Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 81573 |
|---|---|
| ensemblid | ENSG00000118454.13 |
| hgncid | 25374 |
| symbol | ANKRD13C |
| name | ankyrin repeat domain 13C |
| refseq_nuc | NM_030816.5 |
| refseq_prot | NP_110443.3 |
| ensembl_nuc | ENST00000370944.9 |
| ensembl_prot | ENSP00000359982.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 70258999 |
| end | 70354722 |
| strand | - |
| ver | v1.2 |
| region | chr1:70258999-70354722 |
| region5000 | chr1:70253999-70359722 |
| regionname0 | ANKRD13C_chr1_70258999_70354722 |
| regionname5000 | ANKRD13C_chr1_70253999_70359722 |
| 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 | 541 | 347 | 86 | 51 | 158 | 16 | 34 | 125 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0002 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0003 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0004 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0005 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0006 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1626 | 318 | 85 | 43 | 144 | 16 | 28 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0002 | 0/0 | 1626 | 26 | 1 | 6 | 14 | 0 | 5 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0003 | 0/0 | 1626 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0004 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0005 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0006 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0007 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0008 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| c0009 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4033 | 265 | 45 | 36 | 148 | 13 | 21 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0002 | 0/0 | 4033 | 31 | 8 | 9 | 7 | 3 | 4 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0003 | 0/0 | 4033 | 8 | 8 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0004 | 0/0 | 4033 | 6 | 5 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0005 | 0/0 | 4033 | 6 | 3 | 0 | 3 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0006 | 0/0 | 4033 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0007 | 0/0 | 4033 | 4 | 1 | 0 | 0 | 0 | 3 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0008 | 0/0 | 4033 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0009 | 0/0 | 4033 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0010 | 0/0 | 4033 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0011 | 0/0 | 4033 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0012 | 0/0 | 4033 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0013 | 0/0 | 4045 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0014 | 0/0 | 4033 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0015 | 0/0 | 4033 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0016 | 0/0 | 4033 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0017 | 0/0 | 4033 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0018 | 0/0 | 4033 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0019 | 0/0 | 4033 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0020 | 0/0 | 4033 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0021 | 0/0 | 4033 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0022 | 0/0 | 4033 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0023 | 0/0 | 4033 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0024 | 0/0 | 4033 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0025 | 0/0 | 4033 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0026 | 0/0 | 4033 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0027 | 0/0 | 4033 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0028 | 0/0 | 4033 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| t0029 | 0/0 | 4033 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1626 | 318 | 85 | 43 | 144 | 16 | 28 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0002 | 0/0 | 1626 | 26 | 1 | 6 | 14 | 0 | 5 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0003 | 0/0 | 1626 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0005 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0002c0007 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0003c0008 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0004c0006 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0005c0009 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0006c0004 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5658 | 240 | 44 | 31 | 134 | 13 | 16 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0002 | 0/0 | 5658 | 29 | 8 | 7 | 7 | 3 | 4 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0003 | 0/0 | 5658 | 8 | 8 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0004 | 0/0 | 5658 | 6 | 5 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0005 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0006 | 0/0 | 5658 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0007 | 0/0 | 5658 | 4 | 1 | 0 | 0 | 0 | 3 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0008 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0009 | 0/0 | 5658 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0011 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0012 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0013 | 0/0 | 5670 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0014 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0015 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0016 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0017 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0018 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0020 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0021 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0022 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0023 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0025 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0026 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0027 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0028 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0001t0029 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0002t0001 | 0/0 | 5658 | 19 | 1 | 4 | 10 | 0 | 4 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0002t0005 | 0/0 | 5658 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0002t0010 | 0/0 | 5658 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0002t0019 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0002t0024 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0003t0002 | 0/0 | 5658 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0001c0005t0001 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0002c0007t0001 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0003c0008t0001 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0004c0006t0001 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0005c0009t0001 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| a0006c0004t0001 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | copy fasta | chr1 | 70253999 | 70359722 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0011g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0011g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0012g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0012g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0013g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0013g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0017g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0018g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0020g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0021g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0022g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0025g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0026g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0027g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0028g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0001t0029g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0010g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0010g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0019g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0002t0024g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0001c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0002c0007t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0003c0008t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0004c0006t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0005c0009t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| a0006c0004t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | GBR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00639 | hp2 | a0003 | c0008 | t0001 | g0342 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00738 | hp2 | a0001 | c0001 | t0025 | g0115 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01167 | hp1 | a0001 | c0001 | t0020 | g0262 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01175 | hp2 | a0001 | c0002 | t0010 | g0024 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0032 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0033 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01496 | hp1 | a0001 | c0002 | t0010 | g0014 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | IBS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0340 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0199 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01975 | hp1 | a0001 | c0001 | t0018 | g0242 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02015 | hp1 | a0001 | c0001 | t0017 | g0238 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02080 | hp1 | a0005 | c0009 | t0001 | g0343 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CDX | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0104 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0345 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02683 | hp2 | a0001 | c0001 | t0013 | g0349 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02717 | hp1 | a0001 | c0001 | t0028 | g0338 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0348 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0346 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0186 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0195 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0347 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0301 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03516 | hp2 | a0001 | c0001 | t0029 | g0344 | AFR | ESN | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03669 | hp2 | a0001 | c0001 | t0027 | g0097 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03704 | hp1 | a0001 | c0001 | t0021 | g0239 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03704 | hp2 | a0001 | c0001 | t0013 | g0350 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0050 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0003 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | STU | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0022 | SAS | STU | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | YRI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18949 | hp2 | a0001 | c0001 | t0022 | g0215 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18962 | hp1 | a0001 | c0001 | t0016 | g0119 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18966 | hp1 | a0006 | c0004 | t0001 | g0004 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18972 | hp2 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18975 | hp2 | a0001 | c0002 | t0024 | g0025 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18985 | hp2 | a0004 | c0006 | t0001 | g0034 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19000 | hp2 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | LWK | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0045 | AFR | LWK | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | LWK | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19063 | hp1 | a0002 | c0007 | t0001 | g0236 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19086 | hp2 | a0001 | c0002 | t0005 | g0031 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | TSI | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20905 | hp1 | a0001 | c0002 | t0019 | g0009 | SAS | GIH | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | GIH | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02486 | hp2 | a0001 | c0001 | t0023 | g0037 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | ACB | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | USA | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | USA | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | USA | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0085 | REF | REF | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | ANKRD13C_chr1_70253999_70359722 | ANKRD13C | chr1 | 70253999 | 70359722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70315503
|
C | T | 1 | a0002 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.641G>A | p.Arg214Gln | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/13 | 955/5658 | 641/1626 | 214/541 | chr1 | 70315503 | ||
| chr1:70353996
|
C | A | 1 | a0003 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.413G>T | p.Gly138Val | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 727/5658 | 413/1626 | 138/541 | chr1 | 70353996 | ||
| chr1:70354105
|
C | T | 1 | a0004 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.304G>A | p.Ala102Thr | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 618/5658 | 304/1626 | 102/541 | chr1 | 70354105 | ||
| chr1:70354372
|
G | A | 1 | a0005 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.37C>T | p.His13Tyr | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 351/5658 | 37/1626 | 13/541 | chr1 | 70354372 | ||
| chr1:70354402
|
C | T | 1 | a0006 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.7G>A | p.Gly3Arg | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 321/5658 | 7/1626 | 3/541 | chr1 | 70354402 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70274740
|
T | C | 1 | a0001c0005 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1374A>G | p.Glu458Glu | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/13 | 1688/5658 | 1374/1626 | 458/541 | chr1 | 70274740 | ||
| chr1:70354229
|
C | T | 1 | a0001c0003 | 2 | HG01255.hp1 HG01361.hp1 |
synonymous_variant | LOW | c.180G>A | p.Arg60Arg | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 494/5658 | 180/1626 | 60/541 | chr1 | 70354229 | ||
| chr1:70354325
|
C | T | 2 | a0001c0002a0001c0005 | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
synonymous_variant | LOW | c.84G>A | p.Glu28Glu | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 398/5658 | 84/1626 | 28/541 | chr1 | 70354325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70259017
|
C | T | 1 | a0001c0001t0007 | 4 | HG02145.hp2 HG02683.hp1 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3700G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 3700 | chr1 | 70259017 | |||||
| chr1:70259116
|
C | A | 1 | a0001c0001t0009 | 2 | HG01934.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3601G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 3601 | chr1 | 70259116 | |||||
| chr1:70259382
|
G | A | 1 | a0001c0001t0020 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3335C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 3335 | chr1 | 70259382 | |||||
| chr1:70259461
|
A | C | 4 | a0001c0001t0002a0001c0001t0017a0001c0001t0021others(1): Show | 33 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3256T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 3256 | chr1 | 70259461 | |||||
| chr1:70259777
|
A | G | 1 | a0001c0002t0019 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2940T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2940 | chr1 | 70259777 | |||||
| chr1:70259793
|
A | T | 1 | a0001c0001t0018 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2924T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2924 | chr1 | 70259793 | |||||
| chr1:70259888
|
T | G | 1 | a0001c0001t0021 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2829A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2829 | chr1 | 70259888 | |||||
| chr1:70260125
|
T | A | 1 | a0001c0001t0022 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2592A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2592 | chr1 | 70260125 | |||||
| chr1:70260174
|
C | T | 1 | a0001c0001t0017 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2543G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2543 | chr1 | 70260174 | |||||
| chr1:70260403
|
T | C | 1 | a0001c0001t0022 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2314A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2314 | chr1 | 70260403 | |||||
| chr1:70260660
|
T | C | 1 | a0001c0001t0003 | 8 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2057A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 2057 | chr1 | 70260660 | |||||
| chr1:70260831
|
G | C | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1886C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 1886 | chr1 | 70260831 | |||||
| chr1:70261114
|
A | G | 2 | a0001c0001t0004a0001c0001t0015 | 7 | HG01192.hp1 HG02886.hp2 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1603T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 1603 | chr1 | 70261114 | |||||
| chr1:70261230
|
G | A | 1 | a0001c0002t0024 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1487C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 1487 | chr1 | 70261230 | |||||
| chr1:70261346
|
G | A | 1 | a0001c0002t0010 | 2 | HG01175.hp2 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1371C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 1371 | chr1 | 70261346 | |||||
| chr1:70261437
|
A | C | 2 | a0001c0001t0006a0001c0001t0011 | 6 | HG02559.hp2 HG02630.hp2 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1280T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 1280 | chr1 | 70261437 | |||||
| chr1:70261660
|
A | G | 1 | a0001c0001t0016 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 1057 | chr1 | 70261660 | |||||
| chr1:70261838
|
A | G | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 879 | chr1 | 70261838 | |||||
| chr1:70262116
|
A | G | 2 | a0001c0001t0005a0001c0002t0005 | 6 | HG02622.hp2 HG03225.hp2 NA18522.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 601 | chr1 | 70262116 | |||||
| chr1:70262269
|
T | C | 2 | a0001c0001t0005a0001c0002t0005 | 6 | HG02622.hp2 HG03225.hp2 NA18522.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*448A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 448 | chr1 | 70262269 | |||||
| chr1:70262376
|
T | C | 1 | a0001c0001t0025 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 341 | chr1 | 70262376 | |||||
| chr1:70262442
|
A | G | 2 | a0001c0001t0008a0001c0001t0029 | 3 | HG01884.hp2 HG02572.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*275T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 275 | chr1 | 70262442 | |||||
| chr1:70262509
|
T | C | 1 | a0001c0001t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 208 | chr1 | 70262509 | |||||
| chr1:70262538
|
C | A | 1 | a0001c0001t0027 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 179 | chr1 | 70262538 | |||||
| chr1:70262596
|
T | C | 1 | a0001c0001t0028 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 13/13 | 121 | chr1 | 70262596 | |||||
| chr1:70354516
|
C | T | 1 | a0001c0001t0014 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 108 | chr1 | 70354516 | |||||
| chr1:70354630
|
G | A | 3 | a0001c0001t0011a0001c0001t0012a0001c0001t0029 | 5 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-222C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | chr1 | 70354630 | ||||||
| chr1:70354657
|
T | TCGCCGTC others(5): Show |
1 | a0001c0001t0013 | 2 | HG02683.hp2 HG03704.hp2 |
5_prime_UTR_variant | MODIFIER | c.-261_-250dupGCTGCG others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/13 | 250 | chr1 | 70354657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70262874
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1496-27A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262874 | ||||||
| chr1:70262916
|
T | C | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1496-69A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262916 | ||||||
| chr1:70262943
|
T | TA | 41 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0052others(38): Show | 42 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1496-97dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAA | 33 | a0001c0001t0002g0046a0001c0001t0002g0054a0001c0001t0002g0126others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1496-100_1496-97du others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1496-107_1496-97du others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(6): Show |
9 | a0001c0001t0001g0274a0001c0001t0001g0295a0001c0001t0003g0304others(6): Show | 9 | HG00639.hp2 HG02622.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1496-109_1496-97du others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(7): Show |
36 | a0001c0001t0001g0070a0001c0001t0001g0253a0001c0001t0001g0254others(33): Show | 36 | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1496-110_1496-97du others(15): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(8): Show |
21 | a0001c0001t0001g0184a0001c0001t0001g0260a0001c0001t0001g0299others(18): Show | 21 | HG00621.hp2 HG01109.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1496-111_1496-97du others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(9): Show |
12 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198others(9): Show | 12 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1496-112_1496-97du others(17): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(10): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1496-113_1496-97du others(18): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262943
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0321 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1496-97_1496-96ins others(18): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262943 | ||||||
| chr1:70262975
|
A | AAG | 60 | a0001c0001t0001g0184a0001c0001t0001g0253a0001c0001t0001g0254others(57): Show | 60 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1496-130_1496-129d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70262975 | ||||||
| chr1:70263353
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1496-506T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70263353 | ||||||
| chr1:70263502
|
TAC | T | 7 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1496-657_1496-656d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70263502 | ||||||
| chr1:70264054
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0171 | 2 | NA18951.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1496-1207C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264054 | ||||||
| chr1:70264058
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0277 | 2 | NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1496-1211G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264058 | ||||||
| chr1:70264090
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1496-1243G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264090 | ||||||
| chr1:70264159
|
A | G | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1496-1312T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264159 | ||||||
| chr1:70264309
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1496-1462G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264309 | ||||||
| chr1:70264381
|
C | T | 7 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1496-1534G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264381 | ||||||
| chr1:70264407
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0012g0348 | 2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1496-1560G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264407 | ||||||
| chr1:70264432
|
C | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-1585G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264432 | ||||||
| chr1:70264475
|
C | CA | 55 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0041others(52): Show | 56 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1496-1629dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264475 | ||||||
| chr1:70264475
|
C | CAA | 6 | a0001c0001t0001g0060a0001c0001t0001g0128a0001c0001t0001g0171others(3): Show | 6 | HG02165.hp2 HG02809.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-1630_1496-162 others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264475 | ||||||
| chr1:70264475
|
CA | C | 104 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(101): Show | 104 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.1496-1629delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264475 | ||||||
| chr1:70264475
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0003g0132a0001c0001t0003g0294a0001c0001t0003g0300others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1496-1637_1496-162 others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264475 | ||||||
| chr1:70264475
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0305 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1496-1638_1496-162 others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264475 | ||||||
| chr1:70264475
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1496-1641_1496-162 others(17): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264475 | ||||||
| chr1:70264710
|
T | C | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1496-1863A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264710 | ||||||
| chr1:70264870
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1496-2023T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70264870 | ||||||
| chr1:70265000
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0164a0001c0001t0001g0173 | 3 | HG01081.hp1 HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1496-2153G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265000 | ||||||
| chr1:70265335
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1496-2488A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265335 | ||||||
| chr1:70265373
|
A | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-2526T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265373 | ||||||
| chr1:70265508
|
C | T | 1 | a0001c0001t0011g0345 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1496-2661G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265508 | ||||||
| chr1:70265679
|
A | G | 2 | a0001c0001t0002g0258a0001c0001t0002g0264 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1496-2832T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265679 | ||||||
| chr1:70265715
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1496-2868G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265715 | ||||||
| chr1:70265824
|
C | CA | 50 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(47): Show | 50 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1496-2978dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265824 | ||||||
| chr1:70265824
|
CA | C | 17 | a0001c0001t0001g0065a0001c0001t0001g0147a0001c0001t0001g0191others(14): Show | 17 | HG00280.hp1 HG01074.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1496-2978delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265824 | ||||||
| chr1:70265824
|
CAA | C | 14 | a0001c0001t0001g0070a0001c0001t0001g0194a0001c0001t0001g0196others(11): Show | 14 | HG02280.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1496-2979_1496-297 others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265824 | ||||||
| chr1:70265824
|
CAAAAA | C | 8 | a0001c0001t0001g0058a0001c0001t0001g0232a0001c0001t0001g0260others(5): Show | 8 | HG00621.hp2 HG00639.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1496-2982_1496-297 others(9): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265824 | ||||||
| chr1:70265824
|
CAAAAAA | C | 53 | a0001c0001t0001g0184a0001c0001t0001g0254a0001c0001t0001g0256others(50): Show | 53 | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1496-2983_1496-297 others(10): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265824 | ||||||
| chr1:70265842
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1496-3005_1496-299 others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265842 | ||||||
| chr1:70265847
|
A | G | 1 | a0001c0001t0020g0262 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1496-3000T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265847 | ||||||
| chr1:70265864
|
AAAG | A | 3 | a0001c0001t0001g0070a0001c0001t0007g0202a0001c0001t0012g0348 | 3 | HG02145.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1496-3020_1496-301 others(7): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265864 | ||||||
| chr1:70265869
|
AGAAG | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-3026_1496-302 others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265869 | ||||||
| chr1:70265881
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0053 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1496-3034C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265881 | ||||||
| chr1:70265909
|
G | A | 8 | a0001c0001t0003g0132a0001c0001t0003g0294a0001c0001t0003g0300others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1496-3062C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265909 | ||||||
| chr1:70265910
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1496-3063C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265910 | ||||||
| chr1:70265928
|
G | A | 60 | a0001c0001t0001g0184a0001c0001t0001g0253a0001c0001t0001g0254others(57): Show | 60 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1496-3081C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265928 | ||||||
| chr1:70265934
|
G | A | 60 | a0001c0001t0001g0184a0001c0001t0001g0253a0001c0001t0001g0254others(57): Show | 60 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1496-3087C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265934 | ||||||
| chr1:70265936
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1496-3089C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265936 | ||||||
| chr1:70265938
|
G | A | 60 | a0001c0001t0001g0184a0001c0001t0001g0253a0001c0001t0001g0254others(57): Show | 60 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1496-3091C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265938 | ||||||
| chr1:70265940
|
A | AGAAGGAA others(5): Show |
20 | a0001c0001t0001g0070a0001c0001t0001g0163a0001c0001t0001g0168others(17): Show | 20 | HG02145.hp1 HG02257.hp2 HG02809.hp2 others(17): Show |
intron_variant | MODIFIER | c.1496-3105_1496-309 others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265940 | ||||||
| chr1:70265940
|
A | AGAAGGAA others(9): Show |
1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1496-3094_1496-309 others(20): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265940 | ||||||
| chr1:70265940
|
A | G | 60 | a0001c0001t0001g0184a0001c0001t0001g0253a0001c0001t0001g0254others(57): Show | 60 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1496-3093T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70265940 | ||||||
| chr1:70266167
|
G | A | 2 | a0001c0001t0003g0304a0001c0001t0003g0305 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1496-3320C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266167 | ||||||
| chr1:70266202
|
T | G | 127 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0184others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.1496-3355A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266202 | ||||||
| chr1:70266352
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG00280.hp1 HG01109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1496-3505C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266352 | ||||||
| chr1:70266656
|
A | G | 89 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0184others(86): Show | 89 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1496-3809T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266656 | ||||||
| chr1:70266714
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0306 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1496-3867C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266714 | ||||||
| chr1:70266828
|
T | C | 34 | a0001c0001t0002g0046a0001c0001t0002g0054a0001c0001t0002g0126others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1496-3981A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266828 | ||||||
| chr1:70266938
|
C | T | 63 | a0001c0001t0001g0184a0001c0001t0001g0253a0001c0001t0001g0254others(60): Show | 63 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1495+3918G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70266938 | ||||||
| chr1:70267067
|
C | T | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1495+3789G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267067 | ||||||
| chr1:70267108
|
A | G | 1 | a0001c0001t0021g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1495+3748T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267108 | ||||||
| chr1:70267118
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1495+3738A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267118 | ||||||
| chr1:70267217
|
G | A | 62 | a0001c0001t0001g0070a0001c0001t0001g0184a0001c0001t0001g0253others(59): Show | 62 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1495+3639C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267217 | ||||||
| chr1:70267274
|
T | C | 7 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0011others(4): Show | 7 | NA18948.hp2 NA18953.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495+3582A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267274 | ||||||
| chr1:70267301
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1495+3555C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267301 | ||||||
| chr1:70267432
|
C | T | 68 | a0001c0001t0001g0070a0001c0001t0001g0184a0001c0001t0001g0194others(65): Show | 68 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1495+3424G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267432 | ||||||
| chr1:70267468
|
A | G | 172 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0044others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.1495+3388T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267468 | ||||||
| chr1:70267609
|
A | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(30): Show | 34 | HG00280.hp2 HG00544.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1495+3247T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267609 | ||||||
| chr1:70267619
|
T | G | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1495+3237A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267619 | ||||||
| chr1:70267846
|
A | G | 8 | a0001c0001t0003g0132a0001c0001t0003g0294a0001c0001t0003g0300others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1495+3010T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70267846 | ||||||
| chr1:70268037
|
TTTG | T | 3 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051 | 3 | HG02683.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1495+2816_1495+281 others(7): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268037 | ||||||
| chr1:70268069
|
A | C | 2 | a0001c0001t0001g0059a0001c0001t0006g0250 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1495+2787T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268069 | ||||||
| chr1:70268148
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0216others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+2708A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268148 | ||||||
| chr1:70268170
|
T | TA | 3 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051 | 3 | HG02683.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1495+2685_1495+268 others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268170 | ||||||
| chr1:70268171
|
T | A | 3 | a0001c0001t0008g0104a0001c0001t0008g0340a0001c0001t0029g0344 | 3 | HG01884.hp2 HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1495+2685A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268171 | ||||||
| chr1:70268171
|
T | C | 3 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051 | 3 | HG02683.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1495+2685A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268171 | ||||||
| chr1:70268175
|
CG | C | 3 | a0001c0001t0008g0104a0001c0001t0008g0340a0001c0001t0029g0344 | 3 | HG01884.hp2 HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1495+2680delC | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268175 | ||||||
| chr1:70268176
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1495+2680C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268176 | ||||||
| chr1:70268176
|
G | C | 96 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0184others(93): Show | 96 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1495+2680C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268176 | ||||||
| chr1:70268179
|
C | G | 89 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0184others(86): Show | 89 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1495+2677G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268179 | ||||||
| chr1:70268182
|
A | C | 6 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1495+2674T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268182 | ||||||
| chr1:70268314
|
T | C | 10 | a0001c0001t0005g0035a0001c0001t0005g0252a0001c0001t0005g0301others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1495+2542A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268314 | ||||||
| chr1:70268319
|
G | A | 3 | a0001c0001t0008g0104a0001c0001t0008g0340a0001c0001t0029g0344 | 3 | HG01884.hp2 HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1495+2537C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268319 | ||||||
| chr1:70268460
|
C | T | 7 | a0001c0001t0003g0132a0001c0001t0003g0300a0001c0001t0003g0302others(4): Show | 7 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495+2396G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268460 | ||||||
| chr1:70268504
|
A | G | 41 | a0001c0001t0001g0048a0001c0001t0001g0316a0001c0001t0001g0317others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1495+2352T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268504 | ||||||
| chr1:70268522
|
T | C | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1495+2334A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268522 | ||||||
| chr1:70268864
|
AT | A | 7 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495+1991delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268864 | ||||||
| chr1:70268893
|
A | T | 67 | a0001c0001t0001g0070a0001c0001t0001g0083a0001c0001t0001g0108others(64): Show | 67 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1495+1963T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268893 | ||||||
| chr1:70268979
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0187a0001c0001t0001g0233others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+1877C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70268979 | ||||||
| chr1:70269045
|
C | A | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1495+1811G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269045 | ||||||
| chr1:70269223
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1495+1633C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269223 | ||||||
| chr1:70269329
|
C | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1495+1527G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269329 | ||||||
| chr1:70269491
|
G | A | 44 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(41): Show | 44 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.1495+1365C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269491 | ||||||
| chr1:70269623
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1495+1233A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269623 | ||||||
| chr1:70269729
|
CA | C | 16 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0118others(13): Show | 16 | HG01515.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1495+1126delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269729 | ||||||
| chr1:70269802
|
G | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0209a0001c0001t0027g0097 | 3 | HG02602.hp2 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1495+1054C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269802 | ||||||
| chr1:70269909
|
T | A | 1 | a0001c0001t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1495+947A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269909 | ||||||
| chr1:70269945
|
G | A | 6 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0005g0035others(3): Show | 6 | HG02622.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1495+911C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70269945 | ||||||
| chr1:70270109
|
G | T | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+747C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270109 | ||||||
| chr1:70270123
|
C | A | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1495+733G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270123 | ||||||
| chr1:70270198
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0149a0001c0001t0001g0179 | 3 | HG02027.hp2 HG02080.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1495+658T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270198 | ||||||
| chr1:70270209
|
T | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0005g0252others(1): Show | 4 | HG02622.hp1 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+647A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270209 | ||||||
| chr1:70270265
|
A | C | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1495+591T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270265 | ||||||
| chr1:70270404
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1495+452C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270404 | ||||||
| chr1:70270409
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1495+447A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270409 | ||||||
| chr1:70270665
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1495+191G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 12/12 | chr1 | 70270665 | ||||||
| chr1:70271004
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1395-48A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271004 | ||||||
| chr1:70271341
|
A | C | 37 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(34): Show | 37 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1395-385T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271341 | ||||||
| chr1:70271389
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0077others(1): Show | 4 | HG02735.hp1 NA18953.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-433A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271389 | ||||||
| chr1:70271461
|
T | G | 1 | a0001c0001t0002g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1395-505A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271461 | ||||||
| chr1:70271469
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395-513A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271469 | ||||||
| chr1:70271626
|
G | GA | 6 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0005g0035others(3): Show | 6 | HG02622.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-671dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271626 | ||||||
| chr1:70271976
|
C | T | 38 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(35): Show | 38 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1395-1020G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70271976 | ||||||
| chr1:70272097
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0232 | 2 | NA18959.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1395-1141A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272097 | ||||||
| chr1:70272163
|
C | CT | 19 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0003g0132others(16): Show | 19 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1395-1208dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272163 | ||||||
| chr1:70272175
|
T | C | 76 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0048others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.1395-1219A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272175 | ||||||
| chr1:70272175
|
T | TC | 6 | a0001c0001t0001g0308a0001c0002t0001g0016a0001c0002t0001g0017others(3): Show | 6 | HG01175.hp2 HG01496.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-1220dupG | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272175 | ||||||
| chr1:70272231
|
C | CT | 69 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0108others(66): Show | 69 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1395-1276dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272231 | ||||||
| chr1:70272268
|
C | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0274 | 2 | NA19072.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1395-1312G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272268 | ||||||
| chr1:70272318
|
C | T | 14 | a0001c0001t0001g0048a0001c0001t0001g0194a0001c0001t0001g0196others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395-1362G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272318 | ||||||
| chr1:70272513
|
T | C | 45 | a0001c0001t0001g0048a0001c0001t0001g0194a0001c0001t0001g0196others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1395-1557A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272513 | ||||||
| chr1:70272561
|
C | T | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1395-1605G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272561 | ||||||
| chr1:70272587
|
C | CT | 10 | a0001c0001t0001g0299a0001c0001t0001g0316a0001c0001t0001g0317others(7): Show | 10 | HG01109.hp2 HG02155.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395-1632dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272587 | ||||||
| chr1:70272597
|
T | C | 1 | a0001c0001t0012g0346 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1395-1641A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272597 | ||||||
| chr1:70272684
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0315 | 2 | HG02015.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1395-1728C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272684 | ||||||
| chr1:70272786
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1395-1830A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272786 | ||||||
| chr1:70272843
|
C | T | 37 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(34): Show | 37 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1394+1877G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272843 | ||||||
| chr1:70272990
|
A | AAAAT | 27 | a0001c0001t0001g0043a0001c0001t0001g0059a0001c0001t0001g0070others(24): Show | 27 | HG00639.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1394+1726_1394+172 others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272990 | ||||||
| chr1:70272990
|
A | AAAATAAA others(1): Show |
85 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0086others(82): Show | 85 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1394+1722_1394+172 others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272990 | ||||||
| chr1:70272990
|
A | AAAATAAA others(5): Show |
15 | a0001c0001t0001g0036a0001c0001t0001g0267a0001c0001t0001g0272others(12): Show | 15 | HG00642.hp1 HG00741.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1394+1718_1394+172 others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272990 | ||||||
| chr1:70272990
|
A | AAAATAAA others(9): Show |
5 | a0001c0001t0001g0263a0001c0001t0001g0266a0001c0001t0001g0269others(2): Show | 5 | HG01361.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+1714_1394+172 others(20): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70272990 | ||||||
| chr1:70273252
|
G | A | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1394+1468C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273252 | ||||||
| chr1:70273278
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1394+1442G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273278 | ||||||
| chr1:70273283
|
A | T | 2 | a0001c0001t0004g0056a0001c0001t0004g0167 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1394+1437T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273283 | ||||||
| chr1:70273332
|
A | G | 1 | a0001c0001t0003g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1394+1388T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273332 | ||||||
| chr1:70273377
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+1343C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273377 | ||||||
| chr1:70273588
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1394+1132T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273588 | ||||||
| chr1:70273797
|
G | C | 173 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0044others(170): Show | 173 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.1394+923C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273797 | ||||||
| chr1:70273960
|
C | T | 37 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0070others(34): Show | 37 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(34): Show |
intron_variant | MODIFIER | c.1394+760G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70273960 | ||||||
| chr1:70274046
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1394+674G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274046 | ||||||
| chr1:70274212
|
G | A | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1394+508C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274212 | ||||||
| chr1:70274255
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1394+465G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274255 | ||||||
| chr1:70274274
|
T | C | 68 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0070others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.1394+446A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274274 | ||||||
| chr1:70274417
|
T | C | 1 | a0001c0001t0006g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1394+303A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274417 | ||||||
| chr1:70274430
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0212 | 2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1394+290G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274430 | ||||||
| chr1:70274470
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0012g0348 | 2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1394+250A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274470 | ||||||
| chr1:70274473
|
C | CA | 23 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0070others(20): Show | 23 | HG01106.hp1 HG01361.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1394+246dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274473 | ||||||
| chr1:70274473
|
C | CAA | 12 | a0001c0001t0001g0144a0001c0001t0003g0132a0001c0001t0003g0300others(9): Show | 12 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1394+245_1394+246d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274473 | ||||||
| chr1:70274473
|
CA | C | 15 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0065others(12): Show | 15 | HG00673.hp2 HG01081.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1394+246delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274473 | ||||||
| chr1:70274473
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1394+236_1394+246d others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274473 | ||||||
| chr1:70274486
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0008g0104a0001c0001t0029g0344 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1394+223_1394+233d others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274486 | ||||||
| chr1:70274487
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1394+223_1394+232d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274487 | ||||||
| chr1:70274493
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0206 | 3 | HG00544.hp2 HG01167.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1394+227T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274493 | ||||||
| chr1:70274496
|
AG | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+223delC | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274496 | ||||||
| chr1:70274497
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0200a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1394+223C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274497 | ||||||
| chr1:70274589
|
A | G | 20 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0003g0132others(17): Show | 20 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1394+131T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274589 | ||||||
| chr1:70274591
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1394+129A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 11/12 | chr1 | 70274591 | ||||||
| chr1:70275305
|
C | T | 2 | a0001c0001t0008g0104a0001c0001t0008g0340 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1296-487G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275305 | ||||||
| chr1:70275340
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1296-522C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275340 | ||||||
| chr1:70275504
|
C | CT | 7 | a0001c0001t0001g0071a0001c0001t0001g0109a0001c0001t0001g0233others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1296-687dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275504 | ||||||
| chr1:70275551
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1296-733T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275551 | ||||||
| chr1:70275687
|
C | A | 37 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(34): Show | 37 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1296-869G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275687 | ||||||
| chr1:70275773
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1296-955G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275773 | ||||||
| chr1:70275853
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1295+912G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275853 | ||||||
| chr1:70275875
|
G | A | 1 | a0001c0001t0002g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1295+890C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275875 | ||||||
| chr1:70275961
|
C | CA | 41 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0044others(38): Show | 41 | HG00280.hp2 HG01175.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.1295+803dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275961 | ||||||
| chr1:70275961
|
C | CAA | 15 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0182others(12): Show | 15 | HG02055.hp1 HG02602.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1295+802_1295+803d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275961 | ||||||
| chr1:70275978
|
A | C | 1 | a0001c0001t0001g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1295+787T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70275978 | ||||||
| chr1:70276025
|
A | G | 1 | a0001c0001t0027g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1295+740T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276025 | ||||||
| chr1:70276143
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1295+622G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276143 | ||||||
| chr1:70276380
|
G | C | 170 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0044others(167): Show | 170 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.1295+385C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276380 | ||||||
| chr1:70276469
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1295+296C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276469 | ||||||
| chr1:70276479
|
A | G | 2 | a0001c0001t0008g0104a0001c0001t0008g0340 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1295+286T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276479 | ||||||
| chr1:70276505
|
T | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1295+260A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276505 | ||||||
| chr1:70276606
|
T | C | 6 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+159A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276606 | ||||||
| chr1:70276698
|
CAT | C | 5 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0008g0104others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1295+65_1295+66del others(2): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 10/12 | chr1 | 70276698 | ||||||
| chr1:70277120
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1216-276C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277120 | ||||||
| chr1:70277284
|
C | G | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1216-440G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277284 | ||||||
| chr1:70277393
|
G | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1216-549C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277393 | ||||||
| chr1:70277394
|
T | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1216-550A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277394 | ||||||
| chr1:70277456
|
C | CA | 16 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0001t0001g0263others(13): Show | 16 | HG00597.hp2 HG01109.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1216-613dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277456 | ||||||
| chr1:70277535
|
G | A | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1216-691C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277535 | ||||||
| chr1:70277612
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0106 | 2 | NA18992.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1216-768A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277612 | ||||||
| chr1:70277696
|
G | C | 6 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-852C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277696 | ||||||
| chr1:70277769
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1216-925C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70277769 | ||||||
| chr1:70278023
|
TA | T | 16 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0118others(13): Show | 16 | HG01168.hp1 HG01168.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1216-1180delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278023 | ||||||
| chr1:70278038
|
A | C | 1 | a0001c0001t0001g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1216-1194T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278038 | ||||||
| chr1:70278059
|
C | G | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1216-1215G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278059 | ||||||
| chr1:70278094
|
C | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0130a0001c0001t0001g0163others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-1250G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278094 | ||||||
| chr1:70278219
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0233a0001c0001t0001g0307others(1): Show | 4 | HG01928.hp2 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-1375C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278219 | ||||||
| chr1:70278266
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0091others(1): Show | 4 | HG02056.hp1 NA18941.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-1422C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278266 | ||||||
| chr1:70278345
|
T | C | 9 | a0001c0001t0003g0132a0001c0001t0003g0294a0001c0001t0003g0300others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-1501A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278345 | ||||||
| chr1:70278378
|
A | G | 2 | a0001c0001t0011g0347a0001c0001t0029g0344 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1216-1534T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278378 | ||||||
| chr1:70278563
|
A | T | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1216-1719T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278563 | ||||||
| chr1:70278564
|
T | A | 2 | a0001c0001t0009g0195a0001c0001t0009g0199 | 2 | HG01934.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1216-1720A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278564 | ||||||
| chr1:70278824
|
A | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(69): Show | 74 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1216-1980T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278824 | ||||||
| chr1:70278984
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1216-2140A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70278984 | ||||||
| chr1:70279046
|
C | CA | 13 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0006g0047others(10): Show | 13 | HG02258.hp1 HG02559.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1216-2203dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279046 | ||||||
| chr1:70279146
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1216-2302C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279146 | ||||||
| chr1:70279195
|
T | C | 62 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0070others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1216-2351A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279195 | ||||||
| chr1:70279217
|
A | T | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1216-2373T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279217 | ||||||
| chr1:70279221
|
A | AAG | 4 | a0001c0001t0004g0056a0001c0001t0004g0167a0001c0001t0005g0035others(1): Show | 4 | HG02886.hp2 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-2379_1216-237 others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279221 | ||||||
| chr1:70279221
|
AAGAG | A | 5 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0008g0104others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-2381_1216-237 others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279221 | ||||||
| chr1:70279270
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1216-2426G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279270 | ||||||
| chr1:70279271
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1216-2427G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279271 | ||||||
| chr1:70279388
|
T | C | 36 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(33): Show | 36 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1216-2544A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279388 | ||||||
| chr1:70279445
|
T | C | 5 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0008g0104others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-2601A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279445 | ||||||
| chr1:70279500
|
C | CT | 58 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0061others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1216-2657dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279500 | ||||||
| chr1:70279606
|
A | G | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1216-2762T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279606 | ||||||
| chr1:70279741
|
G | C | 1 | a0001c0001t0002g0241 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1216-2897C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279741 | ||||||
| chr1:70279763
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1216-2919T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279763 | ||||||
| chr1:70279786
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1216-2942T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279786 | ||||||
| chr1:70279836
|
G | C | 1 | a0001c0001t0001g0334 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1216-2992C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70279836 | ||||||
| chr1:70280298
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1216-3454C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70280298 | ||||||
| chr1:70280372
|
T | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1216-3528A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70280372 | ||||||
| chr1:70280476
|
A | G | 7 | a0001c0001t0001g0036a0001c0001t0005g0035a0001c0001t0005g0252others(4): Show | 7 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-3632T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70280476 | ||||||
| chr1:70280855
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1216-4011T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70280855 | ||||||
| chr1:70280908
|
G | A | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1216-4064C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70280908 | ||||||
| chr1:70280957
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1216-4113A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70280957 | ||||||
| chr1:70281173
|
C | T | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0007g0202others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-4329G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281173 | ||||||
| chr1:70281289
|
T | A | 1 | a0001c0001t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1216-4445A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281289 | ||||||
| chr1:70281396
|
C | CT | 23 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0048others(20): Show | 23 | HG00733.hp1 HG01255.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1216-4553dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281396 | ||||||
| chr1:70281396
|
CT | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0038others(103): Show | 107 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1216-4553delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281396 | ||||||
| chr1:70281396
|
CTT | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0271a0001c0001t0001g0273others(3): Show | 6 | HG00597.hp2 HG02129.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-4554_1216-455 others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281396 | ||||||
| chr1:70281396
|
CTTTTTTT | C | 6 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-4559_1216-455 others(11): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281396 | ||||||
| chr1:70281414
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1216-4570A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281414 | ||||||
| chr1:70281442
|
A | G | 1 | a0001c0001t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1216-4598T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281442 | ||||||
| chr1:70281565
|
G | C | 7 | a0001c0001t0001g0093a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | NA18945.hp1 NA18951.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.1216-4721C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281565 | ||||||
| chr1:70281573
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1216-4729A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281573 | ||||||
| chr1:70281622
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1216-4778G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281622 | ||||||
| chr1:70281759
|
C | T | 23 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0194others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1216-4915G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281759 | ||||||
| chr1:70281845
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1216-5001C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281845 | ||||||
| chr1:70281870
|
A | G | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0007g0202others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-5026T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281870 | ||||||
| chr1:70281876
|
G | A | 9 | a0001c0001t0003g0132a0001c0001t0003g0294a0001c0001t0003g0300others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-5032C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281876 | ||||||
| chr1:70281944
|
G | A | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1216-5100C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70281944 | ||||||
| chr1:70282054
|
C | CT | 18 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0070others(15): Show | 18 | HG02056.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1216-5211dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282054 | ||||||
| chr1:70282117
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0081 | 2 | NA18949.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1216-5273G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282117 | ||||||
| chr1:70282291
|
G | T | 1 | a0001c0001t0011g0345 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1216-5447C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282291 | ||||||
| chr1:70282386
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1216-5542C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282386 | ||||||
| chr1:70282507
|
T | G | 1 | a0001c0001t0001g0308 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1216-5663A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282507 | ||||||
| chr1:70282603
|
T | C | 1 | a0001c0001t0003g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1216-5759A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282603 | ||||||
| chr1:70282739
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1216-5895T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282739 | ||||||
| chr1:70282964
|
CAAGT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(134): Show | 139 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.1216-6124_1216-612 others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282964 | ||||||
| chr1:70282967
|
G | A | 23 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0194others(20): Show | 23 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1216-6123C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70282967 | ||||||
| chr1:70283094
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1216-6250G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283094 | ||||||
| chr1:70283404
|
G | T | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1216-6560C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283404 | ||||||
| chr1:70283521
|
G | GA | 36 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0098others(33): Show | 36 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1216-6678dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283521 | ||||||
| chr1:70283538
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1216-6694G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283538 | ||||||
| chr1:70283645
|
T | TCTCTA | 5 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG02809.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-6806_1216-680 others(9): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283645 | ||||||
| chr1:70283740
|
G | A | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1216-6896C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283740 | ||||||
| chr1:70283801
|
G | A | 1 | a0001c0001t0012g0346 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1216-6957C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283801 | ||||||
| chr1:70283897
|
T | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG02809.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-7053A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283897 | ||||||
| chr1:70283902
|
A | G | 1 | a0001c0001t0003g0306 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1216-7058T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70283902 | ||||||
| chr1:70284368
|
T | G | 1 | a0001c0001t0001g0313 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1216-7524A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70284368 | ||||||
| chr1:70284874
|
C | T | 35 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0070others(32): Show | 35 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1215+7514G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70284874 | ||||||
| chr1:70284875
|
A | G | 35 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0070others(32): Show | 35 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1215+7513T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70284875 | ||||||
| chr1:70284906
|
C | G | 2 | a0001c0001t0002g0258a0001c0001t0002g0264 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1215+7482G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70284906 | ||||||
| chr1:70284995
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0006g0250 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1215+7393G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70284995 | ||||||
| chr1:70285098
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0209 | 2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1215+7290A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285098 | ||||||
| chr1:70285187
|
C | CT | 42 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0001g0086others(39): Show | 42 | HG00738.hp2 HG01074.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1215+7200dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285187 | ||||||
| chr1:70285187
|
CT | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0277a0001c0001t0001g0334others(16): Show | 19 | HG01168.hp1 HG01256.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.1215+7200delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285187 | ||||||
| chr1:70285355
|
C | T | 1 | a0001c0001t0008g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1215+7033G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285355 | ||||||
| chr1:70285501
|
A | T | 16 | a0001c0001t0001g0059a0001c0001t0001g0194a0001c0001t0001g0196others(13): Show | 16 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1215+6887T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285501 | ||||||
| chr1:70285630
|
C | CT | 19 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0131others(16): Show | 19 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1215+6757dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285630 | ||||||
| chr1:70285630
|
C | CTT | 9 | a0001c0001t0001g0121a0001c0001t0001g0139a0001c0001t0001g0140others(6): Show | 9 | HG01074.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+6756_1215+675 others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285630 | ||||||
| chr1:70285630
|
CT | C | 8 | a0001c0001t0001g0055a0001c0001t0001g0087a0001c0001t0001g0337others(5): Show | 8 | HG01928.hp2 HG02056.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+6757delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285630 | ||||||
| chr1:70285647
|
T | C | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0007g0202others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+6741A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285647 | ||||||
| chr1:70285772
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1215+6616C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285772 | ||||||
| chr1:70285902
|
T | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+6486A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285902 | ||||||
| chr1:70285907
|
A | G | 1 | a0001c0001t0002g0126 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1215+6481T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285907 | ||||||
| chr1:70285922
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+6466G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70285922 | ||||||
| chr1:70286086
|
AC | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+6301delG | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286086 | ||||||
| chr1:70286287
|
T | G | 5 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0129others(2): Show | 5 | HG01081.hp1 HG01106.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+6101A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286287 | ||||||
| chr1:70286320
|
C | T | 6 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+6068G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286320 | ||||||
| chr1:70286469
|
T | A | 4 | a0001c0001t0001g0137a0001c0001t0005g0252a0001c0001t0013g0349others(1): Show | 4 | HG02622.hp2 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+5919A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286469 | ||||||
| chr1:70286470
|
A | T | 2 | a0001c0001t0002g0258a0001c0001t0002g0264 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1215+5918T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286470 | ||||||
| chr1:70286585
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1215+5803C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286585 | ||||||
| chr1:70286685
|
T | C | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+5703A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286685 | ||||||
| chr1:70286714
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1215+5674C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286714 | ||||||
| chr1:70286728
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1215+5660T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286728 | ||||||
| chr1:70286811
|
C | T | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1215+5577G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286811 | ||||||
| chr1:70286847
|
G | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0026 | 3 | HG01168.hp1 HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1215+5541C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286847 | ||||||
| chr1:70286859
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0329 | 2 | NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1215+5529T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286859 | ||||||
| chr1:70286880
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1215+5508C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286880 | ||||||
| chr1:70286896
|
G | T | 65 | a0001c0001t0001g0157a0001c0001t0001g0253a0001c0001t0001g0254others(62): Show | 65 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1215+5492C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286896 | ||||||
| chr1:70286907
|
A | G | 6 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+5481T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70286907 | ||||||
| chr1:70287374
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1215+5014A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287374 | ||||||
| chr1:70287387
|
C | CA | 41 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0316others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.1215+5000dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287387 | ||||||
| chr1:70287394
|
A | T | 73 | a0001c0001t0001g0157a0001c0001t0001g0253a0001c0001t0001g0254others(70): Show | 73 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1215+4994T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287394 | ||||||
| chr1:70287540
|
G | A | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1215+4848C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287540 | ||||||
| chr1:70287559
|
G | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0007g0202others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+4829C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287559 | ||||||
| chr1:70287635
|
G | A | 27 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0002g0046others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1215+4753C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287635 | ||||||
| chr1:70287737
|
TG | T | 3 | a0001c0002t0005g0028a0001c0002t0005g0029a0001c0002t0005g0031 | 3 | NA18972.hp2 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1215+4650delC | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287737 | ||||||
| chr1:70287742
|
C | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1215+4646G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287742 | ||||||
| chr1:70287927
|
G | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0058others(28): Show | 32 | HG00544.hp1 HG00597.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1215+4461C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70287927 | ||||||
| chr1:70288182
|
A | G | 7 | a0001c0001t0001g0118a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG00621.hp1 NA18941.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+4206T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288182 | ||||||
| chr1:70288201
|
G | A | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1215+4187C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288201 | ||||||
| chr1:70288316
|
C | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1215+4072G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288316 | ||||||
| chr1:70288368
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1215+4020A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288368 | ||||||
| chr1:70288437
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1215+3951A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288437 | ||||||
| chr1:70288471
|
G | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1215+3917C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288471 | ||||||
| chr1:70288671
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+3717G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288671 | ||||||
| chr1:70288899
|
C | T | 1 | a0001c0001t0021g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1215+3489G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288899 | ||||||
| chr1:70288900
|
A | T | 1 | a0001c0001t0021g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1215+3488T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70288900 | ||||||
| chr1:70289007
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1215+3381C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289007 | ||||||
| chr1:70289034
|
C | T | 4 | a0001c0001t0002g0133a0001c0001t0002g0169a0001c0001t0002g0176others(1): Show | 4 | HG01106.hp1 HG01243.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+3354G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289034 | ||||||
| chr1:70289198
|
G | A | 11 | a0001c0001t0001g0059a0001c0001t0001g0337a0001c0001t0001g0339others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1215+3190C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289198 | ||||||
| chr1:70289360
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1215+3028T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289360 | ||||||
| chr1:70289475
|
T | A | 45 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0048others(42): Show | 45 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(42): Show |
intron_variant | MODIFIER | c.1215+2913A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289475 | ||||||
| chr1:70289481
|
T | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0070a0001c0001t0003g0294others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1215+2907A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289481 | ||||||
| chr1:70289631
|
T | C | 1 | a0001c0001t0017g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1215+2757A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289631 | ||||||
| chr1:70289633
|
A | AT | 12 | a0001c0001t0001g0266a0001c0001t0001g0283a0001c0001t0001g0310others(9): Show | 12 | HG01934.hp2 HG02027.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1215+2754dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289633 | ||||||
| chr1:70289634
|
T | G | 2 | a0001c0002t0005g0029a0001c0002t0005g0031 | 2 | NA18972.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1215+2754A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289634 | ||||||
| chr1:70289676
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1215+2712G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289676 | ||||||
| chr1:70289704
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1215+2684G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289704 | ||||||
| chr1:70289717
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1215+2671G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289717 | ||||||
| chr1:70289794
|
A | T | 2 | a0001c0001t0013g0349a0001c0001t0013g0350 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1215+2594T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289794 | ||||||
| chr1:70289855
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1215+2533T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70289855 | ||||||
| chr1:70290026
|
A | G | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1215+2362T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290026 | ||||||
| chr1:70290131
|
CACTAA | C | 31 | a0001c0001t0001g0098a0001c0001t0001g0255a0001c0001t0001g0257others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+2252_1215+225 others(9): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290131 | ||||||
| chr1:70290135
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0306 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1215+2253T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290135 | ||||||
| chr1:70290137
|
A | T | 31 | a0001c0001t0001g0098a0001c0001t0001g0255a0001c0001t0001g0257others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+2251T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290137 | ||||||
| chr1:70290138
|
G | T | 31 | a0001c0001t0001g0098a0001c0001t0001g0255a0001c0001t0001g0257others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+2250C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290138 | ||||||
| chr1:70290168
|
A | G | 1 | a0001c0001t0006g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1215+2220T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290168 | ||||||
| chr1:70290471
|
A | G | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1215+1917T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290471 | ||||||
| chr1:70290509
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+1879G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290509 | ||||||
| chr1:70290510
|
A | G | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1215+1878T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290510 | ||||||
| chr1:70290539
|
C | CT | 10 | a0001c0001t0001g0048a0001c0001t0001g0283a0001c0001t0001g0337others(7): Show | 10 | HG02145.hp2 HG02602.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215+1848dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290539 | ||||||
| chr1:70290539
|
CT | C | 13 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0150others(10): Show | 13 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1215+1848delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290539 | ||||||
| chr1:70290698
|
C | T | 1 | a0001c0001t0004g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1215+1690G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290698 | ||||||
| chr1:70290699
|
G | A | 1 | a0001c0001t0013g0350 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1215+1689C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290699 | ||||||
| chr1:70290713
|
T | G | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1215+1675A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290713 | ||||||
| chr1:70290737
|
T | G | 3 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0023g0037 | 3 | HG02486.hp2 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1215+1651A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290737 | ||||||
| chr1:70290825
|
T | C | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1215+1563A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290825 | ||||||
| chr1:70290878
|
A | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(234): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1215+1510T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290878 | ||||||
| chr1:70290918
|
G | GA | 8 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+1469dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70290918 | ||||||
| chr1:70291016
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1215+1372T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291016 | ||||||
| chr1:70291026
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+1362G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291026 | ||||||
| chr1:70291036
|
AT | A | 12 | a0001c0001t0001g0059a0001c0001t0001g0337a0001c0001t0001g0339others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+1351delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291036 | ||||||
| chr1:70291093
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1215+1295G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291093 | ||||||
| chr1:70291127
|
C | T | 35 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0070others(32): Show | 35 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1215+1261G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291127 | ||||||
| chr1:70291153
|
T | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1215+1235A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291153 | ||||||
| chr1:70291155
|
C | T | 7 | a0001c0001t0003g0294a0001c0001t0003g0300a0001c0001t0003g0302others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+1233G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291155 | ||||||
| chr1:70291209
|
C | T | 31 | a0001c0001t0001g0098a0001c0001t0001g0255a0001c0001t0001g0257others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+1179G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291209 | ||||||
| chr1:70291313
|
G | T | 3 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0023g0037 | 3 | HG02486.hp2 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1215+1075C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291313 | ||||||
| chr1:70291320
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1215+1068G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291320 | ||||||
| chr1:70291588
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1215+800A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291588 | ||||||
| chr1:70291689
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1215+699G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291689 | ||||||
| chr1:70291875
|
T | C | 8 | a0001c0001t0001g0059a0001c0001t0006g0047a0001c0001t0006g0103others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+513A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70291875 | ||||||
| chr1:70292056
|
T | G | 3 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0023g0037 | 3 | HG02486.hp2 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1215+332A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 9/12 | chr1 | 70292056 | ||||||
| chr1:70292616
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0005g0252a0001c0001t0023g0037 | 3 | HG02486.hp2 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1054-67A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70292616 | ||||||
| chr1:70292682
|
T | A | 1 | a0001c0005t0001g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1054-133A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70292682 | ||||||
| chr1:70292913
|
C | T | 2 | a0001c0001t0005g0035a0001c0001t0005g0301 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1054-364G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70292913 | ||||||
| chr1:70292997
|
T | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1054-448A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70292997 | ||||||
| chr1:70293011
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1054-462G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293011 | ||||||
| chr1:70293084
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0112a0001c0001t0001g0117others(2): Show | 5 | HG01167.hp2 HG02559.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-535G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293084 | ||||||
| chr1:70293118
|
T | C | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-569A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293118 | ||||||
| chr1:70293204
|
A | G | 27 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0002g0046others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1054-655T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293204 | ||||||
| chr1:70293436
|
G | A | 1 | a0001c0001t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1054-887C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293436 | ||||||
| chr1:70293658
|
A | C | 2 | a0001c0001t0001g0070a0001c0001t0007g0202 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1054-1109T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293658 | ||||||
| chr1:70293770
|
G | A | 1 | a0001c0001t0029g0344 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1054-1221C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293770 | ||||||
| chr1:70293798
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1054-1249G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293798 | ||||||
| chr1:70293966
|
C | T | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054-1417G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70293966 | ||||||
| chr1:70294088
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1054-1539A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70294088 | ||||||
| chr1:70294209
|
A | G | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1054-1660T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70294209 | ||||||
| chr1:70294496
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(222): Show | 227 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.1053+1634T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70294496 | ||||||
| chr1:70294631
|
C | A | 2 | a0001c0001t0011g0347a0001c0001t0029g0344 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1053+1499G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70294631 | ||||||
| chr1:70294753
|
G | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1053+1377C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70294753 | ||||||
| chr1:70294908
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+1222A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70294908 | ||||||
| chr1:70295047
|
T | G | 1 | a0001c0001t0001g0311 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1053+1083A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295047 | ||||||
| chr1:70295112
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1053+1018A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295112 | ||||||
| chr1:70295373
|
G | A | 2 | a0001c0003t0002g0032a0001c0003t0002g0033 | 2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1053+757C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295373 | ||||||
| chr1:70295447
|
C | T | 4 | a0001c0002t0001g0030a0001c0002t0005g0028a0001c0002t0005g0029others(1): Show | 4 | NA18972.hp2 NA19000.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+683G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295447 | ||||||
| chr1:70295482
|
G | A | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1053+648C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295482 | ||||||
| chr1:70295488
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0081 | 2 | NA18949.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1053+642G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295488 | ||||||
| chr1:70295556
|
C | T | 88 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(85): Show | 88 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1053+574G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295556 | ||||||
| chr1:70295581
|
T | C | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1053+549A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295581 | ||||||
| chr1:70295631
|
T | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(30): Show | 34 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1053+499A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295631 | ||||||
| chr1:70295705
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1053+425T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295705 | ||||||
| chr1:70295706
|
C | G | 91 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(88): Show | 91 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1053+424G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295706 | ||||||
| chr1:70295860
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1053+270G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70295860 | ||||||
| chr1:70296028
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1053+102C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70296028 | ||||||
| chr1:70296090
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0190 | 2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1053+40C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 8/12 | chr1 | 70296090 | ||||||
| chr1:70296335
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.922-74G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296335 | ||||||
| chr1:70296403
|
TACTC | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.922-146_922-143del others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296403 | ||||||
| chr1:70296446
|
C | G | 2 | a0001c0001t0011g0347a0001c0001t0029g0344 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.922-185G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296446 | ||||||
| chr1:70296499
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.922-238C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296499 | ||||||
| chr1:70296505
|
C | T | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.922-244G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296505 | ||||||
| chr1:70296506
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.922-245C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296506 | ||||||
| chr1:70296521
|
T | G | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922-260A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296521 | ||||||
| chr1:70296627
|
A | G | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.922-366T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70296627 | ||||||
| chr1:70297006
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.922-745C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297006 | ||||||
| chr1:70297120
|
G | T | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.922-859C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297120 | ||||||
| chr1:70297121
|
A | T | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.922-860T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297121 | ||||||
| chr1:70297280
|
C | A | 1 | a0001c0001t0001g0308 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.922-1019G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297280 | ||||||
| chr1:70297286
|
G | GGTTTT | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.922-1026_922-1025i others(7): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297286 | ||||||
| chr1:70297286
|
G | GGTTTTTT | 4 | a0001c0001t0001g0329a0001c0001t0003g0300a0001c0001t0005g0301others(1): Show | 4 | HG00639.hp2 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.922-1026_922-1025i others(9): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297286 | ||||||
| chr1:70297286
|
G | GGTTTTTT others(1): Show |
41 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0260others(38): Show | 41 | HG00621.hp2 HG01070.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.922-1026_922-1025i others(10): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297286 | ||||||
| chr1:70297286
|
G | GGTTTTTT others(2): Show |
35 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(32): Show | 35 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.922-1026_922-1025i others(11): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297286 | ||||||
| chr1:70297286
|
G | GGTTTTTT others(3): Show |
1 | a0001c0001t0001g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.922-1026_922-1025i others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297286 | ||||||
| chr1:70297286
|
G | GGTTTTTT others(5): Show |
1 | a0001c0001t0001g0275 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.922-1026_922-1025i others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297286 | ||||||
| chr1:70297287
|
A | AT | 53 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0074others(50): Show | 53 | HG01074.hp1 HG01192.hp2 HG01256.hp1 others(50): Show |
intron_variant | MODIFIER | c.922-1027dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297287 | ||||||
| chr1:70297287
|
A | ATT | 7 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0007g0202others(4): Show | 7 | HG00621.hp1 HG01175.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.922-1028_922-1027d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297287 | ||||||
| chr1:70297287
|
A | G | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922-1026T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297287 | ||||||
| chr1:70297287
|
A | T | 89 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(86): Show | 89 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.922-1026T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297287 | ||||||
| chr1:70297287
|
AT | A | 14 | a0001c0001t0001g0041a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 14 | HG01884.hp1 HG01975.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.922-1027delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297287 | ||||||
| chr1:70297289
|
T | G | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922-1028A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297289 | ||||||
| chr1:70297333
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.922-1072C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297333 | ||||||
| chr1:70297386
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922-1125G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297386 | ||||||
| chr1:70297395
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.922-1134T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297395 | ||||||
| chr1:70297403
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.922-1142G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297403 | ||||||
| chr1:70297651
|
C | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0058others(33): Show | 37 | HG00544.hp1 HG00673.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.922-1390G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297651 | ||||||
| chr1:70297743
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0308 | 2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.922-1482C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297743 | ||||||
| chr1:70297837
|
C | T | 1 | a0001c0001t0011g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.922-1576G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297837 | ||||||
| chr1:70297868
|
A | C | 5 | a0001c0001t0004g0056a0001c0001t0004g0063a0001c0001t0004g0120others(2): Show | 5 | HG02886.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-1607T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297868 | ||||||
| chr1:70297915
|
CA | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.922-1655delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297915 | ||||||
| chr1:70297982
|
C | T | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.922-1721G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297982 | ||||||
| chr1:70297992
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.922-1731T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70297992 | ||||||
| chr1:70298155
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.922-1894T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298155 | ||||||
| chr1:70298381
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(29): Show | 33 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.922-2120G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298381 | ||||||
| chr1:70298427
|
A | G | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922-2166T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298427 | ||||||
| chr1:70298482
|
C | T | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.922-2221G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298482 | ||||||
| chr1:70298485
|
ATATG | A | 23 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(20): Show | 23 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.922-2228_922-2225d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298485 | ||||||
| chr1:70298531
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.921+2233A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298531 | ||||||
| chr1:70298695
|
A | G | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.921+2069T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298695 | ||||||
| chr1:70298812
|
T | C | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.921+1952A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70298812 | ||||||
| chr1:70299006
|
G | A | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+1758C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299006 | ||||||
| chr1:70299020
|
T | C | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.921+1744A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299020 | ||||||
| chr1:70299033
|
A | ATGTAACA others(5): Show |
1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.921+1730_921+1731i others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299033 | ||||||
| chr1:70299035
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.921+1729G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299035 | ||||||
| chr1:70299044
|
T | C | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.921+1720A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299044 | ||||||
| chr1:70299136
|
G | C | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.921+1628C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299136 | ||||||
| chr1:70299207
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.921+1557A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299207 | ||||||
| chr1:70299500
|
T | C | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+1264A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299500 | ||||||
| chr1:70299626
|
C | T | 1 | a0001c0001t0016g0119 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.921+1138G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299626 | ||||||
| chr1:70299976
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.921+788C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70299976 | ||||||
| chr1:70300012
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.921+752G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300012 | ||||||
| chr1:70300028
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.921+736T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300028 | ||||||
| chr1:70300248
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.921+516C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300248 | ||||||
| chr1:70300418
|
C | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0099others(2): Show | 5 | HG00544.hp2 HG00673.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+346G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300418 | ||||||
| chr1:70300520
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.921+244C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300520 | ||||||
| chr1:70300652
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0092a0001c0001t0001g0095 | 3 | HG02074.hp1 HG02165.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.921+112T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300652 | ||||||
| chr1:70300680
|
A | C | 1 | a0001c0001t0012g0346 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.921+84T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 7/12 | chr1 | 70300680 | ||||||
| chr1:70301178
|
C | CAT | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(78): Show | 83 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.777-272_777-271dup others(2): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301178 | ||||||
| chr1:70301178
|
CAT | C | 9 | a0001c0001t0001g0048a0001c0001t0001g0156a0001c0001t0001g0163others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-272_777-271del others(2): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301178 | ||||||
| chr1:70301180
|
T | C | 133 | a0001c0001t0001g0036a0001c0001t0001g0194a0001c0001t0001g0196others(130): Show | 133 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.777-272A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301180 | ||||||
| chr1:70301182
|
T | C | 29 | a0001c0001t0003g0302a0001c0001t0005g0301a0001c0002t0001g0005others(26): Show | 29 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.777-274A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301182 | ||||||
| chr1:70301183
|
A | G | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-275T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301183 | ||||||
| chr1:70301198
|
C | CATATGTA others(27): Show |
9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-291_777-290ins others(34): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301198 | ||||||
| chr1:70301340
|
G | A | 3 | a0001c0001t0001g0325a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | NA19011.hp1 NA19062.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.777-432C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301340 | ||||||
| chr1:70301379
|
T | C | 1 | a0001c0001t0009g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.777-471A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301379 | ||||||
| chr1:70301537
|
T | G | 1 | a0001c0001t0002g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777-629A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301537 | ||||||
| chr1:70301555
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.777-647A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301555 | ||||||
| chr1:70301883
|
A | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.777-975T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70301883 | ||||||
| chr1:70302309
|
C | CG | 29 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0055others(26): Show | 29 | HG00544.hp2 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.777-1402dupC | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302309 | ||||||
| chr1:70302312
|
G | C | 1 | a0001c0001t0001g0297 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.777-1404C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302312 | ||||||
| chr1:70302318
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.777-1410C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302318 | ||||||
| chr1:70302379
|
A | G | 11 | a0001c0001t0001g0053a0001c0001t0001g0129a0001c0001t0001g0164others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.777-1471T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302379 | ||||||
| chr1:70302428
|
TAAAAGAA others(316): Show |
T | 94 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(91): Show | 94 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.777-1843_777-1521d others(2): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302428 | ||||||
| chr1:70302443
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.777-1535A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302443 | ||||||
| chr1:70302493
|
A | G | 46 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0148others(43): Show | 46 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.777-1585T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302493 | ||||||
| chr1:70302540
|
A | C | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | NA18960.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.777-1632T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302540 | ||||||
| chr1:70302589
|
A | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-1681T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302589 | ||||||
| chr1:70302632
|
G | A | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-1724C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302632 | ||||||
| chr1:70302725
|
C | CA | 65 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0048others(62): Show | 66 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.777-1818dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302725 | ||||||
| chr1:70302725
|
C | CAA | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0070others(16): Show | 19 | HG00280.hp2 HG01261.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.777-1819_777-1818d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302725 | ||||||
| chr1:70302725
|
C | CAAA | 7 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0092others(4): Show | 8 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.777-1820_777-1818d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302725 | ||||||
| chr1:70302725
|
CA | C | 72 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.777-1818delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302725 | ||||||
| chr1:70302725
|
CAA | C | 16 | a0001c0001t0001g0042a0001c0001t0001g0166a0001c0001t0001g0184others(13): Show | 16 | HG01934.hp1 HG02074.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.777-1819_777-1818d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302725 | ||||||
| chr1:70302772
|
G | A | 25 | a0001c0001t0001g0240a0001c0001t0002g0046a0001c0001t0002g0054others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.777-1864C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302772 | ||||||
| chr1:70302808
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.777-1900A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70302808 | ||||||
| chr1:70303032
|
AAGAC | A | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.777-2128_777-2125d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303032 | ||||||
| chr1:70303098
|
T | C | 10 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-2190A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303098 | ||||||
| chr1:70303148
|
G | C | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.777-2240C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303148 | ||||||
| chr1:70303262
|
C | T | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.777-2354G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303262 | ||||||
| chr1:70303361
|
T | A | 75 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(72): Show | 75 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.777-2453A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303361 | ||||||
| chr1:70303406
|
GAAGA | G | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.777-2502_777-2499d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303406 | ||||||
| chr1:70303412
|
A | G | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.777-2504T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303412 | ||||||
| chr1:70303766
|
A | C | 1 | a0001c0001t0002g0126 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.776+2458T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303766 | ||||||
| chr1:70303921
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+2303A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70303921 | ||||||
| chr1:70304223
|
C | T | 94 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0187others(91): Show | 94 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.776+2001G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70304223 | ||||||
| chr1:70304265
|
AC | A | 6 | a0001c0001t0001g0059a0001c0001t0006g0103a0001c0001t0006g0111others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+1958delG | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70304265 | ||||||
| chr1:70304520
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.776+1704G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70304520 | ||||||
| chr1:70304619
|
G | A | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+1605C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70304619 | ||||||
| chr1:70304695
|
G | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.776+1529C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70304695 | ||||||
| chr1:70304874
|
T | G | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+1350A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70304874 | ||||||
| chr1:70305006
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.776+1218G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70305006 | ||||||
| chr1:70305021
|
G | C | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776+1203C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70305021 | ||||||
| chr1:70305701
|
A | G | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.776+523T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70305701 | ||||||
| chr1:70305789
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.776+435C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70305789 | ||||||
| chr1:70306066
|
T | TTTAAAAA others(6): Show |
1 | a0001c0001t0001g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.776+157_776+158ins others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70306066 | ||||||
| chr1:70306130
|
G | A | 1 | a0001c0001t0009g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.776+94C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 6/12 | chr1 | 70306130 | ||||||
| chr1:70306327
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.710-37G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70306327 | ||||||
| chr1:70306861
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.710-571T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70306861 | ||||||
| chr1:70306949
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(220): Show | 225 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(222): Show |
intron_variant | MODIFIER | c.710-659G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70306949 | ||||||
| chr1:70306986
|
C | T | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-696G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70306986 | ||||||
| chr1:70307367
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.710-1077A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70307367 | ||||||
| chr1:70307415
|
A | C | 1 | a0001c0001t0004g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.710-1125T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70307415 | ||||||
| chr1:70307725
|
T | C | 140 | a0001c0001t0001g0036a0001c0001t0001g0156a0001c0001t0001g0163others(137): Show | 140 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.710-1435A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70307725 | ||||||
| chr1:70307881
|
G | A | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.710-1591C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70307881 | ||||||
| chr1:70307979
|
A | C | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.710-1689T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70307979 | ||||||
| chr1:70308072
|
GAAGT | G | 7 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0011others(4): Show | 7 | NA18948.hp2 NA18953.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-1786_710-1783d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308072 | ||||||
| chr1:70308182
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0182 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.710-1892T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308182 | ||||||
| chr1:70308439
|
G | GA | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(74): Show | 79 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.710-2150dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308439 | ||||||
| chr1:70308506
|
G | A | 1 | a0001c0001t0011g0345 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.710-2216C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308506 | ||||||
| chr1:70308598
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.710-2308C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308598 | ||||||
| chr1:70308651
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.710-2361T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308651 | ||||||
| chr1:70308674
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0022g0215a0002c0007t0001g0236others(1): Show | 4 | NA18949.hp2 NA18966.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-2384T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308674 | ||||||
| chr1:70308738
|
C | CA | 60 | a0001c0001t0001g0048a0001c0001t0001g0095a0001c0001t0001g0112others(57): Show | 60 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.710-2449dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308738 | ||||||
| chr1:70308738
|
C | CAA | 75 | a0001c0001t0001g0036a0001c0001t0001g0253a0001c0001t0001g0254others(72): Show | 75 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.710-2450_710-2449d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308738 | ||||||
| chr1:70308738
|
C | CAAA | 9 | a0001c0001t0001g0263a0001c0001t0001g0268a0001c0001t0001g0269others(6): Show | 9 | HG00733.hp2 HG00741.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.710-2451_710-2449d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70308738 | ||||||
| chr1:70309029
|
C | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG02809.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-2739G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309029 | ||||||
| chr1:70309217
|
C | T | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.710-2927G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309217 | ||||||
| chr1:70309299
|
C | T | 1 | a0004c0006t0001g0034 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.710-3009G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309299 | ||||||
| chr1:70309352
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(73): Show | 78 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.710-3062G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309352 | ||||||
| chr1:70309448
|
G | A | 3 | a0001c0001t0003g0300a0001c0001t0003g0302a0001c0001t0005g0301 | 3 | HG02886.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.710-3158C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309448 | ||||||
| chr1:70309489
|
C | G | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.710-3199G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309489 | ||||||
| chr1:70309533
|
A | T | 1 | a0001c0002t0001g0026 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.710-3243T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309533 | ||||||
| chr1:70309568
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0081 | 2 | NA18949.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.710-3278A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309568 | ||||||
| chr1:70309627
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0007g0202a0001c0001t0023g0037 | 3 | HG02145.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.710-3337C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309627 | ||||||
| chr1:70309715
|
C | CAAA | 6 | a0001c0001t0001g0290a0001c0001t0001g0323a0001c0001t0001g0331others(3): Show | 6 | HG02165.hp1 HG02886.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.710-3428_710-3426d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309715 | ||||||
| chr1:70309715
|
CA | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0145a0001c0001t0001g0222others(3): Show | 6 | HG00140.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-3426delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309715 | ||||||
| chr1:70309726
|
A | AAAT | 7 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0259others(4): Show | 7 | HG01243.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.710-3437_710-3436i others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309726 | ||||||
| chr1:70309726
|
A | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0227a0001c0001t0001g0268others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-3436T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309726 | ||||||
| chr1:70309729
|
A | AAAT | 41 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0260others(38): Show | 41 | HG00597.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.710-3440_710-3439i others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309729 | ||||||
| chr1:70309729
|
A | AT | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(21): Show | 24 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.710-3440_710-3439i others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309729 | ||||||
| chr1:70309729
|
A | T | 88 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0041others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.710-3439T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309729 | ||||||
| chr1:70309730
|
A | T | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.710-3440T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309730 | ||||||
| chr1:70309732
|
A | AAAAT | 17 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(14): Show | 17 | HG02015.hp2 HG02040.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.710-3443_710-3442i others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309732 | ||||||
| chr1:70309732
|
A | AAAT | 10 | a0001c0001t0001g0253a0001c0001t0001g0281a0001c0001t0001g0283others(7): Show | 10 | HG00733.hp2 HG02683.hp2 HG03704.hp2 others(7): Show |
intron_variant | MODIFIER | c.710-3445_710-3443d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309732 | ||||||
| chr1:70309732
|
A | AT | 8 | a0001c0001t0001g0042a0001c0001t0001g0074a0001c0001t0001g0082others(5): Show | 8 | HG00733.hp1 HG01071.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.710-3443_710-3442i others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309732 | ||||||
| chr1:70309732
|
A | T | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.710-3442T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309732 | ||||||
| chr1:70309735
|
T | A | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.710-3445A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309735 | ||||||
| chr1:70309794
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.710-3504T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309794 | ||||||
| chr1:70309821
|
T | G | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-3531A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309821 | ||||||
| chr1:70309978
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.710-3688A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70309978 | ||||||
| chr1:70310060
|
C | A | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.709+3685G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70310060 | ||||||
| chr1:70310205
|
T | C | 25 | a0001c0001t0001g0240a0001c0001t0002g0046a0001c0001t0002g0054others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.709+3540A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70310205 | ||||||
| chr1:70310499
|
A | G | 1 | a0001c0002t0001g0012 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.709+3246T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70310499 | ||||||
| chr1:70310591
|
A | G | 134 | a0001c0001t0001g0036a0001c0001t0001g0194a0001c0001t0001g0196others(131): Show | 134 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.709+3154T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70310591 | ||||||
| chr1:70311000
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.709+2745T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311000 | ||||||
| chr1:70311003
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0220a0001c0001t0001g0249others(1): Show | 4 | NA18981.hp2 NA19007.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+2742C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311003 | ||||||
| chr1:70311137
|
T | C | 119 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(116): Show | 119 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.709+2608A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311137 | ||||||
| chr1:70311154
|
G | C | 2 | a0001c0001t0007g0050a0001c0001t0007g0051 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.709+2591C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311154 | ||||||
| chr1:70311167
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.709+2578G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311167 | ||||||
| chr1:70311168
|
T | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.709+2577A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311168 | ||||||
| chr1:70311261
|
G | A | 2 | a0001c0001t0011g0347a0001c0001t0029g0344 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.709+2484C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311261 | ||||||
| chr1:70311430
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.709+2315C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311430 | ||||||
| chr1:70311512
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.709+2233T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311512 | ||||||
| chr1:70311593
|
T | A | 1 | a0001c0002t0001g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.709+2152A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70311593 | ||||||
| chr1:70312231
|
A | G | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.709+1514T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312231 | ||||||
| chr1:70312256
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.709+1489C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312256 | ||||||
| chr1:70312313
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.709+1432A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312313 | ||||||
| chr1:70312368
|
G | GT | 21 | a0001c0001t0001g0048a0001c0001t0001g0079a0001c0001t0001g0080others(18): Show | 21 | HG00673.hp2 HG01884.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.709+1376dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312368 | ||||||
| chr1:70312579
|
T | G | 29 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0002t0001g0005others(26): Show | 29 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.709+1166A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312579 | ||||||
| chr1:70312631
|
C | T | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.709+1114G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312631 | ||||||
| chr1:70312658
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.709+1087G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312658 | ||||||
| chr1:70312660
|
C | T | 2 | a0002c0007t0001g0236a0006c0004t0001g0004 | 2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.709+1085G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312660 | ||||||
| chr1:70312667
|
C | CA | 126 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0254others(123): Show | 126 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.709+1077dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312667 | ||||||
| chr1:70312710
|
A | T | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+1035T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312710 | ||||||
| chr1:70312830
|
T | A | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.709+915A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312830 | ||||||
| chr1:70312867
|
T | TGAG | 121 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0253others(118): Show | 121 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.709+875_709+877dup others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70312867 | ||||||
| chr1:70313001
|
C | A | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.709+744G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313001 | ||||||
| chr1:70313016
|
C | T | 1 | a0001c0001t0023g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.709+729G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313016 | ||||||
| chr1:70313174
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.709+571A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313174 | ||||||
| chr1:70313355
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.709+390A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313355 | ||||||
| chr1:70313527
|
C | CA | 20 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0127others(17): Show | 20 | HG01081.hp1 HG01106.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.709+217dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313527 | ||||||
| chr1:70313649
|
A | C | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.709+96T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313649 | ||||||
| chr1:70313676
|
G | A | 2 | a0001c0001t0011g0347a0001c0001t0029g0344 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.709+69C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313676 | ||||||
| chr1:70313713
|
A | G | 1 | a0001c0001t0014g0003 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.709+32T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 5/12 | chr1 | 70313713 | ||||||
| chr1:70314032
|
TAATA | T | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-246_664-243del others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314032 | ||||||
| chr1:70314171
|
T | C | 3 | a0001c0001t0003g0300a0001c0001t0003g0302a0001c0001t0005g0301 | 3 | HG02886.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664-381A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314171 | ||||||
| chr1:70314324
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.664-534A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314324 | ||||||
| chr1:70314456
|
C | T | 1 | a0001c0001t0011g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.664-666G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314456 | ||||||
| chr1:70314631
|
A | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0088others(5): Show | 9 | HG00280.hp2 HG01070.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.664-841T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314631 | ||||||
| chr1:70314795
|
A | G | 2 | a0001c0001t0013g0349a0001c0001t0013g0350 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.663+686T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314795 | ||||||
| chr1:70314812
|
C | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.663+669G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314812 | ||||||
| chr1:70314818
|
T | A | 1 | a0001c0001t0001g0341 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.663+663A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70314818 | ||||||
| chr1:70315013
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(67): Show | 72 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.663+468G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70315013 | ||||||
| chr1:70315045
|
C | A | 4 | a0001c0001t0001g0240a0001c0001t0022g0215a0002c0007t0001g0236others(1): Show | 4 | NA18949.hp2 NA18966.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+436G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70315045 | ||||||
| chr1:70315050
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.663+431C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70315050 | ||||||
| chr1:70315211
|
T | C | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.663+270A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70315211 | ||||||
| chr1:70315264
|
T | C | 25 | a0001c0001t0001g0240a0001c0001t0002g0046a0001c0001t0002g0054others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.663+217A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70315264 | ||||||
| chr1:70315425
|
A | G | 5 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0010others(2): Show | 5 | HG01074.hp1 HG01168.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+56T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 4/12 | chr1 | 70315425 | ||||||
| chr1:70315681
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.578-115C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70315681 | ||||||
| chr1:70315809
|
A | G | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.578-243T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70315809 | ||||||
| chr1:70315846
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-280C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70315846 | ||||||
| chr1:70316502
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0135 | 2 | HG00741.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.578-936C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70316502 | ||||||
| chr1:70316520
|
T | TA | 36 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0112others(33): Show | 36 | HG01074.hp1 HG01167.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.578-955dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70316520 | ||||||
| chr1:70316520
|
TA | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0141others(6): Show | 9 | HG02602.hp1 HG02683.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.578-955delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70316520 | ||||||
| chr1:70316650
|
T | A | 2 | a0001c0001t0001g0048a0001c0001t0007g0049 | 2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.578-1084A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70316650 | ||||||
| chr1:70317009
|
C | T | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.578-1443G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317009 | ||||||
| chr1:70317060
|
AT | A | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.578-1495delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317060 | ||||||
| chr1:70317466
|
T | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0005g0035others(1): Show | 4 | HG02622.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-1900A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317466 | ||||||
| chr1:70317718
|
T | A | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.578-2152A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317718 | ||||||
| chr1:70317812
|
T | A | 1 | a0001c0001t0011g0345 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.578-2246A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317812 | ||||||
| chr1:70317850
|
A | G | 92 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(89): Show | 92 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.578-2284T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317850 | ||||||
| chr1:70317853
|
AG | A | 3 | a0001c0001t0001g0071a0001c0001t0002g0218a0001c0001t0002g0229 | 3 | HG02257.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.578-2288delC | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317853 | ||||||
| chr1:70317884
|
AT | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-2319delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70317884 | ||||||
| chr1:70318049
|
T | C | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.578-2483A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318049 | ||||||
| chr1:70318058
|
C | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.578-2492G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318058 | ||||||
| chr1:70318267
|
T | C | 3 | a0001c0001t0003g0300a0001c0001t0003g0302a0001c0001t0005g0301 | 3 | HG02886.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.578-2701A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318267 | ||||||
| chr1:70318296
|
A | G | 1 | a0001c0001t0006g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.578-2730T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318296 | ||||||
| chr1:70318450
|
A | G | 1 | a0001c0001t0012g0346 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.578-2884T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318450 | ||||||
| chr1:70318679
|
G | GT | 17 | a0001c0001t0001g0168a0001c0001t0001g0317a0001c0001t0002g0237others(14): Show | 17 | HG01496.hp1 HG01516.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.578-3114dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318679 | ||||||
| chr1:70318679
|
G | GTT | 59 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(56): Show | 59 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.578-3115_578-3114d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318679 | ||||||
| chr1:70318679
|
G | GTTT | 21 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0263others(18): Show | 21 | HG01361.hp2 HG02080.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.578-3116_578-3114d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318679 | ||||||
| chr1:70318679
|
GT | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.578-3114delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318679 | ||||||
| chr1:70318694
|
T | G | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.578-3128A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318694 | ||||||
| chr1:70318714
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.578-3148G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318714 | ||||||
| chr1:70318808
|
G | C | 1 | a0005c0009t0001g0343 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.578-3242C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318808 | ||||||
| chr1:70318829
|
T | C | 95 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(92): Show | 95 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.578-3263A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318829 | ||||||
| chr1:70318872
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(213): Show | 218 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.578-3306T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70318872 | ||||||
| chr1:70319007
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.578-3441A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319007 | ||||||
| chr1:70319021
|
C | A | 1 | a0001c0005t0001g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.578-3455G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319021 | ||||||
| chr1:70319157
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.578-3591C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319157 | ||||||
| chr1:70319216
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.578-3650G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319216 | ||||||
| chr1:70319228
|
A | G | 4 | a0001c0001t0011g0345a0001c0001t0011g0347a0001c0001t0012g0348others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-3662T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319228 | ||||||
| chr1:70319252
|
T | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(29): Show | 33 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.578-3686A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319252 | ||||||
| chr1:70319270
|
C | T | 2 | a0001c0001t0009g0195a0001c0001t0009g0199 | 2 | HG01934.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.578-3704G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319270 | ||||||
| chr1:70319404
|
A | G | 119 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(116): Show | 119 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.578-3838T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319404 | ||||||
| chr1:70319511
|
G | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.578-3945C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319511 | ||||||
| chr1:70319538
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.578-3972G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319538 | ||||||
| chr1:70319562
|
G | A | 14 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0139others(11): Show | 14 | HG00738.hp2 HG01074.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.578-3996C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319562 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.578-4042_578-4041i others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0003g0305others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-4042_578-4041i others(15): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(7): Show |
41 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0261others(38): Show | 41 | HG00621.hp2 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.578-4042_578-4041i others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(8): Show |
31 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(28): Show | 31 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.578-4042_578-4041i others(17): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(9): Show |
12 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0267others(9): Show | 12 | HG00642.hp1 HG01109.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.578-4042_578-4041i others(18): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0005g0035a0001c0001t0011g0345a0001c0001t0011g0347others(1): Show | 4 | HG02630.hp2 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-4042_578-4041i others(19): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.578-4042_578-4041i others(20): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319607
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.578-4042_578-4041i others(23): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319607 | ||||||
| chr1:70319652
|
C | CT | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(174): Show | 179 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.578-4087dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319652 | ||||||
| chr1:70319652
|
C | CTT | 9 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(6): Show | 9 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.578-4088_578-4087d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319652 | ||||||
| chr1:70319652
|
CT | C | 20 | a0001c0001t0001g0036a0001c0001t0001g0179a0001c0001t0001g0187others(17): Show | 20 | HG00140.hp1 HG01934.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.578-4087delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319652 | ||||||
| chr1:70319760
|
A | T | 1 | a0001c0001t0001g0295 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.578-4194T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319760 | ||||||
| chr1:70319871
|
GTAGGATG others(6): Show |
G | 2 | a0001c0001t0001g0123a0001c0001t0001g0145 | 2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.578-4318_578-4306d others(15): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319871 | ||||||
| chr1:70319975
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.578-4409G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70319975 | ||||||
| chr1:70320296
|
G | A | 4 | a0001c0001t0011g0345a0001c0001t0011g0347a0001c0001t0012g0348others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+4557C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320296 | ||||||
| chr1:70320481
|
A | C | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.577+4372T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320481 | ||||||
| chr1:70320603
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.577+4250C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320603 | ||||||
| chr1:70320779
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.577+4074T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320779 | ||||||
| chr1:70320783
|
T | A | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.577+4070A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320783 | ||||||
| chr1:70320856
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.577+3997G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320856 | ||||||
| chr1:70320918
|
T | C | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.577+3935A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320918 | ||||||
| chr1:70320949
|
C | G | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.577+3904G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320949 | ||||||
| chr1:70320962
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0222 | 2 | NA18950.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.577+3891A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70320962 | ||||||
| chr1:70321100
|
G | A | 3 | a0001c0001t0011g0345a0001c0001t0011g0347a0001c0001t0029g0344 | 3 | HG02630.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.577+3753C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70321100 | ||||||
| chr1:70321164
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0177 | 2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.577+3689A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70321164 | ||||||
| chr1:70321440
|
T | C | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.577+3413A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70321440 | ||||||
| chr1:70321461
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+3392G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70321461 | ||||||
| chr1:70321741
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.577+3112A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70321741 | ||||||
| chr1:70322008
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.577+2845A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322008 | ||||||
| chr1:70322035
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.577+2818G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322035 | ||||||
| chr1:70322036
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.577+2817G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322036 | ||||||
| chr1:70322170
|
T | C | 60 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0053others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.577+2683A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322170 | ||||||
| chr1:70322239
|
A | C | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.577+2614T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322239 | ||||||
| chr1:70322270
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.577+2583C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322270 | ||||||
| chr1:70322313
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.577+2540C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322313 | ||||||
| chr1:70322398
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.577+2455C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322398 | ||||||
| chr1:70322452
|
A | C | 2 | a0001c0001t0002g0258a0001c0001t0002g0264 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.577+2401T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322452 | ||||||
| chr1:70322718
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.577+2135G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322718 | ||||||
| chr1:70322849
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577+2004C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322849 | ||||||
| chr1:70322973
|
A | T | 1 | a0001c0001t0002g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.577+1880T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70322973 | ||||||
| chr1:70323000
|
A | AC | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.577+1852_577+1853i others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323000 | ||||||
| chr1:70323034
|
A | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.577+1819T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323034 | ||||||
| chr1:70323178
|
A | G | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.577+1675T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323178 | ||||||
| chr1:70323363
|
G | A | 94 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.577+1490C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323363 | ||||||
| chr1:70323363
|
G | C | 3 | a0001c0001t0011g0345a0001c0001t0011g0347a0001c0001t0029g0344 | 3 | HG02630.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.577+1490C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323363 | ||||||
| chr1:70323410
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.577+1443G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323410 | ||||||
| chr1:70323411
|
A | G | 92 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(89): Show | 92 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.577+1442T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323411 | ||||||
| chr1:70323546
|
G | A | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.577+1307C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323546 | ||||||
| chr1:70323646
|
C | CA | 10 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0088others(7): Show | 11 | HG00280.hp2 HG01070.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.577+1206dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323646 | ||||||
| chr1:70323648
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.577+1205T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323648 | ||||||
| chr1:70323657
|
A | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.577+1196T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323657 | ||||||
| chr1:70323658
|
T | A | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.577+1195A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323658 | ||||||
| chr1:70323725
|
A | AT | 7 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0144others(4): Show | 7 | HG02074.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+1127dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323725 | ||||||
| chr1:70323811
|
G | A | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.577+1042C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323811 | ||||||
| chr1:70323890
|
A | AT | 23 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(20): Show | 23 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.577+962dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323890 | ||||||
| chr1:70323914
|
C | T | 1 | a0001c0001t0011g0345 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.577+939G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70323914 | ||||||
| chr1:70324260
|
T | A | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577+593A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70324260 | ||||||
| chr1:70324347
|
A | T | 1 | a0001c0001t0021g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.577+506T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70324347 | ||||||
| chr1:70324368
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0058others(32): Show | 36 | HG00544.hp1 HG00673.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.577+485G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 3/12 | chr1 | 70324368 | ||||||
| chr1:70325074
|
C | T | 5 | a0001c0001t0001g0059a0001c0001t0006g0103a0001c0001t0006g0111others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-117G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325074 | ||||||
| chr1:70325165
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.473-208A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325165 | ||||||
| chr1:70325266
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.473-309G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325266 | ||||||
| chr1:70325344
|
G | A | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.473-387C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325344 | ||||||
| chr1:70325394
|
A | G | 84 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(81): Show | 84 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.473-437T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325394 | ||||||
| chr1:70325554
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.473-597A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325554 | ||||||
| chr1:70325600
|
C | A | 2 | a0001c0001t0001g0075a0001c0002t0005g0031 | 2 | NA18964.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.473-643G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325600 | ||||||
| chr1:70325804
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.473-847C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325804 | ||||||
| chr1:70325836
|
G | A | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.473-879C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325836 | ||||||
| chr1:70325894
|
A | T | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.473-937T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70325894 | ||||||
| chr1:70326124
|
G | A | 3 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0019g0009 | 3 | HG03490.hp1 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.473-1167C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326124 | ||||||
| chr1:70326161
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.473-1204C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326161 | ||||||
| chr1:70326231
|
C | CA | 39 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(36): Show | 39 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.473-1275dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
C | CAA | 15 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0137others(12): Show | 15 | HG02027.hp2 HG02055.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.473-1276_473-1275d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CA | C | 25 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0077others(22): Show | 25 | HG00544.hp2 HG01070.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.473-1275delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAA | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(54): Show | 59 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.473-1276_473-1275d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAAA | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0260a0001c0001t0001g0263others(26): Show | 29 | HG00621.hp2 HG01109.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-1277_473-1275d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAAAA | C | 74 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(71): Show | 74 | HG00597.hp2 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.473-1278_473-1275d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAAAAA | C | 12 | a0001c0001t0001g0287a0001c0001t0001g0295a0001c0001t0003g0294others(9): Show | 12 | HG01168.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.473-1279_473-1275d others(7): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAAAAAA | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0337a0001c0001t0001g0339others(5): Show | 8 | HG01192.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-1280_473-1275d others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.473-1284_473-1275d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326231
|
CAAAAAAA others(5): Show |
C | 11 | a0001c0001t0001g0139a0001c0001t0001g0180a0001c0001t0001g0194others(8): Show | 11 | HG01074.hp2 HG01934.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.473-1286_473-1275d others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326231 | ||||||
| chr1:70326370
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.473-1413C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326370 | ||||||
| chr1:70326657
|
G | GTTTAT | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(213): Show | 218 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.473-1701_473-1700i others(7): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326657 | ||||||
| chr1:70326707
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.473-1750G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326707 | ||||||
| chr1:70326872
|
G | GA | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.473-1916dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326872 | ||||||
| chr1:70326987
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.473-2030A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70326987 | ||||||
| chr1:70327010
|
A | AT | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(213): Show | 218 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.473-2054_473-2053i others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70327010 | ||||||
| chr1:70327150
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.473-2193G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70327150 | ||||||
| chr1:70327244
|
G | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-2287C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70327244 | ||||||
| chr1:70327530
|
C | G | 9 | a0001c0001t0001g0263a0001c0001t0001g0266a0001c0001t0001g0267others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.473-2573G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70327530 | ||||||
| chr1:70327735
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.473-2778T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70327735 | ||||||
| chr1:70327819
|
C | G | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.473-2862G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70327819 | ||||||
| chr1:70328161
|
ATGTT | A | 4 | a0001c0002t0001g0030a0001c0002t0005g0028a0001c0002t0005g0029others(1): Show | 4 | NA18972.hp2 NA19000.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-3208_473-3205d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328161 | ||||||
| chr1:70328276
|
T | G | 14 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0139others(11): Show | 14 | HG00738.hp2 HG01074.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-3319A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328276 | ||||||
| chr1:70328298
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.473-3341G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328298 | ||||||
| chr1:70328329
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.473-3372A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328329 | ||||||
| chr1:70328357
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.473-3400G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328357 | ||||||
| chr1:70328434
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02074.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.473-3477C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328434 | ||||||
| chr1:70328619
|
G | A | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.473-3662C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328619 | ||||||
| chr1:70328753
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.473-3796C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328753 | ||||||
| chr1:70328833
|
G | A | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-3876C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328833 | ||||||
| chr1:70328864
|
T | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(75): Show | 80 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.473-3907A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70328864 | ||||||
| chr1:70329057
|
AAAAC | A | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.473-4104_473-4101d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70329057 | ||||||
| chr1:70329327
|
C | T | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.473-4370G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70329327 | ||||||
| chr1:70329696
|
G | T | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(341): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.473-4739C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70329696 | ||||||
| chr1:70329831
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0277 | 2 | NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.473-4874C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70329831 | ||||||
| chr1:70330088
|
C | CA | 6 | a0001c0001t0001g0036a0001c0001t0001g0175a0001c0001t0001g0278others(3): Show | 6 | HG01192.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-5132dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330088 | ||||||
| chr1:70330120
|
A | C | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.473-5163T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330120 | ||||||
| chr1:70330202
|
TA | T | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.473-5246delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330202 | ||||||
| chr1:70330306
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-5349G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330306 | ||||||
| chr1:70330348
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00733.hp1 HG01071.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-5391G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330348 | ||||||
| chr1:70330442
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-5485G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330442 | ||||||
| chr1:70330574
|
C | CA | 64 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(61): Show | 65 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.472+5483dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330574 | ||||||
| chr1:70330574
|
C | CAA | 36 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0048others(33): Show | 37 | HG00544.hp1 HG00673.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.472+5482_472+5483d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330574 | ||||||
| chr1:70330574
|
CA | C | 91 | a0001c0001t0001g0053a0001c0001t0001g0112a0001c0001t0001g0128others(88): Show | 91 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.472+5483delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330574 | ||||||
| chr1:70330574
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.472+5474_472+5483d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330574 | ||||||
| chr1:70330757
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.472+5301A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330757 | ||||||
| chr1:70330758
|
C | T | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.472+5300G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330758 | ||||||
| chr1:70330892
|
CTTACT | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0129a0001c0001t0001g0164others(1): Show | 4 | HG01081.hp1 HG01106.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+5161_472+5165d others(7): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330892 | ||||||
| chr1:70330970
|
T | C | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.472+5088A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70330970 | ||||||
| chr1:70331025
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.472+5033A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331025 | ||||||
| chr1:70331078
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0212 | 2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.472+4980C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331078 | ||||||
| chr1:70331267
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.472+4791C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331267 | ||||||
| chr1:70331317
|
C | T | 90 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(87): Show | 90 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.472+4741G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331317 | ||||||
| chr1:70331659
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.472+4399A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331659 | ||||||
| chr1:70331732
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.472+4326C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331732 | ||||||
| chr1:70331820
|
C | CA | 206 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.472+4237dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331820 | ||||||
| chr1:70331820
|
C | CAA | 15 | a0001c0001t0001g0175a0001c0001t0001g0221a0001c0001t0001g0225others(12): Show | 15 | HG00733.hp1 HG01071.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+4236_472+4237d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331820 | ||||||
| chr1:70331820
|
CA | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0057others(4): Show | 7 | HG02056.hp1 HG02602.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.472+4237delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331820 | ||||||
| chr1:70331820
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.472+4228_472+4237d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331820 | ||||||
| chr1:70331820
|
CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0001g0036a0001c0001t0007g0202a0001c0001t0023g0037others(25): Show | 28 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.472+4227_472+4237d others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331820 | ||||||
| chr1:70331845
|
G | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(29): Show | 33 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.472+4213C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70331845 | ||||||
| chr1:70332098
|
T | TACCAACA others(7): Show |
1 | a0001c0001t0001g0329 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.472+3946_472+3959d others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332098 | ||||||
| chr1:70332186
|
A | G | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+3872T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332186 | ||||||
| chr1:70332501
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.472+3557G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332501 | ||||||
| chr1:70332677
|
G | T | 1 | a0003c0008t0001g0342 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.472+3381C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332677 | ||||||
| chr1:70332729
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.472+3329C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332729 | ||||||
| chr1:70332746
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+3312C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332746 | ||||||
| chr1:70332912
|
T | C | 1 | a0001c0002t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.472+3146A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70332912 | ||||||
| chr1:70333053
|
C | T | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.472+3005G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70333053 | ||||||
| chr1:70333240
|
C | T | 2 | a0001c0001t0011g0345a0001c0001t0012g0346 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.472+2818G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70333240 | ||||||
| chr1:70333365
|
G | C | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.472+2693C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70333365 | ||||||
| chr1:70333648
|
C | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0164a0001c0001t0001g0173 | 3 | HG01081.hp1 HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.472+2410G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70333648 | ||||||
| chr1:70333657
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0122 | 2 | HG01167.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.472+2401A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70333657 | ||||||
| chr1:70333879
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.472+2179G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70333879 | ||||||
| chr1:70334308
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.472+1750C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334308 | ||||||
| chr1:70334579
|
T | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0308 | 2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.472+1479A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334579 | ||||||
| chr1:70334600
|
C | G | 135 | a0001c0001t0001g0036a0001c0001t0001g0194a0001c0001t0001g0196others(132): Show | 135 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.472+1458G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334600 | ||||||
| chr1:70334601
|
C | G | 1 | a0001c0001t0001g0255 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.472+1457G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334601 | ||||||
| chr1:70334603
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.472+1455A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334603 | ||||||
| chr1:70334718
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(213): Show | 218 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.472+1340C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334718 | ||||||
| chr1:70334784
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.472+1274A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334784 | ||||||
| chr1:70334821
|
G | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+1237C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334821 | ||||||
| chr1:70334902
|
A | G | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(341): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.472+1156T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70334902 | ||||||
| chr1:70335049
|
T | C | 1 | a0001c0001t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.472+1009A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335049 | ||||||
| chr1:70335084
|
G | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.472+974C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335084 | ||||||
| chr1:70335116
|
A | C | 1 | a0001c0001t0001g0329 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.472+942T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335116 | ||||||
| chr1:70335309
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0232 | 2 | NA18959.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.472+749G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335309 | ||||||
| chr1:70335333
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.472+725C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335333 | ||||||
| chr1:70335405
|
C | CA | 82 | a0001c0001t0001g0040a0001c0001t0001g0175a0001c0001t0001g0253others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.472+652dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335405 | ||||||
| chr1:70335439
|
A | G | 3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.472+619T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335439 | ||||||
| chr1:70335569
|
G | T | 6 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0265others(3): Show | 6 | HG01070.hp2 HG01071.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+489C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335569 | ||||||
| chr1:70335596
|
GC | G | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.472+461delG | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335596 | ||||||
| chr1:70335643
|
G | T | 4 | a0001c0001t0002g0133a0001c0001t0002g0169a0001c0001t0002g0176others(1): Show | 4 | HG01106.hp1 HG01243.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+415C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70335643 | ||||||
| chr1:70336046
|
A | T | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.472+12T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 2/12 | chr1 | 70336046 | ||||||
| chr1:70336241
|
T | C | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.431-142A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336241 | ||||||
| chr1:70336519
|
T | A | 1 | a0001c0001t0001g0329 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.431-420A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336519 | ||||||
| chr1:70336541
|
G | T | 2 | a0001c0001t0001g0036a0001c0001t0023g0037 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.431-442C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336541 | ||||||
| chr1:70336554
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.431-455G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336554 | ||||||
| chr1:70336555
|
C | T | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.431-456G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336555 | ||||||
| chr1:70336566
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(327): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.431-467A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336566 | ||||||
| chr1:70336626
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.431-527C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336626 | ||||||
| chr1:70336827
|
C | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-728G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336827 | ||||||
| chr1:70336885
|
A | C | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-786T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70336885 | ||||||
| chr1:70337015
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.431-916C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337015 | ||||||
| chr1:70337133
|
C | T | 1 | a0001c0001t0006g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-1034G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337133 | ||||||
| chr1:70337146
|
A | AAC | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.431-1049_431-1048d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
A | AACAC | 46 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0067others(43): Show | 46 | HG00639.hp2 HG00673.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.431-1051_431-1048d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
A | AACACAC | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0314others(6): Show | 9 | HG01167.hp1 HG02132.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1053_431-1048d others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
A | AACACACA others(1): Show |
3 | a0001c0001t0001g0102a0001c0001t0002g0176a0001c0001t0007g0051 | 3 | HG01106.hp1 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.431-1055_431-1048d others(10): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
A | AACACACA others(3): Show |
3 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0004g0251 | 3 | HG01192.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.431-1057_431-1048d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.431-1048_431-1047i others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
AAC | A | 17 | a0001c0001t0001g0040a0001c0001t0001g0221a0001c0001t0001g0223others(14): Show | 17 | HG00733.hp1 HG01071.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.431-1049_431-1048d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337146
|
AACAC | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0196others(9): Show | 12 | HG00280.hp1 HG01934.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.431-1051_431-1048d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337146 | ||||||
| chr1:70337446
|
G | A | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-1347C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337446 | ||||||
| chr1:70337590
|
T | TA | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1492dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337590 | ||||||
| chr1:70337653
|
C | T | 2 | a0001c0002t0001g0005a0001c0002t0001g0010 | 2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.431-1554G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337653 | ||||||
| chr1:70337816
|
T | G | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.431-1717A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337816 | ||||||
| chr1:70337891
|
G | T | 1 | a0001c0001t0001g0329 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.431-1792C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337891 | ||||||
| chr1:70337956
|
A | G | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-1857T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70337956 | ||||||
| chr1:70338016
|
T | A | 2 | a0001c0002t0010g0014a0001c0002t0010g0024 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.431-1917A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338016 | ||||||
| chr1:70338034
|
G | C | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.431-1935C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338034 | ||||||
| chr1:70338124
|
T | G | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-2025A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338124 | ||||||
| chr1:70338225
|
C | A | 1 | a0001c0001t0027g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.431-2126G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338225 | ||||||
| chr1:70338272
|
CA | C | 3 | a0001c0001t0001g0184a0001c0001t0002g0046a0001c0001t0018g0242 | 3 | HG01975.hp1 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.431-2174delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338272 | ||||||
| chr1:70338404
|
T | G | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.431-2305A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338404 | ||||||
| chr1:70338487
|
G | T | 1 | a0001c0001t0001g0328 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.431-2388C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70338487 | ||||||
| chr1:70339143
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0007g0202a0001c0001t0023g0037 | 3 | HG02145.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.431-3044C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339143 | ||||||
| chr1:70339209
|
C | CA | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(78): Show | 83 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.431-3111dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339209 | ||||||
| chr1:70339311
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.431-3212A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339311 | ||||||
| chr1:70339315
|
A | AT | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(87): Show | 92 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.431-3217dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339315 | ||||||
| chr1:70339315
|
AT | A | 78 | a0001c0001t0001g0125a0001c0001t0001g0253a0001c0001t0001g0254others(75): Show | 78 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.431-3217delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339315 | ||||||
| chr1:70339376
|
G | A | 1 | a0001c0002t0010g0024 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431-3277C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339376 | ||||||
| chr1:70339411
|
G | A | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.431-3312C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339411 | ||||||
| chr1:70339447
|
T | C | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.431-3348A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339447 | ||||||
| chr1:70339631
|
T | C | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-3532A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339631 | ||||||
| chr1:70339648
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.431-3549T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339648 | ||||||
| chr1:70339777
|
G | C | 6 | a0001c0001t0005g0035a0001c0001t0011g0345a0001c0001t0011g0347others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-3678C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339777 | ||||||
| chr1:70339811
|
GTTTATTA others(3): Show |
G | 2 | a0001c0001t0001g0044a0001c0001t0001g0163 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.431-3722_431-3713d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339811 | ||||||
| chr1:70339812
|
TTTA | T | 84 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0060others(81): Show | 84 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.431-3716_431-3714d others(5): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTA | T | 69 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0055others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.431-3719_431-3714d others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(2): Show |
T | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0039others(58): Show | 63 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.431-3722_431-3714d others(11): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(5): Show |
T | 3 | a0001c0001t0002g0169a0001c0001t0004g0056a0001c0001t0007g0202 | 3 | HG01496.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.431-3725_431-3714d others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(8): Show |
T | 2 | a0001c0001t0001g0041a0001c0001t0001g0210 | 2 | HG02135.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.431-3728_431-3714d others(17): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(11): Show |
T | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0333others(5): Show | 8 | HG01074.hp1 HG01192.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.431-3731_431-3714d others(20): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(14): Show |
T | 3 | a0001c0001t0001g0036a0001c0001t0001g0292a0001c0001t0023g0037 | 3 | HG02486.hp2 HG02922.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.431-3734_431-3714d others(23): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(17): Show |
T | 84 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(81): Show | 84 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.431-3737_431-3714d others(26): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339812
|
TTTATTAT others(20): Show |
T | 4 | a0001c0001t0001g0303a0001c0001t0001g0307a0001c0001t0003g0306others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-3740_431-3714d others(29): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339812 | ||||||
| chr1:70339817
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.431-3718A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339817 | ||||||
| chr1:70339854
|
ATTATTAT others(4): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-3766_431-3756d others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70339854 | ||||||
| chr1:70340139
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0337a0001c0001t0001g0339others(2): Show | 5 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-4040C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70340139 | ||||||
| chr1:70340338
|
C | G | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-4239G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70340338 | ||||||
| chr1:70340354
|
C | G | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-4255G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70340354 | ||||||
| chr1:70340500
|
A | C | 4 | a0001c0002t0001g0030a0001c0002t0005g0028a0001c0002t0005g0029others(1): Show | 4 | NA18972.hp2 NA19000.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-4401T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70340500 | ||||||
| chr1:70340622
|
G | C | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.431-4523C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70340622 | ||||||
| chr1:70341096
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.431-4997G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341096 | ||||||
| chr1:70341244
|
G | T | 1 | a0002c0007t0001g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.431-5145C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341244 | ||||||
| chr1:70341359
|
G | T | 1 | a0001c0001t0012g0346 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.431-5260C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341359 | ||||||
| chr1:70341362
|
TG | T | 6 | a0001c0001t0003g0294a0001c0001t0003g0300a0001c0001t0003g0302others(3): Show | 6 | HG02257.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-5264delC | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341362 | ||||||
| chr1:70341363
|
G | GT | 19 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0194others(16): Show | 19 | HG00140.hp2 HG01192.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.431-5265dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341363 | ||||||
| chr1:70341363
|
G | T | 1 | a0001c0001t0003g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-5264C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341363 | ||||||
| chr1:70341363
|
GT | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(158): Show | 163 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.431-5265delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341363 | ||||||
| chr1:70341364
|
T | G | 1 | a0001c0001t0007g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.431-5265A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341364 | ||||||
| chr1:70341364
|
T | TG | 3 | a0001c0001t0002g0046a0001c0001t0002g0243a0001c0001t0018g0242 | 3 | HG01928.hp2 HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.431-5266_431-5265i others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341364 | ||||||
| chr1:70341365
|
T | G | 4 | a0001c0001t0001g0048a0001c0001t0007g0049a0001c0001t0007g0050others(1): Show | 4 | HG02602.hp1 HG02683.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-5266A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341365 | ||||||
| chr1:70341370
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.431-5271A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341370 | ||||||
| chr1:70341373
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0203 | 2 | NA18941.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.431-5274A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341373 | ||||||
| chr1:70341515
|
C | T | 4 | a0001c0001t0011g0345a0001c0001t0011g0347a0001c0001t0012g0346others(1): Show | 4 | HG02630.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-5416G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341515 | ||||||
| chr1:70341532
|
T | G | 1 | a0001c0002t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-5433A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341532 | ||||||
| chr1:70341586
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-5487G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341586 | ||||||
| chr1:70341596
|
G | C | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-5497C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341596 | ||||||
| chr1:70341607
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-5508C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341607 | ||||||
| chr1:70341646
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.431-5547G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341646 | ||||||
| chr1:70341778
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.431-5679C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341778 | ||||||
| chr1:70341938
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.431-5839A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341938 | ||||||
| chr1:70341970
|
G | C | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.431-5871C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70341970 | ||||||
| chr1:70342127
|
G | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0122 | 2 | HG01167.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.431-6028C>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342127 | ||||||
| chr1:70342173
|
C | T | 6 | a0001c0001t0001g0059a0001c0001t0004g0063a0001c0001t0006g0103others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-6074G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342173 | ||||||
| chr1:70342411
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.431-6312C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342411 | ||||||
| chr1:70342443
|
C | G | 1 | a0001c0001t0016g0119 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.431-6344G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342443 | ||||||
| chr1:70342536
|
C | T | 4 | a0001c0001t0011g0345a0001c0001t0011g0347a0001c0001t0012g0346others(1): Show | 4 | HG02630.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-6437G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342536 | ||||||
| chr1:70342585
|
T | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0055others(29): Show | 33 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.431-6486A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342585 | ||||||
| chr1:70342611
|
TCAATAGT others(11): Show |
T | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.431-6530_431-6513d others(20): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342611 | ||||||
| chr1:70342618
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.431-6519A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342618 | ||||||
| chr1:70342646
|
A | AGCAATAG others(10): Show |
1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.431-6564_431-6548d others(19): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342646 | ||||||
| chr1:70342670
|
C | T | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.431-6571G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342670 | ||||||
| chr1:70342722
|
AAACACAC others(9): Show |
A | 1 | a0001c0001t0001g0102 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.431-6639_431-6624d others(18): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342722 | ||||||
| chr1:70342723
|
AACACACA others(11): Show |
A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0341 | 3 | HG00544.hp1 HG02056.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.431-6642_431-6625d others(20): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342723 | ||||||
| chr1:70342723
|
AACACACA others(13): Show |
A | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0039others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.431-6644_431-6625d others(22): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342723 | ||||||
| chr1:70342725
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0038 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.431-6640_431-6627d others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342725 | ||||||
| chr1:70342739
|
A | AAC | 43 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0114others(40): Show | 43 | HG00280.hp1 HG01109.hp1 HG01255.hp1 others(40): Show |
intron_variant | MODIFIER | c.431-6642_431-6641d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
A | AACAC | 20 | a0001c0001t0001g0200a0001c0002t0001g0005a0001c0002t0001g0007others(17): Show | 20 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.431-6644_431-6641d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
A | AACACAC | 3 | a0001c0002t0001g0027a0001c0002t0019g0009a0001c0005t0001g0022 | 3 | HG03669.hp1 HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.431-6646_431-6641d others(8): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
A | AACACACA others(5): Show |
1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.431-6652_431-6641d others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
AAC | A | 84 | a0001c0001t0001g0059a0001c0001t0001g0162a0001c0001t0001g0253others(81): Show | 84 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.431-6642_431-6641d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
AACAC | A | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-6644_431-6641d others(6): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
AACACACA others(5): Show |
A | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-6652_431-6641d others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342739
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-6654_431-6641d others(16): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342739 | ||||||
| chr1:70342773
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.431-6674T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342773 | ||||||
| chr1:70342844
|
T | C | 1 | a0001c0001t0006g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.431-6745A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342844 | ||||||
| chr1:70342983
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.431-6884C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70342983 | ||||||
| chr1:70343035
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0232 | 2 | NA18959.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.431-6936C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343035 | ||||||
| chr1:70343249
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(214): Show | 219 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.431-7150G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343249 | ||||||
| chr1:70343362
|
A | T | 1 | a0001c0001t0016g0119 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.431-7263T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343362 | ||||||
| chr1:70343387
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.431-7288G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343387 | ||||||
| chr1:70343560
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431-7461A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343560 | ||||||
| chr1:70343561
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431-7462A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343561 | ||||||
| chr1:70343606
|
G | A | 1 | a0001c0002t0005g0031 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.431-7507C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343606 | ||||||
| chr1:70343637
|
C | A | 1 | a0001c0001t0011g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.431-7538G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343637 | ||||||
| chr1:70343802
|
T | A | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-7703A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343802 | ||||||
| chr1:70343872
|
C | T | 85 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(82): Show | 85 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.431-7773G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70343872 | ||||||
| chr1:70344221
|
C | T | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.431-8122G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344221 | ||||||
| chr1:70344295
|
C | CA | 10 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(7): Show | 10 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.431-8197dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344295
|
C | CAAAAAAA | 9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0259others(6): Show | 9 | HG01070.hp2 HG01168.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-8203_431-8197d others(9): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344295
|
C | CAAAAAAA others(1): Show |
68 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(65): Show | 68 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.431-8204_431-8197d others(10): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344295
|
C | CAAAAAAA others(2): Show |
14 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(11): Show | 14 | HG01928.hp1 HG02129.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.431-8205_431-8197d others(11): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344295
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0291a0001c0001t0008g0340a0001c0002t0001g0007others(3): Show | 6 | HG01074.hp1 HG01168.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-8206_431-8197d others(12): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344295
|
C | CAAAAAAA others(4): Show |
23 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(20): Show | 23 | HG01175.hp2 HG01192.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.431-8207_431-8197d others(13): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344295
|
CA | C | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0057others(7): Show | 10 | HG01167.hp2 HG01256.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.431-8197delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344295 | ||||||
| chr1:70344451
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.431-8352C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344451 | ||||||
| chr1:70344463
|
C | CA | 113 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0163others(110): Show | 113 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.431-8365dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344463 | ||||||
| chr1:70344545
|
G | A | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.431-8446C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344545 | ||||||
| chr1:70344818
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.431-8719A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344818 | ||||||
| chr1:70344994
|
T | G | 6 | a0001c0001t0001g0313a0001c0001t0001g0324a0001c0001t0001g0325others(3): Show | 6 | NA18975.hp1 NA18985.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-8895A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70344994 | ||||||
| chr1:70345138
|
T | C | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.430+8841A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345138 | ||||||
| chr1:70345288
|
G | A | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+8691C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345288 | ||||||
| chr1:70345289
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0007g0202a0001c0001t0023g0037 | 3 | HG02145.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430+8690G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345289 | ||||||
| chr1:70345429
|
CA | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0194a0001c0001t0001g0201others(3): Show | 6 | HG00738.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+8549delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345429 | ||||||
| chr1:70345572
|
T | TC | 91 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(88): Show | 91 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.430+8406_430+8407i others(3): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345572 | ||||||
| chr1:70345638
|
T | C | 2 | a0001c0001t0003g0302a0001c0001t0005g0301 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.430+8341A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345638 | ||||||
| chr1:70345641
|
C | CA | 11 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0164others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+8337dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345641 | ||||||
| chr1:70345900
|
T | C | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+8079A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345900 | ||||||
| chr1:70345935
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+8044A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345935 | ||||||
| chr1:70345962
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.430+8017G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70345962 | ||||||
| chr1:70346034
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.430+7945C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346034 | ||||||
| chr1:70346205
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+7774G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346205 | ||||||
| chr1:70346333
|
T | C | 1 | a0001c0001t0023g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430+7646A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346333 | ||||||
| chr1:70346462
|
G | C | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.430+7517C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346462 | ||||||
| chr1:70346696
|
T | C | 4 | a0001c0002t0001g0030a0001c0002t0005g0028a0001c0002t0005g0029others(1): Show | 4 | NA18972.hp2 NA19000.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+7283A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346696 | ||||||
| chr1:70346858
|
C | T | 1 | a0001c0001t0003g0306 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430+7121G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346858 | ||||||
| chr1:70346963
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+7016C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346963 | ||||||
| chr1:70346986
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02074.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.430+6993C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70346986 | ||||||
| chr1:70347024
|
G | A | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.430+6955C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347024 | ||||||
| chr1:70347091
|
C | CA | 53 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(50): Show | 53 | HG00621.hp1 HG00673.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.430+6887dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347091 | ||||||
| chr1:70347091
|
CA | C | 103 | a0001c0001t0001g0036a0001c0001t0001g0058a0001c0001t0001g0059others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.430+6887delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347091 | ||||||
| chr1:70347091
|
CAA | C | 24 | a0001c0001t0001g0048a0001c0001t0001g0253a0001c0001t0001g0254others(21): Show | 24 | HG01074.hp1 HG01192.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.430+6886_430+6887d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347091 | ||||||
| chr1:70347371
|
CT | C | 83 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(80): Show | 83 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.430+6607delA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347371 | ||||||
| chr1:70347675
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+6304G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347675 | ||||||
| chr1:70347809
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0002g0046 | 2 | HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.430+6170C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347809 | ||||||
| chr1:70347903
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0038others(73): Show | 78 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.430+6076G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70347903 | ||||||
| chr1:70348044
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.430+5935A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348044 | ||||||
| chr1:70348201
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0203 | 2 | NA18941.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.430+5778T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348201 | ||||||
| chr1:70348283
|
A | AT | 14 | a0001c0001t0001g0307a0001c0001t0001g0337a0001c0001t0001g0339others(11): Show | 14 | HG01192.hp1 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.430+5695dupA | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348283 | ||||||
| chr1:70348326
|
T | C | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG02622.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+5653A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348326 | ||||||
| chr1:70348417
|
G | C | 4 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0004g0251others(1): Show | 4 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+5562C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348417 | ||||||
| chr1:70348495
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.430+5484C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348495 | ||||||
| chr1:70348697
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430+5282C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348697 | ||||||
| chr1:70348789
|
C | A | 1 | a0001c0001t0001g0311 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.430+5190G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348789 | ||||||
| chr1:70348899
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.430+5080G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348899 | ||||||
| chr1:70348974
|
C | T | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.430+5005G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70348974 | ||||||
| chr1:70349000
|
G | A | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+4979C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349000 | ||||||
| chr1:70349109
|
A | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0234 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.430+4870T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349109 | ||||||
| chr1:70349414
|
A | C | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+4565T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349414 | ||||||
| chr1:70349483
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.430+4496G>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349483 | ||||||
| chr1:70349500
|
CA | C | 88 | a0001c0001t0001g0048a0001c0001t0001g0253a0001c0001t0001g0254others(85): Show | 88 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.430+4478delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349500 | ||||||
| chr1:70349601
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.430+4378G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349601 | ||||||
| chr1:70349893
|
T | C | 21 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(18): Show | 21 | HG00621.hp2 HG02015.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+4086A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349893 | ||||||
| chr1:70349954
|
G | A | 82 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(79): Show | 82 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.430+4025C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70349954 | ||||||
| chr1:70350132
|
G | A | 27 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(24): Show | 27 | HG01074.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.430+3847C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350132 | ||||||
| chr1:70350512
|
G | A | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+3467C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350512 | ||||||
| chr1:70350611
|
C | T | 1 | a0001c0003t0002g0032 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.430+3368G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350611 | ||||||
| chr1:70350649
|
T | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0187others(4): Show | 7 | HG01891.hp1 HG02809.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+3330A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350649 | ||||||
| chr1:70350676
|
C | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG00280.hp1 HG01109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.430+3303G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350676 | ||||||
| chr1:70350676
|
C | T | 4 | a0001c0001t0001g0307a0001c0001t0003g0306a0001c0001t0005g0252others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+3303G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350676 | ||||||
| chr1:70350677
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.430+3302C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350677 | ||||||
| chr1:70350880
|
A | G | 135 | a0001c0001t0001g0036a0001c0001t0001g0194a0001c0001t0001g0196others(132): Show | 135 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.430+3099T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350880 | ||||||
| chr1:70350888
|
C | T | 9 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01934.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+3091G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350888 | ||||||
| chr1:70350966
|
G | A | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430+3013C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70350966 | ||||||
| chr1:70351085
|
C | T | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+2894G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351085 | ||||||
| chr1:70351260
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2719T>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351260 | ||||||
| chr1:70351334
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+2645A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351334 | ||||||
| chr1:70351384
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0006g0047a0001c0001t0007g0049others(2): Show | 5 | HG02602.hp1 HG02683.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2595G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351384 | ||||||
| chr1:70351540
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.430+2439G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351540 | ||||||
| chr1:70351675
|
C | A | 3 | a0001c0001t0003g0304a0001c0001t0003g0305a0001c0001t0003g0312 | 3 | HG02145.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+2304G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351675 | ||||||
| chr1:70351718
|
G | A | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430+2261C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351718 | ||||||
| chr1:70351848
|
G | GA | 4 | a0001c0002t0001g0030a0001c0002t0005g0028a0001c0002t0005g0029others(1): Show | 4 | NA18972.hp2 NA19000.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2130dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351848 | ||||||
| chr1:70351941
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0003g0306 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.430+2038C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70351941 | ||||||
| chr1:70352245
|
C | T | 1 | a0001c0001t0015g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430+1734G>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352245 | ||||||
| chr1:70352339
|
C | CA | 40 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(37): Show | 40 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.430+1639dupT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352339 | ||||||
| chr1:70352339
|
C | CAA | 19 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0240others(16): Show | 19 | HG00140.hp1 HG00597.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.430+1638_430+1639d others(4): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352339 | ||||||
| chr1:70352339
|
CA | C | 94 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(91): Show | 94 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.430+1639delT | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352339 | ||||||
| chr1:70352339
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0004g0251 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.430+1628_430+1639d others(14): Show |
ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352339 | ||||||
| chr1:70352639
|
A | T | 1 | a0001c0001t0001g0313 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.430+1340T>A | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352639 | ||||||
| chr1:70352815
|
G | A | 21 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(18): Show | 21 | HG00621.hp2 HG02015.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+1164C>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352815 | ||||||
| chr1:70352833
|
G | C | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+1146C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352833 | ||||||
| chr1:70352861
|
T | C | 1 | a0001c0001t0012g0348 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.430+1118A>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352861 | ||||||
| chr1:70352893
|
T | G | 96 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(93): Show | 96 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.430+1086A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352893 | ||||||
| chr1:70352930
|
T | A | 4 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(1): Show | 4 | NA19001.hp1 NA19007.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+1049A>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352930 | ||||||
| chr1:70352992
|
G | C | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0028g0338 | 3 | HG02622.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.430+987C>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70352992 | ||||||
| chr1:70353163
|
A | C | 1 | a0001c0001t0005g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+816T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70353163 | ||||||
| chr1:70353239
|
A | C | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+740T>G | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70353239 | ||||||
| chr1:70353301
|
T | G | 1 | a0001c0001t0008g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+678A>C | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70353301 | ||||||
| chr1:70353854
|
C | A | 1 | a0001c0001t0001g0341 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430+125G>T | ANKRD13C | ENSG00000118454.13 | transcript | ENST00000370944.9 | protein_coding | 1/12 | chr1 | 70353854 |