| geneid | 51306 |
|---|---|
| ensemblid | ENSG00000031003.11 |
| hgncid | 1335 |
| symbol | FAM13B |
| name | family with sequence similarity 13 member B |
| refseq_nuc | NM_001385994.1 |
| refseq_prot | NP_001372923.1 |
| ensembl_nuc | ENST00000689681.1 |
| ensembl_prot | ENSP00000509788.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 137937960 |
| end | 138033079 |
| strand | - |
| ver | v1.2 |
| region | chr5:137937960-138033079 |
| region5000 | chr5:137932960-138038079 |
| regionname0 | FAM13B_chr5_137937960_138033079 |
| regionname5000 | FAM13B_chr5_137932960_138038079 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 937 | 314 | 92 | 74 | 106 | 12 | 28 | 78 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0002 | 0/0 | 937 | 6 | 2 | 1 | 0 | 2 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0003 | 0/0 | 937 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0004 | 0/0 | 937 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2814 | 302 | 83 | 72 | 106 | 12 | 28 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| c0002 | 1/0 | 2814 | 10 | 9 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| c0003 | 0/0 | 2814 | 5 | 2 | 1 | 0 | 1 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| c0004 | 0/0 | 2814 | 2 | 0 | 2 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| c0005 | 0/0 | 2814 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| c0006 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| c0007 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2766 | 203 | 43 | 52 | 80 | 6 | 21 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0002 | 1/0 | 2766 | 82 | 40 | 20 | 7 | 8 | 6 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0003 | 0/0 | 2766 | 16 | 0 | 1 | 14 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0004 | 0/0 | 2766 | 6 | 6 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0005 | 0/0 | 2788 | 2 | 0 | 0 | 2 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0006 | 0/0 | 2766 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0007 | 0/0 | 2766 | 2 | 0 | 2 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0008 | 0/0 | 2766 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0009 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0010 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0011 | 0/0 | 2766 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0012 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0013 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0014 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| t0015 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| 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 | 0/1 | 2814 | 302 | 83 | 72 | 106 | 12 | 28 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0002 | 1/0 | 2814 | 10 | 9 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0004 | 0/0 | 2814 | 2 | 0 | 2 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0002c0003 | 0/0 | 2814 | 5 | 2 | 1 | 0 | 1 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0002c0006 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0003c0005 | 0/0 | 2814 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0004c0007 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5579 | 201 | 43 | 51 | 80 | 6 | 20 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0002 | 0/0 | 5579 | 66 | 29 | 19 | 7 | 6 | 5 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0003 | 0/0 | 5579 | 16 | 0 | 1 | 14 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0004 | 0/0 | 5579 | 6 | 6 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0005 | 0/0 | 5601 | 2 | 0 | 0 | 2 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0006 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0008 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0009 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0010 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0011 | 0/0 | 5579 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0012 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0013 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0014 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0001t0015 | 0/0 | 5579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0002t0002 | 1/0 | 5579 | 10 | 9 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0001c0004t0007 | 0/0 | 5579 | 2 | 0 | 2 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0002c0003t0002 | 0/0 | 5579 | 5 | 2 | 1 | 0 | 1 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0002c0006t0002 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0003c0005t0001 | 0/0 | 5579 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| a0004c0007t0001 | 0/0 | 5579 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | copy fasta | chr5 | 137932960 | 138038079 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0011g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0012g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0014g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0001t0015g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0004t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0001c0004t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0002c0006t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0003c0005t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| a0004c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | GBR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00280 | hp1 | a0002 | c0006 | t0002 | g0005 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00323 | hp1 | a0002 | c0003 | t0002 | g0004 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00738 | hp2 | a0001 | c0004 | t0007 | g0191 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG00741 | hp2 | a0003 | c0005 | t0001 | g0251 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01192 | hp1 | a0001 | c0004 | t0007 | g0189 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0268 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | IBS | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0013 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0221 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | CDX | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0289 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0299 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0297 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0290 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0291 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0105 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02976 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0296 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03710 | hp1 | a0004 | c0007 | t0001 | g0194 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0267 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0320 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03927 | hp2 | a0001 | c0001 | t0014 | g0026 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18969 | hp1 | a0001 | c0001 | t0015 | g0308 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18978 | hp1 | a0001 | c0001 | t0013 | g0236 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | GIH | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0294 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | MSL | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | USA | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | LWK | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0170 | REF | REF | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0295 | REF | REF | FAM13B_chr5_137932960_138038079 | FAM13B | chr5 | 137932960 | 138038079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137940279
|
C | G | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.2760G>C | p.Lys920Asn | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 3260/5579 | 2760/2814 | 920/937 | chr5 | 137940279 | ||
| chr5:137942993
|
T | C | 1 | a0002 | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
missense_variant | MODERATE | c.2470A>G | p.Met824Val | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/24 | 2970/5579 | 2470/2814 | 824/937 | chr5 | 137942993 | ||
| chr5:137960194
|
T | C | 1 | a0004 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1265A>G | p.Asp422Gly | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/24 | 1765/5579 | 1265/2814 | 422/937 | chr5 | 137960194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137940237
|
T | G | 1 | a0001c0004 | 2 | HG00738.hp2 HG01192.hp1 |
synonymous_variant | LOW | c.2802A>C | p.Ser934Ser | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 3302/5579 | 2802/2814 | 934/937 | chr5 | 137940237 | ||
| chr5:137945986
|
T | C | 1 | a0002c0006 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.2256A>G | p.Glu752Glu | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/24 | 2756/5579 | 2256/2814 | 752/937 | chr5 | 137945986 | ||
| chr5:138011809
|
G | A | 6 | a0001c0001a0001c0004a0002c0003others(3): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
synonymous_variant | LOW | c.507C>T | p.Ser169Ser | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/24 | 1007/5579 | 507/2814 | 169/937 | chr5 | 138011809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137938043
|
A | G | 1 | a0001c0001t0011 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2182T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2182 | chr5 | 137938043 | |||||
| chr5:137938089
|
C | T | 1 | a0001c0001t0008 | 2 | HG02895.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2136G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2136 | chr5 | 137938089 | |||||
| chr5:137938090
|
A | T | 2 | a0001c0001t0004a0001c0001t0006 | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2135T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2135 | chr5 | 137938090 | |||||
| chr5:137938192
|
T | C | 1 | a0001c0001t0012 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2033A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 2033 | chr5 | 137938192 | |||||
| chr5:137938342
|
A | C | 2 | a0001c0001t0004a0001c0001t0006 | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1883T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1883 | chr5 | 137938342 | |||||
| chr5:137938528
|
T | C | 1 | a0001c0001t0013 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1697 | chr5 | 137938528 | |||||
| chr5:137938692
|
G | A | 1 | a0001c0001t0015 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1533C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1533 | chr5 | 137938692 | |||||
| chr5:137938781
|
C | G | 1 | a0001c0004t0007 | 2 | HG00738.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1444G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1444 | chr5 | 137938781 | |||||
| chr5:137938797
|
G | T | 1 | a0001c0001t0010 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1428C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 1428 | chr5 | 137938797 | |||||
| chr5:137939426
|
G | A | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*799C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 799 | chr5 | 137939426 | |||||
| chr5:137939510
|
T | C | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 238 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*715A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 715 | chr5 | 137939510 | |||||
| chr5:137939518
|
G | A | 1 | a0001c0001t0008 | 2 | HG02895.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*707C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 707 | chr5 | 137939518 | |||||
| chr5:137939701
|
C | T | 1 | a0001c0001t0009 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 524 | chr5 | 137939701 | |||||
| chr5:137939952
|
G | A | 1 | a0001c0001t0014 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 24/24 | 273 | chr5 | 137939952 | |||||
| chr5:138032801
|
C | A | 2 | a0001c0001t0003a0001c0001t0015 | 17 | HG00544.hp1 HG01433.hp2 HG02071.hp1 others(14): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-222G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/24 | chr5 | 138032801 | ||||||
| chr5:138033062
|
A | AGCGGGAG others(15): Show |
1 | a0001c0001t0005 | 2 | HG00408.hp2 NA18980.hp2 |
5_prime_UTR_variant | MODIFIER | c.-505_-484dupCCGCCA others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/24 | 13952 | chr5 | 138033062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137940443
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2691-95A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940443 | ||||||
| chr5:137940469
|
TA | T | 7 | a0001c0001t0001g0095a0001c0001t0001g0248a0001c0001t0002g0268others(4): Show | 7 | HG01516.hp1 HG01517.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.2691-122delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940469 | ||||||
| chr5:137940710
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0154 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2691-362C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940710 | ||||||
| chr5:137940903
|
T | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2691-555A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940903 | ||||||
| chr5:137940979
|
C | A | 124 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.2691-631G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137940979 | ||||||
| chr5:137941031
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2691-683C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941031 | ||||||
| chr5:137941049
|
G | A | 5 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG00597.hp2 HG02135.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.2691-701C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941049 | ||||||
| chr5:137941063
|
G | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2691-715C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941063 | ||||||
| chr5:137941077
|
T | A | 1 | a0001c0001t0010g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2691-729A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941077 | ||||||
| chr5:137941126
|
T | C | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2691-778A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941126 | ||||||
| chr5:137941692
|
A | C | 4 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2690+252T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 23/23 | chr5 | 137941692 | ||||||
| chr5:137942286
|
A | AAG | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2589-243_2589-242d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942286 | ||||||
| chr5:137942320
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2589-275T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942320 | ||||||
| chr5:137942443
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2589-398G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942443 | ||||||
| chr5:137942729
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2588+146A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942729 | ||||||
| chr5:137942832
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2588+43A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 22/23 | chr5 | 137942832 | ||||||
| chr5:137943044
|
A | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0116 | 2 | HG00733.hp2 HG01168.hp1 |
splice_region_variant&intron_variant | LOW | c.2425-6T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 21/23 | chr5 | 137943044 | ||||||
| chr5:137943058
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2425-20C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 21/23 | chr5 | 137943058 | ||||||
| chr5:137943082
|
G | T | 1 | a0001c0001t0002g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2425-44C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 21/23 | chr5 | 137943082 | ||||||
| chr5:137943301
|
T | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2341-85A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943301 | ||||||
| chr5:137943737
|
T | A | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2341-521A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943737 | ||||||
| chr5:137943740
|
G | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0125 | 2 | NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2341-524C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943740 | ||||||
| chr5:137943744
|
C | CA | 52 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(49): Show | 52 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2341-529dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943744 | ||||||
| chr5:137943841
|
A | G | 2 | a0001c0001t0001g0162a0001c0002t0002g0290 | 2 | HG01358.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2341-625T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943841 | ||||||
| chr5:137943921
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2341-705A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943921 | ||||||
| chr5:137943961
|
C | T | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2341-745G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137943961 | ||||||
| chr5:137944017
|
T | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.2341-801A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944017 | ||||||
| chr5:137944173
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2341-957G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944173 | ||||||
| chr5:137944232
|
G | A | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2341-1016C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944232 | ||||||
| chr5:137944276
|
C | A | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2341-1060G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944276 | ||||||
| chr5:137944486
|
G | A | 1 | a0001c0001t0004g0264 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2341-1270C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944486 | ||||||
| chr5:137944671
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2340+1231A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944671 | ||||||
| chr5:137944763
|
CA | C | 71 | a0001c0001t0001g0168a0001c0001t0001g0181a0001c0001t0001g0193others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2340+1138delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944763 | ||||||
| chr5:137944763
|
CAA | C | 236 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 236 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.2340+1137_2340+113 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944763 | ||||||
| chr5:137944768
|
A | C | 4 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2340+1134T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944768 | ||||||
| chr5:137944769
|
A | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2340+1133T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944769 | ||||||
| chr5:137944777
|
A | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2340+1125T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944777 | ||||||
| chr5:137944955
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02027.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2340+947C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137944955 | ||||||
| chr5:137945075
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0092 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2340+827G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945075 | ||||||
| chr5:137945287
|
A | G | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2340+615T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945287 | ||||||
| chr5:137945438
|
TAA | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0281 | 3 | HG02055.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2340+462_2340+463d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945438 | ||||||
| chr5:137945511
|
C | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2340+391G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 20/23 | chr5 | 137945511 | ||||||
| chr5:137946019
|
A | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2245-22T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 19/23 | chr5 | 137946019 | ||||||
| chr5:137946069
|
T | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG01952.hp2 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2245-72A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 19/23 | chr5 | 137946069 | ||||||
| chr5:137946074
|
G | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0208a0001c0001t0001g0239 | 3 | NA18957.hp2 NA18961.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2245-77C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 19/23 | chr5 | 137946074 | ||||||
| chr5:137946342
|
C | CA | 8 | a0001c0001t0001g0203a0001c0001t0001g0280a0001c0001t0002g0166others(5): Show | 8 | HG01167.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2161-32dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946342 | ||||||
| chr5:137946350
|
A | C | 1 | a0001c0001t0002g0074 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2161-39T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946350 | ||||||
| chr5:137946436
|
G | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.2161-125C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946436 | ||||||
| chr5:137946899
|
T | C | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.2161-588A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137946899 | ||||||
| chr5:137947105
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2161-794G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947105 | ||||||
| chr5:137947117
|
G | A | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2161-806C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947117 | ||||||
| chr5:137947255
|
A | T | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.2161-944T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947255 | ||||||
| chr5:137947361
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2161-1050T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947361 | ||||||
| chr5:137947398
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2161-1087G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947398 | ||||||
| chr5:137947511
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2161-1200T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137947511 | ||||||
| chr5:137948080
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2160+875A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948080 | ||||||
| chr5:137948083
|
TC | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2160+871delG | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948083 | ||||||
| chr5:137948123
|
T | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2160+832A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948123 | ||||||
| chr5:137948180
|
CA | C | 232 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(229): Show | 232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.2160+774delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948180 | ||||||
| chr5:137948401
|
CTTTA | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2160+550_2160+553d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948401 | ||||||
| chr5:137948605
|
G | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0257 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2160+350C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948605 | ||||||
| chr5:137948819
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2160+136A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948819 | ||||||
| chr5:137948855
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2160+100C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948855 | ||||||
| chr5:137948879
|
CTACCCTG others(15): Show |
C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2160+54_2160+75del others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 18/23 | chr5 | 137948879 | ||||||
| chr5:137949212
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1931-28C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949212 | ||||||
| chr5:137949321
|
T | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1931-137A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949321 | ||||||
| chr5:137949473
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1931-289T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949473 | ||||||
| chr5:137949554
|
T | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1931-370A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949554 | ||||||
| chr5:137949567
|
G | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0057 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1931-383C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949567 | ||||||
| chr5:137949609
|
G | A | 1 | a0001c0001t0001g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1931-425C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949609 | ||||||
| chr5:137949660
|
C | T | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1931-476G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949660 | ||||||
| chr5:137949798
|
CA | C | 304 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(301): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1931-615delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949798 | ||||||
| chr5:137949864
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0174 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1931-680C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137949864 | ||||||
| chr5:137950176
|
T | A | 2 | a0001c0001t0008g0105a0001c0001t0008g0108 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1931-992A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950176 | ||||||
| chr5:137950176
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1931-992A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950176 | ||||||
| chr5:137950208
|
C | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1931-1024G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950208 | ||||||
| chr5:137950251
|
G | A | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1931-1067C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950251 | ||||||
| chr5:137950407
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1931-1223T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950407 | ||||||
| chr5:137950431
|
G | A | 243 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(240): Show | 243 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.1931-1247C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950431 | ||||||
| chr5:137950675
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1931-1491C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950675 | ||||||
| chr5:137950841
|
T | C | 2 | a0001c0001t0002g0033a0001c0001t0002g0062 | 2 | NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1931-1657A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137950841 | ||||||
| chr5:137951124
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1930+1504G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951124 | ||||||
| chr5:137951156
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0252 | 2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1930+1472C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951156 | ||||||
| chr5:137951209
|
C | CA | 68 | a0001c0001t0001g0100a0001c0001t0001g0117a0001c0001t0001g0126others(65): Show | 68 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1930+1418dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | ||||||
| chr5:137951209
|
C | CAA | 116 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(113): Show | 116 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1930+1417_1930+141 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | ||||||
| chr5:137951209
|
C | CAAA | 10 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0112others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1930+1416_1930+141 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | ||||||
| chr5:137951209
|
CA | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0178a0001c0001t0002g0268others(9): Show | 12 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1930+1418delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951209 | ||||||
| chr5:137951213
|
A | C | 1 | a0003c0005t0001g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1930+1415T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951213 | ||||||
| chr5:137951233
|
A | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0195a0001c0004t0007g0189others(1): Show | 4 | HG00738.hp2 HG01192.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1930+1395T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951233 | ||||||
| chr5:137951234
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1930+1394C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951234 | ||||||
| chr5:137951235
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1930+1393C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951235 | ||||||
| chr5:137951236
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1930+1392T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951236 | ||||||
| chr5:137951977
|
G | A | 8 | a0001c0001t0001g0168a0001c0001t0001g0181a0001c0001t0001g0183others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.1930+651C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137951977 | ||||||
| chr5:137952124
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1930+504A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137952124 | ||||||
| chr5:137952296
|
C | G | 6 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 6 | HG01978.hp1 HG02109.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930+332G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137952296 | ||||||
| chr5:137952530
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1930+98T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 17/23 | chr5 | 137952530 | ||||||
| chr5:137952931
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0066 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1849-222G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137952931 | ||||||
| chr5:137953027
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1848+309G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953027 | ||||||
| chr5:137953059
|
A | G | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848+277T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953059 | ||||||
| chr5:137953105
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1848+231G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953105 | ||||||
| chr5:137953195
|
C | T | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1848+141G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953195 | ||||||
| chr5:137953323
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+13C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 16/23 | chr5 | 137953323 | ||||||
| chr5:137953505
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1719-40C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953505 | ||||||
| chr5:137953526
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1719-61A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953526 | ||||||
| chr5:137953664
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1719-199G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953664 | ||||||
| chr5:137953720
|
C | A | 1 | a0001c0001t0001g0235 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1719-255G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953720 | ||||||
| chr5:137953901
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0109others(1): Show | 4 | HG01978.hp1 HG02735.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1718+265T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137953901 | ||||||
| chr5:137954041
|
C | CT | 74 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1718+124dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 15/23 | chr5 | 137954041 | ||||||
| chr5:137954505
|
T | TAC | 20 | a0001c0001t0001g0093a0001c0001t0001g0106a0001c0001t0001g0139others(17): Show | 20 | HG01243.hp2 HG01515.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1508-131_1508-130d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954505 | ||||||
| chr5:137954525
|
T | C | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 222 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1508-149A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954525 | ||||||
| chr5:137954527
|
C | T | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 217 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1508-151G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954527 | ||||||
| chr5:137954528
|
ATG | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0217a0001c0001t0001g0240 | 3 | NA18982.hp1 NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1508-154_1508-153d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954528 | ||||||
| chr5:137954529
|
T | C | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 218 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1508-153A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954529 | ||||||
| chr5:137954529
|
T | TAC | 4 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0003g0307others(1): Show | 4 | HG01081.hp2 HG01123.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1508-154_1508-153i others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954529 | ||||||
| chr5:137954530
|
G | A | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 222 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1508-154C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954530 | ||||||
| chr5:137954536
|
GTGTA | G | 67 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1508-164_1508-161d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954536 | ||||||
| chr5:137954538
|
G | A | 17 | a0001c0001t0001g0093a0001c0001t0001g0106a0001c0001t0001g0241others(14): Show | 17 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1508-162C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954538 | ||||||
| chr5:137954601
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1508-225A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954601 | ||||||
| chr5:137954619
|
AT | A | 239 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(236): Show | 239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1508-244delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954619 | ||||||
| chr5:137954644
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1508-268G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954644 | ||||||
| chr5:137954673
|
T | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1508-297A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954673 | ||||||
| chr5:137954692
|
T | G | 1 | a0001c0001t0008g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1508-316A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954692 | ||||||
| chr5:137954700
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1508-324G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954700 | ||||||
| chr5:137954868
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1508-492G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954868 | ||||||
| chr5:137954983
|
T | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(14): Show | 17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1508-607A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137954983 | ||||||
| chr5:137955008
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1508-632A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955008 | ||||||
| chr5:137955072
|
T | TA | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1508-697dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955072 | ||||||
| chr5:137955118
|
T | G | 1 | a0002c0003t0002g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1508-742A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955118 | ||||||
| chr5:137955161
|
T | C | 3 | a0001c0001t0002g0052a0001c0001t0002g0069a0001c0001t0002g0071 | 3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1508-785A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955161 | ||||||
| chr5:137955172
|
CCTCA | C | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1508-800_1508-797d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955172 | ||||||
| chr5:137955362
|
TATAATAT others(8): Show |
T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1508-1001_1508-987 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955362 | ||||||
| chr5:137955507
|
AT | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1507+969delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955507 | ||||||
| chr5:137955633
|
A | G | 1 | a0001c0001t0013g0236 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1507+844T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955633 | ||||||
| chr5:137955900
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1507+577T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955900 | ||||||
| chr5:137955928
|
G | A | 1 | a0001c0001t0015g0308 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1507+549C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137955928 | ||||||
| chr5:137956146
|
A | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1507+331T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956146 | ||||||
| chr5:137956184
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1507+293T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956184 | ||||||
| chr5:137956406
|
G | A | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1507+71C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956406 | ||||||
| chr5:137956444
|
C | CA | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1507+32dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 14/23 | chr5 | 137956444 | ||||||
| chr5:137956706
|
A | AT | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1442-165dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956706 | ||||||
| chr5:137956748
|
A | G | 8 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG00140.hp1 HG00642.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1442-206T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956748 | ||||||
| chr5:137956757
|
A | AG | 18 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0002g0065others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1442-216dupC | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956757 | ||||||
| chr5:137956757
|
A | AGG | 42 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(39): Show | 42 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1442-217_1442-216d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956757 | ||||||
| chr5:137956757
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1442-215T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956757 | ||||||
| chr5:137956766
|
A | G | 53 | a0001c0001t0001g0178a0001c0001t0001g0201a0001c0001t0002g0019others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1442-224T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956766 | ||||||
| chr5:137956767
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1442-225T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956767 | ||||||
| chr5:137956878
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0192 | 2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1442-336A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137956878 | ||||||
| chr5:137957264
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1442-722C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957264 | ||||||
| chr5:137957332
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1442-790C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957332 | ||||||
| chr5:137957398
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1442-856C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957398 | ||||||
| chr5:137957453
|
T | C | 2 | a0001c0001t0001g0245a0001c0001t0002g0075 | 2 | HG02818.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1442-911A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957453 | ||||||
| chr5:137957540
|
C | CA | 50 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0088others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1442-999dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957540 | ||||||
| chr5:137957540
|
CA | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0077a0001c0001t0001g0080others(22): Show | 25 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1442-999delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957540 | ||||||
| chr5:137957682
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0232a0001c0001t0001g0244 | 3 | HG01074.hp1 HG04204.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1442-1140C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957682 | ||||||
| chr5:137957924
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1442-1382C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957924 | ||||||
| chr5:137957927
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1442-1385C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957927 | ||||||
| chr5:137957929
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1442-1387G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137957929 | ||||||
| chr5:137958230
|
T | G | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1441+1386A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137958230 | ||||||
| chr5:137958874
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1441+742A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137958874 | ||||||
| chr5:137959013
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1441+603T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959013 | ||||||
| chr5:137959219
|
T | C | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0237others(1): Show | 4 | NA19009.hp2 NA19010.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441+397A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959219 | ||||||
| chr5:137959230
|
A | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1441+386T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959230 | ||||||
| chr5:137959291
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441+325C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959291 | ||||||
| chr5:137959529
|
G | C | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1441+87C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 13/23 | chr5 | 137959529 | ||||||
| chr5:137959827
|
C | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1294-64G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137959827 | ||||||
| chr5:137959829
|
T | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1294-66A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137959829 | ||||||
| chr5:137959940
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1294-177A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137959940 | ||||||
| chr5:137960134
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1293+32A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 12/23 | chr5 | 137960134 | ||||||
| chr5:137960400
|
A | G | 3 | a0001c0001t0002g0052a0001c0001t0002g0069a0001c0001t0002g0071 | 3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1245-186T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960400 | ||||||
| chr5:137960422
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1245-208A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960422 | ||||||
| chr5:137960837
|
C | T | 4 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245-623G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960837 | ||||||
| chr5:137960876
|
C | A | 1 | a0001c0001t0002g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1245-662G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137960876 | ||||||
| chr5:137961314
|
A | AAACAAC | 21 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 21 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1244+1085_1244+109 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | ||||||
| chr5:137961314
|
A | AAACAACA others(2): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0246a0001c0001t0004g0265 | 3 | HG01175.hp2 HG01975.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1244+1082_1244+109 others(13): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | ||||||
| chr5:137961314
|
A | AAACAACA others(5): Show |
3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1244+1079_1244+109 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | ||||||
| chr5:137961314
|
AAAC | A | 118 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1244+1088_1244+109 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | ||||||
| chr5:137961314
|
AAACAAC | A | 158 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(155): Show | 158 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1244+1085_1244+109 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961314 | ||||||
| chr5:137961708
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1244+697G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961708 | ||||||
| chr5:137961867
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1244+538G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961867 | ||||||
| chr5:137961879
|
ACT | A | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1244+524_1244+525d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137961879 | ||||||
| chr5:137962120
|
A | T | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1244+285T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962120 | ||||||
| chr5:137962150
|
G | C | 1 | a0001c0001t0002g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1244+255C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962150 | ||||||
| chr5:137962152
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1244+253A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962152 | ||||||
| chr5:137962234
|
C | T | 243 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(240): Show | 243 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.1244+171G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 11/23 | chr5 | 137962234 | ||||||
| chr5:137962765
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02895.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1180-296C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962765 | ||||||
| chr5:137962810
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1180-341T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962810 | ||||||
| chr5:137962948
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1180-479C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962948 | ||||||
| chr5:137962975
|
T | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-506A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137962975 | ||||||
| chr5:137963052
|
T | C | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1180-583A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963052 | ||||||
| chr5:137963122
|
A | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-653T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963122 | ||||||
| chr5:137963155
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-686C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963155 | ||||||
| chr5:137963201
|
T | C | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-732A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963201 | ||||||
| chr5:137963481
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1180-1012A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963481 | ||||||
| chr5:137963532
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1180-1063A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963532 | ||||||
| chr5:137963588
|
A | C | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-1119T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963588 | ||||||
| chr5:137963625
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1180-1156A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963625 | ||||||
| chr5:137963658
|
G | A | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-1189C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963658 | ||||||
| chr5:137963663
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0077 | 2 | NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1180-1194G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963663 | ||||||
| chr5:137963749
|
G | A | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1180-1280C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963749 | ||||||
| chr5:137963751
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0304 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1180-1282C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963751 | ||||||
| chr5:137963858
|
T | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-1389A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963858 | ||||||
| chr5:137963903
|
C | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-1434G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963903 | ||||||
| chr5:137963931
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-1462C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963931 | ||||||
| chr5:137963932
|
T | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1180-1463A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137963932 | ||||||
| chr5:137964076
|
T | A | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1180-1607A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964076 | ||||||
| chr5:137964160
|
C | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-1691G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964160 | ||||||
| chr5:137964182
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1180-1713G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964182 | ||||||
| chr5:137964213
|
G | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1180-1744C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964213 | ||||||
| chr5:137964262
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0116 | 2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1180-1793A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964262 | ||||||
| chr5:137964392
|
A | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-1923T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964392 | ||||||
| chr5:137964597
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1180-2128A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964597 | ||||||
| chr5:137964622
|
G | A | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1180-2153C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964622 | ||||||
| chr5:137964716
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0160 | 2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.1180-2247C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964716 | ||||||
| chr5:137964899
|
G | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-2430C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137964899 | ||||||
| chr5:137965101
|
G | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-2632C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965101 | ||||||
| chr5:137965102
|
C | G | 243 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(240): Show | 243 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.1180-2633G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965102 | ||||||
| chr5:137965110
|
G | A | 3 | a0001c0001t0002g0052a0001c0001t0002g0069a0001c0001t0002g0071 | 3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1180-2641C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965110 | ||||||
| chr5:137965178
|
T | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-2709A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965178 | ||||||
| chr5:137965449
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1180-2980G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965449 | ||||||
| chr5:137965495
|
G | A | 2 | a0001c0001t0002g0047a0001c0001t0002g0056 | 2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1180-3026C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965495 | ||||||
| chr5:137965515
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1180-3046A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965515 | ||||||
| chr5:137965547
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1180-3078C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965547 | ||||||
| chr5:137965571
|
A | T | 9 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180-3102T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965571 | ||||||
| chr5:137965776
|
A | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0041 | 2 | NA18957.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1180-3307T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965776 | ||||||
| chr5:137965979
|
C | CA | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-3511dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137965979 | ||||||
| chr5:137966006
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1180-3537G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966006 | ||||||
| chr5:137966100
|
TA | T | 125 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1180-3632delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966100 | ||||||
| chr5:137966100
|
TAA | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1180-3633_1180-363 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966100 | ||||||
| chr5:137966231
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-3762C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966231 | ||||||
| chr5:137966257
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0157a0001c0001t0002g0302others(1): Show | 4 | HG01243.hp1 HG02622.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-3788G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966257 | ||||||
| chr5:137966428
|
G | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-3959C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966428 | ||||||
| chr5:137966459
|
T | TTA | 5 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0215others(2): Show | 5 | HG01891.hp1 HG02004.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-3992_1180-399 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966459
|
T | TTATA | 3 | a0001c0001t0001g0159a0001c0001t0002g0304a0001c0002t0002g0293 | 3 | HG01346.hp2 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1180-3994_1180-399 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966459
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0010g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1180-4000_1180-399 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966459
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1180-4002_1180-399 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966459
|
TTA | T | 25 | a0001c0001t0001g0121a0001c0001t0001g0210a0001c0001t0001g0211others(22): Show | 25 | HG00544.hp1 HG01891.hp2 HG02293.hp2 others(22): Show |
intron_variant | MODIFIER | c.1180-3992_1180-399 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966459
|
TTATA | T | 6 | a0001c0001t0001g0280a0001c0001t0002g0020a0001c0001t0002g0034others(3): Show | 6 | HG01167.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-3994_1180-399 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966459
|
TTATATA | T | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0046others(2): Show | 5 | HG01257.hp1 HG01258.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-3996_1180-399 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966459 | ||||||
| chr5:137966474
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0004g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180-4023_1180-400 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966474 | ||||||
| chr5:137966476
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0004g0265a0001c0001t0006g0262a0001c0001t0006g0263 | 3 | HG02896.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1180-4025_1180-400 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966476 | ||||||
| chr5:137966480
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1180-4011A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | ||||||
| chr5:137966480
|
T | TAGAGAGA others(5): Show |
1 | a0001c0001t0001g0111 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1180-4012_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | ||||||
| chr5:137966480
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0047a0001c0001t0002g0070 | 2 | HG01081.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1180-4021_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | ||||||
| chr5:137966480
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1180-4023_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | ||||||
| chr5:137966480
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0004g0258a0001c0001t0004g0264 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1180-4027_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966480 | ||||||
| chr5:137966482
|
T | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0111a0001c0001t0001g0133others(5): Show | 8 | HG00639.hp2 HG00735.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-4013A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
T | TAGAGAGA others(3): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0142 | 2 | HG00558.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1180-4014_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
T | TAGAGAGA others(5): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0147a0001c0001t0001g0240 | 3 | HG02148.hp2 NA19067.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1180-4014_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
T | TAGAGAGA others(7): Show |
1 | a0001c0001t0003g0322 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1180-4014_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
T | TAGAGAGA others(19): Show |
1 | a0001c0001t0001g0156 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1180-4014_1180-401 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0002g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1180-4023_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0004g0260 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1180-4029_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966482
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0004g0259 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1180-4031_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966482 | ||||||
| chr5:137966484
|
T | G | 21 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0024others(18): Show | 21 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1180-4015A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
T | TAGAGAGA others(1): Show |
5 | a0001c0001t0001g0025a0001c0001t0001g0123a0001c0001t0001g0183others(2): Show | 5 | HG01106.hp2 HG01243.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
T | TAGAGAGA others(3): Show |
6 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0120others(3): Show | 6 | HG01952.hp2 HG02257.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
T | TAGAGAGA others(5): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0225a0001c0004t0007g0189 | 3 | HG01192.hp1 HG02735.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
T | TAGAGAGA others(7): Show |
3 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0249 | 3 | HG03139.hp1 NA18945.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
T | TAGAGAGA others(9): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0193 | 3 | HG01255.hp2 NA19068.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1180-4016_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
TATATAG | T | 18 | a0001c0001t0001g0235a0001c0001t0002g0019a0001c0001t0002g0028others(15): Show | 18 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1180-4021_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
TATATAGA others(3): Show |
T | 1 | a0001c0001t0002g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1180-4025_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966484
|
TATATAGA others(5): Show |
T | 2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1180-4027_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966484 | ||||||
| chr5:137966486
|
T | G | 52 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(49): Show | 52 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1180-4017A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
T | TAGAG | 8 | a0001c0001t0001g0078a0001c0001t0001g0247a0001c0001t0001g0248others(5): Show | 8 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-4018_1180-401 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
T | TAGAGAGA others(1): Show |
5 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0112others(2): Show | 5 | HG00741.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-4018_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
T | TAGAGAGA others(3): Show |
7 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0184others(4): Show | 7 | HG00621.hp2 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-4018_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
T | TAGAGAGA others(7): Show |
1 | a0001c0001t0001g0139 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1180-4018_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
T | TAGAGAGA others(9): Show |
1 | a0001c0001t0001g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1180-4018_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0098 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1180-4018_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
TATAG | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0214a0001c0001t0001g0242others(3): Show | 6 | HG02683.hp2 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-4021_1180-401 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966486
|
TATAGAG | T | 5 | a0001c0001t0002g0033a0001c0001t0002g0049a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-4023_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966486 | ||||||
| chr5:137966488
|
T | G | 96 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(93): Show | 96 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.1180-4019A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TAGAG | 4 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-4023_1180-402 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TAGAGAGA others(3): Show |
5 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0145others(2): Show | 5 | HG02273.hp1 HG02965.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-4029_1180-402 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TAGAGAGA others(5): Show |
5 | a0001c0001t0001g0137a0001c0001t0001g0146a0001c0001t0001g0150others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-4031_1180-402 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TAGAGAGA others(7): Show |
7 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0180others(4): Show | 7 | HG00423.hp2 HG01515.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-4033_1180-402 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1180-4037_1180-402 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATAG | 3 | a0001c0001t0002g0292a0001c0001t0002g0300a0001c0002t0002g0299 | 3 | HG02451.hp2 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATAGAG | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0132 | 3 | HG01123.hp1 HG03017.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATAGAGA others(1): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0093a0001c0001t0001g0095others(2): Show | 5 | HG04228.hp2 NA18957.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATAGAGA others(3): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0153a0001c0001t0001g0168 | 3 | HG00280.hp2 HG03225.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATAGAGA others(5): Show |
1 | a0001c0001t0001g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATAGAGA others(7): Show |
1 | a0004c0007t0001g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATAG | 4 | a0001c0001t0001g0076a0001c0001t0001g0087a0001c0001t0001g0283others(1): Show | 4 | HG00642.hp2 HG01081.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATAGA others(1): Show |
3 | a0001c0001t0001g0113a0001c0001t0001g0161a0002c0003t0002g0008 | 3 | HG03579.hp1 NA18978.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATAGA others(3): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0274 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATAGA others(5): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0160 | 3 | HG00408.hp1 HG00438.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATAGA others(11): Show |
1 | a0001c0001t0001g0187 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATAGA others(13): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0252 | 2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0208 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0124 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0227 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0207 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(9): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0196 | 2 | HG00558.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(11): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0206 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(15): Show |
1 | a0002c0003t0002g0004 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(26): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(19): Show |
1 | a0002c0003t0002g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(25): Show |
1 | a0002c0003t0002g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(36): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1180-4020_1180-401 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(19): Show |
1 | a0002c0003t0002g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
T | TATATATA others(37): Show |
1 | a0002c0006t0002g0005 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1180-4020_1180-401 others(48): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
TAG | T | 34 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1180-4021_1180-402 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
TAGAG | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0217others(6): Show | 9 | HG00323.hp2 HG00741.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-4023_1180-402 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
TAGAGAG | T | 8 | a0001c0001t0001g0115a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-4025_1180-402 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966488
|
TAGAGAGA others(5): Show |
T | 2 | a0001c0001t0002g0051a0001c0001t0002g0053 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1180-4031_1180-402 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966488 | ||||||
| chr5:137966490
|
G | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0169a0001c0001t0001g0172others(13): Show | 16 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.1180-4021C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966490 | ||||||
| chr5:137966492
|
G | T | 28 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(25): Show | 28 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1180-4023C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966492 | ||||||
| chr5:137966494
|
G | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0162others(12): Show | 15 | HG00438.hp2 HG01074.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1180-4025C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966494 | ||||||
| chr5:137966496
|
G | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0162others(3): Show | 6 | HG00438.hp2 HG00738.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-4027C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966496 | ||||||
| chr5:137966498
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0226 | 2 | HG00738.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1180-4029C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966498 | ||||||
| chr5:137966500
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1180-4031C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966500 | ||||||
| chr5:137966524
|
G | GAGAGAGA others(4): Show |
2 | a0001c0001t0001g0094a0001c0004t0007g0191 | 2 | HG00738.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1180-4056_1180-405 others(15): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966524 | ||||||
| chr5:137966525
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0077 | 2 | NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1180-4056C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966525 | ||||||
| chr5:137966636
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1180-4167A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966636 | ||||||
| chr5:137966674
|
A | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-4205T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137966674 | ||||||
| chr5:137967051
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0159 | 2 | HG01346.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1180-4582G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967051 | ||||||
| chr5:137967085
|
T | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-4616A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967085 | ||||||
| chr5:137967200
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1180-4731A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967200 | ||||||
| chr5:137967241
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180-4772A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967241 | ||||||
| chr5:137967522
|
CA | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1180-5054delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967522 | ||||||
| chr5:137967595
|
G | A | 2 | a0001c0001t0005g0001a0001c0001t0005g0002 | 2 | HG00408.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1180-5126C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967595 | ||||||
| chr5:137967606
|
G | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-5137C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967606 | ||||||
| chr5:137967664
|
G | A | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1180-5195C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967664 | ||||||
| chr5:137967705
|
C | A | 2 | a0001c0001t0002g0292a0001c0001t0002g0298 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1180-5236G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967705 | ||||||
| chr5:137967833
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0195 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1180-5364G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967833 | ||||||
| chr5:137967837
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1180-5368C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137967837 | ||||||
| chr5:137968082
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1180-5613G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968082 | ||||||
| chr5:137968099
|
A | G | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-5630T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968099 | ||||||
| chr5:137968109
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1180-5640G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968109 | ||||||
| chr5:137968146
|
C | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-5677G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968146 | ||||||
| chr5:137968219
|
C | CA | 254 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(251): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1180-5751dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968219 | ||||||
| chr5:137968219
|
C | CAA | 52 | a0001c0001t0001g0100a0001c0001t0001g0229a0001c0001t0001g0230others(49): Show | 52 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1180-5752_1180-575 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968219 | ||||||
| chr5:137968266
|
T | C | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-5797A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968266 | ||||||
| chr5:137968438
|
C | CA | 16 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0160others(13): Show | 16 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1180-5970dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968438 | ||||||
| chr5:137968438
|
CA | C | 7 | a0001c0001t0001g0093a0001c0001t0001g0114a0001c0001t0001g0122others(4): Show | 7 | HG01070.hp1 HG01168.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-5970delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968438 | ||||||
| chr5:137968498
|
T | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0062 | 2 | NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1180-6029A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968498 | ||||||
| chr5:137968542
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1180-6073T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968542 | ||||||
| chr5:137968634
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0063 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1180-6165C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968634 | ||||||
| chr5:137968644
|
C | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-6175G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968644 | ||||||
| chr5:137968649
|
C | G | 7 | a0001c0001t0002g0047a0001c0001t0002g0049a0001c0001t0002g0055others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-6180G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968649 | ||||||
| chr5:137968650
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-6181C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968650 | ||||||
| chr5:137968652
|
G | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-6183C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968652 | ||||||
| chr5:137968719
|
T | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-6250A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968719 | ||||||
| chr5:137968760
|
C | T | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-6291G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968760 | ||||||
| chr5:137968902
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1180-6433C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968902 | ||||||
| chr5:137968971
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1180-6502A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137968971 | ||||||
| chr5:137969034
|
A | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1180-6565T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969034 | ||||||
| chr5:137969043
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1180-6574C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969043 | ||||||
| chr5:137969071
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1180-6602T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969071 | ||||||
| chr5:137969089
|
T | G | 1 | a0001c0001t0001g0232 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1180-6620A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969089 | ||||||
| chr5:137969188
|
C | T | 124 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1180-6719G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969188 | ||||||
| chr5:137969397
|
G | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1180-6928C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969397 | ||||||
| chr5:137969439
|
C | T | 124 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1180-6970G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969439 | ||||||
| chr5:137969478
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1180-7009C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969478 | ||||||
| chr5:137969517
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1180-7048C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969517 | ||||||
| chr5:137969573
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180-7104C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969573 | ||||||
| chr5:137969662
|
A | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1180-7193T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969662 | ||||||
| chr5:137969668
|
C | T | 1 | a0002c0003t0002g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1180-7199G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969668 | ||||||
| chr5:137969709
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1180-7240A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969709 | ||||||
| chr5:137969776
|
T | G | 57 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1180-7307A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969776 | ||||||
| chr5:137969854
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1180-7385C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969854 | ||||||
| chr5:137969871
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-7402A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969871 | ||||||
| chr5:137969901
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0063 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1180-7432C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969901 | ||||||
| chr5:137969996
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1180-7527G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137969996 | ||||||
| chr5:137970057
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG00423.hp1 NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1180-7588G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970057 | ||||||
| chr5:137970085
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180-7616C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970085 | ||||||
| chr5:137970103
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1180-7634G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970103 | ||||||
| chr5:137970167
|
C | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG02717.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-7698G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970167 | ||||||
| chr5:137970179
|
C | T | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-7710G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970179 | ||||||
| chr5:137970280
|
G | C | 1 | a0001c0001t0004g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180-7811C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970280 | ||||||
| chr5:137970281
|
G | C | 58 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1180-7812C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970281 | ||||||
| chr5:137970315
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1180-7846A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970315 | ||||||
| chr5:137970319
|
C | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0238 | 2 | HG03516.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1180-7850G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970319 | ||||||
| chr5:137970419
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1180-7950G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970419 | ||||||
| chr5:137970462
|
G | A | 65 | a0001c0001t0001g0272a0001c0001t0002g0019a0001c0001t0002g0020others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1180-7993C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970462 | ||||||
| chr5:137970544
|
T | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-8075A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970544 | ||||||
| chr5:137970555
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1180-8086T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970555 | ||||||
| chr5:137970762
|
G | A | 2 | a0001c0001t0001g0256a0001c0001t0012g0221 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1180-8293C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970762 | ||||||
| chr5:137970806
|
C | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-8337G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970806 | ||||||
| chr5:137970902
|
A | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-8433T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970902 | ||||||
| chr5:137970946
|
C | G | 125 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1180-8477G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970946 | ||||||
| chr5:137970950
|
G | C | 125 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1180-8481C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970950 | ||||||
| chr5:137970954
|
C | G | 1 | a0002c0003t0002g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1180-8485G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137970954 | ||||||
| chr5:137971039
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-8570A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971039 | ||||||
| chr5:137971107
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-8638C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971107 | ||||||
| chr5:137971137
|
C | G | 73 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 73 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1180-8668G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971137 | ||||||
| chr5:137971193
|
T | C | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1180-8724A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971193 | ||||||
| chr5:137971204
|
G | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1180-8735C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971204 | ||||||
| chr5:137971319
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0053 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1180-8850C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971319 | ||||||
| chr5:137971333
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1180-8864G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971333 | ||||||
| chr5:137971375
|
A | G | 9 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180-8906T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971375 | ||||||
| chr5:137971429
|
A | G | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-8960T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971429 | ||||||
| chr5:137971434
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-8965G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971434 | ||||||
| chr5:137971477
|
T | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0053 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1180-9008A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971477 | ||||||
| chr5:137971518
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-9049A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971518 | ||||||
| chr5:137971646
|
C | T | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-9177G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971646 | ||||||
| chr5:137971667
|
C | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-9198G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971667 | ||||||
| chr5:137971709
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-9240G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971709 | ||||||
| chr5:137971756
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-9287C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971756 | ||||||
| chr5:137971789
|
A | G | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-9320T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971789 | ||||||
| chr5:137971796
|
C | A | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-9327G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971796 | ||||||
| chr5:137971796
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1180-9327G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971796 | ||||||
| chr5:137971940
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1180-9471C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137971940 | ||||||
| chr5:137972078
|
C | T | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-9609G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972078 | ||||||
| chr5:137972100
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180-9631A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972100 | ||||||
| chr5:137972110
|
T | G | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1180-9641A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972110 | ||||||
| chr5:137972127
|
C | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-9658G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972127 | ||||||
| chr5:137972147
|
GAGACACA others(25): Show |
G | 1 | a0001c0001t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1180-9710_1180-967 others(36): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972147 | ||||||
| chr5:137972447
|
A | T | 1 | a0001c0001t0002g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1180-9978T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972447 | ||||||
| chr5:137972478
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-10009G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972478 | ||||||
| chr5:137972618
|
G | C | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1180-10149C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972618 | ||||||
| chr5:137972674
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-10205G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972674 | ||||||
| chr5:137972675
|
G | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-10206C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972675 | ||||||
| chr5:137972714
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-10245A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972714 | ||||||
| chr5:137972882
|
C | T | 7 | a0001c0001t0002g0047a0001c0001t0002g0049a0001c0001t0002g0055others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-10413G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972882 | ||||||
| chr5:137972893
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1180-10424T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972893 | ||||||
| chr5:137972915
|
C | T | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1180-10446G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972915 | ||||||
| chr5:137972980
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1180-10511G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137972980 | ||||||
| chr5:137973007
|
C | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-10538G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973007 | ||||||
| chr5:137973012
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1180-10543A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973012 | ||||||
| chr5:137973214
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180-10745A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973214 | ||||||
| chr5:137973239
|
T | C | 2 | a0001c0001t0006g0262a0001c0001t0006g0263 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1180-10770A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973239 | ||||||
| chr5:137973284
|
T | C | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1180-10815A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973284 | ||||||
| chr5:137973340
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0154 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1180-10871G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973340 | ||||||
| chr5:137973395
|
A | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1180-10926T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973395 | ||||||
| chr5:137973519
|
T | C | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-11050A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973519 | ||||||
| chr5:137973582
|
C | A | 9 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180-11113G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973582 | ||||||
| chr5:137973610
|
G | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0126others(3): Show | 6 | NA18612.hp2 NA18959.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-11141C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973610 | ||||||
| chr5:137973675
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0063 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1180-11206C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973675 | ||||||
| chr5:137973791
|
A | G | 307 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1180-11322T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973791 | ||||||
| chr5:137973795
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1180-11326C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973795 | ||||||
| chr5:137973843
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-11374G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973843 | ||||||
| chr5:137973847
|
T | C | 58 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1180-11378A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973847 | ||||||
| chr5:137973861
|
C | T | 4 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-11392G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973861 | ||||||
| chr5:137973901
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1179+11356A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973901 | ||||||
| chr5:137973912
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1179+11345A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973912 | ||||||
| chr5:137973939
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1179+11318T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137973939 | ||||||
| chr5:137974011
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1179+11246A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974011 | ||||||
| chr5:137974048
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1179+11209C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974048 | ||||||
| chr5:137974457
|
T | G | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1179+10800A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974457 | ||||||
| chr5:137974465
|
G | C | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1179+10792C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974465 | ||||||
| chr5:137974471
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+10786T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974471 | ||||||
| chr5:137974481
|
G | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01975.hp1 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+10776C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974481 | ||||||
| chr5:137974599
|
T | TA | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1179+10657dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974599 | ||||||
| chr5:137974623
|
A | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+10634T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974623 | ||||||
| chr5:137974628
|
G | GA | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1179+10628dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974628 | ||||||
| chr5:137974663
|
C | CA | 7 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0119others(4): Show | 7 | HG00423.hp1 HG02145.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+10593dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974663 | ||||||
| chr5:137974663
|
C | CAA | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+10592_1179+10 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974663 | ||||||
| chr5:137974663
|
CA | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01175.hp2 HG01255.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+10593delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974663 | ||||||
| chr5:137974761
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1179+10496C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974761 | ||||||
| chr5:137974868
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0092 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1179+10389G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974868 | ||||||
| chr5:137974975
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1179+10282C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137974975 | ||||||
| chr5:137975128
|
T | C | 1 | a0001c0001t0002g0285 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1179+10129A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975128 | ||||||
| chr5:137975147
|
A | G | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+10110T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975147 | ||||||
| chr5:137975294
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1179+9963A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975294 | ||||||
| chr5:137975309
|
G | A | 1 | a0001c0001t0010g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1179+9948C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975309 | ||||||
| chr5:137975314
|
C | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+9943G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975314 | ||||||
| chr5:137975493
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1179+9764A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975493 | ||||||
| chr5:137975537
|
CCA | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1179+9718_1179+971 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975537 | ||||||
| chr5:137975670
|
T | TA | 9 | a0001c0001t0001g0161a0001c0001t0004g0258a0001c0001t0004g0259others(6): Show | 9 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+9586dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975670 | ||||||
| chr5:137975677
|
AT | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+9579delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975677 | ||||||
| chr5:137975819
|
G | GT | 7 | a0001c0001t0001g0240a0001c0001t0002g0049a0001c0001t0002g0268others(4): Show | 7 | HG01109.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+9437dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975819 | ||||||
| chr5:137975902
|
T | TA | 12 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0101others(9): Show | 12 | HG01106.hp1 HG01978.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1179+9354dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975902 | ||||||
| chr5:137975979
|
C | CT | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0257 | 3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1179+9277_1179+927 others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975979 | ||||||
| chr5:137975980
|
C | CTTTTT | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(218): Show | 221 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1179+9272_1179+927 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTT | 10 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0110others(7): Show | 10 | HG01175.hp2 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1179+9271_1179+927 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTTT others(6): Show |
9 | a0001c0001t0002g0044a0001c0001t0002g0060a0001c0001t0002g0075others(6): Show | 9 | HG01070.hp2 HG01243.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+9264_1179+927 others(17): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTTT others(7): Show |
42 | a0001c0001t0002g0020a0001c0001t0002g0028a0001c0001t0002g0032others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1179+9263_1179+927 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTTT others(8): Show |
10 | a0001c0001t0002g0019a0001c0001t0002g0029a0001c0001t0002g0030others(7): Show | 10 | HG00741.hp1 HG01192.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1179+9262_1179+927 others(19): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1179+9276_1179+927 others(21): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0002g0166a0001c0001t0002g0250 | 2 | HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+9276_1179+927 others(22): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+9276_1179+927 others(23): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975980
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0257 | 3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1179+9277G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975980 | ||||||
| chr5:137975994
|
T | TTTTTTTT others(8): Show |
1 | a0002c0006t0002g0005 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1179+9262_1179+926 others(19): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137975994 | ||||||
| chr5:137976145
|
T | C | 309 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(306): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1179+9112A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976145 | ||||||
| chr5:137976145
|
T | G | 1 | a0001c0001t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+9112A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976145 | ||||||
| chr5:137976191
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0063 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1179+9066C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976191 | ||||||
| chr5:137976216
|
A | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+9041T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976216 | ||||||
| chr5:137976380
|
C | G | 2 | a0001c0001t0002g0300a0001c0001t0002g0304 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1179+8877G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976380 | ||||||
| chr5:137976486
|
T | A | 9 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+8771A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976486 | ||||||
| chr5:137976486
|
T | C | 1 | a0001c0001t0002g0287 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1179+8771A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976486 | ||||||
| chr5:137976759
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1179+8498G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976759 | ||||||
| chr5:137976788
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1179+8469A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976788 | ||||||
| chr5:137976814
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+8443T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976814 | ||||||
| chr5:137976815
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+8442A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976815 | ||||||
| chr5:137976839
|
T | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+8418A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137976839 | ||||||
| chr5:137977014
|
T | G | 1 | a0001c0001t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1179+8243A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977014 | ||||||
| chr5:137977026
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0002g0051a0001c0001t0002g0053 | 3 | HG01167.hp1 HG01169.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1179+8231G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977026 | ||||||
| chr5:137977027
|
G | A | 2 | a0001c0002t0002g0289a0001c0002t0002g0290 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1179+8230C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977027 | ||||||
| chr5:137977460
|
C | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+7797G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977460 | ||||||
| chr5:137977603
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+7654G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977603 | ||||||
| chr5:137977700
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1179+7557T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977700 | ||||||
| chr5:137977707
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0003g0306a0001c0001t0003g0307others(13): Show | 16 | HG00544.hp1 HG01433.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1179+7550T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977707 | ||||||
| chr5:137977889
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1179+7368A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137977889 | ||||||
| chr5:137978266
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1179+6991G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978266 | ||||||
| chr5:137978377
|
A | G | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+6880T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978377 | ||||||
| chr5:137978490
|
C | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+6767G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978490 | ||||||
| chr5:137978711
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1179+6546T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978711 | ||||||
| chr5:137978723
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1179+6534A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978723 | ||||||
| chr5:137978780
|
T | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1179+6477A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978780 | ||||||
| chr5:137978826
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0208a0001c0001t0001g0239 | 3 | NA18957.hp2 NA18961.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1179+6431G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137978826 | ||||||
| chr5:137979114
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1179+6143C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979114 | ||||||
| chr5:137979233
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1179+6024C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979233 | ||||||
| chr5:137979373
|
C | T | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+5884G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979373 | ||||||
| chr5:137979725
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1179+5532A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979725 | ||||||
| chr5:137979845
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1179+5412G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979845 | ||||||
| chr5:137979878
|
T | A | 9 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG01106.hp1 HG01978.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+5379A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979878 | ||||||
| chr5:137979999
|
TA | T | 259 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1179+5257delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979999 | ||||||
| chr5:137979999
|
TAA | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0114a0001c0001t0001g0116others(4): Show | 7 | HG00733.hp2 HG01168.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+5256_1179+525 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137979999 | ||||||
| chr5:137980029
|
C | T | 2 | a0001c0001t0002g0300a0001c0001t0002g0304 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1179+5228G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980029 | ||||||
| chr5:137980116
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1179+5141A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980116 | ||||||
| chr5:137980146
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1179+5111G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980146 | ||||||
| chr5:137980152
|
G | T | 1 | a0001c0001t0002g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1179+5105C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980152 | ||||||
| chr5:137980155
|
A | G | 1 | a0001c0002t0002g0294 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1179+5102T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980155 | ||||||
| chr5:137980168
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1179+5089G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980168 | ||||||
| chr5:137980176
|
G | GAA | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1179+5079_1179+508 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980176 | ||||||
| chr5:137980272
|
T | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1179+4985A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980272 | ||||||
| chr5:137980440
|
CT | C | 281 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(278): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1179+4816delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980440 | ||||||
| chr5:137980440
|
CTT | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0153a0001c0001t0001g0241others(6): Show | 9 | HG01069.hp2 HG01243.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+4815_1179+481 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980440 | ||||||
| chr5:137980454
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1179+4803A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980454 | ||||||
| chr5:137980458
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1179+4799A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980458 | ||||||
| chr5:137980583
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1179+4674G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980583 | ||||||
| chr5:137980847
|
C | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+4410G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980847 | ||||||
| chr5:137980951
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1179+4306G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137980951 | ||||||
| chr5:137981017
|
T | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+4240A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981017 | ||||||
| chr5:137981077
|
A | AT | 11 | a0001c0001t0002g0040a0001c0001t0002g0050a0001c0001t0002g0054others(8): Show | 11 | HG00323.hp2 HG01192.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1179+4179dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | ||||||
| chr5:137981077
|
AT | A | 111 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(108): Show | 111 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1179+4179delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | ||||||
| chr5:137981077
|
ATT | A | 117 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(114): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1179+4178_1179+417 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | ||||||
| chr5:137981077
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1179+4170_1179+417 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | ||||||
| chr5:137981077
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0284 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1179+4166_1179+417 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981077 | ||||||
| chr5:137981177
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+4080T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981177 | ||||||
| chr5:137981218
|
A | G | 2 | a0002c0003t0002g0004a0002c0006t0002g0005 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1179+4039T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981218 | ||||||
| chr5:137981432
|
G | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(14): Show | 17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1179+3825C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981432 | ||||||
| chr5:137981614
|
C | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0066a0001c0001t0002g0070 | 3 | HG00639.hp2 HG00735.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1179+3643G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981614 | ||||||
| chr5:137981771
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1179+3486C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981771 | ||||||
| chr5:137981859
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0127 | 2 | NA18950.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1179+3398C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981859 | ||||||
| chr5:137981871
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+3386C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137981871 | ||||||
| chr5:137982092
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1179+3165C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982092 | ||||||
| chr5:137982351
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1179+2906C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982351 | ||||||
| chr5:137982355
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+2902G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982355 | ||||||
| chr5:137982507
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1179+2750G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982507 | ||||||
| chr5:137982523
|
A | AAAC | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+2731_1179+273 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982523 | ||||||
| chr5:137982545
|
A | AACC | 125 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1179+2709_1179+271 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982545 | ||||||
| chr5:137982662
|
T | TTTA | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+2592_1179+259 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982662 | ||||||
| chr5:137982697
|
G | C | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1179+2560C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982697 | ||||||
| chr5:137982765
|
T | G | 1 | a0001c0001t0004g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1179+2492A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982765 | ||||||
| chr5:137982989
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1179+2268C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137982989 | ||||||
| chr5:137983176
|
T | TA | 7 | a0001c0001t0002g0303a0001c0002t0002g0288a0001c0002t0002g0291others(4): Show | 7 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1179+2080dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0071others(1): Show | 4 | HG00323.hp1 HG01891.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+2071_1179+208 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(4): Show |
T | 5 | a0001c0001t0002g0052a0001c0001t0002g0069a0001c0001t0002g0286others(2): Show | 5 | HG01433.hp1 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+2070_1179+208 others(15): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0062others(1): Show | 4 | HG00140.hp2 HG03225.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+2069_1179+208 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0002g0292a0001c0001t0002g0298a0001c0001t0002g0300 | 3 | HG02451.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+2068_1179+208 others(17): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0002g0047a0001c0001t0002g0056 | 2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1179+2067_1179+208 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(8): Show |
T | 19 | a0001c0001t0001g0010a0001c0001t0001g0154a0001c0001t0001g0161others(16): Show | 19 | HG00423.hp1 HG00597.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1179+2066_1179+208 others(19): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(9): Show |
T | 123 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1179+2065_1179+208 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983176
|
TAAAAAAA others(10): Show |
T | 101 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(98): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1179+2064_1179+208 others(21): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983176 | ||||||
| chr5:137983194
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1179+2063T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983194 | ||||||
| chr5:137983205
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1179+2052T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983205 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0002g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(49): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0002g0074 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(48): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(30): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0002g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(28): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(25): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0040a0001c0001t0002g0049 | 2 | HG01109.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1179+2043_1179+204 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1179+2043_1179+204 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0002g0055a0001c0001t0002g0060 | 2 | HG01070.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1179+2043_1179+204 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | AAAAAC | 6 | a0001c0001t0002g0019a0001c0001t0002g0031a0001c0001t0002g0065others(3): Show | 6 | HG00735.hp2 HG02027.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+2043_1179+204 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983213
|
A | C | 16 | a0001c0001t0002g0020a0001c0001t0002g0032a0001c0001t0002g0033others(13): Show | 16 | HG00140.hp2 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1179+2044T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983213 | ||||||
| chr5:137983312
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1179+1945A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983312 | ||||||
| chr5:137983402
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1179+1855A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983402 | ||||||
| chr5:137983760
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1179+1497G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983760 | ||||||
| chr5:137983900
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1179+1357G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137983900 | ||||||
| chr5:137984086
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1179+1171G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984086 | ||||||
| chr5:137984106
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1179+1151G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984106 | ||||||
| chr5:137984113
|
G | A | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1179+1144C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984113 | ||||||
| chr5:137984199
|
GATTATTT others(7): Show |
G | 1 | a0001c0001t0002g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1179+1044_1179+105 others(18): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984199 | ||||||
| chr5:137984228
|
T | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1179+1029A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984228 | ||||||
| chr5:137984255
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1179+1002A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984255 | ||||||
| chr5:137984512
|
T | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0257 | 3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1179+745A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984512 | ||||||
| chr5:137984594
|
C | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+663G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984594 | ||||||
| chr5:137984633
|
C | T | 1 | a0002c0003t0002g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1179+624G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984633 | ||||||
| chr5:137984634
|
CT | C | 235 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(232): Show | 235 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1179+622delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984634 | ||||||
| chr5:137984736
|
G | A | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1179+521C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984736 | ||||||
| chr5:137984765
|
T | C | 14 | a0001c0001t0002g0039a0001c0001t0002g0041a0001c0001t0002g0047others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1179+492A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984765 | ||||||
| chr5:137984766
|
GT | G | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1179+490delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984766 | ||||||
| chr5:137984766
|
GTTT | G | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179+488_1179+490d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984766 | ||||||
| chr5:137984821
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1179+436A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984821 | ||||||
| chr5:137984963
|
G | A | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1179+294C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984963 | ||||||
| chr5:137984999
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0253 | 3 | HG03130.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1179+258C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137984999 | ||||||
| chr5:137985226
|
A | T | 1 | a0001c0001t0002g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1179+31T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | 137985226 | ||||||
| chr5:137985658
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1047-269C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137985658 | ||||||
| chr5:137985693
|
CATA | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1047-307_1047-305d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137985693 | ||||||
| chr5:137985713
|
C | T | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047-324G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137985713 | ||||||
| chr5:137986001
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1047-612A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986001 | ||||||
| chr5:137986010
|
C | T | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(243): Show | 246 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1047-621G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986010 | ||||||
| chr5:137986029
|
C | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-640G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986029 | ||||||
| chr5:137986076
|
C | CT | 58 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1047-688dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986076 | ||||||
| chr5:137986134
|
G | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-745C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986134 | ||||||
| chr5:137986341
|
T | TA | 11 | a0001c0001t0002g0056a0001c0001t0002g0070a0001c0001t0002g0268others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1047-953dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986341 | ||||||
| chr5:137986426
|
T | TCC | 46 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(43): Show | 46 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1046+1033_1046+103 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986426 | ||||||
| chr5:137986435
|
CA | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1046+1025delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986435 | ||||||
| chr5:137986436
|
A | C | 70 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1046+1025T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986436 | ||||||
| chr5:137986449
|
A | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1046+1012T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986449 | ||||||
| chr5:137986554
|
T | C | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1046+907A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986554 | ||||||
| chr5:137986746
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1046+715A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986746 | ||||||
| chr5:137986813
|
C | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0207 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1046+648G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986813 | ||||||
| chr5:137986965
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1046+496A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137986965 | ||||||
| chr5:137987428
|
A | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1046+33T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 9/23 | chr5 | 137987428 | ||||||
| chr5:137988054
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.890+220T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 8/23 | chr5 | 137988054 | ||||||
| chr5:137988055
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.890+219C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 8/23 | chr5 | 137988055 | ||||||
| chr5:137988431
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.849-116C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988431 | ||||||
| chr5:137988627
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.849-312C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988627 | ||||||
| chr5:137988650
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0257 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.849-335A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988650 | ||||||
| chr5:137988885
|
T | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.849-570A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988885 | ||||||
| chr5:137988974
|
C | T | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250others(3): Show | 6 | HG01516.hp1 HG01517.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-659G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137988974 | ||||||
| chr5:137989004
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0003g0318 | 3 | NA19009.hp2 NA19085.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.849-689A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989004 | ||||||
| chr5:137989078
|
C | G | 2 | a0001c0001t0006g0262a0001c0001t0006g0263 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849-763G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989078 | ||||||
| chr5:137989118
|
G | A | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-803C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989118 | ||||||
| chr5:137989251
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.849-936A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989251 | ||||||
| chr5:137989369
|
CAGTA | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.849-1058_849-1055d others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989369 | ||||||
| chr5:137989405
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0127 | 2 | NA18950.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.849-1090G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989405 | ||||||
| chr5:137989896
|
G | GA | 48 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.849-1582dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989896 | ||||||
| chr5:137989925
|
G | T | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.849-1610C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989925 | ||||||
| chr5:137989954
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.849-1639G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137989954 | ||||||
| chr5:137990429
|
G | C | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-2114C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990429 | ||||||
| chr5:137990715
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.849-2400C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990715 | ||||||
| chr5:137990775
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.849-2460G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990775 | ||||||
| chr5:137990991
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.849-2676G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137990991 | ||||||
| chr5:137991241
|
T | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-2926A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137991241 | ||||||
| chr5:137992112
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-3797T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992112 | ||||||
| chr5:137992159
|
G | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-3844C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992159 | ||||||
| chr5:137992239
|
T | G | 1 | a0001c0001t0002g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.849-3924A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992239 | ||||||
| chr5:137992299
|
G | GA | 27 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(24): Show | 27 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.849-3985dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992299 | ||||||
| chr5:137992365
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0304 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.849-4050C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992365 | ||||||
| chr5:137992378
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849-4063C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992378 | ||||||
| chr5:137992451
|
G | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-4136C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992451 | ||||||
| chr5:137992551
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.849-4236C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992551 | ||||||
| chr5:137992634
|
A | G | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.849-4319T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992634 | ||||||
| chr5:137992908
|
A | C | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.849-4593T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992908 | ||||||
| chr5:137992948
|
G | A | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0243others(1): Show | 4 | HG00621.hp1 NA18961.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-4633C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992948 | ||||||
| chr5:137992949
|
TCCA | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0243others(1): Show | 4 | HG00621.hp1 NA18961.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-4637_849-4635d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992949 | ||||||
| chr5:137992965
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.849-4650A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137992965 | ||||||
| chr5:137993001
|
T | TACA | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.849-4689_849-4687d others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993001 | ||||||
| chr5:137993454
|
G | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.849-5139C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993454 | ||||||
| chr5:137993506
|
A | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.849-5191T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993506 | ||||||
| chr5:137993781
|
C | T | 2 | a0001c0001t0002g0032a0001c0001t0002g0054 | 2 | HG00323.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.849-5466G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137993781 | ||||||
| chr5:137994104
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01975.hp1 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-5789G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994104 | ||||||
| chr5:137994278
|
C | CT | 60 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.849-5964dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994278 | ||||||
| chr5:137994507
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.849-6192A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994507 | ||||||
| chr5:137994665
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.849-6350G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994665 | ||||||
| chr5:137994742
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0038 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.849-6427T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994742 | ||||||
| chr5:137994892
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.849-6577G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994892 | ||||||
| chr5:137994954
|
C | T | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-6639G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137994954 | ||||||
| chr5:137995016
|
A | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.849-6701T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137995016 | ||||||
| chr5:137995152
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0257 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.849-6837C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137995152 | ||||||
| chr5:137995403
|
A | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.849-7088T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137995403 | ||||||
| chr5:137996069
|
C | T | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.849-7754G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996069 | ||||||
| chr5:137996292
|
C | T | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.849-7977G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996292 | ||||||
| chr5:137996329
|
C | T | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.849-8014G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996329 | ||||||
| chr5:137996473
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.849-8158A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996473 | ||||||
| chr5:137996636
|
A | G | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.849-8321T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996636 | ||||||
| chr5:137996717
|
G | A | 2 | a0001c0001t0003g0306a0001c0001t0003g0321 | 2 | HG01433.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.849-8402C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996717 | ||||||
| chr5:137996829
|
C | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.849-8514G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996829 | ||||||
| chr5:137996884
|
A | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.849-8569T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996884 | ||||||
| chr5:137996965
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.849-8650C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996965 | ||||||
| chr5:137996997
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849-8682C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137996997 | ||||||
| chr5:137997003
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.849-8688C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997003 | ||||||
| chr5:137997049
|
C | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(14): Show | 17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.849-8734G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997049 | ||||||
| chr5:137997193
|
G | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.849-8878C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997193 | ||||||
| chr5:137997270
|
G | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.849-8955C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997270 | ||||||
| chr5:137997393
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0244 | 2 | HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.849-9078G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997393 | ||||||
| chr5:137997400
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.849-9085G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997400 | ||||||
| chr5:137997411
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.849-9096C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997411 | ||||||
| chr5:137997424
|
G | A | 1 | a0002c0003t0002g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.849-9109C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997424 | ||||||
| chr5:137997444
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.849-9129C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997444 | ||||||
| chr5:137997474
|
A | AAT | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849-9161_849-9160d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997474 | ||||||
| chr5:137997476
|
T | A | 6 | a0001c0001t0002g0048a0001c0001t0002g0066a0001c0001t0002g0070others(3): Show | 6 | HG00639.hp2 HG00735.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-9161A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997476 | ||||||
| chr5:137997482
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.849-9167A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997482 | ||||||
| chr5:137997700
|
C | T | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.848+9290G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997700 | ||||||
| chr5:137997982
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.848+9008A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137997982 | ||||||
| chr5:137998386
|
C | G | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.848+8604G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998386 | ||||||
| chr5:137998714
|
A | T | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.848+8276T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998714 | ||||||
| chr5:137998752
|
T | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+8238A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998752 | ||||||
| chr5:137998759
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.848+8231C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998759 | ||||||
| chr5:137998866
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+8124G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998866 | ||||||
| chr5:137998924
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.848+8066C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137998924 | ||||||
| chr5:137999102
|
G | A | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.848+7888C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999102 | ||||||
| chr5:137999104
|
C | CT | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 82 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.848+7885dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999104 | ||||||
| chr5:137999118
|
G | T | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.848+7872C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999118 | ||||||
| chr5:137999120
|
C | T | 1 | a0001c0001t0010g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.848+7870G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999120 | ||||||
| chr5:137999126
|
T | C | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.848+7864A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999126 | ||||||
| chr5:137999133
|
A | G | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.848+7857T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999133 | ||||||
| chr5:137999433
|
A | C | 1 | a0001c0001t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.848+7557T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999433 | ||||||
| chr5:137999445
|
A | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.848+7545T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999445 | ||||||
| chr5:137999787
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.848+7203A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999787 | ||||||
| chr5:137999912
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.848+7078C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 137999912 | ||||||
| chr5:138000088
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.848+6902G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000088 | ||||||
| chr5:138000169
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0174 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.848+6821A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000169 | ||||||
| chr5:138000201
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0257 | 3 | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.848+6789A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000201 | ||||||
| chr5:138000293
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848+6697A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000293 | ||||||
| chr5:138000524
|
G | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+6466C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000524 | ||||||
| chr5:138000728
|
C | T | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.848+6262G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000728 | ||||||
| chr5:138000836
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0240 | 2 | NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.848+6154G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000836 | ||||||
| chr5:138000936
|
C | A | 239 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(236): Show | 239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.848+6054G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000936 | ||||||
| chr5:138000943
|
C | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0022others(99): Show | 102 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.848+6047G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000943 | ||||||
| chr5:138000943
|
CA | C | 201 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.848+6046delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000943 | ||||||
| chr5:138000944
|
A | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0022others(96): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.848+6046T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000944 | ||||||
| chr5:138000948
|
A | C | 1 | a0001c0001t0009g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848+6042T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138000948 | ||||||
| chr5:138001120
|
C | CAA | 6 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0187others(3): Show | 6 | HG01257.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+5868_848+5869d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001120 | ||||||
| chr5:138001134
|
A | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+5856T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001134 | ||||||
| chr5:138001455
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.848+5535G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001455 | ||||||
| chr5:138001740
|
G | A | 115 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(112): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.848+5250C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001740 | ||||||
| chr5:138001769
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.848+5221T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001769 | ||||||
| chr5:138001952
|
G | A | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+5038C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138001952 | ||||||
| chr5:138002477
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0003g0318 | 3 | NA19009.hp2 NA19085.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.848+4513G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002477 | ||||||
| chr5:138002530
|
T | C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+4460A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002530 | ||||||
| chr5:138002664
|
A | AT | 277 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(274): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.848+4325dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002664 | ||||||
| chr5:138002664
|
A | ATT | 14 | a0001c0001t0001g0097a0001c0001t0001g0126a0001c0001t0001g0154others(11): Show | 14 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.848+4324_848+4325d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002664 | ||||||
| chr5:138002737
|
C | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+4253G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002737 | ||||||
| chr5:138002832
|
AT | A | 60 | a0001c0001t0001g0115a0001c0001t0002g0019a0001c0001t0002g0020others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.848+4157delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002832 | ||||||
| chr5:138002963
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+4027G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138002963 | ||||||
| chr5:138003054
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+3936G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003054 | ||||||
| chr5:138003161
|
A | G | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.848+3829T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003161 | ||||||
| chr5:138003358
|
A | G | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.848+3632T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003358 | ||||||
| chr5:138003458
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.848+3532A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003458 | ||||||
| chr5:138003483
|
G | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+3507C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003483 | ||||||
| chr5:138003488
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.848+3502C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003488 | ||||||
| chr5:138003644
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.848+3346G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003644 | ||||||
| chr5:138003775
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.848+3215T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003775 | ||||||
| chr5:138003977
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.848+3013G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138003977 | ||||||
| chr5:138004304
|
C | CAATGAAT others(8): Show |
310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.848+2685_848+2686i others(17): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004304 | ||||||
| chr5:138004378
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.848+2612A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004378 | ||||||
| chr5:138004480
|
G | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0029others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+2510C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004480 | ||||||
| chr5:138004513
|
T | C | 9 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+2477A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004513 | ||||||
| chr5:138004529
|
C | A | 53 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.848+2461G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004529 | ||||||
| chr5:138004532
|
G | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+2458C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004532 | ||||||
| chr5:138004608
|
G | A | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.848+2382C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004608 | ||||||
| chr5:138004749
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.848+2241C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004749 | ||||||
| chr5:138004754
|
C | T | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.848+2236G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004754 | ||||||
| chr5:138004898
|
C | T | 2 | a0001c0002t0002g0289a0001c0002t0002g0290 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.848+2092G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004898 | ||||||
| chr5:138004909
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.848+2081T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138004909 | ||||||
| chr5:138005020
|
T | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.848+1970A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005020 | ||||||
| chr5:138005126
|
A | G | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.848+1864T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005126 | ||||||
| chr5:138005127
|
C | G | 1 | a0001c0001t0002g0075 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.848+1863G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005127 | ||||||
| chr5:138005221
|
G | A | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.848+1769C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005221 | ||||||
| chr5:138005269
|
A | G | 1 | a0001c0001t0013g0236 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.848+1721T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005269 | ||||||
| chr5:138005272
|
TTAAAACA others(2): Show |
T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.848+1709_848+1717d others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005272 | ||||||
| chr5:138005403
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848+1587T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005403 | ||||||
| chr5:138005463
|
AT | A | 156 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(153): Show | 156 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.848+1526delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005463 | ||||||
| chr5:138005477
|
G | A | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+1513C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005477 | ||||||
| chr5:138005653
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.848+1337T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005653 | ||||||
| chr5:138005670
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.848+1320C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005670 | ||||||
| chr5:138005845
|
T | C | 242 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(239): Show | 242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.848+1145A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005845 | ||||||
| chr5:138005922
|
G | A | 2 | a0001c0001t0006g0262a0001c0001t0006g0263 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.848+1068C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005922 | ||||||
| chr5:138005938
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.848+1052C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138005938 | ||||||
| chr5:138006045
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+945G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006045 | ||||||
| chr5:138006047
|
C | T | 14 | a0001c0001t0002g0039a0001c0001t0002g0041a0001c0001t0002g0047others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.848+943G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006047 | ||||||
| chr5:138006139
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+851A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006139 | ||||||
| chr5:138006154
|
C | G | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+836G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006154 | ||||||
| chr5:138006188
|
C | T | 9 | a0001c0001t0001g0096a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 9 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+802G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006188 | ||||||
| chr5:138006221
|
C | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.848+769G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006221 | ||||||
| chr5:138006355
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0181a0001c0001t0001g0193 | 3 | HG00280.hp2 HG01255.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.848+635G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006355 | ||||||
| chr5:138006362
|
G | A | 1 | a0001c0001t0004g0264 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.848+628C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006362 | ||||||
| chr5:138006824
|
A | T | 1 | a0001c0001t0001g0025 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.848+166T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006824 | ||||||
| chr5:138006887
|
A | G | 1 | a0001c0001t0009g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.848+103T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006887 | ||||||
| chr5:138006900
|
T | C | 116 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(113): Show | 116 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.848+90A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 7/23 | chr5 | 138006900 | ||||||
| chr5:138007360
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.691-213T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007360 | ||||||
| chr5:138007410
|
T | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0217others(2): Show | 5 | HG00408.hp2 NA18612.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-263A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007410 | ||||||
| chr5:138007427
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0116 | 2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.691-280T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007427 | ||||||
| chr5:138007574
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.691-427C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007574 | ||||||
| chr5:138007701
|
CA | C | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.691-555delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007701 | ||||||
| chr5:138007752
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02027.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.691-605A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138007752 | ||||||
| chr5:138008066
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.691-919A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008066 | ||||||
| chr5:138008084
|
C | A | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.691-937G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008084 | ||||||
| chr5:138008448
|
A | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0125 | 2 | NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.691-1301T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008448 | ||||||
| chr5:138008498
|
C | A | 50 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.691-1351G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008498 | ||||||
| chr5:138008624
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.691-1477A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008624 | ||||||
| chr5:138008658
|
A | G | 1 | a0003c0005t0001g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.691-1511T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008658 | ||||||
| chr5:138008739
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0244 | 2 | HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.691-1592A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008739 | ||||||
| chr5:138008999
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0005g0001others(1): Show | 4 | HG00408.hp2 NA18612.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1852G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138008999 | ||||||
| chr5:138009344
|
G | T | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.690+1664C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009344 | ||||||
| chr5:138009445
|
G | A | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.690+1563C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009445 | ||||||
| chr5:138009488
|
C | CA | 7 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0109others(4): Show | 7 | HG01069.hp1 HG02735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+1519dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009488 | ||||||
| chr5:138009778
|
T | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.690+1230A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009778 | ||||||
| chr5:138009784
|
G | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.690+1224C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009784 | ||||||
| chr5:138009802
|
C | CA | 177 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.690+1205dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009802 | ||||||
| chr5:138009802
|
C | CAA | 6 | a0001c0001t0001g0107a0001c0001t0001g0246a0001c0001t0002g0053others(3): Show | 6 | HG01167.hp1 HG01175.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+1204_690+1205d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009802 | ||||||
| chr5:138009869
|
G | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0203others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+1139C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138009869 | ||||||
| chr5:138010085
|
A | G | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.690+923T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010085 | ||||||
| chr5:138010106
|
C | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.690+902G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010106 | ||||||
| chr5:138010224
|
AC | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.690+783delG | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010224 | ||||||
| chr5:138010556
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.690+452T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010556 | ||||||
| chr5:138010717
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0056 | 2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.690+291T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010717 | ||||||
| chr5:138010724
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.690+284A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010724 | ||||||
| chr5:138010854
|
A | C | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.690+154T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010854 | ||||||
| chr5:138010957
|
T | TA | 178 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.690+50dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010957 | ||||||
| chr5:138010957
|
T | TAA | 104 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(101): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.690+49_690+50dupTT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 6/23 | chr5 | 138010957 | ||||||
| chr5:138011379
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.549-230A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011379 | ||||||
| chr5:138011664
|
C | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.548+104G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011664 | ||||||
| chr5:138011714
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.548+54C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011714 | ||||||
| chr5:138011751
|
T | A | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.548+17A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 5/23 | chr5 | 138011751 | ||||||
| chr5:138012028
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0244 | 2 | HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.371-83G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012028 | ||||||
| chr5:138012089
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.371-144G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012089 | ||||||
| chr5:138012117
|
ATGGAGAA others(4): Show |
A | 1 | a0001c0002t0002g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.371-183_371-173del others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012117 | ||||||
| chr5:138012216
|
C | CT | 205 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.371-272dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012216 | ||||||
| chr5:138012216
|
C | CTT | 11 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0210others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.371-273_371-272dup others(2): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012216 | ||||||
| chr5:138012216
|
CTTTTTT | C | 50 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(47): Show | 50 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.371-277_371-272del others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012216 | ||||||
| chr5:138012224
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.371-279A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012224 | ||||||
| chr5:138012303
|
A | G | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-358T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012303 | ||||||
| chr5:138012328
|
G | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.371-383C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012328 | ||||||
| chr5:138012508
|
A | C | 58 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.371-563T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012508 | ||||||
| chr5:138012527
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-582C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012527 | ||||||
| chr5:138012608
|
G | A | 242 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(239): Show | 242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.371-663C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012608 | ||||||
| chr5:138012730
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.371-785G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012730 | ||||||
| chr5:138012905
|
CA | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0182a0001c0001t0002g0300others(4): Show | 7 | HG01243.hp1 HG01256.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-961delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138012905 | ||||||
| chr5:138013270
|
G | C | 1 | a0001c0001t0002g0046 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.371-1325C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013270 | ||||||
| chr5:138013283
|
T | C | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.371-1338A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013283 | ||||||
| chr5:138013454
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.371-1509A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013454 | ||||||
| chr5:138013501
|
C | CA | 232 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(229): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.371-1557dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013501 | ||||||
| chr5:138013501
|
C | CAA | 8 | a0001c0001t0001g0117a0001c0001t0001g0147a0001c0001t0001g0180others(5): Show | 8 | HG01515.hp2 HG02559.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.371-1558_371-1557d others(4): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013501 | ||||||
| chr5:138013517
|
A | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-1572T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013517 | ||||||
| chr5:138013694
|
C | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA19003.hp2 NA19056.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.371-1749G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138013694 | ||||||
| chr5:138014015
|
C | G | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-2070G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014015 | ||||||
| chr5:138014031
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.371-2086C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014031 | ||||||
| chr5:138014050
|
C | T | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.371-2105G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014050 | ||||||
| chr5:138014291
|
G | A | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.371-2346C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014291 | ||||||
| chr5:138014599
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.371-2654C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014599 | ||||||
| chr5:138014789
|
T | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.371-2844A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138014789 | ||||||
| chr5:138015273
|
G | A | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.370+3029C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015273 | ||||||
| chr5:138015304
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.370+2998G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015304 | ||||||
| chr5:138015388
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.370+2914C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015388 | ||||||
| chr5:138015429
|
G | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370+2873C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015429 | ||||||
| chr5:138015459
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.370+2843G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015459 | ||||||
| chr5:138015470
|
A | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0168a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.370+2832T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015470 | ||||||
| chr5:138015478
|
A | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.370+2824T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138015478 | ||||||
| chr5:138016148
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.370+2154A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016148 | ||||||
| chr5:138016459
|
T | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0072others(1): Show | 4 | HG00741.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+1843A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016459 | ||||||
| chr5:138016460
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0092 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.370+1842T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016460 | ||||||
| chr5:138016507
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370+1795C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016507 | ||||||
| chr5:138016613
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(5): Show | 8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.370+1689C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138016613 | ||||||
| chr5:138017343
|
A | G | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.370+959T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017343 | ||||||
| chr5:138017391
|
T | C | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0281 | 3 | HG02055.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.370+911A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017391 | ||||||
| chr5:138017852
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.370+450A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017852 | ||||||
| chr5:138017979
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.370+323G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138017979 | ||||||
| chr5:138018278
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.370+24A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 4/23 | chr5 | 138018278 | ||||||
| chr5:138018792
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+163C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 3/23 | chr5 | 138018792 | ||||||
| chr5:138019162
|
C | CA | 62 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(59): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-35-17dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019162 | ||||||
| chr5:138019162
|
CA | C | 239 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(236): Show | 239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-35-17delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019162 | ||||||
| chr5:138019247
|
A | G | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-101T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019247 | ||||||
| chr5:138019440
|
T | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG03490.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-35-294A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019440 | ||||||
| chr5:138019591
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-35-445C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019591 | ||||||
| chr5:138019682
|
AT | A | 270 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-35-537delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019682 | ||||||
| chr5:138019813
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0257 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-35-667C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019813 | ||||||
| chr5:138019841
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0192 | 3 | HG00639.hp1 HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-35-695C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019841 | ||||||
| chr5:138019932
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-35-786C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138019932 | ||||||
| chr5:138020196
|
G | A | 1 | a0001c0001t0013g0236 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-36+835C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020196 | ||||||
| chr5:138020210
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-36+821C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020210 | ||||||
| chr5:138020287
|
T | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0117a0001c0001t0001g0119others(2): Show | 5 | NA18953.hp2 NA19011.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+744A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020287 | ||||||
| chr5:138020323
|
C | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-36+708G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020323 | ||||||
| chr5:138020324
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-36+707C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020324 | ||||||
| chr5:138020663
|
A | G | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-36+368T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020663 | ||||||
| chr5:138020850
|
A | C | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+181T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 2/23 | chr5 | 138020850 | ||||||
| chr5:138021523
|
C | CATG | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-327_-202-326i others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138021523 | ||||||
| chr5:138021768
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0162 | 3 | HG00738.hp1 HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-202-571C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138021768 | ||||||
| chr5:138021846
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-202-649A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138021846 | ||||||
| chr5:138022087
|
C | T | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-890G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022087 | ||||||
| chr5:138022112
|
CAAAAAAA others(2): Show |
C | 239 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(236): Show | 239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-202-924_-202-916d others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022112 | ||||||
| chr5:138022294
|
T | C | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-202-1097A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022294 | ||||||
| chr5:138022324
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-202-1127A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022324 | ||||||
| chr5:138022628
|
C | T | 7 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0046others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-202-1431G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022628 | ||||||
| chr5:138022847
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-1650C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022847 | ||||||
| chr5:138022863
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-202-1666G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022863 | ||||||
| chr5:138022946
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-202-1749C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022946 | ||||||
| chr5:138022954
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-1757T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022954 | ||||||
| chr5:138022993
|
G | T | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-202-1796C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138022993 | ||||||
| chr5:138023065
|
C | G | 5 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0059others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-1868G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023065 | ||||||
| chr5:138023235
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-2038T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023235 | ||||||
| chr5:138023401
|
C | A | 3 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0303 | 3 | HG01243.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-202-2204G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023401 | ||||||
| chr5:138023404
|
T | C | 64 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0028others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-202-2207A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023404 | ||||||
| chr5:138023551
|
T | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0187others(3): Show | 6 | HG01257.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-2354A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023551 | ||||||
| chr5:138023676
|
C | G | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-202-2479G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023676 | ||||||
| chr5:138023765
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-202-2568C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023765 | ||||||
| chr5:138023856
|
G | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-2659C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023856 | ||||||
| chr5:138023894
|
C | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-202-2697G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138023894 | ||||||
| chr5:138024068
|
T | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-2871A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024068 | ||||||
| chr5:138024194
|
A | C | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-202-2997T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024194 | ||||||
| chr5:138024314
|
C | G | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-202-3117G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024314 | ||||||
| chr5:138024329
|
G | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-3132C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024329 | ||||||
| chr5:138024359
|
T | C | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-202-3162A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024359 | ||||||
| chr5:138024477
|
T | G | 116 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(113): Show | 116 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-202-3280A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024477 | ||||||
| chr5:138024579
|
T | TA | 305 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(302): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-202-3383dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024579 | ||||||
| chr5:138024632
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-202-3435A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024632 | ||||||
| chr5:138024683
|
G | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(5): Show | 8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-3486C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024683 | ||||||
| chr5:138024786
|
A | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-3589T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024786 | ||||||
| chr5:138024810
|
C | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-3613G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024810 | ||||||
| chr5:138024812
|
C | G | 4 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-202-3615G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | ||||||
| chr5:138024812
|
CAG | C | 68 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-202-3617_-202-361 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | ||||||
| chr5:138024812
|
CAGAG | C | 122 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(119): Show | 122 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-202-3619_-202-361 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | ||||||
| chr5:138024812
|
CAGAGAG | C | 116 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 116 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-202-3621_-202-361 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024812 | ||||||
| chr5:138024816
|
G | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02523.hp1 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-202-3619C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024816 | ||||||
| chr5:138024818
|
G | C | 126 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(123): Show | 126 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-202-3621C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024818 | ||||||
| chr5:138024820
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0198 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-202-3623C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024820 | ||||||
| chr5:138024834
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-202-3637C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024834 | ||||||
| chr5:138024836
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-202-3639T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024836 | ||||||
| chr5:138024902
|
ACT | A | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-3707_-202-370 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024902 | ||||||
| chr5:138024922
|
G | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0187others(3): Show | 6 | HG01257.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-3725C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138024922 | ||||||
| chr5:138025011
|
T | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG00423.hp1 HG00438.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-202-3814A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025011 | ||||||
| chr5:138025093
|
C | G | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-3896G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025093 | ||||||
| chr5:138025093
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-202-3896G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025093 | ||||||
| chr5:138025288
|
C | CATATAT | 5 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(2): Show | 5 | HG01069.hp1 HG01070.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4097_-202-409 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | ||||||
| chr5:138025288
|
C | CATATATA others(1): Show |
20 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0032others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-202-4099_-202-409 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | ||||||
| chr5:138025288
|
C | CATATATA others(3): Show |
18 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0030others(15): Show | 18 | HG01257.hp1 HG01258.hp2 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.-202-4101_-202-409 others(14): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | ||||||
| chr5:138025288
|
C | CATATATA others(5): Show |
2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG00140.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-202-4103_-202-409 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | ||||||
| chr5:138025288
|
CATAT | C | 16 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(13): Show | 16 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-202-4095_-202-409 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | ||||||
| chr5:138025288
|
CATATAT | C | 84 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(81): Show | 84 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-202-4097_-202-409 others(10): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025288 | ||||||
| chr5:138025304
|
TATATA | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG00597.hp1 NA18948.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4112_-202-410 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025304 | ||||||
| chr5:138025305
|
A | G | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(130): Show | 133 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-202-4108T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025305 | ||||||
| chr5:138025306
|
TATATG | T | 116 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-202-4114_-202-411 others(9): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025306 | ||||||
| chr5:138025306
|
TATATGTA | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0078others(14): Show | 17 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.-202-4116_-202-411 others(11): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025306 | ||||||
| chr5:138025307
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-4110T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025307 | ||||||
| chr5:138025309
|
A | G | 11 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(8): Show | 11 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-202-4112T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025309 | ||||||
| chr5:138025310
|
T | G | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG00597.hp1 NA18948.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4113A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025310 | ||||||
| chr5:138025311
|
G | A | 9 | a0001c0001t0002g0033a0001c0001t0002g0059a0001c0001t0002g0060others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.-202-4114C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025311 | ||||||
| chr5:138025311
|
G | T | 11 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0202others(8): Show | 11 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-202-4114C>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025311 | ||||||
| chr5:138025313
|
A | AT | 7 | a0001c0001t0002g0166a0001c0001t0002g0300a0001c0001t0002g0301others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-202-4117dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025313 | ||||||
| chr5:138025313
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-202-4116T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025313 | ||||||
| chr5:138025313
|
A | T | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 222 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-202-4116T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025313 | ||||||
| chr5:138025315
|
T | A | 1 | a0002c0003t0002g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-202-4118A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025315 | ||||||
| chr5:138025319
|
T | G | 1 | a0001c0001t0013g0236 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-202-4122A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025319 | ||||||
| chr5:138025322
|
T | G | 80 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-202-4125A>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025322 | ||||||
| chr5:138025516
|
G | A | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-202-4319C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025516 | ||||||
| chr5:138025705
|
A | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-4508T>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025705 | ||||||
| chr5:138025729
|
C | T | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-4532G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025729 | ||||||
| chr5:138025775
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0117 | 2 | NA18953.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-202-4578G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138025775 | ||||||
| chr5:138026009
|
A | T | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4812T>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026009 | ||||||
| chr5:138026233
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-202-5036A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026233 | ||||||
| chr5:138026254
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0116 | 2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-202-5057G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026254 | ||||||
| chr5:138026270
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-202-5073A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026270 | ||||||
| chr5:138026572
|
T | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-5375A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026572 | ||||||
| chr5:138026628
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-202-5431G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | ||||||
| chr5:138026628
|
C | CA | 54 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-202-5432dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | ||||||
| chr5:138026628
|
C | CAA | 45 | a0001c0001t0001g0237a0001c0001t0001g0245a0001c0001t0001g0282others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-202-5433_-202-543 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | ||||||
| chr5:138026628
|
C | CAAA | 9 | a0001c0001t0001g0280a0001c0001t0002g0019a0001c0001t0002g0063others(6): Show | 9 | HG00735.hp2 HG01167.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-202-5434_-202-543 others(7): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | ||||||
| chr5:138026628
|
CA | C | 13 | a0001c0001t0001g0095a0001c0001t0001g0114a0001c0001t0001g0115others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-5432delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026628 | ||||||
| chr5:138026655
|
A | AC | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-202-5459_-202-545 others(5): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026655 | ||||||
| chr5:138026655
|
A | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(10): Show | 13 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-5458T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026655 | ||||||
| chr5:138026689
|
C | CA | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-202-5493dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026689 | ||||||
| chr5:138026742
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-202-5545G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026742 | ||||||
| chr5:138026757
|
T | A | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-202-5560A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026757 | ||||||
| chr5:138026858
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-202-5661C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026858 | ||||||
| chr5:138026938
|
C | CAAAT | 23 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(20): Show | 23 | HG00280.hp2 HG00733.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-202-5745_-202-574 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026938
|
C | CAAATAAA others(1): Show |
8 | a0001c0001t0001g0093a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-5749_-202-574 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026938
|
CAAAT | C | 119 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0089others(116): Show | 119 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-202-5745_-202-574 others(8): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026938
|
CAAATAAA others(1): Show |
C | 15 | a0001c0001t0001g0091a0001c0001t0001g0243a0001c0001t0001g0244others(12): Show | 15 | HG00621.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-202-5749_-202-574 others(12): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026938
|
CAAATAAA others(5): Show |
C | 15 | a0001c0001t0002g0020a0001c0001t0002g0072a0001c0001t0002g0073others(12): Show | 15 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-5753_-202-574 others(16): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026938
|
CAAATAAA others(9): Show |
C | 1 | a0001c0001t0002g0074 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-202-5757_-202-574 others(20): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026938
|
CAAATAAA others(13): Show |
C | 1 | a0001c0001t0002g0075 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-202-5761_-202-574 others(24): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026938 | ||||||
| chr5:138026999
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+5783C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138026999 | ||||||
| chr5:138027383
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-203+5399A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027383 | ||||||
| chr5:138027484
|
T | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-203+5298A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027484 | ||||||
| chr5:138027496
|
T | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-203+5286A>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027496 | ||||||
| chr5:138027514
|
G | A | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+5268C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027514 | ||||||
| chr5:138027542
|
T | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | HG02258.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-203+5240A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027542 | ||||||
| chr5:138027589
|
T | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-203+5193A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027589 | ||||||
| chr5:138027625
|
C | G | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-203+5157G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027625 | ||||||
| chr5:138027785
|
T | C | 8 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-203+4997A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027785 | ||||||
| chr5:138027969
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-203+4813T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138027969 | ||||||
| chr5:138028408
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-203+4374A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028408 | ||||||
| chr5:138028494
|
GA | G | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+4287delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028494 | ||||||
| chr5:138028549
|
G | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+4233C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028549 | ||||||
| chr5:138028592
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-203+4190C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028592 | ||||||
| chr5:138028607
|
G | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-203+4175C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028607 | ||||||
| chr5:138028637
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-203+4145G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028637 | ||||||
| chr5:138028752
|
T | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+4030A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028752 | ||||||
| chr5:138028800
|
C | T | 2 | a0001c0002t0002g0289a0001c0002t0002g0290 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-203+3982G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028800 | ||||||
| chr5:138028968
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-203+3814C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138028968 | ||||||
| chr5:138029029
|
GA | G | 19 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00558.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+3752delT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029029 | ||||||
| chr5:138029106
|
C | T | 19 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0001g0181others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+3676G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029106 | ||||||
| chr5:138029133
|
T | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+3649A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029133 | ||||||
| chr5:138029241
|
T | C | 4 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-203+3541A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029241 | ||||||
| chr5:138029323
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-203+3459T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029323 | ||||||
| chr5:138029328
|
T | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+3454A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029328 | ||||||
| chr5:138029432
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-203+3350C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138029432 | ||||||
| chr5:138030279
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-203+2503G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030279 | ||||||
| chr5:138030334
|
A | C | 240 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(237): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-203+2448T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030334 | ||||||
| chr5:138030410
|
C | CT | 14 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.-203+2371dupA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030410 | ||||||
| chr5:138030410
|
CT | C | 114 | a0001c0001t0001g0009a0001c0001t0001g0076a0001c0001t0001g0077others(111): Show | 114 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-203+2371delA | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030410 | ||||||
| chr5:138030691
|
G | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0250 | 3 | HG02145.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-203+2091C>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030691 | ||||||
| chr5:138030711
|
T | TC | 108 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-203+2070dupG | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030711 | ||||||
| chr5:138030711
|
T | TCC | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0252others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.-203+2069_-203+207 others(6): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030711 | ||||||
| chr5:138030722
|
C | CA | 8 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+2059dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030722 | ||||||
| chr5:138030723
|
A | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(8): Show | 11 | HG00735.hp1 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.-203+2059T>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030723 | ||||||
| chr5:138030758
|
G | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+2024C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030758 | ||||||
| chr5:138030837
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-203+1945G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030837 | ||||||
| chr5:138030893
|
C | A | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270 | 3 | HG01516.hp1 HG01517.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-203+1889G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030893 | ||||||
| chr5:138030925
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-203+1857G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030925 | ||||||
| chr5:138030948
|
G | A | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-203+1834C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138030948 | ||||||
| chr5:138031030
|
C | CA | 6 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270others(3): Show | 6 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+1751dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031030 | ||||||
| chr5:138031113
|
C | A | 2 | a0002c0003t0002g0007a0002c0003t0002g0008 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-203+1669G>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031113 | ||||||
| chr5:138031232
|
T | TA | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG01496.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+1549dupT | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031232 | ||||||
| chr5:138031322
|
C | G | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-203+1460G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031322 | ||||||
| chr5:138031426
|
G | A | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+1356C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031426 | ||||||
| chr5:138031451
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG00642.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-203+1331C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031451 | ||||||
| chr5:138031474
|
G | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287 | 3 | HG02559.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-203+1308C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031474 | ||||||
| chr5:138031742
|
C | T | 310 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(307): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-203+1040G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031742 | ||||||
| chr5:138031908
|
C | G | 1 | a0001c0001t0001g0009 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-203+874G>C | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138031908 | ||||||
| chr5:138032020
|
T | C | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+762A>G | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032020 | ||||||
| chr5:138032479
|
C | T | 6 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0006others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+303G>A | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032479 | ||||||
| chr5:138032714
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+68C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032714 | ||||||
| chr5:138032732
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-203+50C>T | FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | 138032732 |