a0001c0004t0003g0016others(3): Show | 6 | HG00597.hp2 HG01515.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.873+1589delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70492656 | |||||
| chr6:70492681
|
T | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+1598T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492681 | ||||||
| chr6:70492861
|
A | G | 1 | a0002c0006t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.873+1778A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492861 | ||||||
| chr6:70492939
|
CTT | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+1857_873+1858d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492939 | ||||||
| chr6:70493081
|
A | G | 8 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+1998A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493081 | ||||||
| chr6:70493145
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.873+2062C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493145 | ||||||
| chr6:70493160
|
G | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.873+2077G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493160 | ||||||
| chr6:70493221
|
A | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.873+2138A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493221 | ||||||
| chr6:70493385
|
C | T | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.873+2302C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493385 | ||||||
| chr6:70493390
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.873+2307G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493390 | ||||||
| chr6:70493869
|
A | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.873+2786A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493869 | ||||||
| chr6:70494033
|
G | A | 49 | a0002c0003t0001g0002a0002c0003t0001g0022a0002c0003t0001g0030others(46): Show | 49 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.873+2950G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494033 | ||||||
| chr6:70494053
|
CA | C | 60 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(57): Show | 60 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.873+2991delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70494053 | |||||
| chr6:70494053
|
CAA | C | 79 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(76): Show | 79 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.873+2990_873+2991d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70494053 | |||||
| chr6:70494053
|
CAAA | C | 9 | a0001c0002t0002g0183a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 9 | HG01099.hp1 HG02109.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.873+2989_873+2991d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70494053 | |||||
| chr6:70494125
|
A | G | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.873+3042A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494125 | ||||||
| chr6:70494295
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+3212G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494295 | ||||||
| chr6:70494347
|
T | C | 5 | a0002c0003t0001g0045a0002c0003t0001g0046a0002c0003t0001g0120others(2): Show | 5 | HG02083.hp1 HG02523.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+3264T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494347 | ||||||
| chr6:70494450
|
T | C | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.873+3367T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494450 | ||||||
| chr6:70494803
|
A | T | 1 | a0002c0003t0001g0042 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.873+3720A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494803 | ||||||
| chr6:70494806
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+3723A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494806 | ||||||
| chr6:70494889
|
T | C | 1 | a0002c0003t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.873+3806T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494889 | ||||||
| chr6:70494898
|
A | G | 5 | a0002c0003t0001g0002a0002c0003t0001g0039a0002c0003t0001g0041others(2): Show | 5 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.873+3815A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494898 | ||||||
| chr6:70495149
|
T | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+4066T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495149 | ||||||
| chr6:70495559
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+4476G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495559 | ||||||
| chr6:70495707
|
G | A | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.873+4624G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495707 | ||||||
| chr6:70495747
|
C | T | 1 | a0005c0008t0004g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.873+4664C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495747 | ||||||
| chr6:70495768
|
A | G | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.873+4685A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495768 | ||||||
| chr6:70495996
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00642.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.873+4913C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495996 | ||||||
| chr6:70496105
|
C | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+5022C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496105 | ||||||
| chr6:70496334
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+5251G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496334 | ||||||
| chr6:70496365
|
G | A | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.873+5282G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496365 | ||||||
| chr6:70496458
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0158 | 3 | HG02145.hp2 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.873+5375G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496458 | ||||||
| chr6:70496461
|
C | A | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+5378C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496461 | ||||||
| chr6:70496469
|
T | TGA | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.873+5388_873+5389d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70496469 | |||||
| chr6:70496554
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.873+5471T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496554 | ||||||
| chr6:70496572
|
T | C | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+5489T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496572 | ||||||
| chr6:70496609
|
G | A | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.873+5526G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496609 | ||||||
| chr6:70496631
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873+5548G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496631 | ||||||
| chr6:70496772
|
AT | A | 21 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 21 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.873+5702delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70496772 | |||||
| chr6:70496790
|
A | G | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+5707A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496790 | ||||||
| chr6:70497081
|
A | G | 22 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.874-5555A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497081 | ||||||
| chr6:70497226
|
A | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.874-5410A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497226 | ||||||
| chr6:70497255
|
C | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-5381C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497255 | ||||||
| chr6:70497403
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.874-5233C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497403 | ||||||
| chr6:70497473
|
T | C | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.874-5163T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497473 | ||||||
| chr6:70497504
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-5132A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497504 | ||||||
| chr6:70497589
|
A | G | 1 | a0002c0003t0001g0042 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.874-5047A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497589 | ||||||
| chr6:70497762
|
C | T | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.874-4874C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497762 | ||||||
| chr6:70497839
|
G | A | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-4797G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497839 | ||||||
| chr6:70497874
|
G | A | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.874-4762G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497874 | ||||||
| chr6:70497877
|
A | T | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.874-4759A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497877 | ||||||
| chr6:70498073
|
A | C | 28 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.874-4563A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498073 | ||||||
| chr6:70498095
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.874-4541G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498095 | ||||||
| chr6:70498155
|
T | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.874-4481T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498155 | ||||||
| chr6:70498212
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.874-4424T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498212 | ||||||
| chr6:70498216
|
T | C | 1 | a0001c0002t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.874-4420T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498216 | ||||||
| chr6:70498269
|
T | A | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-4367T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498269 | ||||||
| chr6:70498276
|
T | C | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-4360T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498276 | ||||||
| chr6:70498325
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.874-4311T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498325 | ||||||
| chr6:70498460
|
C | T | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.874-4176C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498460 | ||||||
| chr6:70498467
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.874-4169C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498467 | ||||||
| chr6:70498567
|
TAC | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.874-4067_874-4066d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70498567 | |||||
| chr6:70498650
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.874-3986T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498650 | ||||||
| chr6:70498726
|
G | T | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.874-3910G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498726 | ||||||
| chr6:70498748
|
A | C | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-3888A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498748 | ||||||
| chr6:70498752
|
G | A | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.874-3884G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498752 | ||||||
| chr6:70498825
|
A | G | 17 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0178others(14): Show | 17 | HG00597.hp1 HG01993.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.874-3811A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498825 | ||||||
| chr6:70498940
|
ATG | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-3694_874-3693d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70498940 | |||||
| chr6:70498960
|
G | A | 2 | a0001c0002t0002g0253a0001c0002t0002g0263 | 2 | HG00280.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.874-3676G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498960 | ||||||
| chr6:70499047
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.874-3589A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499047 | ||||||
| chr6:70499132
|
T | G | 1 | a0002c0003t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.874-3504T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499132 | ||||||
| chr6:70499159
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-3477C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499159 | ||||||
| chr6:70499410
|
A | G | 1 | a0001c0002t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.874-3226A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499410 | ||||||
| chr6:70499613
|
T | G | 5 | a0002c0003t0001g0045a0002c0003t0001g0046a0002c0003t0001g0120others(2): Show | 5 | HG02083.hp1 HG02523.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.874-3023T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499613 | ||||||
| chr6:70500151
|
A | G | 1 | a0002c0006t0001g0149 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.874-2485A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500151 | ||||||
| chr6:70500200
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.874-2436A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500200 | ||||||
| chr6:70500249
|
T | C | 1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.874-2387T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500249 | ||||||
| chr6:70500309
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0158 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.874-2327G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500309 | ||||||
| chr6:70500327
|
C | T | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.874-2309C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500327 | ||||||
| chr6:70500428
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.874-2208G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500428 | ||||||
| chr6:70500457
|
A | G | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.874-2179A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500457 | ||||||
| chr6:70500523
|
G | A | 4 | a0002c0003t0001g0051a0002c0003t0001g0107a0002c0003t0001g0114others(1): Show | 4 | HG01243.hp1 HG01358.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-2113G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500523 | ||||||
| chr6:70500582
|
A | C | 1 | a0001c0002t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.874-2054A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500582 | ||||||
| chr6:70500791
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.874-1845C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500791 | ||||||
| chr6:70500811
|
G | A | 2 | a0001c0004t0003g0010a0001c0004t0003g0013 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.874-1825G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500811 | ||||||
| chr6:70500917
|
G | A | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.874-1719G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500917 | ||||||
| chr6:70501063
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.874-1573G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501063 | ||||||
| chr6:70501260
|
GC | G | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.874-1373delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70501260 | |||||
| chr6:70501263
|
C | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.874-1373C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501263 | ||||||
| chr6:70501432
|
C | T | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.874-1204C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501432 | ||||||
| chr6:70501609
|
A | G | 143 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(140): Show | 143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.874-1027A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501609 | ||||||
| chr6:70501691
|
G | A | 46 | a0001c0002t0002g0167a0001c0002t0002g0169a0001c0002t0002g0176others(43): Show | 46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.874-945G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501691 | ||||||
| chr6:70501736
|
C | T | 2 | a0001c0004t0003g0010a0001c0004t0003g0013 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.874-900C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501736 | ||||||
| chr6:70501872
|
T | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.874-764T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501872 | ||||||
| chr6:70501971
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.874-665C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501971 | ||||||
| chr6:70502117
|
A | G | 1 | a0002c0003t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.874-519A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502117 | ||||||
| chr6:70502142
|
T | C | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.874-494T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502142 | ||||||
| chr6:70502275
|
ACT | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-357_874-356del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70502275 | |||||
| chr6:70502430
|
T | TAAAAATT others(309): Show |
2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.874-206_874-205ins others(316): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502430 | ||||||
| chr6:70502431
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.874-205G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502431 | ||||||
| chr6:70502504
|
G | GCA | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-129_874-128dup others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70502504 | |||||
| chr6:70502615
|
T | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-21T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502615 | ||||||
| chr6:70502826
|
A | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1029+35A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70502826 | ||||||
| chr6:70502889
|
A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1029+98A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70502889 | ||||||
| chr6:70503168
|
T | C | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1029+377T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503168 | ||||||
| chr6:70503211
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1029+420C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503211 | ||||||
| chr6:70503350
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0055 | 2 | HG02015.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1029+559T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503350 | ||||||
| chr6:70503375
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1029+584A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503375 | ||||||
| chr6:70503437
|
A | T | 1 | a0006c0010t0003g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1029+646A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503437 | ||||||
| chr6:70503443
|
ATTT | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+656_1029+658d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70503443 | |||||
| chr6:70503485
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1029+694A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503485 | ||||||
| chr6:70503532
|
G | A | 1 | a0002c0003t0001g0002 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1029+741G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503532 | ||||||
| chr6:70503765
|
A | C | 5 | a0002c0003t0001g0035a0002c0003t0001g0134a0002c0003t0001g0137others(2): Show | 5 | HG01168.hp1 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+974A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503765 | ||||||
| chr6:70503771
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+980C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503771 | ||||||
| chr6:70503811
|
T | G | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1029+1020T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503811 | ||||||
| chr6:70503849
|
T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+1058T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503849 | ||||||
| chr6:70504145
|
C | T | 57 | a0002c0003t0001g0002a0002c0003t0001g0022a0002c0003t0001g0030others(54): Show | 57 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1029+1354C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504145 | ||||||
| chr6:70504281
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1029+1490G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504281 | ||||||
| chr6:70504352
|
T | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1029+1561T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504352 | ||||||
| chr6:70504498
|
A | G | 15 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(12): Show | 15 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1029+1707A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504498 | ||||||
| chr6:70504547
|
A | G | 1 | a0002c0006t0001g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1029+1756A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504547 | ||||||
| chr6:70504718
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1029+1927G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504718 | ||||||
| chr6:70504842
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+2051G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504842 | ||||||
| chr6:70504969
|
A | C | 1 | a0002c0003t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1029+2178A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504969 | ||||||
| chr6:70505073
|
CAT | C | 166 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0036others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1029+2299_1029+230 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505073 | |||||
| chr6:70505073
|
CATAT | C | 98 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(95): Show | 98 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1029+2297_1029+230 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505073 | |||||
| chr6:70505077
|
T | C | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1029+2286T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505077 | ||||||
| chr6:70505156
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+2365C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505156 | ||||||
| chr6:70505210
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+2419A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505210 | ||||||
| chr6:70505295
|
G | A | 220 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1029+2504G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505295 | ||||||
| chr6:70505371
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+2580A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505371 | ||||||
| chr6:70505535
|
A | AT | 51 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(48): Show | 51 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1029+2753dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505535 | |||||
| chr6:70505544
|
T | TC | 5 | a0001c0002t0002g0168a0001c0002t0002g0171a0001c0002t0002g0172others(2): Show | 5 | HG00673.hp2 NA18939.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+2754dupC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505544 | |||||
| chr6:70505805
|
T | C | 221 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(218): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1029+3014T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505805 | ||||||
| chr6:70505882
|
T | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02615.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029+3091T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505882 | ||||||
| chr6:70506064
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1029+3273G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506064 | ||||||
| chr6:70506121
|
G | T | 8 | a0002c0003t0001g0002a0002c0003t0001g0039a0002c0003t0001g0040others(5): Show | 8 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+3330G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506121 | ||||||
| chr6:70506201
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1029+3410C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506201 | ||||||
| chr6:70506230
|
G | C | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1029+3439G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506230 | ||||||
| chr6:70506479
|
A | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+3688A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506479 | ||||||
| chr6:70506834
|
G | T | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1029+4043G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506834 | ||||||
| chr6:70506855
|
T | C | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1029+4064T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506855 | ||||||
| chr6:70506929
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1029+4138A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506929 | ||||||
| chr6:70506966
|
A | C | 1 | a0002c0003t0001g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1029+4175A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506966 | ||||||
| chr6:70507095
|
G | A | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1029+4304G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507095 | ||||||
| chr6:70507108
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0105 | 3 | HG01074.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1029+4317C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507108 | ||||||
| chr6:70507120
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1029+4329G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507120 | ||||||
| chr6:70507209
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+4418C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507209 | ||||||
| chr6:70507445
|
T | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+4654T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507445 | ||||||
| chr6:70507467
|
A | G | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1029+4676A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507467 | ||||||
| chr6:70507511
|
G | A | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1029+4720G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507511 | ||||||
| chr6:70507571
|
T | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+4780T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507571 | ||||||
| chr6:70507572
|
T | G | 1 | a0001c0004t0003g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1029+4781T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507572 | ||||||
| chr6:70507921
|
C | G | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1029+5130C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507921 | ||||||
| chr6:70507969
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1029+5178A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507969 | ||||||
| chr6:70508055
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1029+5264T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508055 | ||||||
| chr6:70508085
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+5294G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508085 | ||||||
| chr6:70508296
|
G | C | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1029+5505G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508296 | ||||||
| chr6:70508351
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0095others(3): Show | 6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1029+5560A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508351 | ||||||
| chr6:70508846
|
C | G | 1 | a0001c0002t0002g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1029+6055C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508846 | ||||||
| chr6:70508878
|
T | C | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1029+6087T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508878 | ||||||
| chr6:70508880
|
G | A | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+6089G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508880 | ||||||
| chr6:70508938
|
C | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+6147C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508938 | ||||||
| chr6:70508996
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+6205G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508996 | ||||||
| chr6:70509168
|
T | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1029+6377T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509168 | ||||||
| chr6:70509354
|
A | T | 135 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1029+6563A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509354 | ||||||
| chr6:70509374
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1029+6583G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509374 | ||||||
| chr6:70509382
|
A | T | 1 | a0002c0003t0001g0128 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1029+6591A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509382 | ||||||
| chr6:70509544
|
T | C | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+6753T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509544 | ||||||
| chr6:70509602
|
C | T | 1 | a0002c0003t0001g0035 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1029+6811C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509602 | ||||||
| chr6:70509662
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1029+6871A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509662 | ||||||
| chr6:70509761
|
C | T | 30 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(27): Show | 30 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.1029+6970C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509761 | ||||||
| chr6:70509817
|
A | G | 1 | a0001c0002t0002g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1029+7026A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509817 | ||||||
| chr6:70509852
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+7061C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509852 | ||||||
| chr6:70509867
|
G | A | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1029+7076G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509867 | ||||||
| chr6:70510067
|
C | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+7276C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510067 | ||||||
| chr6:70510107
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1029+7316T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510107 | ||||||
| chr6:70510169
|
G | A | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+7378G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510169 | ||||||
| chr6:70510177
|
G | A | 1 | a0001c0004t0003g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1029+7386G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510177 | ||||||
| chr6:70510304
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1029+7513T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510304 | ||||||
| chr6:70510333
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+7542A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510333 | ||||||
| chr6:70510367
|
T | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+7576T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510367 | ||||||
| chr6:70510480
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+7689G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510480 | ||||||
| chr6:70510691
|
A | G | 3 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0166 | 3 | NA18990.hp2 NA19055.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1029+7900A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510691 | ||||||
| chr6:70510757
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+7966G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510757 | ||||||
| chr6:70510853
|
C | T | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+8062C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510853 | ||||||
| chr6:70510873
|
A | C | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+8082A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510873 | ||||||
| chr6:70510967
|
G | A | 15 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(12): Show | 15 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1029+8176G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510967 | ||||||
| chr6:70511164
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+8373A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511164 | ||||||
| chr6:70511223
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+8432A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511223 | ||||||
| chr6:70511454
|
A | G | 1 | a0001c0002t0002g0187 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1029+8663A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511454 | ||||||
| chr6:70511576
|
TA | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+8791delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70511576 | |||||
| chr6:70511577
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1029+8786A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511577 | ||||||
| chr6:70511744
|
A | G | 6 | a0002c0003t0001g0128a0002c0006t0001g0034a0002c0006t0001g0129others(3): Show | 6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1029+8953A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511744 | ||||||
| chr6:70511971
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1029+9180C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511971 | ||||||
| chr6:70512146
|
G | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1029+9355G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512146 | ||||||
| chr6:70512244
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+9453G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512244 | ||||||
| chr6:70512452
|
T | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1029+9661T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512452 | ||||||
| chr6:70512454
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+9663G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512454 | ||||||
| chr6:70512484
|
G | A | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1029+9693G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512484 | ||||||
| chr6:70512871
|
T | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-9642T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512871 | ||||||
| chr6:70512985
|
C | CT | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1030-9518dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70512985 | |||||
| chr6:70512985
|
CT | C | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-9518delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70512985 | |||||
| chr6:70513218
|
C | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1030-9295C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513218 | ||||||
| chr6:70513259
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1030-9254C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513259 | ||||||
| chr6:70513316
|
AT | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1030-9194delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513316 | |||||
| chr6:70513322
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-9191C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513322 | ||||||
| chr6:70513388
|
CT | C | 45 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0147others(42): Show | 45 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.1030-9107delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513388 | |||||
| chr6:70513388
|
CTT | C | 22 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1030-9108_1030-910 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513388 | |||||
| chr6:70513581
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1030-8932C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513581 | ||||||
| chr6:70513632
|
T | C | 2 | a0001c0002t0002g0171a0001c0002t0002g0172 | 2 | HG00673.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1030-8881T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513632 | ||||||
| chr6:70513707
|
C | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1030-8806C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513707 | ||||||
| chr6:70513778
|
G | A | 2 | a0002c0003t0001g0108a0002c0003t0001g0115 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1030-8735G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513778 | ||||||
| chr6:70513852
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1030-8661T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513852 | ||||||
| chr6:70513853
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1030-8660G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513853 | ||||||
| chr6:70513990
|
GT | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-8514delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513990 | |||||
| chr6:70514145
|
G | A | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1030-8368G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514145 | ||||||
| chr6:70514343
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-8170C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514343 | ||||||
| chr6:70514354
|
T | C | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1030-8159T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514354 | ||||||
| chr6:70514387
|
C | T | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-8126C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514387 | ||||||
| chr6:70514494
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1030-8019T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514494 | ||||||
| chr6:70514501
|
C | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-8012C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514501 | ||||||
| chr6:70514521
|
T | G | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1030-7992T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514521 | ||||||
| chr6:70514528
|
G | A | 1 | a0002c0003t0001g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1030-7985G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514528 | ||||||
| chr6:70514593
|
C | T | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1030-7920C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514593 | ||||||
| chr6:70514602
|
T | C | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1030-7911T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514602 | ||||||
| chr6:70514644
|
G | T | 1 | a0002c0006t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1030-7869G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514644 | ||||||
| chr6:70514711
|
G | GA | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1030-7801dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70514711 | |||||
| chr6:70514821
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-7692A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514821 | ||||||
| chr6:70514926
|
T | C | 15 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0178others(12): Show | 15 | HG01993.hp1 HG02004.hp1 HG03491.hp2 others(12): Show |
intron_variant | MODIFIER | c.1030-7587T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514926 | ||||||
| chr6:70514966
|
C | G | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1030-7547C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514966 | ||||||
| chr6:70514991
|
C | G | 1 | a0002c0003t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1030-7522C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514991 | ||||||
| chr6:70515070
|
C | G | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1030-7443C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515070 | ||||||
| chr6:70515070
|
C | T | 112 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(109): Show | 112 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1030-7443C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515070 | ||||||
| chr6:70515323
|
T | C | 1 | a0001c0002t0002g0256 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1030-7190T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515323 | ||||||
| chr6:70515462
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1030-7051A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515462 | ||||||
| chr6:70515582
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-6931C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515582 | ||||||
| chr6:70515880
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1030-6633G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515880 | ||||||
| chr6:70515998
|
T | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1030-6515T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515998 | ||||||
| chr6:70516021
|
G | C | 143 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(140): Show | 143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1030-6492G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516021 | ||||||
| chr6:70516259
|
G | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1030-6254G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516259 | ||||||
| chr6:70516361
|
T | G | 3 | a0001c0004t0003g0250a0001c0004t0003g0251a0001c0004t0003g0252 | 3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1030-6152T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516361 | ||||||
| chr6:70516453
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-6060G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516453 | ||||||
| chr6:70516502
|
T | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1030-6011T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516502 | ||||||
| chr6:70516527
|
TTTC | T | 7 | a0001c0009t0001g0212a0003c0005t0001g0242a0003c0005t0001g0243others(4): Show | 7 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1030-5983_1030-598 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516527 | |||||
| chr6:70516530
|
C | CT | 11 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 11 | HG01934.hp1 HG02027.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1030-5960dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | |||||
| chr6:70516530
|
CT | C | 48 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(45): Show | 48 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1030-5960delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | |||||
| chr6:70516530
|
CTT | C | 14 | a0001c0001t0001g0151a0001c0004t0003g0001a0001c0004t0003g0230others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1030-5961_1030-596 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | |||||
| chr6:70516530
|
CTTT | C | 5 | a0001c0002t0002g0175a0001c0002t0002g0178a0001c0002t0002g0207others(2): Show | 5 | HG03516.hp2 HG03540.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.1030-5962_1030-596 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | |||||
| chr6:70516530
|
CTTTT | C | 50 | a0001c0001t0001g0267a0001c0002t0002g0167a0001c0002t0002g0168others(47): Show | 50 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1030-5963_1030-596 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | |||||
| chr6:70516534
|
T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-5979T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516534 | ||||||
| chr6:70516575
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1030-5938A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516575 | ||||||
| chr6:70516622
|
G | A | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-5891G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516622 | ||||||
| chr6:70516628
|
T | C | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1030-5885T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516628 | ||||||
| chr6:70516634
|
C | CA | 40 | a0001c0002t0002g0167a0001c0002t0002g0176a0001c0002t0002g0177others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1030-5878dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516634 | |||||
| chr6:70516647
|
A | G | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1030-5866A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516647 | ||||||
| chr6:70516680
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-5833A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516680 | ||||||
| chr6:70516798
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0104 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1030-5715G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516798 | ||||||
| chr6:70516848
|
T | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-5665T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516848 | ||||||
| chr6:70516885
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-5628G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516885 | ||||||
| chr6:70516932
|
A | G | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1030-5581A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516932 | ||||||
| chr6:70517009
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1030-5504A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517009 | ||||||
| chr6:70517132
|
G | A | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1030-5381G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517132 | ||||||
| chr6:70517147
|
A | G | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-5366A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517147 | ||||||
| chr6:70517281
|
A | T | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1030-5232A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517281 | ||||||
| chr6:70517346
|
G | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1030-5167G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517346 | ||||||
| chr6:70517347
|
A | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1030-5166A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517347 | ||||||
| chr6:70517357
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-5156C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517357 | ||||||
| chr6:70517415
|
C | CT | 27 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0082others(24): Show | 27 | HG00621.hp2 HG01069.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1030-5077dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70517415 | |||||
| chr6:70517415
|
C | CTT | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1030-5078_1030-507 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70517415 | |||||
| chr6:70517415
|
CT | C | 53 | a0001c0001t0001g0075a0001c0001t0001g0153a0001c0002t0002g0167others(50): Show | 53 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1030-5077delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70517415 | |||||
| chr6:70517448
|
T | C | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-5065T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517448 | ||||||
| chr6:70517449
|
G | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-5064G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517449 | ||||||
| chr6:70517680
|
T | A | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-4833T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517680 | ||||||
| chr6:70517785
|
A | G | 1 | a0003c0005t0001g0243 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1030-4728A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517785 | ||||||
| chr6:70517826
|
A | T | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030-4687A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517826 | ||||||
| chr6:70517837
|
A | C | 2 | a0001c0002t0002g0255a0001c0002t0002g0257 | 2 | HG00639.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1030-4676A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517837 | ||||||
| chr6:70517944
|
G | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-4569G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517944 | ||||||
| chr6:70517946
|
C | T | 2 | a0002c0003t0001g0039a0002c0003t0001g0042 | 2 | HG01123.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1030-4567C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517946 | ||||||
| chr6:70517996
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1030-4517A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517996 | ||||||
| chr6:70518055
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1030-4458G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518055 | ||||||
| chr6:70518093
|
A | G | 1 | a0002c0003t0001g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1030-4420A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518093 | ||||||
| chr6:70518164
|
A | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1030-4349A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518164 | ||||||
| chr6:70518281
|
CTT | C | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-4229_1030-422 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70518281 | |||||
| chr6:70518461
|
T | G | 3 | a0002c0003t0001g0051a0002c0003t0001g0114a0002c0003t0001g0135 | 3 | HG01243.hp1 HG01358.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1030-4052T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518461 | ||||||
| chr6:70518857
|
C | A | 3 | a0001c0004t0003g0250a0001c0004t0003g0251a0001c0004t0003g0252 | 3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1030-3656C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518857 | ||||||
| chr6:70518912
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1030-3601C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518912 | ||||||
| chr6:70519022
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1030-3491G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519022 | ||||||
| chr6:70519051
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1030-3462A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519051 | ||||||
| chr6:70519064
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0013t0001g0085 | 3 | HG01175.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1030-3449T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519064 | ||||||
| chr6:70519167
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-3346A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519167 | ||||||
| chr6:70519176
|
G | C | 70 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1030-3337G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519176 | ||||||
| chr6:70519271
|
CATT | C | 3 | a0001c0004t0003g0235a0001c0004t0003g0238a0001c0004t0003g0239 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1030-3239_1030-323 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70519271 | |||||
| chr6:70519307
|
A | G | 1 | a0006c0010t0003g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1030-3206A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519307 | ||||||
| chr6:70519446
|
T | C | 1 | a0002c0003t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1030-3067T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519446 | ||||||
| chr6:70519449
|
A | G | 14 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-3064A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519449 | ||||||
| chr6:70519521
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1030-2992G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519521 | ||||||
| chr6:70519568
|
T | G | 69 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(66): Show | 69 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1030-2945T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519568 | ||||||
| chr6:70519580
|
T | C | 223 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(220): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1030-2933T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519580 | ||||||
| chr6:70519637
|
G | C | 152 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(149): Show | 152 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.1030-2876G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519637 | ||||||
| chr6:70519647
|
G | T | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1030-2866G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519647 | ||||||
| chr6:70519738
|
TAAG | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-2773_1030-277 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70519738 | |||||
| chr6:70519885
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-2628C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519885 | ||||||
| chr6:70519909
|
G | GATAT | 101 | a0001c0001t0001g0164a0001c0001t0001g0210a0001c0001t0001g0267others(98): Show | 101 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1030-2599_1030-259 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70519909 | |||||
| chr6:70519918
|
G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-2595G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519918 | ||||||
| chr6:70519921
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-2592A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519921 | ||||||
| chr6:70519956
|
G | A | 118 | a0001c0001t0001g0164a0001c0001t0001g0210a0001c0001t0001g0267others(115): Show | 118 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1030-2557G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519956 | ||||||
| chr6:70520105
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0056 | 2 | HG03831.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1030-2408A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520105 | ||||||
| chr6:70520113
|
C | G | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1030-2400C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520113 | ||||||
| chr6:70520169
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1030-2344C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520169 | ||||||
| chr6:70520228
|
A | G | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1030-2285A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520228 | ||||||
| chr6:70520292
|
GAGTT | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-2217_1030-221 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70520292 | |||||
| chr6:70520315
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-2198A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520315 | ||||||
| chr6:70520579
|
G | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0105 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1030-1934G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520579 | ||||||
| chr6:70520654
|
AATAC | A | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-1851_1030-184 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70520654 | |||||
| chr6:70520773
|
T | A | 1 | a0001c0004t0003g0236 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1030-1740T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520773 | ||||||
| chr6:70520998
|
G | C | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1030-1515G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520998 | ||||||
| chr6:70521060
|
A | G | 1 | a0004c0007t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1030-1453A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521060 | ||||||
| chr6:70521143
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-1370G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521143 | ||||||
| chr6:70521224
|
A | G | 1 | a0002c0003t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1030-1289A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521224 | ||||||
| chr6:70521293
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-1220C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521293 | ||||||
| chr6:70521319
|
G | A | 16 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(13): Show | 16 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1030-1194G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521319 | ||||||
| chr6:70521319
|
G | GT | 13 | a0001c0002t0002g0209a0001c0002t0002g0253a0001c0002t0002g0254others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-1187dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70521319 | |||||
| chr6:70521334
|
T | C | 1 | a0001c0002t0002g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1030-1179T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521334 | ||||||
| chr6:70521415
|
A | C | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-1098A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521415 | ||||||
| chr6:70521978
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG00280.hp2 HG00639.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1030-535G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521978 | ||||||
| chr6:70522019
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-494C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522019 | ||||||
| chr6:70522062
|
A | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-451A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522062 | ||||||
| chr6:70522182
|
T | G | 80 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-331T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522182 | ||||||
| chr6:70522209
|
G | A | 1 | a0002c0003t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1030-304G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522209 | ||||||
| chr6:70522217
|
C | T | 56 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-296C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522217 | ||||||
| chr6:70522311
|
GTTTATA | G | 69 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(66): Show | 69 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1030-194_1030-189d others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70522311 | |||||
| chr6:70522369
|
A | G | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1030-144A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522369 | ||||||
| chr6:70522494
|
C | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-19C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522494 | ||||||
| chr6:70522705
|
T | A | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1103+119T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70522705 | ||||||
| chr6:70523142
|
A | AG | 113 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(110): Show | 113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1103+556_1103+557i others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523142 | ||||||
| chr6:70523358
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086 | 3 | NA18961.hp2 NA18962.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1104-609G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523358 | ||||||
| chr6:70523399
|
A | G | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1104-568A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523399 | ||||||
| chr6:70523439
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104-528T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523439 | ||||||
| chr6:70523468
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1104-499G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523468 | ||||||
| chr6:70523609
|
A | T | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1104-358A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523609 | ||||||
| chr6:70523641
|
T | C | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1104-326T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523641 | ||||||
| chr6:70523645
|
T | C | 11 | a0001c0004t0007g0265a0001c0009t0001g0211a0001c0009t0001g0212others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1104-322T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523645 | ||||||
| chr6:70523788
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1104-179A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523788 | ||||||
| chr6:70523848
|
G | T | 69 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(66): Show | 69 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1104-119G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523848 | ||||||
| chr6:70523860
|
A | G | 1 | a0001c0002t0002g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1104-107A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523860 | ||||||
| chr6:70523942
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1104-25A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523942 | ||||||
| chr6:70524133
|
C | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1258+12C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 14/21 | chr6 | 70524133 | ||||||
| chr6:70526748
|
TATACACA others(5): Show |
T | 1 | a0001c0002t0002g0224 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3614+52_3614+63del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526748 | |||||
| chr6:70526748
|
TATACACA others(13): Show |
T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.3614+52_3614+71del others(20): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526748 | |||||
| chr6:70526750
|
T | TACACACA others(13): Show |
1 | a0001c0004t0003g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3614+67_3614+68ins others(20): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526750 | |||||
| chr6:70526750
|
TACACACA others(7): Show |
T | 3 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206 | 3 | NA18522.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3614+54_3614+67del others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526750 | |||||
| chr6:70526752
|
C | CACACACA others(9): Show |
1 | a0001c0004t0003g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3614+67_3614+68ins others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526752 | |||||
| chr6:70526752
|
C | T | 43 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(40): Show | 43 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.3614+54C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526752 | ||||||
| chr6:70526754
|
C | CACACACA others(7): Show |
1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3614+67_3614+68ins others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526754 | |||||
| chr6:70526754
|
CACACACA others(5): Show |
C | 46 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(43): Show | 46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.3614+68_3614+79del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526754 | |||||
| chr6:70526756
|
CACACACA others(3): Show |
C | 3 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0199 | 3 | HG00741.hp2 HG01167.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3614+68_3614+77del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526756 | |||||
| chr6:70526762
|
CACAT | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0142others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+68_3614+71del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526762 | |||||
| chr6:70526766
|
T | C | 4 | a0001c0002t0002g0224a0001c0004t0003g0250a0001c0004t0003g0251others(1): Show | 4 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+68T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526766 | ||||||
| chr6:70526766
|
T | TAC | 12 | a0001c0001t0001g0098a0001c0001t0001g0105a0002c0003t0001g0030others(9): Show | 12 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.3614+104_3614+105d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526766
|
T | TACAC | 4 | a0001c0001t0001g0104a0001c0004t0004g0015a0005c0008t0004g0003others(1): Show | 4 | HG01074.hp2 HG01346.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+102_3614+105d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526766
|
T | TACACACA others(3): Show |
1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3614+96_3614+105du others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526766
|
T | TACACACA others(7): Show |
1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3614+92_3614+105du others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526766
|
TAC | T | 33 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(30): Show | 33 | HG01069.hp1 HG01168.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.3614+104_3614+105d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526766
|
TACAC | T | 3 | a0001c0001t0001g0147a0001c0009t0001g0211a0001c0009t0001g0212 | 3 | HG02258.hp2 HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3614+102_3614+105d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526766
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0053a0001c0004t0003g0009 | 2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3614+96_3614+105de others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | |||||
| chr6:70526768
|
C | T | 4 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0142others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+70C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526768 | ||||||
| chr6:70526770
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3614+72C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526770 | ||||||
| chr6:70526792
|
CACACACA others(7): Show |
C | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+96_3614+109de others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526792 | |||||
| chr6:70526794
|
C | T | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3614+96C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526794 | ||||||
| chr6:70526796
|
C | T | 71 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(68): Show | 71 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.3614+98C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526796 | ||||||
| chr6:70526798
|
C | T | 78 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(75): Show | 78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3614+100C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526798 | ||||||
| chr6:70526800
|
C | T | 78 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(75): Show | 78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3614+102C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526800 | ||||||
| chr6:70526802
|
C | T | 92 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(89): Show | 92 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.3614+104C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526802 | ||||||
| chr6:70526804
|
T | C | 4 | a0001c0004t0004g0015a0001c0004t0006g0019a0005c0008t0004g0003others(1): Show | 4 | HG01074.hp2 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+106T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526804 | ||||||
| chr6:70527040
|
C | T | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.3614+342C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527040 | ||||||
| chr6:70527073
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3614+375A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527073 | ||||||
| chr6:70527133
|
G | A | 1 | a0002c0003t0001g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3614+435G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527133 | ||||||
| chr6:70527372
|
T | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3614+674T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527372 | ||||||
| chr6:70527431
|
A | G | 67 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3614+733A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527431 | ||||||
| chr6:70527518
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3615-774G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527518 | ||||||
| chr6:70527835
|
G | A | 1 | a0002c0006t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3615-457G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527835 | ||||||
| chr6:70527857
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3615-435A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527857 | ||||||
| chr6:70527862
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3615-430G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527862 | ||||||
| chr6:70528024
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3615-268T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528024 | ||||||
| chr6:70528039
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3615-253G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528039 | ||||||
| chr6:70528114
|
A | G | 3 | a0002c0003t0001g0137a0002c0003t0001g0138a0002c0003t0001g0139 | 3 | HG01358.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3615-178A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528114 | ||||||
| chr6:70528136
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3615-156C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528136 | ||||||
| chr6:70528548
|
G | T | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3775+96G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528548 | ||||||
| chr6:70528666
|
C | T | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3775+214C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528666 | ||||||
| chr6:70528674
|
C | T | 135 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.3775+222C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528674 | ||||||
| chr6:70528702
|
A | AT | 219 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(216): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.3775+260dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70528702 | |||||
| chr6:70528813
|
T | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3775+361T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528813 | ||||||
| chr6:70528850
|
T | C | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3775+398T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528850 | ||||||
| chr6:70528851
|
G | A | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.3775+399G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528851 | ||||||
| chr6:70529002
|
G | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0155a0007c0019t0001g0083 | 3 | HG02083.hp2 HG02523.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3775+550G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529002 | ||||||
| chr6:70529438
|
T | TA | 6 | a0001c0001t0001g0058a0001c0001t0001g0210a0001c0002t0002g0171others(3): Show | 6 | HG02300.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3775+1002dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70529438 | |||||
| chr6:70529669
|
C | T | 1 | a0002c0003t0001g0216 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3775+1217C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529669 | ||||||
| chr6:70529789
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3775+1337G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529789 | ||||||
| chr6:70529866
|
T | G | 1 | a0001c0002t0002g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3775+1414T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529866 | ||||||
| chr6:70529889
|
C | T | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3775+1437C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529889 | ||||||
| chr6:70530030
|
C | G | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3775+1578C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530030 | ||||||
| chr6:70530063
|
CA | C | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.3775+1622delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70530063 | |||||
| chr6:70530070
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3775+1618A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530070 | ||||||
| chr6:70530072
|
A | T | 4 | a0001c0004t0003g0250a0001c0004t0003g0251a0001c0004t0003g0252others(1): Show | 4 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3775+1620A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530072 | ||||||
| chr6:70530195
|
G | C | 1 | a0002c0003t0001g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3775+1743G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530195 | ||||||
| chr6:70530244
|
C | T | 1 | a0006c0010t0003g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3775+1792C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530244 | ||||||
| chr6:70530331
|
A | G | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3775+1879A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530331 | ||||||
| chr6:70530363
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3775+1911T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530363 | ||||||
| chr6:70530389
|
A | T | 1 | a0001c0002t0002g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3775+1937A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530389 | ||||||
| chr6:70530390
|
A | C | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3775+1938A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530390 | ||||||
| chr6:70530397
|
A | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3775+1945A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530397 | ||||||
| chr6:70530493
|
G | A | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.3775+2041G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530493 | ||||||
| chr6:70530606
|
G | T | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3775+2154G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530606 | ||||||
| chr6:70531145
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3776-2015G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531145 | ||||||
| chr6:70531186
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3776-1974A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531186 | ||||||
| chr6:70531497
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3776-1663A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531497 | ||||||
| chr6:70531502
|
G | A | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.3776-1658G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531502 | ||||||
| chr6:70531531
|
A | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3776-1629A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531531 | ||||||
| chr6:70531731
|
C | T | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3776-1429C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531731 | ||||||
| chr6:70531800
|
C | T | 15 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(12): Show | 15 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3776-1360C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531800 | ||||||
| chr6:70531888
|
C | CT | 15 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(12): Show | 15 | HG00621.hp2 HG00735.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.3776-1247dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70531888
|
CT | C | 18 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01099.hp2 HG01168.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.3776-1247delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70531888
|
CTT | C | 14 | a0001c0001t0001g0210a0001c0004t0001g0160a0001c0004t0001g0161others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.3776-1248_3776-124 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70531888
|
CTTT | C | 9 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(6): Show | 9 | HG00741.hp2 HG01167.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3776-1249_3776-124 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70531888
|
CTTTT | C | 48 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(45): Show | 48 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.3776-1250_3776-124 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70531888
|
CTTTTT | C | 14 | a0001c0002t0002g0221a0001c0002t0002g0253a0001c0002t0002g0255others(11): Show | 14 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.3776-1251_3776-124 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70531888
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.3776-1254_3776-124 others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | |||||
| chr6:70532233
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3776-927A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532233 | ||||||
| chr6:70532242
|
T | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3776-918T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532242 | ||||||
| chr6:70532246
|
A | G | 1 | a0001c0002t0002g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3776-914A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532246 | ||||||
| chr6:70532298
|
A | G | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3776-862A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532298 | ||||||
| chr6:70532378
|
A | G | 7 | a0001c0001t0001g0027a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3776-782A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532378 | ||||||
| chr6:70532708
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3776-452G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532708 | ||||||
| chr6:70532748
|
C | T | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.3776-412C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532748 | ||||||
| chr6:70532844
|
A | G | 3 | a0001c0004t0003g0250a0001c0004t0003g0251a0001c0004t0003g0252 | 3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3776-316A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532844 | ||||||
| chr6:70533382
|
GTA | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.3867+135_3867+136d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 70533382 | |||||
| chr6:70533384
|
A | G | 1 | a0002c0003t0001g0035 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3867+133A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533384 | ||||||
| chr6:70533403
|
A | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3867+152A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533403 | ||||||
| chr6:70533408
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3867+157T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533408 | ||||||
| chr6:70533432
|
C | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3867+181C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533432 | ||||||
| chr6:70533566
|
C | T | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3868-191C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533566 | ||||||
| chr6:70533649
|
A | G | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3868-108A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533649 | ||||||
| chr6:70533681
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3868-76A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533681 | ||||||
| chr6:70534062
|
G | A | 1 | a0002c0003t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3965+208G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534062 | ||||||
| chr6:70534227
|
G | A | 2 | a0002c0003t0001g0108a0002c0003t0001g0115 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3965+373G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534227 | ||||||
| chr6:70534241
|
CATATATG others(6): Show |
C | 144 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(141): Show | 144 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.3965+415_3965+427d others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534241 | |||||
| chr6:70534312
|
C | CT | 30 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0060others(27): Show | 30 | HG00621.hp2 HG00735.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3965+483dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTT | 7 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(4): Show | 7 | HG00280.hp1 HG00639.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3965+479_3965+483d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTT | 5 | a0001c0002t0002g0258a0001c0002t0002g0262a0001c0002t0002g0263others(2): Show | 5 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3965+478_3965+483d others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3965+474_3965+483d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(4): Show |
10 | a0001c0002t0002g0168a0001c0002t0002g0190a0001c0002t0002g0191others(7): Show | 10 | HG01975.hp1 HG01993.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.3965+473_3965+483d others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(5): Show |
20 | a0001c0002t0002g0169a0001c0002t0002g0171a0001c0002t0002g0172others(17): Show | 20 | HG00597.hp1 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.3965+472_3965+483d others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(6): Show |
23 | a0001c0002t0002g0167a0001c0002t0002g0173a0001c0002t0002g0174others(20): Show | 23 | HG00621.hp1 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.3965+471_3965+483d others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(7): Show |
3 | a0001c0002t0002g0186a0001c0002t0002g0208a0003c0005t0001g0249 | 3 | HG01255.hp2 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3965+470_3965+483d others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3965+469_3965+483d others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(25): Show |
1 | a0003c0005t0001g0245 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3965+483_3965+484i others(34): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(26): Show |
2 | a0003c0005t0001g0243a0003c0005t0001g0246 | 2 | HG02293.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3965+483_3965+484i others(35): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
C | CTTTTTTT others(30): Show |
1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3965+483_3965+484i others(39): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534312
|
CT | C | 11 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(8): Show | 11 | HG00639.hp2 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.3965+483delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | |||||
| chr6:70534426
|
C | T | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.3965+572C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534426 | ||||||
| chr6:70534444
|
C | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3965+590C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534444 | ||||||
| chr6:70534582
|
G | C | 67 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3965+728G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534582 | ||||||
| chr6:70534626
|
C | A | 1 | a0002c0006t0001g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3965+772C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534626 | ||||||
| chr6:70535220
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3966-1040C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535220 | ||||||
| chr6:70535317
|
A | G | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3966-943A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535317 | ||||||
| chr6:70535423
|
G | A | 23 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3966-837G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535423 | ||||||
| chr6:70535571
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3966-689G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535571 | ||||||
| chr6:70535614
|
G | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3966-646G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535614 | ||||||
| chr6:70535684
|
A | G | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3966-576A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535684 | ||||||
| chr6:70535729
|
A | G | 1 | a0002c0003t0001g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3966-531A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535729 | ||||||
| chr6:70535762
|
A | T | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3966-498A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535762 | ||||||
| chr6:70535805
|
A | G | 23 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3966-455A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535805 | ||||||
| chr6:70535833
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3966-427A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535833 | ||||||
| chr6:70535864
|
G | A | 7 | a0002c0003t0001g0035a0002c0003t0001g0134a0002c0003t0001g0136others(4): Show | 7 | HG00140.hp2 HG01168.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.3966-396G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535864 | ||||||
| chr6:70535981
|
C | T | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3966-279C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535981 | ||||||
| chr6:70535982
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3966-278G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535982 | ||||||
| chr6:70536033
|
ATGT | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3966-222_3966-220d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70536033 | |||||
| chr6:70536072
|
G | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3966-188G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70536072 | ||||||
| chr6:70536090
|
ACATTTTT others(6): Show |
A | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3966-169_3966-157d others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70536090 | ||||||
| chr6:70536503
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.4117+92G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536503 | ||||||
| chr6:70536797
|
G | T | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4117+386G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536797 | ||||||
| chr6:70536802
|
A | G | 1 | a0001c0002t0002g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4117+391A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536802 | ||||||
| chr6:70536837
|
G | A | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4117+426G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536837 | ||||||
| chr6:70536932
|
T | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4117+521T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536932 | ||||||
| chr6:70536934
|
A | AT | 60 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0267others(57): Show | 60 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.4117+543dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70536934 | |||||
| chr6:70536934
|
A | ATT | 7 | a0001c0002t0002g0169a0001c0002t0002g0174a0001c0002t0002g0175others(4): Show | 7 | HG00741.hp2 HG01433.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.4117+542_4117+543d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70536934 | |||||
| chr6:70536934
|
AT | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0099a0001c0002t0002g0255others(2): Show | 5 | HG02004.hp2 NA19055.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4117+543delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70536934 | |||||
| chr6:70537060
|
G | A | 11 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(8): Show | 11 | HG00609.hp1 HG00621.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.4117+649G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537060 | ||||||
| chr6:70537238
|
T | C | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4117+827T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537238 | ||||||
| chr6:70537273
|
G | T | 1 | a0002c0003t0001g0035 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4117+862G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537273 | ||||||
| chr6:70537346
|
T | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4117+935T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537346 | ||||||
| chr6:70537488
|
G | C | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4118-803G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537488 | ||||||
| chr6:70537602
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4118-689A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537602 | ||||||
| chr6:70537628
|
T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4118-663T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537628 | ||||||
| chr6:70537637
|
A | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4118-654A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537637 | ||||||
| chr6:70537671
|
G | C | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4118-620G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537671 | ||||||
| chr6:70537682
|
A | G | 78 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(75): Show | 78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4118-609A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537682 | ||||||
| chr6:70537684
|
A | G | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4118-607A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537684 | ||||||
| chr6:70537737
|
C | T | 23 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4118-554C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537737 | ||||||
| chr6:70537869
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4118-422A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537869 | ||||||
| chr6:70537960
|
ATCT | A | 23 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4118-323_4118-321d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70537960 | |||||
| chr6:70538036
|
G | C | 1 | a0008c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4118-255G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538036 | ||||||
| chr6:70538084
|
A | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4118-207A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538084 | ||||||
| chr6:70538126
|
A | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4118-165A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538126 | ||||||
| chr6:70538129
|
G | A | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4118-162G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538129 | ||||||
| chr6:70538160
|
T | C | 23 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4118-131T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538160 | ||||||
| chr6:70538448
|
TA | T | 55 | a0001c0001t0001g0071a0001c0002t0002g0167a0001c0002t0002g0168others(52): Show | 55 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.4228+53delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538448 | |||||
| chr6:70538603
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+202G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538603 | ||||||
| chr6:70538660
|
T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+259T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538660 | ||||||
| chr6:70538667
|
C | T | 55 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(52): Show | 55 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.4228+266C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538667 | ||||||
| chr6:70538690
|
A | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+289A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538690 | ||||||
| chr6:70538762
|
T | G | 1 | a0007c0019t0001g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4228+361T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538762 | ||||||
| chr6:70538787
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4228+386A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538787 | ||||||
| chr6:70538795
|
ATTATG | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0002t0002g0255others(8): Show | 11 | HG00642.hp2 HG01109.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.4228+404_4228+408d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538795 | |||||
| chr6:70538800
|
G | GTTATA | 2 | a0001c0002t0002g0254a0001c0002t0002g0263 | 2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4228+403_4228+404i others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538800
|
G | GTTATATT others(3): Show |
2 | a0001c0002t0002g0253a0001c0002t0002g0257 | 2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.4228+403_4228+404i others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538800
|
G | GTTATATT others(8): Show |
1 | a0001c0002t0002g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4228+403_4228+404i others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538800
|
GTTATGTT others(3): Show |
G | 29 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0050others(26): Show | 29 | HG01069.hp1 HG01074.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.4228+404_4228+413d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538800
|
GTTATGTT others(8): Show |
G | 7 | a0001c0001t0001g0148a0001c0004t0003g0237a0001c0004t0003g0250others(4): Show | 7 | HG01192.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4228+404_4228+418d others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538800
|
GTTATGTT others(13): Show |
G | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0004t0003g0233 | 3 | HG02622.hp2 HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4228+404_4228+423d others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538800
|
GTTATGTT others(28): Show |
G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+404_4228+438d others(37): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | |||||
| chr6:70538805
|
G | A | 23 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0253others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.4228+404G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538805 | ||||||
| chr6:70538805
|
G | GTTATA | 18 | a0001c0001t0001g0058a0001c0001t0001g0073a0001c0001t0001g0096others(15): Show | 18 | HG00280.hp2 HG00621.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.4228+456_4228+460d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | |||||
| chr6:70538805
|
G | GTTATATT others(3): Show |
7 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0002t0002g0208others(4): Show | 7 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4228+451_4228+460d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | |||||
| chr6:70538805
|
GTTATA | G | 45 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0055others(42): Show | 45 | HG00597.hp1 HG00609.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.4228+456_4228+460d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | |||||
| chr6:70538805
|
GTTATATT others(3): Show |
G | 14 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0094others(11): Show | 14 | HG00673.hp1 HG01123.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.4228+451_4228+460d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | |||||
| chr6:70538805
|
GTTATATT others(8): Show |
G | 5 | a0001c0001t0001g0091a0001c0002t0002g0188a0001c0002t0002g0189others(2): Show | 5 | HG03195.hp2 NA18953.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.4228+446_4228+460d others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | |||||
| chr6:70538805
|
GTTATATT others(13): Show |
G | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4228+441_4228+460d others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | |||||
| chr6:70538835
|
A | ATTATATT others(8): Show |
6 | a0003c0005t0001g0242a0003c0005t0001g0244a0003c0005t0001g0245others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+448_4228+449i others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538835 | |||||
| chr6:70538835
|
A | ATTATATT others(3): Show |
2 | a0003c0005t0001g0243a0003c0005t0001g0249 | 2 | HG02293.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.4228+443_4228+444i others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538835 | |||||
| chr6:70538842
|
TATATTAT others(4): Show |
T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+442_4228+452d others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538842 | ||||||
| chr6:70538851
|
TTA | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4228+454_4228+455d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538851 | |||||
| chr6:70538917
|
C | CTTTTTTT others(176): Show |
1 | a0001c0002t0002g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4228+517_4228+518i others(185): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538917 | |||||
| chr6:70538917
|
C | CTTTTTTT others(177): Show |
8 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(5): Show | 8 | HG00280.hp1 HG00642.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+517_4228+518i others(186): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538917 | |||||
| chr6:70538917
|
C | CTTTTTTT others(178): Show |
4 | a0001c0002t0002g0256a0001c0002t0002g0260a0001c0002t0002g0262others(1): Show | 4 | HG02257.hp2 HG02698.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.4228+517_4228+518i others(187): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538917 | |||||
| chr6:70538919
|
A | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+518A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538919 | ||||||
| chr6:70538920
|
C | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+519C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538920 | ||||||
| chr6:70538921
|
A | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+520A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538921 | ||||||
| chr6:70539298
|
C | G | 32 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(29): Show | 32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.4228+897C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539298 | ||||||
| chr6:70539485
|
A | G | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4228+1084A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539485 | ||||||
| chr6:70539596
|
C | T | 1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4228+1195C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539596 | ||||||
| chr6:70539718
|
G | A | 5 | a0001c0002t0002g0254a0001c0002t0002g0258a0001c0002t0002g0259others(2): Show | 5 | HG00642.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4228+1317G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539718 | ||||||
| chr6:70539797
|
C | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.4228+1396C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539797 | ||||||
| chr6:70539853
|
A | G | 220 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(217): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.4228+1452A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539853 | ||||||
| chr6:70539920
|
T | C | 1 | a0001c0002t0002g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4228+1519T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539920 | ||||||
| chr6:70539945
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4228+1544G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539945 | ||||||
| chr6:70539991
|
G | A | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+1590G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539991 | ||||||
| chr6:70540063
|
G | A | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+1662G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540063 | ||||||
| chr6:70540130
|
T | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4228+1729T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540130 | ||||||
| chr6:70540217
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4228+1816A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540217 | ||||||
| chr6:70540228
|
A | G | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.4228+1827A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540228 | ||||||
| chr6:70540230
|
G | A | 143 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(140): Show | 143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.4228+1829G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540230 | ||||||
| chr6:70540257
|
T | C | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+1856T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540257 | ||||||
| chr6:70540318
|
C | CT | 111 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0047others(108): Show | 111 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+1941dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | |||||
| chr6:70540318
|
C | CTT | 20 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0079others(17): Show | 20 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.4228+1940_4228+194 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | |||||
| chr6:70540318
|
C | CTTTTT | 6 | a0003c0005t0001g0242a0003c0005t0001g0244a0003c0005t0001g0246others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+1937_4228+194 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | |||||
| chr6:70540318
|
CT | C | 11 | a0001c0002t0002g0254a0001c0002t0002g0255a0001c0002t0002g0256others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.4228+1941delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | |||||
| chr6:70540386
|
A | G | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+1985A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540386 | ||||||
| chr6:70540406
|
G | A | 2 | a0010c0015t0005g0005a0012c0018t0005g0006 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4228+2005G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540406 | ||||||
| chr6:70540474
|
G | A | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4228+2073G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540474 | ||||||
| chr6:70540546
|
C | T | 1 | a0001c0002t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4228+2145C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540546 | ||||||
| chr6:70540568
|
G | A | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4228+2167G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540568 | ||||||
| chr6:70540635
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+2234A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540635 | ||||||
| chr6:70540749
|
T | A | 1 | a0002c0003t0001g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4228+2348T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540749 | ||||||
| chr6:70540951
|
C | T | 3 | a0001c0001t0001g0028a0006c0010t0003g0007a0006c0010t0003g0008 | 3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+2550C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540951 | ||||||
| chr6:70540952
|
A | T | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+2551A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540952 | ||||||
| chr6:70541017
|
A | G | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.4228+2616A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541017 | ||||||
| chr6:70541226
|
T | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4228+2825T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541226 | ||||||
| chr6:70541718
|
T | C | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+3317T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541718 | ||||||
| chr6:70541840
|
G | T | 1 | a0001c0004t0003g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4228+3439G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541840 | ||||||
| chr6:70542018
|
A | G | 1 | a0002c0003t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4228+3617A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542018 | ||||||
| chr6:70542130
|
C | G | 11 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(8): Show | 11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.4228+3729C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542130 | ||||||
| chr6:70542248
|
G | GCA | 62 | a0001c0001t0001g0047a0001c0001t0001g0105a0001c0001t0001g0112others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.4228+3875_4228+387 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACA | 13 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(10): Show | 13 | HG00741.hp2 HG01167.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+3873_4228+387 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACA | 9 | a0001c0002t0002g0169a0001c0002t0002g0204a0001c0002t0002g0205others(6): Show | 9 | HG01192.hp2 HG01433.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.4228+3871_4228+387 others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACAC others(3): Show |
3 | a0001c0002t0002g0256a0001c0002t0002g0258a0001c0002t0002g0264 | 3 | HG00642.hp2 HG02735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4228+3867_4228+387 others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACAC others(5): Show |
8 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(5): Show | 8 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+3865_4228+387 others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACAC others(7): Show |
2 | a0001c0002t0002g0262a0001c0004t0003g0234 | 2 | HG01069.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4228+3863_4228+387 others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACAC others(9): Show |
13 | a0001c0004t0003g0230a0001c0004t0003g0233a0001c0004t0003g0235others(10): Show | 13 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+3861_4228+387 others(20): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACAC others(11): Show |
6 | a0001c0004t0003g0231a0001c0004t0003g0241a0003c0005t0001g0243others(3): Show | 6 | HG02293.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+3859_4228+387 others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
G | GCACACAC others(13): Show |
2 | a0001c0004t0003g0001a0009c0014t0003g0001 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4228+3857_4228+387 others(24): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542248
|
GCA | G | 18 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.4228+3875_4228+387 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | |||||
| chr6:70542276
|
A | ACACACAC others(19): Show |
1 | a0001c0004t0003g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(30): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | |||||
| chr6:70542276
|
A | ACACACAC others(15): Show |
1 | a0001c0004t0003g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(26): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | |||||
| chr6:70542276
|
A | ACACACAC others(11): Show |
5 | a0001c0004t0003g0011a0001c0004t0003g0012a0001c0004t0003g0250others(2): Show | 5 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4228+3876_4228+387 others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | |||||
| chr6:70542276
|
A | ACACACAC others(7): Show |
1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | |||||
| chr6:70542276
|
A | ACACACAC others(3): Show |
1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | |||||
| chr6:70542277
|
C | CACACACA others(10): Show |
1 | a0001c0004t0003g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(21): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542277 | ||||||
| chr6:70542278
|
C | A | 10 | a0001c0004t0003g0016a0001c0004t0003g0017a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+3877C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542278 | ||||||
| chr6:70542331
|
C | CTTTTTGT others(98): Show |
1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+3989_4228+399 others(109): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542331 | |||||
| chr6:70542333
|
T | C | 1 | a0006c0010t0003g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4228+3932T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542333 | ||||||
| chr6:70542344
|
CTCATGTG others(8): Show |
C | 3 | a0001c0002t0002g0171a0001c0009t0001g0211a0001c0009t0001g0212 | 3 | HG02559.hp2 HG03453.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.4228+3962_4228+397 others(19): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542344 | |||||
| chr6:70542374
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+3973A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542374 | ||||||
| chr6:70542661
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+4260A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542661 | ||||||
| chr6:70542762
|
G | A | 2 | a0005c0008t0004g0003a0005c0008t0004g0004 | 2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4228+4361G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542762 | ||||||
| chr6:70542972
|
A | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0105 | 3 | HG01074.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.4228+4571A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542972 | ||||||
| chr6:70543057
|
T | C | 80 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(77): Show | 80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.4228+4656T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543057 | ||||||
| chr6:70543093
|
G | A | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4228+4692G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543093 | ||||||
| chr6:70543323
|
G | A | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+4922G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543323 | ||||||
| chr6:70543579
|
TTACAAAA others(6): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4228+5187_4228+519 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70543579 | |||||
| chr6:70543615
|
G | A | 128 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(125): Show | 128 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.4228+5214G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543615 | ||||||
| chr6:70543681
|
T | C | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4228+5280T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543681 | ||||||
| chr6:70543769
|
C | A | 111 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(108): Show | 111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+5368C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543769 | ||||||
| chr6:70543825
|
T | G | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4228+5424T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543825 | ||||||
| chr6:70543887
|
T | G | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4228+5486T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543887 | ||||||
| chr6:70543998
|
C | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+5597C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543998 | ||||||
| chr6:70544108
|
T | TA | 68 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(65): Show | 68 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.4228+5720dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70544108 | |||||
| chr6:70544118
|
A | G | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+5717A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544118 | ||||||
| chr6:70544150
|
C | G | 1 | a0002c0003t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4228+5749C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544150 | ||||||
| chr6:70544150
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4228+5749C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544150 | ||||||
| chr6:70544169
|
G | A | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4228+5768G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544169 | ||||||
| chr6:70544183
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4228+5782A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544183 | ||||||
| chr6:70544220
|
G | A | 1 | a0002c0003t0001g0124 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4228+5819G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544220 | ||||||
| chr6:70544373
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4228+5972A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544373 | ||||||
| chr6:70544529
|
A | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4228+6128A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544529 | ||||||
| chr6:70544530
|
A | G | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+6129A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544530 | ||||||
| chr6:70544724
|
G | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+6323G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544724 | ||||||
| chr6:70544746
|
T | TA | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+6354dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70544746 | |||||
| chr6:70544799
|
C | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+6398C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544799 | ||||||
| chr6:70544819
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+6418G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544819 | ||||||
| chr6:70544868
|
TG | T | 6 | a0002c0003t0001g0128a0002c0006t0001g0034a0002c0006t0001g0129others(3): Show | 6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+6469delG | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70544868 | |||||
| chr6:70545017
|
C | A | 67 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4228+6616C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545017 | ||||||
| chr6:70545038
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4228+6637T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545038 | ||||||
| chr6:70545080
|
C | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+6679C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545080 | ||||||
| chr6:70545721
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+7320G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545721 | ||||||
| chr6:70545730
|
G | A | 68 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(65): Show | 68 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.4228+7329G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545730 | ||||||
| chr6:70545733
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+7332A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545733 | ||||||
| chr6:70545763
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4228+7362C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545763 | ||||||
| chr6:70545992
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4228+7591C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545992 | ||||||
| chr6:70545992
|
C | G | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+7591C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545992 | ||||||
| chr6:70546009
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+7608C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546009 | ||||||
| chr6:70546051
|
G | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+7650G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546051 | ||||||
| chr6:70546062
|
G | A | 2 | a0002c0003t0001g0116a0002c0003t0001g0118 | 2 | NA19010.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.4228+7661G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546062 | ||||||
| chr6:70546108
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4228+7707A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546108 | ||||||
| chr6:70546125
|
G | T | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+7724G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546125 | ||||||
| chr6:70546445
|
A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+8044A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546445 | ||||||
| chr6:70546502
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+8101C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546502 | ||||||
| chr6:70546651
|
A | T | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+8250A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546651 | ||||||
| chr6:70546857
|
T | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.4228+8456T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546857 | ||||||
| chr6:70546901
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4228+8500G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546901 | ||||||
| chr6:70546935
|
G | C | 1 | a0002c0006t0001g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4228+8534G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546935 | ||||||
| chr6:70547019
|
G | T | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4228+8618G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547019 | ||||||
| chr6:70547473
|
A | G | 3 | a0001c0002t0002g0177a0001c0002t0002g0192a0001c0002t0002g0199 | 3 | NA18993.hp2 NA19070.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4228+9072A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547473 | ||||||
| chr6:70547698
|
A | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG00738.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4229-9052A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547698 | ||||||
| chr6:70547733
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-9017A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547733 | ||||||
| chr6:70547921
|
C | T | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4229-8829C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547921 | ||||||
| chr6:70548023
|
G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-8727G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548023 | ||||||
| chr6:70548439
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4229-8311A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548439 | ||||||
| chr6:70548442
|
A | G | 1 | a0002c0006t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4229-8308A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548442 | ||||||
| chr6:70548520
|
C | T | 1 | a0002c0003t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4229-8230C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548520 | ||||||
| chr6:70548538
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4229-8212T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548538 | ||||||
| chr6:70548604
|
A | G | 2 | a0001c0002t0002g0173a0001c0002t0002g0174 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.4229-8146A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548604 | ||||||
| chr6:70548701
|
A | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-8049A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548701 | ||||||
| chr6:70548727
|
GA | G | 67 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4229-8020delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70548727 | |||||
| chr6:70549055
|
A | G | 12 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0052others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4229-7695A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549055 | ||||||
| chr6:70549286
|
C | T | 12 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.4229-7464C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549286 | ||||||
| chr6:70549387
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4229-7363A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549387 | ||||||
| chr6:70549432
|
T | A | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4229-7318T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549432 | ||||||
| chr6:70549712
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4229-7038G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549712 | ||||||
| chr6:70549730
|
T | C | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4229-7020T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549730 | ||||||
| chr6:70549764
|
A | C | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4229-6986A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549764 | ||||||
| chr6:70549800
|
A | C | 1 | a0002c0006t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4229-6950A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549800 | ||||||
| chr6:70550554
|
T | A | 67 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4229-6196T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550554 | ||||||
| chr6:70550578
|
A | G | 1 | a0002c0003t0001g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4229-6172A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550578 | ||||||
| chr6:70550717
|
G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-6033G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550717 | ||||||
| chr6:70550759
|
G | C | 27 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0054others(24): Show | 27 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.4229-5991G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550759 | ||||||
| chr6:70550761
|
A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-5989A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550761 | ||||||
| chr6:70550863
|
T | C | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4229-5887T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550863 | ||||||
| chr6:70550929
|
C | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5821C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550929 | ||||||
| chr6:70550931
|
C | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5819C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550931 | ||||||
| chr6:70550932
|
T | A | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5818T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550932 | ||||||
| chr6:70550933
|
T | C | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5817T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550933 | ||||||
| chr6:70550934
|
T | A | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5816T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550934 | ||||||
| chr6:70550940
|
T | G | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5810T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550940 | ||||||
| chr6:70550944
|
G | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5806G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550944 | ||||||
| chr6:70550945
|
A | T | 1 | a0002c0003t0001g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5805A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550945 | ||||||
| chr6:70551446
|
A | C | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-5304A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551446 | ||||||
| chr6:70551497
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4229-5253G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551497 | ||||||
| chr6:70551518
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4229-5232G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551518 | ||||||
| chr6:70551701
|
C | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-5049C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551701 | ||||||
| chr6:70552033
|
A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-4717A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552033 | ||||||
| chr6:70552073
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4229-4677G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552073 | ||||||
| chr6:70552218
|
G | C | 1 | a0002c0006t0001g0130 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4229-4532G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552218 | ||||||
| chr6:70552290
|
GCTTTATA others(6): Show |
G | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4229-4433_4229-442 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552290 | |||||
| chr6:70552387
|
C | T | 14 | a0001c0004t0003g0001a0001c0004t0003g0230a0001c0004t0003g0231others(11): Show | 14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4229-4363C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552387 | ||||||
| chr6:70552418
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4229-4332G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552418 | ||||||
| chr6:70552465
|
C | CT | 8 | a0001c0001t0001g0064a0001c0001t0001g0094a0001c0001t0001g0101others(5): Show | 8 | HG00673.hp1 HG01109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.4229-4264dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | |||||
| chr6:70552465
|
CT | C | 118 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.4229-4264delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | |||||
| chr6:70552465
|
CTT | C | 88 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(85): Show | 88 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.4229-4265_4229-426 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | |||||
| chr6:70552465
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0003t0001g0124 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4229-4276_4229-426 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | |||||
| chr6:70552491
|
C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-4259C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552491 | ||||||
| chr6:70552555
|
G | A | 1 | a0004c0007t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4229-4195G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552555 | ||||||
| chr6:70552571
|
C | T | 2 | a0001c0009t0001g0211a0001c0009t0001g0212 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4229-4179C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552571 | ||||||
| chr6:70552759
|
C | T | 1 | a0002c0003t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4229-3991C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552759 | ||||||
| chr6:70553155
|
C | A | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-3595C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553155 | ||||||
| chr6:70553193
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0104 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4229-3557T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553193 | ||||||
| chr6:70553303
|
G | A | 1 | a0001c0002t0002g0181 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4229-3447G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553303 | ||||||
| chr6:70553339
|
A | G | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4229-3411A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553339 | ||||||
| chr6:70553695
|
T | A | 11 | a0001c0004t0007g0265a0001c0009t0001g0211a0001c0009t0001g0212others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.4229-3055T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553695 | ||||||
| chr6:70553695
|
T | TTAAA | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-3055_4229-305 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553695 | ||||||
| chr6:70553696
|
A | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-3054A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553696 | ||||||
| chr6:70553700
|
A | AAAAG | 65 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(62): Show | 65 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.4229-3050_4229-304 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553700 | ||||||
| chr6:70553700
|
A | G | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-3050A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553700 | ||||||
| chr6:70553727
|
C | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-3023C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553727 | ||||||
| chr6:70553813
|
C | T | 67 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4229-2937C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553813 | ||||||
| chr6:70553931
|
C | A | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-2819C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553931 | ||||||
| chr6:70554045
|
G | A | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4229-2705G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554045 | ||||||
| chr6:70554087
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4229-2663G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554087 | ||||||
| chr6:70554146
|
G | C | 2 | a0004c0007t0001g0123a0004c0007t0001g0152 | 2 | NA18950.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.4229-2604G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554146 | ||||||
| chr6:70554157
|
C | T | 28 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(25): Show | 28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.4229-2593C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554157 | ||||||
| chr6:70554168
|
G | A | 1 | a0002c0003t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4229-2582G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554168 | ||||||
| chr6:70554174
|
AAAGT | A | 8 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(5): Show | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4229-2571_4229-256 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70554174 | |||||
| chr6:70554299
|
T | G | 1 | a0002c0003t0001g0111 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4229-2451T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554299 | ||||||
| chr6:70554458
|
G | A | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4229-2292G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554458 | ||||||
| chr6:70554590
|
G | A | 4 | a0001c0004t0001g0160a0001c0004t0001g0161a0001c0004t0001g0162others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4229-2160G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554590 | ||||||
| chr6:70554631
|
T | C | 5 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0142others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4229-2119T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554631 | ||||||
| chr6:70554667
|
G | A | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4229-2083G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554667 | ||||||
| chr6:70554713
|
C | T | 5 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206others(2): Show | 5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.4229-2037C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554713 | ||||||
| chr6:70554740
|
G | T | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-2010G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554740 | ||||||
| chr6:70554847
|
G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-1903G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554847 | ||||||
| chr6:70554978
|
G | A | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4229-1772G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554978 | ||||||
| chr6:70555028
|
C | T | 1 | a0011c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4229-1722C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555028 | ||||||
| chr6:70555043
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.4229-1707C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555043 | ||||||
| chr6:70555331
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-1419C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555331 | ||||||
| chr6:70555408
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4229-1342T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555408 | ||||||
| chr6:70555488
|
G | A | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4229-1262G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555488 | ||||||
| chr6:70555696
|
G | C | 2 | a0006c0010t0003g0007a0006c0010t0003g0008 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4229-1054G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555696 | ||||||
| chr6:70555728
|
AG | A | 10 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-1014delG | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70555728 | |||||
| chr6:70556000
|
T | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-750T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556000 | ||||||
| chr6:70556226
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4229-524G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556226 | ||||||
| chr6:70556239
|
A | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-511A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556239 | ||||||
| chr6:70556349
|
G | A | 1 | a0001c0002t0002g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4229-401G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556349 | ||||||
| chr6:70556355
|
T | C | 1 | a0002c0016t0002g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4229-395T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556355 | ||||||
| chr6:70556519
|
C | T | 7 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.4229-231C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556519 | ||||||
| chr6:70556681
|
TATG | T | 10 | a0001c0009t0001g0211a0001c0009t0001g0212a0003c0005t0001g0242others(7): Show | 10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-66_4229-64del others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70556681 | |||||
| chr6:70556922
|
T | G | 5 | a0002c0003t0001g0035a0002c0003t0001g0134a0002c0003t0001g0137others(2): Show | 5 | HG01168.hp1 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4342+59T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70556922 | ||||||
| chr6:70557275
|
A | C | 54 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(51): Show | 54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4342+412A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557275 | ||||||
| chr6:70557379
|
C | G | 1 | a0002c0003t0001g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4342+516C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557379 | ||||||
| chr6:70557551
|
G | A | 8 | a0001c0004t0003g0010a0001c0004t0003g0011a0001c0004t0003g0012others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.4342+688G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557551 | ||||||
| chr6:70557601
|
C | T | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4342+738C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557601 | ||||||
| chr6:70557626
|
A | G | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4342+763A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557626 | ||||||
| chr6:70557694
|
C | CA | 63 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(60): Show | 63 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.4342+855dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | |||||
| chr6:70557694
|
C | CAA | 69 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(66): Show | 69 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.4342+854_4342+855d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | |||||
| chr6:70557694
|
C | CAAA | 31 | a0001c0002t0002g0172a0001c0002t0002g0175a0001c0002t0002g0176others(28): Show | 31 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.4342+853_4342+855d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | |||||
| chr6:70557694
|
C | CAAAA | 6 | a0001c0002t0002g0197a0001c0002t0002g0258a0001c0002t0002g0259others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4342+852_4342+855d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | |||||
| chr6:70557702
|
A | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0095others(3): Show | 6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.4342+839A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557702 | ||||||
| chr6:70557707
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4342+844A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557707 | ||||||
| chr6:70557812
|
G | A | 1 | a0002c0003t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4342+949G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557812 | ||||||
| chr6:70557863
|
G | A | 117 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0002t0002g0167others(114): Show | 117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4342+1000G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557863 | ||||||
| chr6:70557963
|
G | A | 13 | a0001c0002t0002g0253a0001c0002t0002g0254a0001c0002t0002g0255others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4342+1100G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557963 | ||||||
| chr6:70557972
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4342+1109A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557972 | ||||||
| chr6:70558066
|
A | G | 78 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(75): Show | 78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4342+1203A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558066 | ||||||
| chr6:70558536
|
G | A | 12 | a0001c0004t0003g0009a0001c0004t0003g0010a0001c0004t0003g0011others(9): Show | 12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.4343-1180G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558536 | ||||||
| chr6:70558708
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0055 | 2 | HG02015.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.4343-1008C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558708 | ||||||
| chr6:70558710
|
T | C | 78 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(75): Show | 78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4343-1006T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558710 | ||||||
| chr6:70558778
|
C | T | 2 | a0001c0004t0003g0016a0001c0004t0003g0017 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4343-938C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558778 | ||||||
| chr6:70559138
|
G | A | 30 | a0001c0004t0003g0001a0001c0004t0003g0009a0001c0004t0003g0010others(27): Show | 30 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.4343-578G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559138 | ||||||
| chr6:70559212
|
G | A | 8 | a0001c0002t0002g0220a0001c0002t0002g0223a0001c0002t0002g0224others(5): Show | 8 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.4343-504G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559212 | ||||||
| chr6:70559260
|
G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4343-456G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559260 | ||||||
| chr6:70559452
|
A | T | 1 | a0002c0016t0002g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4343-264A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559452 |