| geneid | 132001 |
|---|---|
| ensemblid | ENSG00000144559.11 |
| hgncid | 25187 |
| symbol | TAMM41 |
| name | TAM41 mitochondrial translocator assembly and maintenance homolog |
| refseq_nuc | NM_001284401.2 |
| refseq_prot | NP_001271330.1 |
| ensembl_nuc | ENST00000455809.6 |
| ensembl_prot | ENSP00000398596.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 11790442 |
| end | 11846885 |
| strand | - |
| ver | v1.2 |
| region | chr3:11790442-11846885 |
| region5000 | chr3:11785442-11851885 |
| regionname0 | TAMM41_chr3_11790442_11846885 |
| regionname5000 | TAMM41_chr3_11785442_11851885 |
| 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 | 337 | 282 | 71 | 54 | 119 | 11 | 26 | 88 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002 | 0/0 | 337 | 73 | 14 | 11 | 33 | 3 | 12 | 27 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0003 | 0/1 | 337 | 10 | 0 | 3 | 2 | 3 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0004 | 0/0 | 337 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0005 | 0/0 | 337 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0006 | 0/0 | 337 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0007 | 0/0 | 337 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| 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 | 1014 | 193 | 40 | 31 | 100 | 4 | 17 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0002 | 0/0 | 1014 | 86 | 29 | 23 | 18 | 7 | 9 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0003 | 0/0 | 1014 | 43 | 5 | 2 | 26 | 1 | 9 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0004 | 0/0 | 1014 | 30 | 9 | 9 | 7 | 2 | 3 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0005 | 0/1 | 1014 | 8 | 0 | 2 | 2 | 3 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0006 | 0/0 | 1014 | 3 | 0 | 1 | 0 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0007 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0008 | 0/0 | 1014 | 2 | 0 | 1 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0009 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0010 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0011 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| c0012 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| 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 | 1/0 | 313 | 187 | 47 | 21 | 101 | 2 | 15 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| t0002 | 0/0 | 313 | 94 | 33 | 17 | 27 | 5 | 12 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| t0003 | 0/1 | 313 | 50 | 4 | 21 | 12 | 7 | 5 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| t0004 | 0/0 | 313 | 40 | 3 | 11 | 14 | 4 | 8 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| t0005 | 0/0 | 313 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| 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 | 6 | 0 | 1 | 5 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| 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 | 1014 | 193 | 40 | 31 | 100 | 4 | 17 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0002 | 0/0 | 1014 | 86 | 29 | 23 | 18 | 7 | 9 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0007 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0012 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0003 | 0/0 | 1014 | 43 | 5 | 2 | 26 | 1 | 9 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0004 | 0/0 | 1014 | 30 | 9 | 9 | 7 | 2 | 3 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0003c0005 | 0/1 | 1014 | 8 | 0 | 2 | 2 | 3 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0003c0008 | 0/0 | 1014 | 2 | 0 | 1 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0004c0006 | 0/0 | 1014 | 3 | 0 | 1 | 0 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0005c0009 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0006c0011 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0007c0010 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1326 | 167 | 36 | 18 | 95 | 2 | 15 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0001t0003 | 0/0 | 1326 | 26 | 4 | 13 | 5 | 2 | 2 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0002t0002 | 0/0 | 1326 | 71 | 27 | 15 | 17 | 5 | 7 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0002t0004 | 0/0 | 1326 | 14 | 1 | 8 | 1 | 2 | 2 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0002t0005 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0007t0001 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0001c0012t0001 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0003t0002 | 0/0 | 1326 | 20 | 3 | 2 | 10 | 0 | 5 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0003t0003 | 0/0 | 1326 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0003t0004 | 0/0 | 1326 | 20 | 2 | 0 | 13 | 1 | 4 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0004t0001 | 0/0 | 1326 | 15 | 8 | 2 | 5 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0004t0002 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0002c0004t0003 | 0/0 | 1326 | 14 | 0 | 7 | 2 | 2 | 3 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0003c0005t0001 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0003c0005t0003 | 0/1 | 1326 | 7 | 0 | 1 | 2 | 3 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0003c0008t0004 | 0/0 | 1326 | 2 | 0 | 1 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0004c0006t0004 | 0/0 | 1326 | 3 | 0 | 1 | 0 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0005c0009t0002 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0006c0011t0004 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| a0007c0010t0001 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | copy fasta | chr3 | 11785442 | 11851885 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0007t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0007t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0012t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0008t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0008t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0004c0006t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0004c0006t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0004c0006t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0005c0009t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0005c0009t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0006c0011t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0007c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0174 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00099 | hp2 | a0004 | c0006 | t0004 | g0142 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00140 | hp1 | a0003 | c0005 | t0003 | g0252 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00140 | hp2 | a0002 | c0003 | t0004 | g0115 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0124 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00323 | hp1 | a0002 | c0004 | t0003 | g0184 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00323 | hp2 | a0003 | c0005 | t0003 | g0303 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00438 | hp2 | a0002 | c0003 | t0004 | g0053 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00544 | hp1 | a0002 | c0003 | t0004 | g0061 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00639 | hp1 | a0003 | c0008 | t0004 | g0112 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00738 | hp1 | a0006 | c0011 | t0004 | g0070 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0117 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01070 | hp2 | a0002 | c0004 | t0003 | g0185 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0257 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0260 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01109 | hp2 | a0002 | c0004 | t0003 | g0165 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01192 | hp1 | a0004 | c0006 | t0004 | g0141 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01192 | hp2 | a0002 | c0004 | t0003 | g0182 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0091 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01256 | hp2 | a0002 | c0004 | t0003 | g0010 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01257 | hp2 | a0002 | c0004 | t0003 | g0015 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01258 | hp1 | a0002 | c0004 | t0003 | g0015 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01258 | hp2 | a0002 | c0004 | t0003 | g0010 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01261 | hp2 | a0003 | c0005 | t0003 | g0253 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01358 | hp2 | a0003 | c0005 | t0001 | g0240 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0097 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0320 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0009 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0181 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0009 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0085 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0324 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0039 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0086 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0066 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0119 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0092 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0094 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02055 | hp2 | a0005 | c0009 | t0002 | g0036 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02071 | hp1 | a0002 | c0004 | t0001 | g0343 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02080 | hp1 | a0002 | c0003 | t0004 | g0075 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02080 | hp2 | a0003 | c0005 | t0003 | g0201 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0149 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0145 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02148 | hp2 | a0001 | c0002 | t0004 | g0088 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02165 | hp2 | a0002 | c0004 | t0001 | g0220 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0309 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0144 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0087 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02280 | hp1 | a0002 | c0004 | t0001 | g0262 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0052 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0089 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0310 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0028 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02738 | hp1 | a0002 | c0003 | t0004 | g0064 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0140 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0261 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02976 | hp1 | a0002 | c0004 | t0001 | g0225 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0110 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0069 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0074 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0230 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03225 | hp2 | a0001 | c0007 | t0001 | g0146 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03239 | hp2 | a0003 | c0008 | t0004 | g0051 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03486 | hp1 | a0005 | c0009 | t0002 | g0035 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03490 | hp1 | a0002 | c0004 | t0003 | g0183 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0027 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0136 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03654 | hp2 | a0002 | c0003 | t0002 | g0057 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0067 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0127 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03710 | hp2 | a0002 | c0004 | t0003 | g0258 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0128 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0111 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0073 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04115 | hp1 | a0002 | c0003 | t0004 | g0056 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04184 | hp2 | a0002 | c0003 | t0004 | g0048 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0109 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04199 | hp2 | a0004 | c0006 | t0004 | g0143 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04204 | hp1 | a0002 | c0003 | t0004 | g0114 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04204 | hp2 | a0002 | c0004 | t0003 | g0164 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0118 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | CHB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18906 | hp2 | a0002 | c0003 | t0004 | g0137 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0055 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18945 | hp2 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18946 | hp2 | a0002 | c0004 | t0001 | g0256 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18951 | hp2 | a0002 | c0004 | t0003 | g0196 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0148 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18953 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18954 | hp1 | a0002 | c0003 | t0002 | g0059 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0054 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18966 | hp2 | a0002 | c0004 | t0001 | g0340 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18972 | hp2 | a0002 | c0004 | t0003 | g0206 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18974 | hp1 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18982 | hp1 | a0002 | c0003 | t0002 | g0058 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18984 | hp1 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18986 | hp2 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18988 | hp1 | a0002 | c0003 | t0004 | g0060 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18990 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18991 | hp1 | a0001 | c0012 | t0001 | g0212 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0047 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18999 | hp1 | a0002 | c0003 | t0002 | g0046 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19001 | hp2 | a0002 | c0003 | t0004 | g0068 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19004 | hp2 | a0002 | c0003 | t0004 | g0105 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19007 | hp2 | a0002 | c0003 | t0004 | g0063 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19009 | hp1 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0102 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19043 | hp2 | a0007 | c0010 | t0001 | g0147 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19054 | hp2 | a0002 | c0003 | t0004 | g0062 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19078 | hp1 | a0002 | c0003 | t0004 | g0098 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19080 | hp2 | a0002 | c0003 | t0003 | g0150 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0100 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19083 | hp1 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0103 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ASW | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0084 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20752 | hp2 | a0002 | c0004 | t0003 | g0151 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20805 | hp1 | a0003 | c0005 | t0003 | g0254 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0123 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0113 | SAS | GIH | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02559 | hp2 | a0002 | c0003 | t0004 | g0026 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0259 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18955 | hp2 | a0003 | c0005 | t0003 | g0244 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0005 | t0003 | g0304 | REF | REF | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0307 | REF | REF | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11829741
|
T | C | 2 | a0003a0006 | 11 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(8): Show |
missense_variant | MODERATE | c.535A>G | p.Ile179Val | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/8 | 784/1326 | 535/1014 | 179/337 | chr3 | 11829741 | ||
| chr3:11839286
|
T | C | 2 | a0002a0006 | 74 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
missense_variant | MODERATE | c.347A>G | p.Asn116Ser | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/8 | 596/1326 | 347/1014 | 116/337 | chr3 | 11839286 | ||
| chr3:11844075
|
T | C | 1 | a0005 | 2 | HG02055.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.272A>G | p.Tyr91Cys | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/8 | 521/1326 | 272/1014 | 91/337 | chr3 | 11844075 | ||
| chr3:11846519
|
G | A | 1 | a0004 | 3 | HG00099.hp2 HG01192.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.118C>T | p.Pro40Ser | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 367/1326 | 118/1014 | 40/337 | chr3 | 11846519 | ||
| chr3:11846599
|
A | T | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.38T>A | p.Phe13Tyr | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 287/1326 | 38/1014 | 13/337 | chr3 | 11846599 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11829769
|
G | A | 1 | a0001c0012 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.507C>T | p.Pro169Pro | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/8 | 756/1326 | 507/1014 | 169/337 | chr3 | 11829769 | ||
| chr3:11846517
|
C | G | 6 | a0001c0002a0002c0003a0003c0008others(3): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
synonymous_variant | LOW | c.120G>C | p.Pro40Pro | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 369/1326 | 120/1014 | 40/337 | chr3 | 11846517 | ||
| chr3:11846628
|
C | T | 1 | a0001c0007 | 2 | HG02145.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.9G>A | p.Leu3Leu | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 258/1326 | 9/1014 | 3/337 | chr3 | 11846628 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11790479
|
C | T | 9 | a0001c0001t0003a0001c0002t0004a0002c0003t0003others(6): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 8/8 | 26 | chr3 | 11790479 | |||||
| chr3:11846707
|
T | C | 1 | a0001c0002t0005 | 1 | HG02258.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | chr3 | 11846707 | ||||||
| chr3:11846785
|
C | G | 10 | a0001c0002t0002a0001c0002t0004a0001c0002t0005others(7): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
5_prime_UTR_variant | MODIFIER | c.-149G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 149 | chr3 | 11846785 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11790613
|
T | C | 1 | a0001c0002t0002g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.938-32A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790613 | ||||||
| chr3:11790617
|
G | A | 1 | a0002c0003t0003g0148 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.938-36C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790617 | ||||||
| chr3:11790697
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0191 | 3 | HG02109.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.938-116G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790697 | ||||||
| chr3:11790894
|
C | A | 1 | a0001c0002t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.938-313G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790894 | ||||||
| chr3:11791106
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.938-525A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791106 | ||||||
| chr3:11791124
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.938-543A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791124 | ||||||
| chr3:11791130
|
G | A | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.938-549C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791130 | ||||||
| chr3:11791136
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(105): Show | 122 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.938-555C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791136 | ||||||
| chr3:11791214
|
C | T | 6 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.938-633G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791214 | ||||||
| chr3:11791229
|
C | T | 1 | a0001c0002t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.938-648G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791229 | ||||||
| chr3:11791299
|
G | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.938-718C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791299 | ||||||
| chr3:11791324
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.938-743A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791324 | ||||||
| chr3:11791721
|
C | T | 75 | a0001c0001t0001g0169a0001c0001t0001g0187a0001c0001t0003g0011others(72): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.938-1140G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791721 | ||||||
| chr3:11791797
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0191a0002c0003t0004g0137 | 4 | HG02109.hp2 HG02280.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-1216G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791797 | ||||||
| chr3:11791801
|
T | G | 1 | a0001c0002t0002g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.938-1220A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791801 | ||||||
| chr3:11791819
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.938-1238A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791819 | ||||||
| chr3:11791999
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(182): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.938-1418G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791999 | ||||||
| chr3:11792018
|
A | G | 1 | a0001c0002t0002g0107 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.938-1437T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792018 | ||||||
| chr3:11792058
|
A | G | 2 | a0002c0004t0001g0309a0002c0004t0001g0310 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.938-1477T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792058 | ||||||
| chr3:11792155
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.938-1574C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792155 | ||||||
| chr3:11792163
|
C | T | 8 | a0001c0001t0001g0319a0001c0001t0001g0331a0001c0002t0002g0041others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.938-1582G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792163 | ||||||
| chr3:11792173
|
A | AT | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(106): Show | 124 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.938-1593dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792173 | ||||||
| chr3:11792183
|
T | G | 9 | a0002c0003t0002g0066a0002c0003t0002g0091a0002c0004t0001g0225others(6): Show | 9 | HG01109.hp1 HG01243.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.938-1602A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792183 | ||||||
| chr3:11792185
|
TG | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-1605delC | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792185 | ||||||
| chr3:11792186
|
G | T | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-1605C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792186 | ||||||
| chr3:11792208
|
C | T | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-1627G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792208 | ||||||
| chr3:11792486
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0329 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.938-1905T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792486 | ||||||
| chr3:11792705
|
A | T | 1 | a0002c0003t0004g0006 | 2 | NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.938-2124T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792705 | ||||||
| chr3:11792815
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.938-2234T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792815 | ||||||
| chr3:11792875
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.938-2294G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792875 | ||||||
| chr3:11792955
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(83): Show | 99 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.938-2374C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792955 | ||||||
| chr3:11793010
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0197a0001c0001t0001g0198others(9): Show | 14 | NA18906.hp2 NA18943.hp1 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.938-2429C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793010 | ||||||
| chr3:11793018
|
G | A | 1 | a0002c0003t0002g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.938-2437C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793018 | ||||||
| chr3:11793059
|
C | CA | 28 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0198others(25): Show | 29 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.938-2479dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
C | CAA | 24 | a0001c0001t0001g0243a0001c0001t0001g0269a0001c0001t0001g0292others(21): Show | 25 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.938-2480_938-2479d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
C | CAAA | 61 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(58): Show | 70 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.938-2481_938-2479d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
C | CAAAA | 30 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 35 | HG00621.hp2 HG01074.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.938-2482_938-2479d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-2488_938-2479d others(12): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
CA | C | 13 | a0001c0001t0001g0163a0001c0001t0001g0186a0001c0001t0001g0203others(10): Show | 13 | HG00099.hp2 HG00642.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.938-2479delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
CAA | C | 22 | a0001c0001t0001g0169a0001c0001t0001g0187a0001c0001t0001g0326others(19): Show | 24 | HG00099.hp1 HG00733.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.938-2480_938-2479d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
CAAA | C | 52 | a0001c0001t0003g0021a0001c0001t0003g0171a0001c0001t0003g0255others(49): Show | 57 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.938-2481_938-2479d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793059
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.938-2486_938-2479d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | ||||||
| chr3:11793081
|
A | AG | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-2501_938-2500i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793081 | ||||||
| chr3:11793083
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.938-2503_938-2502i others(31): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793083 | ||||||
| chr3:11793083
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0002g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.938-2503_938-2502i others(18): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793083 | ||||||
| chr3:11793083
|
A | G | 81 | a0001c0001t0001g0169a0001c0001t0001g0187a0001c0001t0001g0316others(78): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.938-2502T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793083 | ||||||
| chr3:11793162
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0214a0001c0001t0001g0221 | 4 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-2581T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793162 | ||||||
| chr3:11793226
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.938-2645C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793226 | ||||||
| chr3:11793271
|
A | G | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.938-2690T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793271 | ||||||
| chr3:11793274
|
T | A | 2 | a0003c0005t0003g0252a0006c0011t0004g0070 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.938-2693A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793274 | ||||||
| chr3:11793310
|
A | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(12): Show | 16 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.938-2729T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793310 | ||||||
| chr3:11793430
|
CA | C | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-2850delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793430 | ||||||
| chr3:11793580
|
A | T | 1 | a0001c0002t0002g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.938-2999T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793580 | ||||||
| chr3:11793583
|
A | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-3002T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793583 | ||||||
| chr3:11793598
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.938-3017G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793598 | ||||||
| chr3:11793657
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-3076T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793657 | ||||||
| chr3:11793678
|
A | G | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.938-3097T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793678 | ||||||
| chr3:11793687
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(240): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.938-3106T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793687 | ||||||
| chr3:11793718
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(119): Show | 137 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.938-3137C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793718 | ||||||
| chr3:11793728
|
G | A | 1 | a0001c0002t0002g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.938-3147C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793728 | ||||||
| chr3:11793769
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(107): Show | 125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.938-3188G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793769 | ||||||
| chr3:11793822
|
C | T | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.938-3241G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793822 | ||||||
| chr3:11794058
|
A | C | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.938-3477T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794058 | ||||||
| chr3:11794059
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.938-3478G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794059 | ||||||
| chr3:11794065
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.938-3484G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794065 | ||||||
| chr3:11794148
|
A | AT | 11 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0001g0236others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.938-3568dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794148 | ||||||
| chr3:11794148
|
A | ATT | 9 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(6): Show | 10 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.938-3569_938-3568d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794148 | ||||||
| chr3:11794155
|
T | TA | 121 | a0001c0001t0001g0162a0001c0001t0001g0169a0001c0001t0001g0176others(118): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.938-3575_938-3574i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794155 | ||||||
| chr3:11794161
|
T | A | 41 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(38): Show | 41 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.938-3580A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794161 | ||||||
| chr3:11794187
|
A | G | 1 | a0002c0003t0004g0006 | 2 | NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.938-3606T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794187 | ||||||
| chr3:11794229
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.938-3648A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794229 | ||||||
| chr3:11794589
|
T | TAAAAC | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-4009_938-4008i others(7): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794589 | ||||||
| chr3:11794591
|
G | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-4010C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794591 | ||||||
| chr3:11794621
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.938-4040G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794621 | ||||||
| chr3:11794823
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.938-4242A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794823 | ||||||
| chr3:11794912
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.938-4331A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794912 | ||||||
| chr3:11794944
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.938-4363T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794944 | ||||||
| chr3:11794975
|
T | C | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-4394A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794975 | ||||||
| chr3:11795040
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-4459C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795040 | ||||||
| chr3:11795112
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.938-4531T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795112 | ||||||
| chr3:11795169
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.938-4588A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795169 | ||||||
| chr3:11795208
|
G | A | 3 | a0001c0001t0001g0249a0001c0001t0001g0329a0001c0001t0001g0338 | 3 | HG02074.hp1 HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.938-4627C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795208 | ||||||
| chr3:11795299
|
G | A | 5 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180others(2): Show | 5 | HG01192.hp1 HG01257.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.938-4718C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795299 | ||||||
| chr3:11795588
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-5007C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795588 | ||||||
| chr3:11795662
|
T | C | 3 | a0001c0001t0001g0237a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG00741.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.938-5081A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795662 | ||||||
| chr3:11795730
|
C | G | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-5149G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795730 | ||||||
| chr3:11795738
|
T | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(5): Show | 9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.938-5157A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795738 | ||||||
| chr3:11795923
|
G | A | 7 | a0001c0002t0004g0049a0001c0002t0004g0086a0001c0002t0004g0087others(4): Show | 7 | HG00438.hp2 HG01358.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.938-5342C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795923 | ||||||
| chr3:11796035
|
C | T | 3 | a0001c0001t0001g0217a0001c0002t0002g0134a0001c0002t0002g0135 | 3 | HG02615.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.938-5454G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796035 | ||||||
| chr3:11796108
|
G | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(10): Show | 14 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.938-5527C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796108 | ||||||
| chr3:11796538
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.938-5957G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796538 | ||||||
| chr3:11796643
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.938-6062C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796643 | ||||||
| chr3:11796671
|
G | C | 1 | a0001c0001t0003g0177 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.938-6090C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796671 | ||||||
| chr3:11796710
|
A | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(12): Show | 16 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.938-6129T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796710 | ||||||
| chr3:11796884
|
C | CA | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.938-6304dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796884 | ||||||
| chr3:11797035
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.938-6454A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797035 | ||||||
| chr3:11797250
|
T | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-6669A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797250 | ||||||
| chr3:11797330
|
G | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-6749C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797330 | ||||||
| chr3:11797357
|
T | G | 129 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0163others(126): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.938-6776A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797357 | ||||||
| chr3:11797456
|
G | A | 2 | a0001c0001t0001g0322a0002c0003t0004g0137 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.938-6875C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797456 | ||||||
| chr3:11797461
|
T | C | 1 | a0002c0004t0003g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.938-6880A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797461 | ||||||
| chr3:11797484
|
C | T | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-6903G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797484 | ||||||
| chr3:11797525
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.938-6944G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797525 | ||||||
| chr3:11797570
|
TAAG | T | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-6992_938-6990d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797570 | ||||||
| chr3:11797608
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.938-7027C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797608 | ||||||
| chr3:11797769
|
A | T | 1 | a0001c0001t0003g0251 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.938-7188T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797769 | ||||||
| chr3:11797896
|
A | G | 1 | a0002c0004t0001g0256 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.938-7315T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797896 | ||||||
| chr3:11798195
|
A | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.938-7614T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798195 | ||||||
| chr3:11798292
|
T | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0276 | 2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.938-7711A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798292 | ||||||
| chr3:11798418
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.938-7837T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798418 | ||||||
| chr3:11798457
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(117): Show | 134 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.938-7876G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798457 | ||||||
| chr3:11798492
|
A | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.938-7911T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798492 | ||||||
| chr3:11798568
|
T | C | 2 | a0002c0003t0002g0073a0002c0003t0002g0074 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.938-7987A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798568 | ||||||
| chr3:11798726
|
G | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.938-8145C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798726 | ||||||
| chr3:11798801
|
A | G | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.938-8220T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798801 | ||||||
| chr3:11798811
|
T | C | 1 | a0003c0005t0001g0240 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.938-8230A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798811 | ||||||
| chr3:11798996
|
C | T | 1 | a0002c0004t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.938-8415G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798996 | ||||||
| chr3:11799042
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.938-8461G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799042 | ||||||
| chr3:11799157
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.938-8576G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799157 | ||||||
| chr3:11799203
|
C | A | 34 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(31): Show | 34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.938-8622G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799203 | ||||||
| chr3:11799238
|
C | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+8595G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799238 | ||||||
| chr3:11799259
|
A | AT | 41 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0001t0003g0286others(38): Show | 45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.937+8573_937+8574i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799259 | ||||||
| chr3:11799345
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+8488C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799345 | ||||||
| chr3:11799429
|
A | G | 128 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0163others(125): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.937+8404T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799429 | ||||||
| chr3:11799455
|
C | T | 114 | a0001c0001t0001g0162a0001c0001t0001g0169a0001c0001t0001g0176others(111): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.937+8378G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799455 | ||||||
| chr3:11799504
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937+8329G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799504 | ||||||
| chr3:11799514
|
C | A | 1 | a0001c0001t0001g0313 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.937+8319G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799514 | ||||||
| chr3:11799594
|
C | T | 10 | a0001c0001t0001g0200a0001c0001t0001g0207a0001c0001t0001g0332others(7): Show | 10 | HG00423.hp2 HG00621.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.937+8239G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799594 | ||||||
| chr3:11799608
|
A | G | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.937+8225T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799608 | ||||||
| chr3:11799609
|
T | C | 1 | a0002c0004t0001g0220 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.937+8224A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799609 | ||||||
| chr3:11799637
|
G | C | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+8196C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799637 | ||||||
| chr3:11799685
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0273a0001c0001t0001g0290others(1): Show | 5 | HG00621.hp2 HG02040.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+8148T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799685 | ||||||
| chr3:11799970
|
C | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(238): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.937+7863G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799970 | ||||||
| chr3:11800337
|
C | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.937+7496G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800337 | ||||||
| chr3:11800475
|
T | C | 2 | a0002c0003t0002g0027a0002c0003t0002g0028 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.937+7358A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800475 | ||||||
| chr3:11800536
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.937+7297A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800536 | ||||||
| chr3:11800547
|
TA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0020others(79): Show | 87 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.937+7285delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | ||||||
| chr3:11800547
|
TAA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(112): Show | 129 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.937+7284_937+7285d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | ||||||
| chr3:11800547
|
TAAA | T | 119 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0163others(116): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.937+7283_937+7285d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | ||||||
| chr3:11800547
|
TAAAA | T | 9 | a0002c0003t0002g0039a0002c0004t0001g0225a0002c0004t0001g0230others(6): Show | 9 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.937+7282_937+7285d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | ||||||
| chr3:11800729
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(239): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.937+7104C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800729 | ||||||
| chr3:11800763
|
G | A | 34 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(31): Show | 34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.937+7070C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800763 | ||||||
| chr3:11800880
|
T | C | 125 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0163others(122): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.937+6953A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800880 | ||||||
| chr3:11801098
|
G | GA | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(237): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.937+6734dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801098 | ||||||
| chr3:11801124
|
C | T | 1 | a0002c0003t0002g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.937+6709G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801124 | ||||||
| chr3:11801290
|
T | C | 1 | a0002c0004t0003g0015 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.937+6543A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801290 | ||||||
| chr3:11801347
|
CCT | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(108): Show | 125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.937+6484_937+6485d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801347 | ||||||
| chr3:11801381
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.937+6452A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801381 | ||||||
| chr3:11801386
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.937+6447A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801386 | ||||||
| chr3:11801387
|
A | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0197a0001c0001t0001g0198others(8): Show | 13 | NA18943.hp1 NA18956.hp1 NA18977.hp2 others(10): Show |
intron_variant | MODIFIER | c.937+6446T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801387 | ||||||
| chr3:11801400
|
C | T | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+6433G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801400 | ||||||
| chr3:11801401
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+6432C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801401 | ||||||
| chr3:11801408
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(108): Show | 125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.937+6425G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801408 | ||||||
| chr3:11801409
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(236): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.937+6424T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801409 | ||||||
| chr3:11801493
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.937+6340G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801493 | ||||||
| chr3:11801538
|
C | T | 3 | a0001c0002t0002g0004a0001c0002t0002g0023a0001c0002t0002g0025 | 4 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+6295G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801538 | ||||||
| chr3:11801625
|
C | T | 1 | a0001c0002t0002g0107 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.937+6208G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801625 | ||||||
| chr3:11801776
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(8): Show | 12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.937+6057A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801776 | ||||||
| chr3:11801807
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+6026C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801807 | ||||||
| chr3:11801829
|
A | G | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+6004T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801829 | ||||||
| chr3:11801954
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937+5879G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801954 | ||||||
| chr3:11801979
|
G | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(83): Show | 99 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.937+5854C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801979 | ||||||
| chr3:11801980
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+5853C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801980 | ||||||
| chr3:11802205
|
G | C | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+5628C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802205 | ||||||
| chr3:11802420
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(104): Show | 121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.937+5413T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802420 | ||||||
| chr3:11802434
|
A | G | 133 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(130): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.937+5399T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802434 | ||||||
| chr3:11802555
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+5278A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802555 | ||||||
| chr3:11802623
|
A | G | 1 | a0001c0002t0002g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.937+5210T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802623 | ||||||
| chr3:11802671
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.937+5162C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802671 | ||||||
| chr3:11802703
|
C | T | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+5130G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802703 | ||||||
| chr3:11802732
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+5101C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802732 | ||||||
| chr3:11802738
|
A | C | 1 | a0001c0001t0001g0268 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.937+5095T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802738 | ||||||
| chr3:11802880
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+4953C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802880 | ||||||
| chr3:11802897
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.937+4936A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802897 | ||||||
| chr3:11803007
|
T | C | 1 | a0001c0001t0001g0333 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.937+4826A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803007 | ||||||
| chr3:11803011
|
C | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+4822G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803011 | ||||||
| chr3:11803062
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(104): Show | 121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.937+4771T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803062 | ||||||
| chr3:11803216
|
G | A | 1 | a0004c0006t0004g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.937+4617C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803216 | ||||||
| chr3:11803281
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(103): Show | 120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.937+4552C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803281 | ||||||
| chr3:11803288
|
G | A | 1 | a0001c0001t0001g0323 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.937+4545C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803288 | ||||||
| chr3:11803536
|
A | G | 4 | a0002c0003t0002g0066a0002c0003t0002g0091a0002c0004t0001g0340others(1): Show | 4 | HG01243.hp2 HG01978.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+4297T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803536 | ||||||
| chr3:11803577
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(237): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.937+4256T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803577 | ||||||
| chr3:11803623
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.937+4210C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803623 | ||||||
| chr3:11803685
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.937+4148T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803685 | ||||||
| chr3:11803714
|
A | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+4119T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803714 | ||||||
| chr3:11803732
|
C | CA | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+4100dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803732 | ||||||
| chr3:11803774
|
T | A | 1 | a0002c0003t0004g0115 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.937+4059A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803774 | ||||||
| chr3:11803811
|
G | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(241): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.937+4022C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803811 | ||||||
| chr3:11804016
|
G | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(103): Show | 120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.937+3817C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804016 | ||||||
| chr3:11804442
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937+3391G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804442 | ||||||
| chr3:11804824
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937+3009G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804824 | ||||||
| chr3:11804858
|
T | C | 11 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(8): Show | 11 | HG02074.hp1 HG02129.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.937+2975A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804858 | ||||||
| chr3:11804868
|
A | AT | 9 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0345others(6): Show | 9 | HG02965.hp1 HG03098.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+2964dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804868 | ||||||
| chr3:11804868
|
AT | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+2964delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804868 | ||||||
| chr3:11804996
|
C | CT | 71 | a0001c0001t0001g0020a0001c0001t0001g0154a0001c0001t0001g0158others(68): Show | 73 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.937+2836dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | ||||||
| chr3:11804996
|
C | CTT | 7 | a0001c0001t0001g0189a0001c0001t0001g0209a0001c0001t0001g0329others(4): Show | 7 | HG02074.hp1 HG02698.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+2835_937+2836d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | ||||||
| chr3:11804996
|
CT | C | 10 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0219others(7): Show | 11 | HG00544.hp1 HG02071.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.937+2836delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | ||||||
| chr3:11804996
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0004g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.937+2826_937+2836d others(13): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | ||||||
| chr3:11804999
|
T | TTG | 8 | a0001c0001t0001g0231a0001c0001t0001g0282a0001c0001t0001g0316others(5): Show | 8 | HG01981.hp2 HG02257.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+2833_937+2834i others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804999 | ||||||
| chr3:11805000
|
T | TG | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(96): Show | 113 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.937+2832_937+2833i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805000 | ||||||
| chr3:11805001
|
T | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0301 | 2 | HG01256.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.937+2832A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805001 | ||||||
| chr3:11805002
|
T | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+2831A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805002 | ||||||
| chr3:11805003
|
T | G | 2 | a0001c0001t0001g0219a0001c0002t0002g0032 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+2830A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805003 | ||||||
| chr3:11805009
|
T | G | 3 | a0001c0001t0001g0231a0001c0001t0001g0282a0001c0001t0001g0331 | 3 | HG01981.hp2 HG06807.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.937+2824A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805009 | ||||||
| chr3:11805010
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+2823A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805010 | ||||||
| chr3:11805011
|
T | G | 1 | a0001c0001t0001g0301 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.937+2822A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805011 | ||||||
| chr3:11805012
|
T | G | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2821A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805012 | ||||||
| chr3:11805053
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(238): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.937+2780T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805053 | ||||||
| chr3:11805062
|
G | A | 1 | a0001c0002t0002g0103 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.937+2771C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805062 | ||||||
| chr3:11805124
|
C | T | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+2709G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805124 | ||||||
| chr3:11805150
|
T | C | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(2): Show | 5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+2683A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805150 | ||||||
| chr3:11805244
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(122): Show | 140 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.937+2589A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805244 | ||||||
| chr3:11805338
|
T | C | 1 | a0002c0003t0002g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.937+2495A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805338 | ||||||
| chr3:11805519
|
G | A | 1 | a0001c0002t0004g0086 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.937+2314C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805519 | ||||||
| chr3:11805564
|
G | A | 2 | a0001c0001t0001g0166a0001c0002t0002g0109 | 2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.937+2269C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805564 | ||||||
| chr3:11805607
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(109): Show | 126 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.937+2226G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805607 | ||||||
| chr3:11805656
|
T | C | 1 | a0002c0004t0003g0206 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.937+2177A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805656 | ||||||
| chr3:11805728
|
G | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2105C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805728 | ||||||
| chr3:11805730
|
T | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2103A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805730 | ||||||
| chr3:11805731
|
C | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2102G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805731 | ||||||
| chr3:11805747
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(104): Show | 121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.937+2086G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805747 | ||||||
| chr3:11805776
|
C | A | 1 | a0001c0001t0003g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.937+2057G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805776 | ||||||
| chr3:11805825
|
C | G | 133 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(130): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.937+2008G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805825 | ||||||
| chr3:11805930
|
T | C | 10 | a0001c0001t0001g0231a0001c0001t0001g0241a0001c0001t0001g0288others(7): Show | 10 | HG01256.hp1 HG01515.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.937+1903A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805930 | ||||||
| chr3:11806063
|
G | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+1770C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806063 | ||||||
| chr3:11806223
|
C | T | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.937+1610G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806223 | ||||||
| chr3:11806338
|
T | C | 1 | a0002c0004t0001g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.937+1495A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806338 | ||||||
| chr3:11806377
|
C | T | 1 | a0001c0002t0002g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.937+1456G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806377 | ||||||
| chr3:11806466
|
AAG | A | 5 | a0001c0001t0003g0242a0001c0002t0004g0118a0001c0002t0004g0119others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+1365_937+1366d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806466 | ||||||
| chr3:11806468
|
G | C | 1 | a0002c0004t0001g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.937+1365C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806468 | ||||||
| chr3:11806488
|
T | G | 2 | a0001c0002t0002g0029a0001c0002t0002g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.937+1345A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806488 | ||||||
| chr3:11806705
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0228a0001c0001t0001g0234others(2): Show | 6 | HG02074.hp2 HG03834.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.937+1128A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806705 | ||||||
| chr3:11807059
|
C | T | 4 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+774G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807059 | ||||||
| chr3:11807107
|
C | T | 1 | a0001c0002t0002g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.937+726G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807107 | ||||||
| chr3:11807110
|
C | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+723G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807110 | ||||||
| chr3:11807162
|
C | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.937+671G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807162 | ||||||
| chr3:11807338
|
C | A | 4 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+495G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807338 | ||||||
| chr3:11807366
|
T | C | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.937+467A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807366 | ||||||
| chr3:11807388
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.937+445G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807388 | ||||||
| chr3:11807400
|
G | C | 41 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0001t0003g0286others(38): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.937+433C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807400 | ||||||
| chr3:11807404
|
C | T | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+429G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807404 | ||||||
| chr3:11807449
|
CCACT | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+380_937+383del others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807449 | ||||||
| chr3:11807611
|
A | G | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+222T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807611 | ||||||
| chr3:11807910
|
C | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(5): Show | 9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.875-15G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11807910 | ||||||
| chr3:11808070
|
G | C | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.875-175C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808070 | ||||||
| chr3:11808075
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.875-180G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808075 | ||||||
| chr3:11808102
|
G | A | 5 | a0002c0003t0002g0057a0002c0003t0002g0067a0002c0003t0002g0069others(2): Show | 5 | HG03017.hp1 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.875-207C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808102 | ||||||
| chr3:11808141
|
C | T | 4 | a0001c0001t0001g0167a0001c0002t0002g0083a0001c0002t0002g0085others(1): Show | 4 | HG00735.hp2 HG01175.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.875-246G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808141 | ||||||
| chr3:11808270
|
C | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0316a0001c0001t0001g0317others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.875-375G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808270 | ||||||
| chr3:11808303
|
G | A | 9 | a0001c0001t0003g0011a0001c0001t0003g0016a0001c0001t0003g0171others(6): Show | 11 | HG00639.hp2 HG01069.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.875-408C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808303 | ||||||
| chr3:11808333
|
A | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.875-438T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808333 | ||||||
| chr3:11808436
|
T | C | 76 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0187others(73): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.875-541A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808436 | ||||||
| chr3:11808437
|
A | T | 76 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0187others(73): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.875-542T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808437 | ||||||
| chr3:11808438
|
AAC | A | 76 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0187others(73): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.875-545_875-544del others(2): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808438 | ||||||
| chr3:11808501
|
G | T | 80 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0187others(77): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.875-606C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808501 | ||||||
| chr3:11808518
|
C | T | 4 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038others(1): Show | 4 | HG02559.hp1 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.875-623G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808518 | ||||||
| chr3:11808530
|
C | T | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.875-635G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808530 | ||||||
| chr3:11808589
|
T | C | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-694A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808589 | ||||||
| chr3:11808749
|
T | C | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.874+768A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808749 | ||||||
| chr3:11808801
|
T | C | 3 | a0001c0001t0001g0161a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.874+716A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808801 | ||||||
| chr3:11808893
|
G | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(238): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.874+624C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808893 | ||||||
| chr3:11808918
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.874+599C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808918 | ||||||
| chr3:11809077
|
G | A | 8 | a0002c0003t0002g0039a0002c0004t0001g0225a0002c0004t0001g0230others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.874+440C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809077 | ||||||
| chr3:11809079
|
G | A | 35 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(32): Show | 35 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.874+438C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809079 | ||||||
| chr3:11809092
|
G | C | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.874+425C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809092 | ||||||
| chr3:11809513
|
G | A | 1 | a0002c0004t0001g0343 | 1 | HG02071.hp1 | splice_region_variant&intron_variant | LOW | c.874+4C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809513 | ||||||
| chr3:11809742
|
C | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0322a0001c0002t0002g0126 | 3 | HG02559.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.709-60G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11809742 | ||||||
| chr3:11810004
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.709-322A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810004 | ||||||
| chr3:11810023
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.709-341G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810023 | ||||||
| chr3:11810067
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.709-385A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810067 | ||||||
| chr3:11810258
|
A | G | 1 | a0003c0005t0003g0303 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.709-576T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810258 | ||||||
| chr3:11810285
|
C | T | 11 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(8): Show | 11 | HG02074.hp1 HG02129.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.709-603G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810285 | ||||||
| chr3:11810467
|
A | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(240): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.709-785T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810467 | ||||||
| chr3:11810641
|
G | A | 1 | a0001c0001t0003g0287 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.709-959C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810641 | ||||||
| chr3:11810644
|
G | C | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-962C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810644 | ||||||
| chr3:11810894
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.709-1212C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810894 | ||||||
| chr3:11810902
|
G | GA | 39 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0020others(36): Show | 43 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.709-1221dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810902 | ||||||
| chr3:11810902
|
GA | G | 41 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(38): Show | 41 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.709-1221delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810902 | ||||||
| chr3:11810914
|
G | C | 2 | a0001c0001t0001g0326a0001c0002t0002g0125 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.709-1232C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810914 | ||||||
| chr3:11811004
|
G | A | 45 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(42): Show | 45 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.709-1322C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811004 | ||||||
| chr3:11811023
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.709-1341C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811023 | ||||||
| chr3:11811236
|
T | C | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.709-1554A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811236 | ||||||
| chr3:11811415
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.709-1733T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811415 | ||||||
| chr3:11811512
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.709-1830T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811512 | ||||||
| chr3:11811567
|
T | C | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.709-1885A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811567 | ||||||
| chr3:11811596
|
G | A | 2 | a0002c0003t0002g0047a0002c0003t0002g0100 | 2 | NA18994.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.709-1914C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811596 | ||||||
| chr3:11811653
|
T | C | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.709-1971A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811653 | ||||||
| chr3:11811693
|
T | C | 129 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(126): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.709-2011A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811693 | ||||||
| chr3:11811788
|
G | A | 1 | a0002c0004t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.709-2106C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811788 | ||||||
| chr3:11811789
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(108): Show | 125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.709-2107T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811789 | ||||||
| chr3:11811962
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(234): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.709-2280G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811962 | ||||||
| chr3:11811989
|
G | A | 1 | a0001c0002t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.709-2307C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811989 | ||||||
| chr3:11811990
|
C | T | 1 | a0002c0003t0002g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.709-2308G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811990 | ||||||
| chr3:11812073
|
G | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-2391C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812073 | ||||||
| chr3:11812164
|
C | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.709-2482G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812164 | ||||||
| chr3:11812242
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.709-2560C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812242 | ||||||
| chr3:11812324
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(103): Show | 120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.709-2642G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812324 | ||||||
| chr3:11812372
|
C | T | 4 | a0001c0001t0001g0312a0001c0001t0001g0314a0001c0001t0001g0315others(1): Show | 4 | HG01884.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.709-2690G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812372 | ||||||
| chr3:11812423
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(108): Show | 125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.709-2741C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812423 | ||||||
| chr3:11812462
|
G | A | 1 | a0001c0002t0004g0088 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.709-2780C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812462 | ||||||
| chr3:11812617
|
C | T | 34 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(31): Show | 34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.709-2935G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812617 | ||||||
| chr3:11812900
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.709-3218C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812900 | ||||||
| chr3:11812909
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.709-3227C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812909 | ||||||
| chr3:11813029
|
T | C | 1 | a0002c0003t0004g0063 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.709-3347A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813029 | ||||||
| chr3:11813043
|
T | G | 11 | a0001c0001t0001g0243a0001c0001t0001g0327a0001c0001t0001g0344others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.709-3361A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813043 | ||||||
| chr3:11813146
|
C | T | 2 | a0001c0007t0001g0145a0001c0007t0001g0146 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.709-3464G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813146 | ||||||
| chr3:11813177
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.709-3495T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813177 | ||||||
| chr3:11813203
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.709-3521G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813203 | ||||||
| chr3:11813385
|
C | T | 1 | a0001c0002t0004g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.709-3703G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813385 | ||||||
| chr3:11813488
|
C | T | 3 | a0003c0005t0003g0253a0003c0005t0003g0254a0003c0005t0003g0303 | 3 | HG00323.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.708+3704G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813488 | ||||||
| chr3:11813729
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.708+3463C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813729 | ||||||
| chr3:11813828
|
A | ATG | 59 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0001g0176others(56): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.708+3362_708+3363d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
A | ATGTG | 30 | a0001c0001t0001g0161a0001c0001t0001g0169a0001c0001t0001g0187others(27): Show | 32 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.708+3360_708+3363d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
A | ATGTGTG | 15 | a0001c0001t0001g0163a0001c0001t0003g0021a0001c0001t0003g0172others(12): Show | 16 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.708+3358_708+3363d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
A | ATGTGTGT others(1): Show |
30 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0191others(27): Show | 31 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.708+3356_708+3363d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
A | ATGTGTGT others(3): Show |
5 | a0001c0002t0002g0104a0002c0003t0002g0058a0002c0003t0002g0059others(2): Show | 5 | HG02071.hp1 HG03017.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+3354_708+3363d others(12): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
A | ATGTGTGT others(5): Show |
10 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG01891.hp2 HG01978.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.708+3352_708+3363d others(14): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
A | G | 2 | a0003c0005t0003g0254a0003c0005t0003g0303 | 2 | HG00323.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.708+3364T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813828
|
ATG | A | 6 | a0001c0001t0001g0293a0001c0001t0001g0302a0001c0002t0002g0045others(3): Show | 6 | HG03491.hp2 NA18991.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+3362_708+3363d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | ||||||
| chr3:11813850
|
GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+3334_708+3341d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813850 | ||||||
| chr3:11813852
|
GTGTGTA | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032others(1): Show | 4 | HG03098.hp2 HG03471.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+3334_708+3339d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813852 | ||||||
| chr3:11813858
|
A | G | 5 | a0001c0001t0001g0326a0001c0001t0003g0177a0001c0002t0002g0037others(2): Show | 5 | HG00733.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+3334T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813858 | ||||||
| chr3:11813862
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.708+3330T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813862 | ||||||
| chr3:11813866
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.708+3326T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813866 | ||||||
| chr3:11813866
|
ATATATAT others(1): Show |
A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0334 | 3 | HG01070.hp1 HG01071.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.708+3318_708+3325d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813866 | ||||||
| chr3:11813868
|
A | G | 3 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0125 | 3 | HG03195.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.708+3324T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813868 | ||||||
| chr3:11813870
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.708+3322T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813870 | ||||||
| chr3:11813870
|
ATATG | A | 3 | a0001c0002t0002g0037a0001c0002t0002g0038a0001c0002t0002g0125 | 3 | HG03195.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.708+3318_708+3321d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813870 | ||||||
| chr3:11813888
|
A | ATGTGTAT others(13): Show |
1 | a0001c0001t0001g0329 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.708+3284_708+3303d others(22): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813888 | ||||||
| chr3:11813904
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0186 | 2 | HG00733.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.708+3288T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813904 | ||||||
| chr3:11813904
|
ATATG | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+3284_708+3287d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813904 | ||||||
| chr3:11813920
|
GTA | G | 5 | a0001c0001t0001g0316a0001c0001t0001g0336a0001c0002t0002g0008others(2): Show | 6 | HG00438.hp1 HG00673.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.708+3270_708+3271d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813920 | ||||||
| chr3:11813924
|
ATATG | A | 7 | a0001c0001t0001g0213a0002c0003t0002g0047a0002c0003t0002g0058others(4): Show | 7 | HG02165.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+3264_708+3267d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813924 | ||||||
| chr3:11813991
|
T | TAC | 78 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(75): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.708+3199_708+3200d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | ||||||
| chr3:11813991
|
T | TACAC | 16 | a0001c0001t0001g0161a0001c0002t0002g0038a0001c0002t0004g0049others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.708+3197_708+3200d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | ||||||
| chr3:11813991
|
TAC | T | 32 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(29): Show | 34 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.708+3199_708+3200d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | ||||||
| chr3:11813991
|
TACAC | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0191a0001c0002t0002g0032others(1): Show | 5 | HG02109.hp2 HG02280.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+3197_708+3200d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | ||||||
| chr3:11813991
|
TACACAC | T | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0322others(2): Show | 5 | HG02257.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+3195_708+3200d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | ||||||
| chr3:11814302
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.708+2890G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814302 | ||||||
| chr3:11814494
|
G | A | 8 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0316others(5): Show | 8 | HG02257.hp2 HG03098.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.708+2698C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814494 | ||||||
| chr3:11814524
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.708+2668C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814524 | ||||||
| chr3:11814688
|
C | T | 2 | a0001c0001t0001g0326a0001c0002t0002g0125 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.708+2504G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814688 | ||||||
| chr3:11814689
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.708+2503C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814689 | ||||||
| chr3:11814782
|
G | A | 1 | a0001c0001t0001g0014 | 2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.708+2410C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814782 | ||||||
| chr3:11814806
|
C | T | 1 | a0002c0004t0002g0140 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.708+2386G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814806 | ||||||
| chr3:11814955
|
C | T | 2 | a0001c0007t0001g0145a0001c0007t0001g0146 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.708+2237G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814955 | ||||||
| chr3:11815045
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(112): Show | 130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+2147T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815045 | ||||||
| chr3:11815096
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(244): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.708+2096T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815096 | ||||||
| chr3:11815106
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(112): Show | 130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+2086A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815106 | ||||||
| chr3:11815197
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(112): Show | 130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+1995T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815197 | ||||||
| chr3:11815247
|
C | T | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(2): Show | 5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+1945G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815247 | ||||||
| chr3:11815248
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.708+1944C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815248 | ||||||
| chr3:11815673
|
T | G | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.708+1519A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815673 | ||||||
| chr3:11815728
|
T | TA | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+1463dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815728 | ||||||
| chr3:11815820
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.708+1372T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815820 | ||||||
| chr3:11815899
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.708+1293C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815899 | ||||||
| chr3:11815962
|
G | A | 6 | a0002c0003t0002g0057a0002c0003t0002g0065a0002c0003t0002g0067others(3): Show | 6 | HG03017.hp1 HG03017.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+1230C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815962 | ||||||
| chr3:11815986
|
C | A | 1 | a0001c0002t0002g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.708+1206G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815986 | ||||||
| chr3:11816137
|
C | T | 6 | a0001c0001t0001g0239a0001c0002t0002g0082a0001c0002t0002g0121others(3): Show | 6 | HG00280.hp1 HG01243.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+1055G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816137 | ||||||
| chr3:11816154
|
C | T | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(2): Show | 5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+1038G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816154 | ||||||
| chr3:11816217
|
G | GA | 39 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0234others(36): Show | 40 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.708+974dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816217 | ||||||
| chr3:11816299
|
G | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+893C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816299 | ||||||
| chr3:11816344
|
TAAAC | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(82): Show | 98 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.708+844_708+847del others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816344 | ||||||
| chr3:11816356
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.708+836C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816356 | ||||||
| chr3:11816384
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(112): Show | 130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+808A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816384 | ||||||
| chr3:11816390
|
C | T | 2 | a0002c0004t0001g0309a0002c0004t0001g0310 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.708+802G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816390 | ||||||
| chr3:11816398
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.708+794A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816398 | ||||||
| chr3:11816521
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.708+671A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816521 | ||||||
| chr3:11816678
|
A | C | 3 | a0001c0002t0002g0004a0001c0002t0002g0023a0001c0002t0002g0025 | 4 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+514T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816678 | ||||||
| chr3:11816750
|
G | GC | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(2): Show | 5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+441_708+442ins others(1): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816750 | ||||||
| chr3:11816775
|
A | C | 1 | a0001c0002t0004g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.708+417T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816775 | ||||||
| chr3:11816791
|
AC | A | 6 | a0001c0001t0001g0223a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+400delG | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816791 | ||||||
| chr3:11816792
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(103): Show | 120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.708+400G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816792 | ||||||
| chr3:11816851
|
G | A | 1 | a0002c0004t0003g0010 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.708+341C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816851 | ||||||
| chr3:11816926
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(111): Show | 129 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.708+266A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816926 | ||||||
| chr3:11817414
|
T | C | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.563-77A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817414 | ||||||
| chr3:11817731
|
T | C | 1 | a0002c0003t0002g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.563-394A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817731 | ||||||
| chr3:11817857
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(5): Show | 9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.563-520T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817857 | ||||||
| chr3:11817871
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.563-534A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817871 | ||||||
| chr3:11817956
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.563-619G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817956 | ||||||
| chr3:11817971
|
G | A | 1 | a0002c0003t0002g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.563-634C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817971 | ||||||
| chr3:11817990
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.563-653G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817990 | ||||||
| chr3:11818179
|
G | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(241): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.563-842C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818179 | ||||||
| chr3:11818241
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-904T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818241 | ||||||
| chr3:11818242
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-905T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818242 | ||||||
| chr3:11818248
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-911A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818248 | ||||||
| chr3:11818311
|
G | A | 3 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0181 | 3 | HG00099.hp1 HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.563-974C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818311 | ||||||
| chr3:11818322
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-985A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818322 | ||||||
| chr3:11818360
|
T | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG02148.hp1 HG02293.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-1023A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818360 | ||||||
| chr3:11818415
|
C | G | 1 | a0002c0003t0004g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.563-1078G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818415 | ||||||
| chr3:11818635
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.563-1298T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818635 | ||||||
| chr3:11818663
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.563-1326C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818663 | ||||||
| chr3:11818703
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(117): Show | 135 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.563-1366A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818703 | ||||||
| chr3:11818746
|
A | C | 2 | a0002c0003t0002g0027a0002c0003t0002g0028 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.563-1409T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818746 | ||||||
| chr3:11818746
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(117): Show | 135 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.563-1409T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818746 | ||||||
| chr3:11818794
|
G | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.563-1457C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818794 | ||||||
| chr3:11818797
|
G | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.563-1460C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818797 | ||||||
| chr3:11818798
|
G | T | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.563-1461C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818798 | ||||||
| chr3:11818800
|
C | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.563-1463G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818800 | ||||||
| chr3:11818801
|
C | G | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.563-1464G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818801 | ||||||
| chr3:11818833
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.563-1496C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818833 | ||||||
| chr3:11818893
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(117): Show | 135 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.563-1556T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818893 | ||||||
| chr3:11818897
|
C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(115): Show | 133 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.563-1561dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818897 | ||||||
| chr3:11819023
|
A | G | 1 | a0006c0011t0004g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.563-1686T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819023 | ||||||
| chr3:11819033
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.563-1696A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819033 | ||||||
| chr3:11819050
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.563-1713T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819050 | ||||||
| chr3:11819067
|
T | G | 1 | a0001c0001t0001g0299 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.563-1730A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819067 | ||||||
| chr3:11819141
|
A | G | 5 | a0002c0003t0002g0066a0002c0003t0002g0091a0002c0003t0004g0056others(2): Show | 5 | HG01243.hp2 HG01978.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-1804T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819141 | ||||||
| chr3:11819183
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(111): Show | 129 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.563-1846G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819183 | ||||||
| chr3:11819208
|
A | G | 1 | a0002c0004t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.563-1871T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819208 | ||||||
| chr3:11819290
|
T | G | 2 | a0001c0001t0003g0286a0001c0001t0003g0287 | 2 | NA18612.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.563-1953A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819290 | ||||||
| chr3:11819296
|
G | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-1959C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819296 | ||||||
| chr3:11819384
|
A | T | 1 | a0001c0001t0001g0235 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.563-2047T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819384 | ||||||
| chr3:11819461
|
T | C | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.563-2124A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819461 | ||||||
| chr3:11819466
|
C | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.563-2129G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819466 | ||||||
| chr3:11819693
|
G | A | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.563-2356C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819693 | ||||||
| chr3:11819712
|
T | C | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.563-2375A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819712 | ||||||
| chr3:11819986
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.563-2649G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819986 | ||||||
| chr3:11820160
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.563-2823A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820160 | ||||||
| chr3:11820176
|
C | T | 2 | a0003c0005t0003g0252a0006c0011t0004g0070 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.563-2839G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820176 | ||||||
| chr3:11820241
|
G | A | 1 | a0001c0002t0002g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.563-2904C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820241 | ||||||
| chr3:11820386
|
T | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(101): Show | 118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.563-3049A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820386 | ||||||
| chr3:11820424
|
A | C | 3 | a0001c0001t0001g0239a0001c0002t0002g0121a0001c0002t0002g0122 | 3 | HG02683.hp2 HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.563-3087T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820424 | ||||||
| chr3:11820492
|
G | A | 34 | a0001c0001t0001g0162a0001c0001t0001g0213a0001c0001t0001g0249others(31): Show | 34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.563-3155C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820492 | ||||||
| chr3:11820558
|
A | G | 6 | a0001c0002t0004g0049a0001c0002t0004g0086a0001c0002t0004g0087others(3): Show | 6 | HG01358.hp1 HG01975.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-3221T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820558 | ||||||
| chr3:11820947
|
T | C | 1 | a0001c0002t0004g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.563-3610A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820947 | ||||||
| chr3:11820969
|
C | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.563-3632G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820969 | ||||||
| chr3:11821242
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.563-3905A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821242 | ||||||
| chr3:11821365
|
G | T | 1 | a0002c0003t0004g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.563-4028C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821365 | ||||||
| chr3:11821499
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.563-4162T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821499 | ||||||
| chr3:11821511
|
T | C | 1 | a0002c0004t0001g0256 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.563-4174A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821511 | ||||||
| chr3:11821589
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.563-4252C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821589 | ||||||
| chr3:11821666
|
G | A | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(2): Show | 5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-4329C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821666 | ||||||
| chr3:11821732
|
T | C | 1 | a0003c0005t0003g0254 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.563-4395A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821732 | ||||||
| chr3:11821891
|
T | C | 2 | a0001c0001t0001g0326a0001c0002t0002g0125 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.563-4554A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821891 | ||||||
| chr3:11821952
|
G | A | 2 | a0001c0001t0001g0326a0001c0002t0002g0125 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.563-4615C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821952 | ||||||
| chr3:11822006
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(109): Show | 126 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.563-4669A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822006 | ||||||
| chr3:11822461
|
A | G | 3 | a0002c0003t0002g0027a0002c0003t0002g0028a0002c0004t0002g0140 | 3 | HG02622.hp2 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.563-5124T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822461 | ||||||
| chr3:11822559
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.563-5222C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822559 | ||||||
| chr3:11822758
|
T | C | 1 | a0001c0002t0002g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.563-5421A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822758 | ||||||
| chr3:11822846
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(101): Show | 118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.563-5509C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822846 | ||||||
| chr3:11822953
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(242): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.563-5616C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822953 | ||||||
| chr3:11823038
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.563-5701A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823038 | ||||||
| chr3:11823127
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(105): Show | 122 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.563-5790G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823127 | ||||||
| chr3:11823254
|
G | GT | 16 | a0001c0001t0001g0020a0001c0001t0001g0161a0001c0001t0001g0198others(13): Show | 17 | HG00738.hp2 HG00741.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.563-5918dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823254 | ||||||
| chr3:11823256
|
T | TG | 5 | a0001c0001t0001g0200a0001c0001t0001g0217a0001c0001t0001g0278others(2): Show | 5 | HG00621.hp1 HG03516.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-5920_563-5919i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823256 | ||||||
| chr3:11823257
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(87): Show | 103 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.563-5920A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823257 | ||||||
| chr3:11823260
|
T | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0199a0001c0001t0001g0218others(16): Show | 20 | HG00621.hp2 HG02027.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.563-5923A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823260 | ||||||
| chr3:11823406
|
C | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-6069G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823406 | ||||||
| chr3:11823448
|
G | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.563-6111C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823448 | ||||||
| chr3:11823660
|
C | CT | 102 | a0001c0001t0001g0012a0001c0001t0001g0161a0001c0001t0001g0163others(99): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.562+6053dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823660 | ||||||
| chr3:11823660
|
C | CTT | 9 | a0001c0001t0001g0169a0001c0001t0001g0218a0001c0001t0001g0219others(6): Show | 9 | HG01361.hp2 HG01433.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.562+6052_562+6053d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823660 | ||||||
| chr3:11823678
|
T | G | 2 | a0002c0003t0002g0027a0002c0003t0002g0028 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.562+6036A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823678 | ||||||
| chr3:11823701
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.562+6013G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823701 | ||||||
| chr3:11823795
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.562+5919C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823795 | ||||||
| chr3:11823825
|
C | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0314 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.562+5889G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823825 | ||||||
| chr3:11823829
|
C | CT | 161 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(158): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.562+5884dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823829 | ||||||
| chr3:11823829
|
C | CTT | 8 | a0001c0001t0001g0218a0001c0001t0001g0292a0001c0001t0001g0338others(5): Show | 8 | HG01109.hp2 HG01361.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.562+5883_562+5884d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823829 | ||||||
| chr3:11823829
|
C | CTTT | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(95): Show | 112 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.562+5882_562+5884d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823829 | ||||||
| chr3:11823862
|
G | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.562+5852C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823862 | ||||||
| chr3:11824213
|
C | CA | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+5500dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824213 | ||||||
| chr3:11824240
|
G | C | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(1): Show | 4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+5474C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824240 | ||||||
| chr3:11824357
|
A | AT | 150 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0163others(147): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.562+5356dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824357 | ||||||
| chr3:11824357
|
A | ATT | 10 | a0001c0001t0001g0161a0001c0001t0003g0284a0001c0002t0002g0101others(7): Show | 10 | HG00544.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.562+5355_562+5356d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824357 | ||||||
| chr3:11824357
|
AT | A | 8 | a0001c0001t0001g0222a0001c0001t0001g0278a0001c0001t0001g0297others(5): Show | 9 | HG01070.hp1 HG01106.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.562+5356delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824357 | ||||||
| chr3:11824481
|
A | G | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+5233T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824481 | ||||||
| chr3:11824785
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.562+4929T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824785 | ||||||
| chr3:11824793
|
T | G | 3 | a0001c0002t0002g0004a0001c0002t0002g0023a0001c0002t0002g0025 | 4 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+4921A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824793 | ||||||
| chr3:11824807
|
C | T | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+4907G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824807 | ||||||
| chr3:11824919
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+4795T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824919 | ||||||
| chr3:11825083
|
C | G | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+4631G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825083 | ||||||
| chr3:11825092
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.562+4622G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825092 | ||||||
| chr3:11825141
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.562+4573T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825141 | ||||||
| chr3:11825279
|
T | C | 1 | a0003c0005t0003g0304 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.562+4435A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825279 | ||||||
| chr3:11825320
|
G | A | 2 | a0001c0007t0001g0145a0001c0007t0001g0146 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.562+4394C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825320 | ||||||
| chr3:11825345
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(104): Show | 121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.562+4369G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825345 | ||||||
| chr3:11825362
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.562+4352G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825362 | ||||||
| chr3:11825560
|
A | C | 3 | a0001c0001t0001g0217a0001c0002t0002g0134a0001c0002t0002g0135 | 3 | HG02615.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.562+4154T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825560 | ||||||
| chr3:11825705
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+4009C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825705 | ||||||
| chr3:11826027
|
C | T | 1 | a0004c0006t0004g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.562+3687G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826027 | ||||||
| chr3:11826251
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.562+3463G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826251 | ||||||
| chr3:11826260
|
G | A | 1 | a0001c0001t0003g0251 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.562+3454C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826260 | ||||||
| chr3:11826304
|
C | T | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.562+3410G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826304 | ||||||
| chr3:11826354
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(100): Show | 117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.562+3360C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826354 | ||||||
| chr3:11826397
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(99): Show | 116 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.562+3317G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826397 | ||||||
| chr3:11826433
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+3281C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826433 | ||||||
| chr3:11826530
|
C | CA | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(181): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.562+3183dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826530 | ||||||
| chr3:11826530
|
C | CAA | 58 | a0001c0001t0001g0162a0001c0001t0001g0176a0001c0001t0001g0213others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.562+3182_562+3183d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826530 | ||||||
| chr3:11826574
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.562+3140C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826574 | ||||||
| chr3:11826576
|
A | T | 1 | a0001c0002t0004g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.562+3138T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826576 | ||||||
| chr3:11826712
|
AG | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.562+3001delC | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826712 | ||||||
| chr3:11827011
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.562+2703A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827011 | ||||||
| chr3:11827309
|
CT | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(239): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.562+2404delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827309 | ||||||
| chr3:11827335
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.562+2379T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827335 | ||||||
| chr3:11827556
|
G | T | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+2158C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827556 | ||||||
| chr3:11827636
|
G | GA | 16 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(13): Show | 17 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.562+2077dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827636 | ||||||
| chr3:11827636
|
GA | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(105): Show | 121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.562+2077delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827636 | ||||||
| chr3:11827667
|
G | A | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.562+2047C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827667 | ||||||
| chr3:11827691
|
A | G | 2 | a0001c0001t0001g0014a0002c0003t0002g0054 | 3 | NA18945.hp1 NA18966.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.562+2023T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827691 | ||||||
| chr3:11827908
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(101): Show | 118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.562+1806C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827908 | ||||||
| chr3:11827913
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+1801C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827913 | ||||||
| chr3:11828058
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+1656C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828058 | ||||||
| chr3:11828075
|
C | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+1639G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828075 | ||||||
| chr3:11828108
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(97): Show | 113 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.562+1606G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828108 | ||||||
| chr3:11828177
|
C | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.562+1537G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828177 | ||||||
| chr3:11828188
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+1526C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828188 | ||||||
| chr3:11828216
|
A | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.562+1498T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828216 | ||||||
| chr3:11828343
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.562+1371A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828343 | ||||||
| chr3:11828483
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+1231G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828483 | ||||||
| chr3:11828640
|
A | G | 2 | a0001c0002t0002g0029a0001c0002t0002g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.562+1074T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828640 | ||||||
| chr3:11828801
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.562+913T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828801 | ||||||
| chr3:11828849
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+865C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828849 | ||||||
| chr3:11829023
|
T | C | 5 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0336others(2): Show | 5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+691A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829023 | ||||||
| chr3:11829312
|
G | A | 38 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0187others(35): Show | 41 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.562+402C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829312 | ||||||
| chr3:11829332
|
A | G | 2 | a0001c0001t0001g0326a0001c0002t0002g0125 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.562+382T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829332 | ||||||
| chr3:11829447
|
T | C | 1 | a0001c0001t0003g0021 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.562+267A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829447 | ||||||
| chr3:11829541
|
G | A | 1 | a0002c0004t0001g0262 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.562+173C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829541 | ||||||
| chr3:11829908
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.412-44C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11829908 | ||||||
| chr3:11829965
|
T | C | 1 | a0001c0002t0002g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.412-101A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11829965 | ||||||
| chr3:11830212
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.412-348G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830212 | ||||||
| chr3:11830234
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.412-370A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830234 | ||||||
| chr3:11830424
|
T | C | 117 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(114): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.412-560A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830424 | ||||||
| chr3:11830510
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412-646G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830510 | ||||||
| chr3:11830813
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-949C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830813 | ||||||
| chr3:11830881
|
C | CA | 96 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0020others(93): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.412-1018dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830881 | ||||||
| chr3:11830881
|
C | CAA | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(190): Show | 211 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.412-1019_412-1018d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830881 | ||||||
| chr3:11830881
|
C | CAAA | 8 | a0001c0001t0001g0281a0001c0001t0001g0293a0001c0001t0001g0321others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-1020_412-1018d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830881 | ||||||
| chr3:11830908
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(244): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.412-1044A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830908 | ||||||
| chr3:11831162
|
G | A | 2 | a0002c0003t0002g0027a0002c0003t0002g0028 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.412-1298C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831162 | ||||||
| chr3:11831257
|
C | T | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.412-1393G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831257 | ||||||
| chr3:11831302
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.412-1438A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831302 | ||||||
| chr3:11831428
|
C | T | 3 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0002t0002g0081 | 3 | NA19006.hp1 NA19006.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.412-1564G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831428 | ||||||
| chr3:11831511
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.412-1647A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831511 | ||||||
| chr3:11831644
|
C | A | 5 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180others(2): Show | 5 | HG01192.hp1 HG01257.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1780G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831644 | ||||||
| chr3:11831906
|
T | C | 1 | a0002c0003t0002g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.412-2042A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831906 | ||||||
| chr3:11831940
|
G | A | 1 | a0002c0003t0002g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.412-2076C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831940 | ||||||
| chr3:11832280
|
AAAC | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.412-2419_412-2417d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832280 | ||||||
| chr3:11832281
|
AAC | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(219): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.412-2419_412-2418d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832281 | ||||||
| chr3:11832282
|
AC | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(13): Show | 17 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.412-2419delG | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832282 | ||||||
| chr3:11832385
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0191a0001c0001t0001g0345others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-2521G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832385 | ||||||
| chr3:11832717
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-2853C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832717 | ||||||
| chr3:11833103
|
T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0191others(6): Show | 10 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.412-3239A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833103 | ||||||
| chr3:11833105
|
G | C | 1 | a0001c0002t0002g0124 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.412-3241C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833105 | ||||||
| chr3:11833138
|
A | G | 1 | a0001c0002t0002g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.412-3274T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833138 | ||||||
| chr3:11833157
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.412-3293T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833157 | ||||||
| chr3:11833211
|
C | A | 1 | a0002c0003t0002g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.412-3347G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833211 | ||||||
| chr3:11833214
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.412-3350G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833214 | ||||||
| chr3:11833221
|
A | C | 1 | a0002c0003t0004g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.412-3357T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833221 | ||||||
| chr3:11833256
|
G | A | 1 | a0001c0002t0002g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.412-3392C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833256 | ||||||
| chr3:11833288
|
G | A | 38 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0187others(35): Show | 41 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.412-3424C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833288 | ||||||
| chr3:11833350
|
C | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0319others(1): Show | 4 | HG02622.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-3486G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833350 | ||||||
| chr3:11833404
|
A | G | 2 | a0001c0002t0002g0116a0001c0002t0002g0133 | 2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.412-3540T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833404 | ||||||
| chr3:11833465
|
C | T | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.412-3601G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833465 | ||||||
| chr3:11833797
|
T | C | 24 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0239others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.412-3933A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833797 | ||||||
| chr3:11833860
|
T | C | 2 | a0001c0001t0001g0166a0001c0002t0002g0109 | 2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.412-3996A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833860 | ||||||
| chr3:11833879
|
A | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-4015T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833879 | ||||||
| chr3:11833966
|
G | C | 1 | a0001c0002t0002g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.412-4102C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833966 | ||||||
| chr3:11833970
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(244): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.412-4106T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833970 | ||||||
| chr3:11833980
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.412-4116A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833980 | ||||||
| chr3:11834167
|
C | A | 1 | a0003c0005t0003g0303 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.412-4303G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834167 | ||||||
| chr3:11834345
|
A | T | 11 | a0001c0001t0001g0243a0001c0001t0001g0327a0001c0001t0001g0344others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.412-4481T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834345 | ||||||
| chr3:11834369
|
C | T | 8 | a0001c0002t0002g0116a0001c0002t0002g0117a0001c0002t0002g0127others(5): Show | 9 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-4505G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834369 | ||||||
| chr3:11834495
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(101): Show | 118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.412-4631T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834495 | ||||||
| chr3:11834718
|
G | A | 3 | a0002c0003t0002g0039a0002c0004t0001g0324a0002c0004t0002g0140 | 3 | HG01884.hp1 HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.411+4504C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834718 | ||||||
| chr3:11834833
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(241): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.411+4389G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834833 | ||||||
| chr3:11834842
|
T | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.411+4380A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834842 | ||||||
| chr3:11834843
|
C | T | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.411+4379G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834843 | ||||||
| chr3:11834847
|
T | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.411+4375A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834847 | ||||||
| chr3:11834908
|
G | A | 5 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+4314C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834908 | ||||||
| chr3:11835038
|
A | C | 1 | a0002c0003t0002g0100 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.411+4184T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835038 | ||||||
| chr3:11835116
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+4106C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835116 | ||||||
| chr3:11835128
|
A | G | 1 | a0002c0003t0002g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.411+4094T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835128 | ||||||
| chr3:11835248
|
T | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.411+3974A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835248 | ||||||
| chr3:11835399
|
T | C | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.411+3823A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835399 | ||||||
| chr3:11835615
|
C | A | 1 | a0001c0001t0003g0181 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.411+3607G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835615 | ||||||
| chr3:11835990
|
C | CT | 117 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0163others(114): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.411+3231dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835990 | ||||||
| chr3:11835990
|
C | CTT | 12 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(9): Show | 12 | HG02080.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.411+3230_411+3231d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835990 | ||||||
| chr3:11836020
|
C | T | 1 | a0001c0002t0002g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.411+3202G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836020 | ||||||
| chr3:11836045
|
G | A | 3 | a0001c0001t0001g0288a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG03516.hp1 NA18959.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.411+3177C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836045 | ||||||
| chr3:11836126
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+3096C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836126 | ||||||
| chr3:11836142
|
C | T | 123 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0001g0156others(120): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.411+3080G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836142 | ||||||
| chr3:11836172
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411+3050C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836172 | ||||||
| chr3:11836260
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.411+2962C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836260 | ||||||
| chr3:11836427
|
C | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0214a0001c0001t0001g0221others(1): Show | 5 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+2795G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836427 | ||||||
| chr3:11836620
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.411+2602G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836620 | ||||||
| chr3:11836711
|
G | A | 116 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(113): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.411+2511C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836711 | ||||||
| chr3:11836711
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0214a0001c0001t0001g0221 | 4 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2511C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836711 | ||||||
| chr3:11836753
|
A | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(114): Show | 131 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.411+2469T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836753 | ||||||
| chr3:11837006
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+2216A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837006 | ||||||
| chr3:11837208
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+2014A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837208 | ||||||
| chr3:11837214
|
C | T | 115 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(112): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.411+2008G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837214 | ||||||
| chr3:11837258
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(244): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.411+1964A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837258 | ||||||
| chr3:11837330
|
T | C | 1 | a0001c0001t0003g0255 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.411+1892A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837330 | ||||||
| chr3:11837405
|
G | GA | 9 | a0001c0001t0001g0019a0001c0001t0001g0199a0001c0001t0001g0289others(6): Show | 10 | HG00438.hp1 HG00621.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+1816dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837405 | ||||||
| chr3:11837521
|
G | C | 2 | a0002c0003t0002g0073a0002c0003t0002g0074 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.411+1701C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837521 | ||||||
| chr3:11837615
|
A | C | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+1607T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837615 | ||||||
| chr3:11837638
|
T | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+1584A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837638 | ||||||
| chr3:11837730
|
C | T | 3 | a0001c0002t0002g0032a0003c0005t0003g0201a0003c0005t0003g0244 | 3 | HG02080.hp2 NA18955.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+1492G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837730 | ||||||
| chr3:11837760
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.411+1462G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837760 | ||||||
| chr3:11837861
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411+1361A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837861 | ||||||
| chr3:11837875
|
G | T | 1 | a0001c0001t0001g0341 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.411+1347C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837875 | ||||||
| chr3:11837968
|
C | T | 1 | a0002c0003t0004g0053 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.411+1254G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837968 | ||||||
| chr3:11838003
|
T | C | 1 | a0001c0001t0001g0341 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.411+1219A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838003 | ||||||
| chr3:11838225
|
T | C | 1 | a0002c0004t0001g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.411+997A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838225 | ||||||
| chr3:11838251
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18954.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.411+971C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838251 | ||||||
| chr3:11838276
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0002t0002g0032 | 3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+946C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838276 | ||||||
| chr3:11838289
|
A | G | 1 | a0001c0002t0002g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.411+933T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838289 | ||||||
| chr3:11838349
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0214a0001c0001t0001g0221others(1): Show | 5 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+873C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838349 | ||||||
| chr3:11838373
|
G | A | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.411+849C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838373 | ||||||
| chr3:11838422
|
T | C | 1 | a0002c0003t0004g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.411+800A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838422 | ||||||
| chr3:11838461
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411+761C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838461 | ||||||
| chr3:11838528
|
T | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.411+694A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838528 | ||||||
| chr3:11838641
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.411+581G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838641 | ||||||
| chr3:11838647
|
T | C | 6 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0319others(3): Show | 6 | HG02622.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+575A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838647 | ||||||
| chr3:11838702
|
C | CT | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(101): Show | 118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.411+519dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838702 | ||||||
| chr3:11839342
|
C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(184): Show | 203 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.319-28G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11839342 | ||||||
| chr3:11839557
|
A | G | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-243T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11839557 | ||||||
| chr3:11839671
|
A | G | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.319-357T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11839671 | ||||||
| chr3:11840027
|
C | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.319-713G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840027 | ||||||
| chr3:11840190
|
C | A | 7 | a0001c0001t0001g0217a0001c0001t0001g0344a0001c0002t0002g0041others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-876G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840190 | ||||||
| chr3:11840236
|
A | AT | 147 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0167others(144): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.319-923dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840236 | ||||||
| chr3:11840236
|
AT | A | 7 | a0001c0001t0001g0215a0001c0002t0002g0101a0001c0002t0002g0102others(4): Show | 7 | HG00323.hp2 HG01891.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-923delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840236 | ||||||
| chr3:11840319
|
G | A | 8 | a0001c0001t0001g0217a0001c0001t0001g0344a0001c0002t0002g0040others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.319-1005C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840319 | ||||||
| chr3:11840380
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.319-1066C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840380 | ||||||
| chr3:11840391
|
T | A | 1 | a0001c0001t0001g0323 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319-1077A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840391 | ||||||
| chr3:11840530
|
C | T | 1 | a0001c0001t0001g0014 | 2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.319-1216G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840530 | ||||||
| chr3:11840646
|
T | A | 2 | a0001c0002t0002g0037a0001c0002t0002g0038 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.319-1332A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840646 | ||||||
| chr3:11840806
|
G | C | 2 | a0001c0001t0001g0306a0003c0005t0003g0304 | 2 | HG01993.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.319-1492C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840806 | ||||||
| chr3:11840822
|
C | G | 1 | a0002c0004t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.319-1508G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840822 | ||||||
| chr3:11841067
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.319-1753T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841067 | ||||||
| chr3:11841073
|
A | AT | 19 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(16): Show | 19 | HG00741.hp2 HG01175.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.319-1760dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
A | ATT | 36 | a0001c0001t0001g0002a0001c0001t0001g0153a0001c0001t0001g0154others(33): Show | 39 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.319-1761_319-1760d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
A | ATTT | 10 | a0001c0001t0001g0013a0001c0001t0001g0152a0001c0001t0001g0161others(7): Show | 11 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-1762_319-1760d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
AT | A | 12 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0322others(9): Show | 13 | HG01993.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1760delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATT | A | 7 | a0001c0002t0002g0045a0001c0002t0002g0108a0001c0002t0002g0109others(4): Show | 7 | HG01358.hp1 HG04184.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-1761_319-1760d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATTT | A | 87 | a0001c0001t0001g0345a0001c0002t0002g0007a0001c0002t0002g0008others(84): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.319-1762_319-1760d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATTTT | A | 12 | a0001c0001t0001g0166a0001c0002t0002g0099a0001c0002t0002g0127others(9): Show | 13 | HG00642.hp1 HG00735.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1763_319-1760d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATTTTT | A | 29 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0176others(26): Show | 30 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.319-1764_319-1760d others(7): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATTTTTT | A | 20 | a0001c0001t0001g0187a0001c0001t0001g0325a0001c0001t0001g0326others(17): Show | 20 | HG00423.hp2 HG01099.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.319-1765_319-1760d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATTTTTTT | A | 6 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(3): Show | 6 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-1766_319-1760d others(9): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841073
|
ATTTTTTT others(3): Show |
A | 10 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-1769_319-1760d others(12): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | ||||||
| chr3:11841170
|
C | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.319-1856G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841170 | ||||||
| chr3:11841240
|
A | G | 105 | a0001c0001t0001g0345a0001c0002t0002g0007a0001c0002t0002g0008others(102): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.319-1926T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841240 | ||||||
| chr3:11841471
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG00423.hp1 HG00673.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.319-2157G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841471 | ||||||
| chr3:11841632
|
G | A | 2 | a0001c0002t0002g0033a0001c0002t0002g0034 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.319-2318C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841632 | ||||||
| chr3:11841748
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0003g0021 | 3 | HG02965.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.318+2281G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841748 | ||||||
| chr3:11841754
|
T | C | 3 | a0001c0002t0002g0134a0001c0002t0002g0135a0001c0002t0002g0136 | 3 | HG02615.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.318+2275A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841754 | ||||||
| chr3:11841795
|
G | T | 3 | a0001c0002t0002g0037a0001c0002t0002g0038a0002c0003t0002g0039 | 3 | HG01891.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.318+2234C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841795 | ||||||
| chr3:11841893
|
C | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0191a0001c0001t0001g0192others(16): Show | 21 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.318+2136G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841893 | ||||||
| chr3:11841971
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0152others(191): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.318+2058C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841971 | ||||||
| chr3:11842124
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0152others(192): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.318+1905A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842124 | ||||||
| chr3:11842314
|
A | G | 1 | a0002c0004t0003g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.318+1715T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842314 | ||||||
| chr3:11842318
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0152others(191): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.318+1711A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842318 | ||||||
| chr3:11842327
|
G | A | 1 | a0004c0006t0004g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+1702C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842327 | ||||||
| chr3:11842353
|
C | A | 104 | a0001c0001t0001g0345a0001c0002t0002g0007a0001c0002t0002g0008others(101): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.318+1676G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842353 | ||||||
| chr3:11842394
|
CA | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(142): Show | 161 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(158): Show |
intron_variant | MODIFIER | c.318+1634delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842394 | ||||||
| chr3:11842394
|
CAA | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0152others(192): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.318+1633_318+1634d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842394 | ||||||
| chr3:11842420
|
C | A | 7 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+1609G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842420 | ||||||
| chr3:11842428
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 5 | HG00558.hp1 HG02165.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1601C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842428 | ||||||
| chr3:11842464
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02109.hp1 HG02559.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.318+1565A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842464 | ||||||
| chr3:11842509
|
C | T | 1 | a0001c0002t0002g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.318+1520G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842509 | ||||||
| chr3:11842514
|
C | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+1515G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842514 | ||||||
| chr3:11842555
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.318+1474C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842555 | ||||||
| chr3:11842594
|
T | A | 2 | a0001c0001t0001g0322a0001c0001t0003g0021 | 3 | HG02965.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.318+1435A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842594 | ||||||
| chr3:11842707
|
G | GA | 105 | a0001c0001t0001g0320a0001c0001t0001g0345a0001c0002t0002g0007others(102): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.318+1321dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842707 | ||||||
| chr3:11842796
|
G | A | 1 | a0001c0001t0001g0321 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.318+1233C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842796 | ||||||
| chr3:11842877
|
A | G | 16 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(13): Show | 17 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.318+1152T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842877 | ||||||
| chr3:11843073
|
G | A | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.318+956C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843073 | ||||||
| chr3:11843075
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | NA18951.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.318+954C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843075 | ||||||
| chr3:11843092
|
G | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+937C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843092 | ||||||
| chr3:11843104
|
T | C | 4 | a0001c0001t0001g0339a0001c0001t0001g0341a0001c0001t0001g0342others(1): Show | 4 | NA18941.hp2 NA18966.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+925A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843104 | ||||||
| chr3:11843213
|
A | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0152others(190): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.318+816T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843213 | ||||||
| chr3:11843278
|
G | A | 20 | a0001c0001t0001g0323a0001c0001t0001g0325a0001c0001t0001g0326others(17): Show | 20 | HG00423.hp2 HG01884.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.318+751C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843278 | ||||||
| chr3:11843388
|
A | AG | 19 | a0001c0001t0001g0012a0001c0001t0001g0191a0001c0001t0001g0192others(16): Show | 21 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.318+640dupC | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843388 | ||||||
| chr3:11843435
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02683.hp1 HG02698.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.318+594G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843435 | ||||||
| chr3:11843562
|
C | A | 2 | a0001c0001t0001g0322a0001c0001t0003g0021 | 3 | HG02965.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.318+467G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843562 | ||||||
| chr3:11843666
|
C | T | 25 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(22): Show | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+363G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843666 | ||||||
| chr3:11843825
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.318+204T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843825 | ||||||
| chr3:11843903
|
G | A | 4 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0103others(1): Show | 4 | HG01891.hp2 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+126C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843903 | ||||||
| chr3:11843946
|
C | G | 1 | a0001c0002t0002g0045 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.318+83G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843946 | ||||||
| chr3:11844246
|
T | G | 23 | a0001c0001t0001g0323a0001c0001t0001g0325a0001c0001t0001g0326others(20): Show | 23 | HG00423.hp2 HG01884.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.136-35A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844246 | ||||||
| chr3:11844341
|
T | C | 119 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(116): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.136-130A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844341 | ||||||
| chr3:11844442
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0007t0001g0145others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-231G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844442 | ||||||
| chr3:11844605
|
C | A | 1 | a0002c0003t0004g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.136-394G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844605 | ||||||
| chr3:11844642
|
C | T | 1 | a0002c0004t0003g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-431G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844642 | ||||||
| chr3:11844742
|
C | T | 105 | a0001c0001t0001g0345a0001c0002t0002g0007a0001c0002t0002g0008others(102): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.136-531G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844742 | ||||||
| chr3:11844744
|
C | A | 2 | a0001c0002t0002g0138a0001c0002t0002g0139 | 2 | HG01074.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.136-533G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844744 | ||||||
| chr3:11844891
|
T | C | 108 | a0001c0001t0001g0345a0001c0002t0002g0007a0001c0002t0002g0008others(105): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.136-680A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844891 | ||||||
| chr3:11844977
|
G | A | 39 | a0001c0001t0001g0345a0001c0002t0002g0106a0001c0002t0002g0107others(36): Show | 40 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.136-766C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844977 | ||||||
| chr3:11845176
|
G | C | 7 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-965C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845176 | ||||||
| chr3:11845270
|
C | G | 7 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-1059G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845270 | ||||||
| chr3:11845277
|
G | A | 108 | a0001c0001t0001g0345a0001c0002t0002g0007a0001c0002t0002g0008others(105): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.136-1066C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845277 | ||||||
| chr3:11845515
|
C | T | 1 | a0002c0004t0002g0140 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.135+987G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845515 | ||||||
| chr3:11845570
|
A | T | 117 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0002t0002g0007others(114): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+932T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845570 | ||||||
| chr3:11845575
|
G | A | 117 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0002t0002g0007others(114): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+927C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845575 | ||||||
| chr3:11845591
|
C | A | 117 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0002t0002g0007others(114): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+911G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845591 | ||||||
| chr3:11845651
|
G | C | 117 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0002t0002g0007others(114): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+851C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845651 | ||||||
| chr3:11845756
|
C | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+746G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845756 | ||||||
| chr3:11845877
|
G | C | 133 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0002t0002g0004others(130): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.135+625C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845877 | ||||||
| chr3:11846020
|
A | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 6 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+482T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11846020 |