Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 121006 |
|---|---|
| ensemblid | ENSG00000185958.10 |
| hgncid | 26980 |
| symbol | FAM186A |
| name | family with sequence similarity 186 member A |
| refseq_nuc | NM_001145475.3 |
| refseq_prot | NP_001138947.1 |
| ensembl_nuc | ENST00000327337.6 |
| ensembl_prot | ENSP00000329995.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 50327309 |
| end | 50396609 |
| strand | - |
| ver | v1.2 |
| region | chr12:50327309-50396609 |
| region5000 | chr12:50322309-50401609 |
| regionname0 | FAM186A_chr12_50327309_50396609 |
| regionname5000 | FAM186A_chr12_50322309_50401609 |
| 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 | 0/0 | 2387 | 93 | 6 | 27 | 45 | 5 | 10 | 34 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002 | 0/0 | 2387 | 91 | 20 | 12 | 55 | 0 | 4 | 45 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003 | 0/1 | 2351 | 75 | 18 | 12 | 33 | 1 | 10 | 25 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0004 | 0/0 | 2351 | 14 | 1 | 8 | 0 | 3 | 2 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0005 | 1/0 | 2351 | 13 | 12 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0006 | 0/0 | 2387 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0007 | 0/0 | 2387 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0008 | 0/0 | 2351 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0009 | 0/0 | 2387 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0010 | 0/0 | 2387 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0011 | 0/0 | 2351 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0012 | 0/0 | 2339 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0013 | 0/0 | 2387 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0014 | 0/0 | 2387 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0015 | 0/0 | 2387 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0016 | 0/0 | 2387 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0017 | 0/0 | 2387 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0018 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0019 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0020 | 0/0 | 1213 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0021 | 0/0 | 2351 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0022 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0023 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0024 | 0/0 | 2387 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0025 | 0/0 | 2387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0026 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0027 | 0/0 | 2387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0028 | 0/0 | 2387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0029 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0030 | 0/0 | 2209 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0031 | 0/0 | 2387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0032 | 0/0 | 2351 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0033 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 7164 | 91 | 6 | 26 | 44 | 5 | 10 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0002 | 0/0 | 7164 | 73 | 16 | 2 | 51 | 0 | 4 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0003 | 0/1 | 7056 | 72 | 16 | 12 | 32 | 1 | 10 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0004 | 0/0 | 7056 | 13 | 1 | 8 | 0 | 3 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0005 | 1/0 | 7056 | 13 | 12 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0006 | 0/0 | 7164 | 11 | 0 | 7 | 4 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0007 | 0/0 | 7164 | 5 | 4 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0008 | 0/0 | 7164 | 4 | 4 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0009 | 0/0 | 7056 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0010 | 0/0 | 7164 | 3 | 0 | 3 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0011 | 0/0 | 7164 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0012 | 0/0 | 7164 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0013 | 0/0 | 7056 | 2 | 0 | 0 | 0 | 0 | 2 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0014 | 0/0 | 7056 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0015 | 0/0 | 7020 | 2 | 0 | 0 | 2 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0016 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0017 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0018 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0019 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0020 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0021 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0022 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0023 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0024 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0025 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0026 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0027 | 0/0 | 7056 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0028 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0029 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0030 | 0/0 | 7056 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0031 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0032 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0033 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0034 | 0/0 | 7164 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0035 | 0/0 | 7164 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0036 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0037 | 0/0 | 7056 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0038 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0039 | 0/0 | 7164 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0040 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0041 | 0/0 | 7164 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0042 | 0/0 | 7164 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| c0043 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| 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 | 200 | 332 | 86 | 62 | 140 | 10 | 32 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 7164 | 91 | 6 | 26 | 44 | 5 | 10 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0001c0039 | 0/0 | 7164 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0001c0042 | 0/0 | 7164 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0002 | 0/0 | 7164 | 73 | 16 | 2 | 51 | 0 | 4 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0006 | 0/0 | 7164 | 11 | 0 | 7 | 4 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0010 | 0/0 | 7164 | 3 | 0 | 3 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0011 | 0/0 | 7164 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0033 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003c0003 | 0/1 | 7056 | 72 | 16 | 12 | 32 | 1 | 10 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003c0014 | 0/0 | 7056 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003c0020 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0004c0004 | 0/0 | 7056 | 13 | 1 | 8 | 0 | 3 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0004c0027 | 0/0 | 7056 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0005c0005 | 1/0 | 7056 | 13 | 12 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0006c0007 | 0/0 | 7164 | 5 | 4 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0007c0008 | 0/0 | 7164 | 4 | 4 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0007c0023 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0008c0009 | 0/0 | 7056 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0009c0012 | 0/0 | 7164 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0010c0019 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0011c0013 | 0/0 | 7056 | 2 | 0 | 0 | 0 | 0 | 2 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0012c0015 | 0/0 | 7020 | 2 | 0 | 0 | 2 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0013c0017 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0014c0018 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0015c0016 | 0/0 | 7164 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0016c0022 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0017c0043 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0018c0026 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0019c0032 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0020c0031 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0021c0030 | 0/0 | 7056 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0022c0029 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0023c0028 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0024c0036 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0025c0035 | 0/0 | 7164 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0026c0034 | 0/0 | 7164 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0027c0038 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0028c0024 | 0/0 | 7164 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0029c0025 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0030c0040 | 0/0 | 7164 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0031c0041 | 0/0 | 7164 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0032c0037 | 0/0 | 7056 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0033c0021 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7363 | 91 | 6 | 26 | 44 | 5 | 10 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0001c0039t0001 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0001c0042t0001 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0002t0001 | 0/0 | 7363 | 73 | 16 | 2 | 51 | 0 | 4 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0006t0001 | 0/0 | 7363 | 11 | 0 | 7 | 4 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0010t0001 | 0/0 | 7363 | 3 | 0 | 3 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0011t0001 | 0/0 | 7363 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0002c0033t0001 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003c0003t0001 | 0/1 | 7255 | 72 | 16 | 12 | 32 | 1 | 10 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003c0014t0001 | 0/0 | 7255 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0003c0020t0001 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0004c0004t0001 | 0/0 | 7255 | 13 | 1 | 8 | 0 | 3 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0004c0027t0001 | 0/0 | 7255 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0005c0005t0001 | 1/0 | 7255 | 13 | 12 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0006c0007t0001 | 0/0 | 7363 | 5 | 4 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0007c0008t0001 | 0/0 | 7363 | 4 | 4 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0007c0023t0001 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0008c0009t0001 | 0/0 | 7255 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0009c0012t0001 | 0/0 | 7363 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0010c0019t0001 | 0/0 | 7363 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0011c0013t0001 | 0/0 | 7255 | 2 | 0 | 0 | 0 | 0 | 2 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0012c0015t0001 | 0/0 | 7219 | 2 | 0 | 0 | 2 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0013c0017t0001 | 0/0 | 7363 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0014c0018t0001 | 0/0 | 7363 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0015c0016t0001 | 0/0 | 7363 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0016c0022t0001 | 0/0 | 7363 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0017c0043t0001 | 0/0 | 7363 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0018c0026t0001 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0019c0032t0001 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0020c0031t0001 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0021c0030t0001 | 0/0 | 7255 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0022c0029t0001 | 0/0 | 7255 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0023c0028t0001 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0024c0036t0001 | 0/0 | 7363 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0025c0035t0001 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0026c0034t0001 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0027c0038t0001 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0028c0024t0001 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0029c0025t0001 | 0/0 | 7291 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0030c0040t0001 | 0/0 | 7363 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0031c0041t0001 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0032c0037t0001 | 0/0 | 7255 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| a0033c0021t0001 | 0/0 | 7255 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | copy fasta | chr12 | 50322309 | 50401609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0039t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0001c0042t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0006t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0010t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0010t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0010t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0011t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0011t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0002c0033t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0014t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0014t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0003c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0004c0027t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0005c0005t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0006c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0006c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0006c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0006c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0006c0007t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0007c0008t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0007c0008t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0007c0008t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0007c0008t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0007c0023t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0008c0009t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0008c0009t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0008c0009t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0009c0012t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0009c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0009c0012t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0010c0019t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0010c0019t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0011c0013t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0011c0013t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0012c0015t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0012c0015t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0013c0017t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0013c0017t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0014c0018t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0014c0018t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0015c0016t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0015c0016t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0016c0022t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0017c0043t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0018c0026t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0019c0032t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0020c0031t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0021c0030t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0022c0029t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0023c0028t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0024c0036t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0025c0035t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0026c0034t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0027c0038t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0028c0024t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0029c0025t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0030c0040t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0031c0041t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0032c0037t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| a0033c0021t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0278 | EUR | GBR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | GBR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0030 | EUR | GBR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00323 | hp1 | a0030 | c0040 | t0001 | g0290 | EUR | FIN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00408 | hp1 | a0018 | c0026 | t0001 | g0200 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00438 | hp2 | a0003 | c0003 | t0001 | g0125 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0270 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00642 | hp2 | a0002 | c0010 | t0001 | g0197 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00673 | hp2 | a0003 | c0020 | t0001 | g0001 | EAS | CHS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00738 | hp1 | a0002 | c0006 | t0001 | g0159 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01071 | hp2 | a0004 | c0004 | t0001 | g0281 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0272 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0277 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0324 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0232 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01167 | hp1 | a0006 | c0007 | t0001 | g0194 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0100 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0289 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01192 | hp1 | a0004 | c0004 | t0001 | g0284 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01255 | hp2 | a0004 | c0004 | t0001 | g0279 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01256 | hp1 | a0004 | c0004 | t0001 | g0276 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01257 | hp1 | a0031 | c0041 | t0001 | g0299 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01261 | hp1 | a0002 | c0006 | t0001 | g0163 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0078 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0273 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0328 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0282 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0205 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01361 | hp2 | a0001 | c0039 | t0001 | g0064 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0253 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0254 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01515 | hp2 | a0004 | c0004 | t0001 | g0274 | EUR | IBS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01517 | hp2 | a0004 | c0004 | t0001 | g0275 | EUR | IBS | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01884 | hp1 | a0007 | c0008 | t0001 | g0088 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01891 | hp2 | a0002 | c0011 | t0001 | g0119 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01928 | hp1 | a0002 | c0010 | t0001 | g0140 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01928 | hp2 | a0032 | c0037 | t0001 | g0031 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01934 | hp1 | a0002 | c0010 | t0001 | g0147 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01943 | hp1 | a0002 | c0006 | t0001 | g0151 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0027 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0287 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01978 | hp2 | a0002 | c0006 | t0001 | g0122 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01981 | hp1 | a0002 | c0006 | t0001 | g0160 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02055 | hp1 | a0013 | c0017 | t0001 | g0003 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02055 | hp2 | a0007 | c0023 | t0001 | g0054 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0204 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0316 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02145 | hp1 | a0013 | c0017 | t0001 | g0131 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0086 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02148 | hp2 | a0002 | c0006 | t0001 | g0192 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | CDX | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | CDX | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CDX | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02257 | hp1 | a0014 | c0018 | t0001 | g0011 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02257 | hp2 | a0033 | c0021 | t0001 | g0002 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02258 | hp1 | a0010 | c0019 | t0001 | g0322 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02258 | hp2 | a0005 | c0005 | t0001 | g0106 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02280 | hp1 | a0003 | c0014 | t0001 | g0089 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02293 | hp2 | a0002 | c0006 | t0001 | g0177 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02300 | hp1 | a0004 | c0004 | t0001 | g0255 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02572 | hp1 | a0008 | c0009 | t0001 | g0111 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02572 | hp2 | a0005 | c0005 | t0001 | g0218 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0295 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02615 | hp1 | a0015 | c0016 | t0001 | g0005 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02615 | hp2 | a0004 | c0004 | t0001 | g0256 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02622 | hp1 | a0005 | c0005 | t0001 | g0223 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0098 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02630 | hp1 | a0006 | c0007 | t0001 | g0038 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02647 | hp2 | a0007 | c0008 | t0001 | g0248 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0294 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02717 | hp1 | a0009 | c0012 | t0001 | g0233 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02717 | hp2 | a0008 | c0009 | t0001 | g0139 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0326 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02809 | hp2 | a0002 | c0033 | t0001 | g0321 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0090 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02818 | hp2 | a0005 | c0005 | t0001 | g0220 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0325 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0155 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02896 | hp1 | a0005 | c0005 | t0001 | g0226 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02896 | hp2 | a0005 | c0005 | t0001 | g0222 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02897 | hp1 | a0005 | c0005 | t0001 | g0251 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02897 | hp2 | a0003 | c0014 | t0001 | g0107 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02922 | hp1 | a0015 | c0016 | t0001 | g0004 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02922 | hp2 | a0005 | c0005 | t0001 | g0109 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0055 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02965 | hp2 | a0006 | c0007 | t0001 | g0164 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0050 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0327 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02976 | hp2 | a0009 | c0012 | t0001 | g0235 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0099 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0085 | AFR | GWD | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03130 | hp1 | a0005 | c0005 | t0001 | g0225 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03130 | hp2 | a0009 | c0012 | t0001 | g0234 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03209 | hp1 | a0029 | c0025 | t0001 | g0243 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0097 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0081 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03225 | hp2 | a0008 | c0009 | t0001 | g0112 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03239 | hp1 | a0017 | c0043 | t0001 | g0306 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0288 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03453 | hp1 | a0023 | c0028 | t0001 | g0317 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03486 | hp1 | a0010 | c0019 | t0001 | g0323 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03490 | hp1 | a0004 | c0027 | t0001 | g0285 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0266 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03516 | hp1 | a0006 | c0007 | t0001 | g0150 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0330 | AFR | ESN | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0049 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0331 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0286 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03927 | hp1 | a0004 | c0004 | t0001 | g0280 | SAS | BEB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | BEB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03942 | hp1 | a0021 | c0030 | t0001 | g0264 | SAS | BEB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0262 | SAS | BEB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0269 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04115 | hp2 | a0016 | c0022 | t0001 | g0171 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04199 | hp1 | a0011 | c0013 | t0001 | g0035 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0260 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04204 | hp2 | a0011 | c0013 | t0001 | g0084 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0051 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG04228 | hp2 | a0024 | c0036 | t0001 | g0188 | SAS | STU | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | CHB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | CHB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18906 | hp1 | a0005 | c0005 | t0001 | g0318 | AFR | YRI | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18943 | hp2 | a0020 | c0031 | t0001 | g0207 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0315 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0314 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18961 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18966 | hp1 | a0002 | c0006 | t0001 | g0157 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18975 | hp1 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0213 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18991 | hp1 | a0002 | c0006 | t0001 | g0162 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18992 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18997 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18998 | hp1 | a0001 | c0042 | t0001 | g0077 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19000 | hp2 | a0012 | c0015 | t0001 | g0214 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0211 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19004 | hp2 | a0002 | c0006 | t0001 | g0156 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0268 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | LWK | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0096 | AFR | LWK | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | LWK | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19043 | hp2 | a0005 | c0005 | t0001 | g0108 | AFR | LWK | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19058 | hp1 | a0003 | c0003 | t0001 | g0212 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19058 | hp2 | a0025 | c0035 | t0001 | g0060 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19060 | hp2 | a0026 | c0034 | t0001 | g0136 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19065 | hp1 | a0022 | c0029 | t0001 | g0201 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0203 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19080 | hp1 | a0002 | c0006 | t0001 | g0161 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19084 | hp1 | a0012 | c0015 | t0001 | g0216 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | YRI | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | YRI | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA20129 | hp1 | a0002 | c0011 | t0001 | g0166 | AFR | ASW | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA20129 | hp2 | a0006 | c0007 | t0001 | g0193 | AFR | ASW | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0082 | SAS | GIH | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG01123 | hp2 | a0004 | c0004 | t0001 | g0283 | AMR | CLM | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02109 | hp1 | a0005 | c0005 | t0001 | g0224 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02109 | hp2 | a0007 | c0008 | t0001 | g0246 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0128 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0022 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02559 | hp1 | a0028 | c0024 | t0001 | g0244 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03471 | hp1 | a0014 | c0018 | t0001 | g0219 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG03471 | hp2 | a0007 | c0008 | t0001 | g0247 | AFR | MSL | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG06807 | hp1 | a0002 | c0011 | t0001 | g0118 | AFR | USA | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| HG06807 | hp2 | a0027 | c0038 | t0001 | g0006 | AFR | USA | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0083 | AFR | LWK | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| NA21309 | hp2 | a0019 | c0032 | t0001 | g0231 | AFR | LWK | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0265 | REF | REF | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| homoSapiens_grch38 | hp1 | a0005 | c0005 | t0001 | g0221 | REF | REF | FAM186A_chr12_50322309_50401609 | FAM186A | chr12 | 50322309 | 50401609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50330667
|
A | T | 3 | a0013a0015a0027 | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
missense_variant | MODERATE | c.6940T>A | p.Trp2314Arg | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/8 | 7065/7255 | 6940/7056 | 2314/2351 | chr12 | 50330667 | ||
| chr12:50333923
|
G | C | 11 | a0003a0004a0011others(8): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
missense_variant | MODERATE | c.6684C>G | p.His2228Gln | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/8 | 6809/7255 | 6684/7056 | 2228/2351 | chr12 | 50333923 | ||
| chr12:50334028
|
C | T | 1 | a0004 | 14 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
missense_variant | MODERATE | c.6579G>A | p.Met2193Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/8 | 6704/7255 | 6579/7056 | 2193/2351 | chr12 | 50334028 | ||
| chr12:50334087
|
G | A | 1 | a0030 | 1 | HG00323.hp1 | stop_gained | HIGH | c.6520C>T | p.Arg2174* | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/8 | 6645/7255 | 6520/7056 | 2174/2351 | chr12 | 50334087 | ||
| chr12:50350336
|
G | A | 19 | a0001a0002a0006others(16): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
missense_variant | MODERATE | c.6496C>T | p.His2166Tyr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 6621/7255 | 6496/7056 | 2166/2351 | chr12 | 50350336 | ||
| chr12:50350500
|
G | A | 1 | a0009 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.6332C>T | p.Ala2111Val | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 6457/7255 | 6332/7056 | 2111/2351 | chr12 | 50350500 | ||
| chr12:50350734
|
T | C | 1 | a0023 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.6098A>G | p.Asp2033Gly | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 6223/7255 | 6098/7056 | 2033/2351 | chr12 | 50350734 | ||
| chr12:50351136
|
T | C | 1 | a0022 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.5696A>G | p.Tyr1899Cys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5821/7255 | 5696/7056 | 1899/2351 | chr12 | 50351136 | ||
| chr12:50351311
|
C | G | 3 | a0007a0028a0029 | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
missense_variant | MODERATE | c.5521G>C | p.Gly1841Arg | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5646/7255 | 5521/7056 | 1841/2351 | chr12 | 50351311 | ||
| chr12:50351439
|
G | C | 1 | a0021 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.5393C>G | p.Ser1798Cys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5518/7255 | 5393/7056 | 1798/2351 | chr12 | 50351439 | ||
| chr12:50351632
|
G | C | 1 | a0014 | 2 | HG02257.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.5200C>G | p.Pro1734Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5325/7255 | 5200/7056 | 1734/2351 | chr12 | 50351632 | ||
| chr12:50351674
|
C | A | 1 | a0030 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.5158G>T | p.Ala1720Ser | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5283/7255 | 5158/7056 | 1720/2351 | chr12 | 50351674 | ||
| chr12:50351853
|
G | A | 1 | a0010 | 2 | HG02258.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.4979C>T | p.Ala1660Val | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5104/7255 | 4979/7056 | 1660/2351 | chr12 | 50351853 | ||
| chr12:50351890
|
C | T | 1 | a0006 | 5 | HG01167.hp1 HG02630.hp1 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.4942G>A | p.Gly1648Arg | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5067/7255 | 4942/7056 | 1648/2351 | chr12 | 50351890 | ||
| chr12:50352003
|
G | GCCTGCAC others(101): Show |
1 | a0031 | 1 | HG01257.hp1 | conservative_inframe_insertion | MODERATE | c.4828_4829insAACTGG others(102): Show |
p.Gln1609_Ala1610ins others(108): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4953/7255 | 4828/7056 | 1610/2351 | chr12 | 50352003 | ||
| chr12:50352003
|
G | GCCTGCGC others(101): Show |
17 | a0001a0002a0006others(14): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
conservative_inframe_insertion | MODERATE | c.4828_4829insAACTGG others(102): Show |
p.Gln1609_Ala1610ins others(108): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4953/7255 | 4828/7056 | 1610/2351 | chr12 | 50352003 | ||
| chr12:50352028
|
G | A | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4804C>T | p.Pro1602Ser | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4929/7255 | 4804/7056 | 1602/2351 | chr12 | 50352028 | ||
| chr12:50352038
|
T | A | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4794A>T | p.Glu1598Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4919/7255 | 4794/7056 | 1598/2351 | chr12 | 50352038 | ||
| chr12:50352039
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4793A>C | p.Glu1598Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4918/7255 | 4793/7056 | 1598/2351 | chr12 | 50352039 | ||
| chr12:50352074
|
T | G | 19 | a0001a0002a0006others(16): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
missense_variant | MODERATE | c.4758A>C | p.Glu1586Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4883/7255 | 4758/7056 | 1586/2351 | chr12 | 50352074 | ||
| chr12:50352075
|
T | G | 19 | a0001a0002a0006others(16): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
missense_variant | MODERATE | c.4757A>C | p.Glu1586Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4882/7255 | 4757/7056 | 1586/2351 | chr12 | 50352075 | ||
| chr12:50352111
|
G | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4721C>A | p.Ala1574Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4846/7255 | 4721/7056 | 1574/2351 | chr12 | 50352111 | ||
| chr12:50352141
|
T | C | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4691A>G | p.Glu1564Gly | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4816/7255 | 4691/7056 | 1564/2351 | chr12 | 50352141 | ||
| chr12:50352159
|
G | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4673C>A | p.Pro1558Gln | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4798/7255 | 4673/7056 | 1558/2351 | chr12 | 50352159 | ||
| chr12:50352165
|
A | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4667T>C | p.Ile1556Thr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4792/7255 | 4667/7056 | 1556/2351 | chr12 | 50352165 | ||
| chr12:50352189
|
A | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4643T>C | p.Val1548Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4768/7255 | 4643/7056 | 1548/2351 | chr12 | 50352189 | ||
| chr12:50352213
|
C | CCCAGGGC others(29): Show |
1 | a0029 | 1 | HG03209.hp1 | conservative_inframe_insertion | MODERATE | c.4618_4619insAGATCC others(30): Show |
p.Leu1539_Gly1540ins others(36): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4743/7255 | 4618/7056 | 1540/2351 | chr12 | 50352213 | ||
| chr12:50352261
|
G | A | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4571C>T | p.Ala1524Val | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4696/7255 | 4571/7056 | 1524/2351 | chr12 | 50352261 | ||
| chr12:50352315
|
A | G | 32 | a0001a0002a0003others(29): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
missense_variant | MODERATE | c.4517T>C | p.Leu1506Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4642/7255 | 4517/7056 | 1506/2351 | chr12 | 50352315 | ||
| chr12:50352447
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4385A>C | p.Gln1462Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4510/7255 | 4385/7056 | 1462/2351 | chr12 | 50352447 | ||
| chr12:50352453
|
G | A | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4379C>T | p.Thr1460Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4504/7255 | 4379/7056 | 1460/2351 | chr12 | 50352453 | ||
| chr12:50352460
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4372A>C | p.Thr1458Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4497/7255 | 4372/7056 | 1458/2351 | chr12 | 50352460 | ||
| chr12:50352470
|
C | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4362G>C | p.Glu1454Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4487/7255 | 4362/7056 | 1454/2351 | chr12 | 50352470 | ||
| chr12:50352471
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4361A>C | p.Glu1454Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4486/7255 | 4361/7056 | 1454/2351 | chr12 | 50352471 | ||
| chr12:50352487
|
C | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4345G>C | p.Ala1449Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4470/7255 | 4345/7056 | 1449/2351 | chr12 | 50352487 | ||
| chr12:50352497
|
C | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4335G>C | p.Met1445Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4460/7255 | 4335/7056 | 1445/2351 | chr12 | 50352497 | ||
| chr12:50352507
|
G | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4325C>A | p.Ala1442Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4450/7255 | 4325/7056 | 1442/2351 | chr12 | 50352507 | ||
| chr12:50352537
|
T | C | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4295A>G | p.Glu1432Gly | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4420/7255 | 4295/7056 | 1432/2351 | chr12 | 50352537 | ||
| chr12:50352540
|
T | A | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4292A>T | p.Gln1431Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4417/7255 | 4292/7056 | 1431/2351 | chr12 | 50352540 | ||
| chr12:50352543
|
G | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4289C>A | p.Ala1430Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4414/7255 | 4289/7056 | 1430/2351 | chr12 | 50352543 | ||
| chr12:50352559
|
G | C | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4273C>G | p.Pro1425Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4398/7255 | 4273/7056 | 1425/2351 | chr12 | 50352559 | ||
| chr12:50352565
|
A | G | 32 | a0001a0002a0003others(29): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
missense_variant | MODERATE | c.4267T>C | p.Phe1423Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4392/7255 | 4267/7056 | 1423/2351 | chr12 | 50352565 | ||
| chr12:50352569
|
G | C | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4263C>G | p.Ile1421Met | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4388/7255 | 4263/7056 | 1421/2351 | chr12 | 50352569 | ||
| chr12:50352578
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4254A>C | p.Glu1418Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4379/7255 | 4254/7056 | 1418/2351 | chr12 | 50352578 | ||
| chr12:50352579
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4253A>C | p.Glu1418Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4378/7255 | 4253/7056 | 1418/2351 | chr12 | 50352579 | ||
| chr12:50352589
|
G | A | 1 | a0026 | 1 | NA19060.hp2 | stop_gained | HIGH | c.4243C>T | p.Gln1415* | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4368/7255 | 4243/7056 | 1415/2351 | chr12 | 50352589 | ||
| chr12:50352604
|
G | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4228C>A | p.Pro1410Thr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4353/7255 | 4228/7056 | 1410/2351 | chr12 | 50352604 | ||
| chr12:50352609
|
C | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4223G>A | p.Gly1408Glu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4348/7255 | 4223/7056 | 1408/2351 | chr12 | 50352609 | ||
| chr12:50352612
|
A | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4220T>A | p.Leu1407Gln | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4345/7255 | 4220/7056 | 1407/2351 | chr12 | 50352612 | ||
| chr12:50352614
|
T | A | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4218A>T | p.Glu1406Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4343/7255 | 4218/7056 | 1406/2351 | chr12 | 50352614 | ||
| chr12:50352615
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4217A>C | p.Glu1406Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4342/7255 | 4217/7056 | 1406/2351 | chr12 | 50352615 | ||
| chr12:50352631
|
T | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4201A>C | p.Thr1401Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4326/7255 | 4201/7056 | 1401/2351 | chr12 | 50352631 | ||
| chr12:50352641
|
C | G | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4191G>C | p.Met1397Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4316/7255 | 4191/7056 | 1397/2351 | chr12 | 50352641 | ||
| chr12:50352651
|
G | T | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4181C>A | p.Ala1394Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4306/7255 | 4181/7056 | 1394/2351 | chr12 | 50352651 | ||
| chr12:50352677
|
GATCCCCA others(29): Show |
G | 1 | a0012 | 2 | NA19000.hp2 NA19084.hp1 |
disruptive_inframe_deletion | MODERATE | c.4119_4154delGCCTCT others(30): Show |
p.Met1373_Gly1384del | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4279/7255 | 4119/7056 | 1373/2351 | chr12 | 50352677 | ||
| chr12:50352731
|
G | C | 1 | a0029 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4101C>G | p.His1367Gln | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4226/7255 | 4101/7056 | 1367/2351 | chr12 | 50352731 | ||
| chr12:50353134
|
A | G | 19 | a0001a0002a0006others(16): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
missense_variant | MODERATE | c.3698T>C | p.Leu1233Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3823/7255 | 3698/7056 | 1233/2351 | chr12 | 50353134 | ||
| chr12:50353147
|
T | G | 2 | a0028a0029 | 2 | HG02559.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.3685A>C | p.Ile1229Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3810/7255 | 3685/7056 | 1229/2351 | chr12 | 50353147 | ||
| chr12:50353192
|
C | A | 1 | a0020 | 1 | NA18943.hp2 | stop_gained | HIGH | c.3640G>T | p.Glu1214* | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3765/7255 | 3640/7056 | 1214/2351 | chr12 | 50353192 | ||
| chr12:50353222
|
T | C | 18 | a0001a0002a0006others(15): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
missense_variant | MODERATE | c.3610A>G | p.Arg1204Gly | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3735/7255 | 3610/7056 | 1204/2351 | chr12 | 50353222 | ||
| chr12:50353461
|
G | A | 1 | a0025 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.3371C>T | p.Thr1124Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3496/7255 | 3371/7056 | 1124/2351 | chr12 | 50353461 | ||
| chr12:50353560
|
T | A | 1 | a0024 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.3272A>T | p.Gln1091Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3397/7255 | 3272/7056 | 1091/2351 | chr12 | 50353560 | ||
| chr12:50354097
|
T | C | 1 | a0014 | 2 | HG02257.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.2735A>G | p.Gln912Arg | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 2860/7255 | 2735/7056 | 912/2351 | chr12 | 50354097 | ||
| chr12:50354226
|
T | C | 1 | a0008 | 3 | HG02572.hp1 HG02717.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.2606A>G | p.Gln869Arg | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 2731/7255 | 2606/7056 | 869/2351 | chr12 | 50354226 | ||
| chr12:50354272
|
A | G | 6 | a0007a0013a0015others(3): Show | 12 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
missense_variant | MODERATE | c.2560T>C | p.Tyr854His | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 2685/7255 | 2560/7056 | 854/2351 | chr12 | 50354272 | ||
| chr12:50354783
|
T | A | 1 | a0010 | 2 | HG02258.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.2049A>T | p.Lys683Asn | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 2174/7255 | 2049/7056 | 683/2351 | chr12 | 50354783 | ||
| chr12:50355101
|
C | G | 1 | a0027 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1731G>C | p.Glu577Asp | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1856/7255 | 1731/7056 | 577/2351 | chr12 | 50355101 | ||
| chr12:50355438
|
G | C | 30 | a0001a0002a0003others(27): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
missense_variant | MODERATE | c.1394C>G | p.Ala465Gly | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1519/7255 | 1394/7056 | 465/2351 | chr12 | 50355438 | ||
| chr12:50355444
|
T | G | 32 | a0001a0002a0003others(29): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
missense_variant | MODERATE | c.1388A>C | p.Lys463Thr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1513/7255 | 1388/7056 | 463/2351 | chr12 | 50355444 | ||
| chr12:50355538
|
C | T | 1 | a0015 | 2 | HG02615.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.1294G>A | p.Glu432Lys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1419/7255 | 1294/7056 | 432/2351 | chr12 | 50355538 | ||
| chr12:50355771
|
G | T | 6 | a0002a0006a0016others(3): Show | 100 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(97): Show |
missense_variant | MODERATE | c.1061C>A | p.Pro354His | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1186/7255 | 1061/7056 | 354/2351 | chr12 | 50355771 | ||
| chr12:50355983
|
G | T | 1 | a0018 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.849C>A | p.Asn283Lys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 974/7255 | 849/7056 | 283/2351 | chr12 | 50355983 | ||
| chr12:50356242
|
C | T | 1 | a0011 | 2 | HG04199.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.590G>A | p.Arg197Lys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 715/7255 | 590/7056 | 197/2351 | chr12 | 50356242 | ||
| chr12:50360780
|
T | G | 20 | a0001a0002a0006others(17): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
missense_variant | MODERATE | c.559A>C | p.Lys187Gln | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/8 | 684/7255 | 559/7056 | 187/2351 | chr12 | 50360780 | ||
| chr12:50360794
|
G | C | 1 | a0017 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.545C>G | p.Ser182Cys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/8 | 670/7255 | 545/7056 | 182/2351 | chr12 | 50360794 | ||
| chr12:50363218
|
C | T | 1 | a0016 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.339G>A | p.Met113Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/8 | 464/7255 | 339/7056 | 113/2351 | chr12 | 50363218 | ||
| chr12:50363229
|
G | A | 1 | a0010 | 2 | HG02258.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.328C>T | p.Leu110Phe | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/8 | 453/7255 | 328/7056 | 110/2351 | chr12 | 50363229 | ||
| chr12:50396316
|
C | T | 1 | a0033 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.169G>A | p.Ala57Thr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/8 | 294/7255 | 169/7056 | 57/2351 | chr12 | 50396316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50350388
|
T | C | 26 | a0001c0001a0001c0039a0001c0042others(23): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
synonymous_variant | LOW | c.6444A>G | p.Thr2148Thr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 6569/7255 | 6444/7056 | 2148/2351 | chr12 | 50350388 | ||
| chr12:50350970
|
T | C | 26 | a0001c0001a0001c0039a0001c0042others(23): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
synonymous_variant | LOW | c.5862A>G | p.Lys1954Lys | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5987/7255 | 5862/7056 | 1954/2351 | chr12 | 50350970 | ||
| chr12:50351420
|
G | A | 1 | a0007c0023 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.5412C>T | p.Tyr1804Tyr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5537/7255 | 5412/7056 | 1804/2351 | chr12 | 50351420 | ||
| chr12:50351696
|
A | G | 1 | a0002c0033 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.5136T>C | p.His1712His | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 5261/7255 | 5136/7056 | 1712/2351 | chr12 | 50351696 | ||
| chr12:50352037
|
G | A | 25 | a0001c0001a0001c0039a0001c0042others(22): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
synonymous_variant | LOW | c.4795C>T | p.Leu1599Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4920/7255 | 4795/7056 | 1599/2351 | chr12 | 50352037 | ||
| chr12:50352044
|
C | A | 25 | a0001c0001a0001c0039a0001c0042others(22): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
synonymous_variant | LOW | c.4788G>T | p.Ala1596Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4913/7255 | 4788/7056 | 1596/2351 | chr12 | 50352044 | ||
| chr12:50352044
|
C | G | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4788G>C | p.Ala1596Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4913/7255 | 4788/7056 | 1596/2351 | chr12 | 50352044 | ||
| chr12:50352068
|
C | A | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4764G>T | p.Gly1588Gly | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4889/7255 | 4764/7056 | 1588/2351 | chr12 | 50352068 | ||
| chr12:50352080
|
C | G | 26 | a0001c0001a0001c0039a0001c0042others(23): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
synonymous_variant | LOW | c.4752G>C | p.Ala1584Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4877/7255 | 4752/7056 | 1584/2351 | chr12 | 50352080 | ||
| chr12:50352110
|
G | T | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4722C>A | p.Ala1574Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4847/7255 | 4722/7056 | 1574/2351 | chr12 | 50352110 | ||
| chr12:50352116
|
G | C | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4716C>G | p.Ala1572Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4841/7255 | 4716/7056 | 1572/2351 | chr12 | 50352116 | ||
| chr12:50352239
|
C | G | 4 | a0013c0017a0015c0016a0027c0038others(1): Show | 6 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.4593G>C | p.Leu1531Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4718/7255 | 4593/7056 | 1531/2351 | chr12 | 50352239 | ||
| chr12:50352302
|
C | T | 1 | a0002c0011 | 3 | HG01891.hp2 HG06807.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.4530G>A | p.Pro1510Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4655/7255 | 4530/7056 | 1510/2351 | chr12 | 50352302 | ||
| chr12:50352311
|
G | C | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4521C>G | p.Leu1507Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4646/7255 | 4521/7056 | 1507/2351 | chr12 | 50352311 | ||
| chr12:50352476
|
A | G | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4356T>C | p.Ala1452Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4481/7255 | 4356/7056 | 1452/2351 | chr12 | 50352476 | ||
| chr12:50352505
|
G | A | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4327C>T | p.Leu1443Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4452/7255 | 4327/7056 | 1443/2351 | chr12 | 50352505 | ||
| chr12:50352506
|
G | T | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4326C>A | p.Ala1442Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4451/7255 | 4326/7056 | 1442/2351 | chr12 | 50352506 | ||
| chr12:50352512
|
G | A | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4320C>T | p.Ala1440Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4445/7255 | 4320/7056 | 1440/2351 | chr12 | 50352512 | ||
| chr12:50352542
|
A | C | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4290T>G | p.Ala1430Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4415/7255 | 4290/7056 | 1430/2351 | chr12 | 50352542 | ||
| chr12:50352548
|
T | A | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4284A>T | p.Ala1428Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4409/7255 | 4284/7056 | 1428/2351 | chr12 | 50352548 | ||
| chr12:50352577
|
A | G | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4255T>C | p.Leu1419Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4380/7255 | 4255/7056 | 1419/2351 | chr12 | 50352577 | ||
| chr12:50352584
|
A | G | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4248T>C | p.Ala1416Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4373/7255 | 4248/7056 | 1416/2351 | chr12 | 50352584 | ||
| chr12:50352620
|
A | T | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4212T>A | p.Ala1404Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4337/7255 | 4212/7056 | 1404/2351 | chr12 | 50352620 | ||
| chr12:50352650
|
G | T | 1 | a0029c0025 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4182C>A | p.Ala1394Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4307/7255 | 4182/7056 | 1394/2351 | chr12 | 50352650 | ||
| chr12:50352872
|
C | T | 1 | a0002c0010 | 3 | HG00642.hp2 HG01928.hp1 HG01934.hp1 |
synonymous_variant | LOW | c.3960G>A | p.Ala1320Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 4085/7255 | 3960/7056 | 1320/2351 | chr12 | 50352872 | ||
| chr12:50353088
|
C | T | 4 | a0007c0008a0007c0023a0028c0024others(1): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
synonymous_variant | LOW | c.3744G>A | p.Ala1248Ala | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3869/7255 | 3744/7056 | 1248/2351 | chr12 | 50353088 | ||
| chr12:50353661
|
G | A | 4 | a0007c0008a0007c0023a0028c0024others(1): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
synonymous_variant | LOW | c.3171C>T | p.Ser1057Ser | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3296/7255 | 3171/7056 | 1057/2351 | chr12 | 50353661 | ||
| chr12:50353676
|
G | C | 1 | a0009c0012 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.3156C>G | p.Pro1052Pro | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3281/7255 | 3156/7056 | 1052/2351 | chr12 | 50353676 | ||
| chr12:50353700
|
C | T | 1 | a0002c0006 | 11 | HG00738.hp1 HG01261.hp1 HG01943.hp1 others(8): Show |
synonymous_variant | LOW | c.3132G>A | p.Glu1044Glu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 3257/7255 | 3132/7056 | 1044/2351 | chr12 | 50353700 | ||
| chr12:50354375
|
T | C | 1 | a0001c0042 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.2457A>G | p.Glu819Glu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 2582/7255 | 2457/7056 | 819/2351 | chr12 | 50354375 | ||
| chr12:50354489
|
A | G | 1 | a0001c0039 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.2343T>C | p.Tyr781Tyr | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 2468/7255 | 2343/7056 | 781/2351 | chr12 | 50354489 | ||
| chr12:50354981
|
G | T | 1 | a0004c0027 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.1851C>A | p.Ile617Ile | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1976/7255 | 1851/7056 | 617/2351 | chr12 | 50354981 | ||
| chr12:50355511
|
A | G | 14 | a0003c0003a0003c0014a0003c0020others(11): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
synonymous_variant | LOW | c.1321T>C | p.Leu441Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1446/7255 | 1321/7056 | 441/2351 | chr12 | 50355511 | ||
| chr12:50355893
|
A | G | 2 | a0003c0014a0033c0021 | 3 | HG02257.hp2 HG02280.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.939T>C | p.Asn313Asn | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/8 | 1064/7255 | 939/7056 | 313/2351 | chr12 | 50355893 | ||
| chr12:50360925
|
A | G | 4 | a0007c0008a0007c0023a0028c0024others(1): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.414T>C | p.Asn138Asn | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/8 | 539/7255 | 414/7056 | 138/2351 | chr12 | 50360925 | ||
| chr12:50396377
|
C | T | 1 | a0003c0020 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.108G>A | p.Leu36Leu | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/8 | 233/7255 | 108/7056 | 36/2351 | chr12 | 50396377 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50327540
|
C | CT | 41 | a0001c0001t0001g0229a0002c0002t0001g0124a0002c0002t0001g0198others(38): Show | 41 | HG00438.hp2 HG00597.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.7035-137dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50327540 | ||||||
| chr12:50327560
|
G | T | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.7035-156C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50327560 | ||||||
| chr12:50327919
|
T | G | 2 | a0009c0012t0001g0234a0009c0012t0001g0235 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.7035-515A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50327919 | ||||||
| chr12:50328177
|
A | G | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7035-773T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328177 | ||||||
| chr12:50328290
|
C | G | 1 | a0002c0002t0001g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7035-886G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328290 | ||||||
| chr12:50328362
|
C | T | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.7035-958G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328362 | ||||||
| chr12:50328515
|
A | T | 1 | a0010c0019t0001g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7035-1111T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328515 | ||||||
| chr12:50328520
|
A | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7035-1116T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328520 | ||||||
| chr12:50328527
|
A | ATTTTTTT others(4): Show |
1 | a0010c0019t0001g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7035-1124_7035-112 others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328527 | ||||||
| chr12:50328527
|
A | T | 1 | a0010c0019t0001g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7035-1123T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328527 | ||||||
| chr12:50328538
|
GTC | G | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.7035-1136_7035-113 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328538 | ||||||
| chr12:50328546
|
T | C | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7035-1142A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328546 | ||||||
| chr12:50328570
|
C | T | 1 | a0003c0003t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7035-1166G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328570 | ||||||
| chr12:50328645
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.7035-1241G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328645 | ||||||
| chr12:50328809
|
C | G | 1 | a0002c0002t0001g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7035-1405G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328809 | ||||||
| chr12:50328813
|
G | A | 2 | a0003c0003t0001g0052a0003c0003t0001g0087 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.7035-1409C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328813 | ||||||
| chr12:50328838
|
G | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7035-1434C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328838 | ||||||
| chr12:50328926
|
G | A | 7 | a0002c0002t0001g0126a0002c0002t0001g0135a0002c0002t0001g0180others(4): Show | 7 | NA18942.hp1 NA18979.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.7035-1522C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50328926 | ||||||
| chr12:50329114
|
C | T | 1 | a0002c0002t0001g0326 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7034+1459G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329114 | ||||||
| chr12:50329120
|
G | A | 1 | a0030c0040t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.7034+1453C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329120 | ||||||
| chr12:50329586
|
T | C | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7034+987A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329586 | ||||||
| chr12:50329599
|
C | CT | 6 | a0008c0009t0001g0111a0008c0009t0001g0112a0009c0012t0001g0233others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.7034+973dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329599 | ||||||
| chr12:50329741
|
C | T | 1 | a0002c0033t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7034+832G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329741 | ||||||
| chr12:50329782
|
G | A | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.7034+791C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329782 | ||||||
| chr12:50329834
|
G | C | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7034+739C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329834 | ||||||
| chr12:50329843
|
G | T | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.7034+730C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50329843 | ||||||
| chr12:50330000
|
T | A | 1 | a0003c0003t0001g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7034+573A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50330000 | ||||||
| chr12:50330210
|
A | G | 94 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.7034+363T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50330210 | ||||||
| chr12:50330319
|
T | A | 1 | a0030c0040t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.7034+254A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50330319 | ||||||
| chr12:50330478
|
A | G | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.7034+95T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50330478 | ||||||
| chr12:50330482
|
A | G | 6 | a0002c0002t0001g0116a0002c0002t0001g0172a0002c0002t0001g0173others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.7034+91T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50330482 | ||||||
| chr12:50330560
|
G | T | 1 | a0003c0003t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7034+13C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 7/7 | chr12 | 50330560 | ||||||
| chr12:50331007
|
C | T | 1 | a0003c0003t0001g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6849-249G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 6/7 | chr12 | 50331007 | ||||||
| chr12:50331046
|
G | T | 1 | a0002c0002t0001g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6849-288C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 6/7 | chr12 | 50331046 | ||||||
| chr12:50331084
|
A | C | 9 | a0005c0005t0001g0218a0005c0005t0001g0220a0005c0005t0001g0222others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.6849-326T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 6/7 | chr12 | 50331084 | ||||||
| chr12:50331308
|
C | G | 1 | a0001c0001t0001g0015 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6848+362G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 6/7 | chr12 | 50331308 | ||||||
| chr12:50331576
|
A | T | 1 | a0003c0003t0001g0262 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6848+94T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 6/7 | chr12 | 50331576 | ||||||
| chr12:50331635
|
G | A | 1 | a0023c0028t0001g0317 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6848+35C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 6/7 | chr12 | 50331635 | ||||||
| chr12:50331971
|
C | A | 5 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.6697-150G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50331971 | ||||||
| chr12:50332103
|
T | C | 1 | a0003c0003t0001g0267 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6697-282A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50332103 | ||||||
| chr12:50332182
|
T | C | 131 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(128): Show | 131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.6697-361A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50332182 | ||||||
| chr12:50332288
|
A | G | 7 | a0002c0002t0001g0138a0002c0002t0001g0178a0002c0002t0001g0179others(4): Show | 7 | HG02155.hp2 NA18957.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.6697-467T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50332288 | ||||||
| chr12:50332296
|
C | T | 2 | a0009c0012t0001g0234a0009c0012t0001g0235 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6697-475G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50332296 | ||||||
| chr12:50332523
|
C | T | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.6697-702G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50332523 | ||||||
| chr12:50333020
|
C | A | 9 | a0005c0005t0001g0218a0005c0005t0001g0220a0005c0005t0001g0222others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.6696+891G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50333020 | ||||||
| chr12:50333400
|
T | C | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.6696+511A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50333400 | ||||||
| chr12:50333738
|
G | A | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.6696+173C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50333738 | ||||||
| chr12:50333870
|
T | A | 1 | a0015c0016t0001g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6696+41A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 5/7 | chr12 | 50333870 | ||||||
| chr12:50334189
|
A | T | 3 | a0002c0011t0001g0118a0002c0011t0001g0119a0002c0011t0001g0166 | 3 | HG01891.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.6504-86T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50334189 | ||||||
| chr12:50334331
|
C | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6504-228G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50334331 | ||||||
| chr12:50334440
|
G | A | 1 | a0003c0003t0001g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.6504-337C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50334440 | ||||||
| chr12:50335116
|
G | C | 1 | a0003c0003t0001g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.6504-1013C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335116 | ||||||
| chr12:50335190
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.6504-1087G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335190 | ||||||
| chr12:50335204
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.6504-1101C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335204 | ||||||
| chr12:50335399
|
A | C | 1 | a0003c0003t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6504-1296T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335399 | ||||||
| chr12:50335537
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG00140.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.6504-1434C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335537 | ||||||
| chr12:50335593
|
G | A | 1 | a0030c0040t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6504-1490C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335593 | ||||||
| chr12:50335672
|
G | A | 2 | a0003c0003t0001g0049a0003c0003t0001g0050 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6504-1569C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335672 | ||||||
| chr12:50335739
|
C | G | 222 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.6504-1636G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335739 | ||||||
| chr12:50335847
|
CG | C | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6504-1745delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335847 | ||||||
| chr12:50335908
|
G | A | 2 | a0002c0011t0001g0118a0002c0011t0001g0119 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6504-1805C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335908 | ||||||
| chr12:50335913
|
C | A | 1 | a0002c0002t0001g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.6504-1810G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335913 | ||||||
| chr12:50335932
|
T | C | 1 | a0008c0009t0001g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6504-1829A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335932 | ||||||
| chr12:50335935
|
C | T | 1 | a0003c0003t0001g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.6504-1832G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335935 | ||||||
| chr12:50335953
|
G | A | 1 | a0002c0010t0001g0147 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6504-1850C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50335953 | ||||||
| chr12:50336048
|
C | A | 1 | a0002c0033t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6504-1945G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336048 | ||||||
| chr12:50336124
|
C | CA | 195 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.6504-2022dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336124 | ||||||
| chr12:50336460
|
C | T | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.6504-2357G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336460 | ||||||
| chr12:50336675
|
C | T | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.6504-2572G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336675 | ||||||
| chr12:50336785
|
G | A | 1 | a0004c0004t0001g0279 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6504-2682C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336785 | ||||||
| chr12:50336795
|
G | T | 1 | a0003c0003t0001g0213 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.6504-2692C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336795 | ||||||
| chr12:50336821
|
T | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6504-2718A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336821 | ||||||
| chr12:50336895
|
G | A | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6504-2792C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50336895 | ||||||
| chr12:50337054
|
G | A | 3 | a0013c0017t0001g0003a0015c0016t0001g0004a0015c0016t0001g0005 | 3 | HG02055.hp1 HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6504-2951C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337054 | ||||||
| chr12:50337257
|
C | G | 1 | a0003c0003t0001g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6504-3154G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337257 | ||||||
| chr12:50337289
|
C | CT | 109 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0020others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.6504-3187dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337289 | ||||||
| chr12:50337289
|
C | CTT | 19 | a0001c0001t0001g0070a0003c0003t0001g0022a0003c0003t0001g0029others(16): Show | 19 | HG00597.hp2 HG00673.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.6504-3188_6504-318 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337289 | ||||||
| chr12:50337289
|
CT | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0063a0001c0001t0001g0094others(4): Show | 7 | HG01069.hp2 HG02293.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.6504-3187delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337289 | ||||||
| chr12:50337340
|
G | A | 94 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.6504-3237C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337340 | ||||||
| chr12:50337459
|
A | AT | 20 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0056others(17): Show | 20 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.6504-3357dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337459 | ||||||
| chr12:50337459
|
AT | A | 7 | a0001c0001t0001g0094a0002c0002t0001g0143a0002c0002t0001g0170others(4): Show | 7 | HG02572.hp1 HG03225.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.6504-3357delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337459 | ||||||
| chr12:50337460
|
T | A | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6504-3357A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337460 | ||||||
| chr12:50337491
|
G | A | 2 | a0015c0016t0001g0004a0015c0016t0001g0005 | 2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6504-3388C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337491 | ||||||
| chr12:50337541
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6504-3438G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337541 | ||||||
| chr12:50337804
|
G | C | 9 | a0005c0005t0001g0218a0005c0005t0001g0220a0005c0005t0001g0222others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.6504-3701C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337804 | ||||||
| chr12:50337853
|
G | A | 1 | a0003c0003t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6504-3750C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337853 | ||||||
| chr12:50337915
|
T | TAAAC | 116 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.6504-3816_6504-381 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337915 | ||||||
| chr12:50337915
|
TAAAC | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(45): Show | 48 | HG00438.hp1 HG01109.hp2 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.6504-3816_6504-381 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50337915 | ||||||
| chr12:50338480
|
C | T | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.6504-4377G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338480 | ||||||
| chr12:50338481
|
A | G | 231 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.6504-4378T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338481 | ||||||
| chr12:50338481
|
A | T | 2 | a0007c0008t0001g0088a0007c0023t0001g0054 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.6504-4378T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338481 | ||||||
| chr12:50338533
|
C | T | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6504-4430G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338533 | ||||||
| chr12:50338551
|
A | G | 1 | a0007c0008t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6504-4448T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338551 | ||||||
| chr12:50338593
|
G | A | 2 | a0003c0003t0001g0272a0003c0003t0001g0273 | 2 | HG01081.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.6504-4490C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338593 | ||||||
| chr12:50338615
|
T | C | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.6504-4512A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338615 | ||||||
| chr12:50338761
|
G | A | 9 | a0005c0005t0001g0218a0005c0005t0001g0220a0005c0005t0001g0222others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.6504-4658C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338761 | ||||||
| chr12:50338788
|
G | A | 1 | a0003c0003t0001g0262 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6504-4685C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338788 | ||||||
| chr12:50338893
|
A | G | 9 | a0005c0005t0001g0218a0005c0005t0001g0220a0005c0005t0001g0222others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.6504-4790T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50338893 | ||||||
| chr12:50339071
|
G | A | 1 | a0003c0003t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6504-4968C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339071 | ||||||
| chr12:50339173
|
C | T | 1 | a0003c0003t0001g0217 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6504-5070G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339173 | ||||||
| chr12:50339175
|
C | G | 7 | a0005c0005t0001g0218a0005c0005t0001g0220a0005c0005t0001g0222others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.6504-5072G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339175 | ||||||
| chr12:50339297
|
G | A | 1 | a0002c0002t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6504-5194C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339297 | ||||||
| chr12:50339741
|
T | TAC | 19 | a0002c0002t0001g0149a0002c0002t0001g0154a0002c0002t0001g0169others(16): Show | 19 | HG00642.hp2 HG01928.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.6504-5640_6504-563 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
T | TACAC | 13 | a0002c0002t0001g0124a0002c0002t0001g0126a0002c0002t0001g0132others(10): Show | 13 | HG00597.hp1 HG01943.hp1 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.6504-5642_6504-563 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
T | TACACAC | 25 | a0002c0002t0001g0073a0002c0002t0001g0114a0002c0002t0001g0115others(22): Show | 25 | HG00738.hp1 HG01261.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.6504-5644_6504-563 others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
T | TACACACA others(1): Show |
27 | a0002c0002t0001g0113a0002c0002t0001g0117a0002c0002t0001g0133others(24): Show | 27 | HG00408.hp2 HG00673.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.6504-5646_6504-563 others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
T | TACACACA others(3): Show |
9 | a0002c0002t0001g0120a0002c0002t0001g0155a0002c0002t0001g0168others(6): Show | 9 | HG01167.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.6504-5648_6504-563 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
T | TACACACA others(5): Show |
2 | a0002c0002t0001g0245a0002c0006t0001g0161 | 2 | NA18957.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.6504-5650_6504-563 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
TAC | T | 6 | a0002c0002t0001g0175a0005c0005t0001g0226a0005c0005t0001g0251others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.6504-5640_6504-563 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
TACAC | T | 15 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0063others(12): Show | 15 | HG00544.hp1 HG01361.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.6504-5642_6504-563 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
TACACAC | T | 96 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.6504-5644_6504-563 others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0046a0001c0001t0001g0227a0003c0003t0001g0087 | 3 | NA18943.hp1 NA18969.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.6504-5646_6504-563 others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
TACACACA others(3): Show |
T | 87 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.6504-5648_6504-563 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339741
|
TACACACA others(7): Show |
T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0013c0017t0001g0131 | 3 | HG02145.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6504-5652_6504-563 others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339741 | ||||||
| chr12:50339920
|
C | G | 5 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.6504-5817G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50339920 | ||||||
| chr12:50340140
|
T | C | 92 | a0001c0001t0001g0101a0001c0001t0001g0196a0002c0002t0001g0073others(89): Show | 92 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.6504-6037A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340140 | ||||||
| chr12:50340155
|
C | T | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6504-6052G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340155 | ||||||
| chr12:50340416
|
T | A | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.6504-6313A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340416 | ||||||
| chr12:50340613
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6510A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340613 | ||||||
| chr12:50340646
|
G | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6543C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340646 | ||||||
| chr12:50340669
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6566A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340669 | ||||||
| chr12:50340677
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6574A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340677 | ||||||
| chr12:50340679
|
A | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6576T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340679 | ||||||
| chr12:50340682
|
A | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6579T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340682 | ||||||
| chr12:50340683
|
A | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6580T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340683 | ||||||
| chr12:50340687
|
A | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6584T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340687 | ||||||
| chr12:50340692
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6589A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340692 | ||||||
| chr12:50340719
|
G | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6616C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340719 | ||||||
| chr12:50340727
|
A | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6624T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340727 | ||||||
| chr12:50340739
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6636A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340739 | ||||||
| chr12:50340742
|
T | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6639A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340742 | ||||||
| chr12:50340743
|
G | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6640C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340743 | ||||||
| chr12:50340750
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6647A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340750 | ||||||
| chr12:50340753
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6650A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340753 | ||||||
| chr12:50340754
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6651A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340754 | ||||||
| chr12:50340756
|
A | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6653T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340756 | ||||||
| chr12:50340760
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6657A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340760 | ||||||
| chr12:50340784
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6681A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340784 | ||||||
| chr12:50340788
|
C | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6685G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340788 | ||||||
| chr12:50340795
|
T | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6692A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340795 | ||||||
| chr12:50340796
|
C | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6693G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340796 | ||||||
| chr12:50340799
|
AT | A | 308 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.6504-6697delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340799 | ||||||
| chr12:50340799
|
ATT | A | 7 | a0002c0002t0001g0073a0002c0002t0001g0153a0002c0002t0001g0329others(4): Show | 7 | HG02572.hp1 HG03139.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.6504-6698_6504-669 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340799 | ||||||
| chr12:50340802
|
TTTTTTTT others(6): Show |
T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6712_6504-670 others(17): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340802 | ||||||
| chr12:50340817
|
G | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6714C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340817 | ||||||
| chr12:50340823
|
G | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6720C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340823 | ||||||
| chr12:50340833
|
G | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6730C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340833 | ||||||
| chr12:50340834
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6731A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340834 | ||||||
| chr12:50340836
|
G | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6733C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340836 | ||||||
| chr12:50340837
|
C | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6734G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340837 | ||||||
| chr12:50340838
|
C | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6735G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340838 | ||||||
| chr12:50340842
|
G | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6739C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340842 | ||||||
| chr12:50340856
|
G | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6753C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340856 | ||||||
| chr12:50340857
|
T | G | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6754A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340857 | ||||||
| chr12:50340858
|
G | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6755C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340858 | ||||||
| chr12:50340860
|
G | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6757C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340860 | ||||||
| chr12:50340874
|
G | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6771C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340874 | ||||||
| chr12:50340907
|
C | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6804G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340907 | ||||||
| chr12:50340908
|
T | C | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6805A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340908 | ||||||
| chr12:50340911
|
C | T | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6808G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340911 | ||||||
| chr12:50340912
|
T | A | 1 | a0003c0003t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6504-6809A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50340912 | ||||||
| chr12:50341032
|
G | A | 5 | a0006c0007t0001g0038a0006c0007t0001g0150a0006c0007t0001g0164others(2): Show | 5 | HG01167.hp1 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.6504-6929C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50341032 | ||||||
| chr12:50341428
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6504-7325T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50341428 | ||||||
| chr12:50341520
|
A | G | 1 | a0003c0003t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6504-7417T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50341520 | ||||||
| chr12:50341733
|
G | A | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6504-7630C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50341733 | ||||||
| chr12:50342245
|
G | T | 1 | a0003c0003t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6503+8084C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342245 | ||||||
| chr12:50342289
|
A | G | 322 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.6503+8040T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342289 | ||||||
| chr12:50342309
|
AAAAAACA others(5): Show |
A | 1 | a0003c0020t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.6503+8008_6503+801 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342309 | ||||||
| chr12:50342432
|
A | G | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6503+7897T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342432 | ||||||
| chr12:50342482
|
A | T | 218 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.6503+7847T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342482 | ||||||
| chr12:50342506
|
G | T | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.6503+7823C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342506 | ||||||
| chr12:50342544
|
G | A | 12 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.6503+7785C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342544 | ||||||
| chr12:50342586
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0312 | 2 | HG01168.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.6503+7743C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342586 | ||||||
| chr12:50342709
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6503+7620C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342709 | ||||||
| chr12:50342719
|
C | T | 1 | a0014c0018t0001g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6503+7610G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342719 | ||||||
| chr12:50342772
|
C | CT | 108 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.6503+7556dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342772 | ||||||
| chr12:50342938
|
AT | A | 304 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(301): Show | 304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.6503+7390delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342938 | ||||||
| chr12:50342938
|
ATT | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0301others(10): Show | 13 | HG00099.hp2 HG01884.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.6503+7389_6503+739 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50342938 | ||||||
| chr12:50343015
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.6503+7314G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343015 | ||||||
| chr12:50343529
|
C | T | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6503+6800G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343529 | ||||||
| chr12:50343655
|
G | A | 5 | a0001c0001t0001g0061a0005c0005t0001g0106a0005c0005t0001g0108others(2): Show | 5 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.6503+6674C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343655 | ||||||
| chr12:50343764
|
G | T | 96 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.6503+6565C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343764 | ||||||
| chr12:50343836
|
T | C | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6503+6493A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343836 | ||||||
| chr12:50343854
|
C | T | 1 | a0006c0007t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6503+6475G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343854 | ||||||
| chr12:50343918
|
C | CT | 9 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0229others(6): Show | 9 | HG00741.hp1 HG00741.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.6503+6410dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343918 | ||||||
| chr12:50343918
|
CT | C | 96 | a0002c0002t0001g0073a0002c0002t0001g0113a0002c0002t0001g0114others(93): Show | 96 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.6503+6410delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50343918 | ||||||
| chr12:50344056
|
A | AT | 75 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0076others(72): Show | 75 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.6503+6272dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344056 | ||||||
| chr12:50344216
|
G | A | 1 | a0003c0003t0001g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6503+6113C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344216 | ||||||
| chr12:50344341
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.6503+5988G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344341 | ||||||
| chr12:50344548
|
T | A | 1 | a0002c0002t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6503+5781A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344548 | ||||||
| chr12:50344652
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0075others(1): Show | 4 | HG02071.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.6503+5677C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344652 | ||||||
| chr12:50344653
|
G | A | 98 | a0002c0002t0001g0073a0002c0002t0001g0113a0002c0002t0001g0114others(95): Show | 98 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.6503+5676C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344653 | ||||||
| chr12:50344819
|
A | G | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.6503+5510T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50344819 | ||||||
| chr12:50345225
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.6503+5104G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345225 | ||||||
| chr12:50345243
|
T | C | 2 | a0002c0011t0001g0118a0002c0011t0001g0119 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6503+5086A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345243 | ||||||
| chr12:50345254
|
G | A | 1 | a0002c0002t0001g0073 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6503+5075C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345254 | ||||||
| chr12:50345422
|
C | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.6503+4907G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345422 | ||||||
| chr12:50345573
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6503+4756G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345573 | ||||||
| chr12:50345636
|
T | G | 2 | a0003c0003t0001g0206a0003c0003t0001g0208 | 2 | NA18961.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.6503+4693A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345636 | ||||||
| chr12:50345652
|
G | T | 1 | a0001c0001t0001g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.6503+4677C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345652 | ||||||
| chr12:50345659
|
G | A | 1 | a0003c0003t0001g0212 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.6503+4670C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345659 | ||||||
| chr12:50345864
|
T | C | 1 | a0002c0002t0001g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6503+4465A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345864 | ||||||
| chr12:50345899
|
A | C | 1 | a0002c0006t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6503+4430T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345899 | ||||||
| chr12:50345984
|
C | T | 1 | a0003c0020t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.6503+4345G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345984 | ||||||
| chr12:50345997
|
C | CA | 16 | a0002c0002t0001g0113a0002c0002t0001g0123a0002c0002t0001g0132others(13): Show | 16 | HG02083.hp1 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.6503+4331dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345997 | ||||||
| chr12:50345997
|
C | CAA | 94 | a0001c0001t0001g0015a0002c0002t0001g0114a0002c0002t0001g0115others(91): Show | 94 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.6503+4330_6503+433 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345997 | ||||||
| chr12:50345997
|
C | CAAA | 102 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.6503+4329_6503+433 others(7): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345997 | ||||||
| chr12:50345997
|
C | CAAAA | 13 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0059others(10): Show | 13 | HG01175.hp1 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.6503+4328_6503+433 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345997 | ||||||
| chr12:50345997
|
CA | C | 97 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.6503+4331delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50345997 | ||||||
| chr12:50346033
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6503+4296C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346033 | ||||||
| chr12:50346201
|
A | AAGAGAGA others(1): Show |
4 | a0001c0001t0001g0013a0003c0003t0001g0085a0003c0003t0001g0099others(1): Show | 4 | HG01168.hp1 HG01255.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6503+4120_6503+412 others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346201 | ||||||
| chr12:50346201
|
A | AG | 3 | a0001c0001t0001g0297a0002c0006t0001g0156a0002c0006t0001g0163 | 3 | HG00741.hp2 HG01261.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.6503+4127_6503+412 others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346201 | ||||||
| chr12:50346201
|
A | G | 1 | a0003c0003t0001g0217 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6503+4128T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346201 | ||||||
| chr12:50346211
|
G | GAGACAGA others(23): Show |
1 | a0015c0016t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6503+4117_6503+411 others(34): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346211 | ||||||
| chr12:50346211
|
G | GAGACAGA others(31): Show |
1 | a0015c0016t0001g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6503+4117_6503+411 others(42): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346211 | ||||||
| chr12:50346211
|
G | GAGACAGA others(35): Show |
2 | a0013c0017t0001g0131a0027c0038t0001g0006 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6503+4117_6503+411 others(46): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346211 | ||||||
| chr12:50346215
|
G | A | 4 | a0013c0017t0001g0131a0015c0016t0001g0004a0015c0016t0001g0005others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.6503+4114C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAAG others(3): Show |
1 | a0009c0012t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAAG others(19): Show |
1 | a0009c0012t0001g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(30): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAAG others(23): Show |
1 | a0009c0012t0001g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(34): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAAG others(35): Show |
1 | a0002c0002t0001g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(46): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(13): Show |
1 | a0003c0003t0001g0217 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(24): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(17): Show |
1 | a0002c0011t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(28): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(21): Show |
1 | a0002c0011t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(32): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(34): Show |
1 | a0002c0002t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(45): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(29): Show |
1 | a0002c0002t0001g0325 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(40): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(16): Show |
1 | a0002c0002t0001g0240 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(27): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(24): Show |
1 | a0002c0002t0001g0179 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(35): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(32): Show |
1 | a0002c0002t0001g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(43): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(11): Show |
1 | a0002c0002t0001g0168 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(22): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(15): Show |
5 | a0002c0002t0001g0134a0002c0002t0001g0165a0002c0002t0001g0327others(2): Show | 5 | HG00408.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(26): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(19): Show |
17 | a0002c0002t0001g0113a0002c0002t0001g0123a0002c0002t0001g0132others(14): Show | 17 | HG01167.hp1 HG01346.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(30): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(23): Show |
20 | a0002c0002t0001g0009a0002c0002t0001g0124a0002c0002t0001g0133others(17): Show | 20 | HG00597.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(34): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(27): Show |
22 | a0002c0002t0001g0073a0002c0002t0001g0115a0002c0002t0001g0117others(19): Show | 22 | HG01884.hp2 HG01978.hp2 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(38): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(31): Show |
20 | a0002c0002t0001g0114a0002c0002t0001g0121a0002c0002t0001g0144others(17): Show | 20 | HG00673.hp1 HG01358.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(42): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(35): Show |
5 | a0002c0002t0001g0126a0002c0002t0001g0183a0002c0002t0001g0259others(2): Show | 5 | NA18906.hp1 NA18954.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(46): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(39): Show |
2 | a0002c0002t0001g0153a0002c0002t0001g0158 | 2 | HG03139.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(50): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(43): Show |
1 | a0025c0035t0001g0060 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(54): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(30): Show |
1 | a0002c0002t0001g0187 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(41): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(29): Show |
1 | a0002c0006t0001g0162 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(40): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(26): Show |
1 | a0001c0001t0001g0036 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(37): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(32): Show |
1 | a0001c0001t0001g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(43): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(19): Show |
1 | a0020c0031t0001g0207 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(30): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(31): Show |
2 | a0001c0001t0001g0061a0002c0002t0001g0138 | 2 | NA18986.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(42): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(26): Show |
1 | a0001c0001t0001g0190 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(37): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(13): Show |
6 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0314others(3): Show | 6 | HG02132.hp2 NA18954.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(24): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(17): Show |
8 | a0001c0001t0001g0229a0001c0001t0001g0293a0001c0001t0001g0309others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(28): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(21): Show |
11 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0075others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(32): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(25): Show |
26 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0023others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(36): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(29): Show |
31 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(40): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(33): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0017others(18): Show | 21 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(44): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(37): Show |
10 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0041others(7): Show | 10 | HG01192.hp2 HG02132.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(48): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(41): Show |
1 | a0001c0001t0001g0063 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(52): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(40): Show |
1 | a0001c0001t0001g0227 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(51): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(26): Show |
1 | a0001c0001t0001g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(37): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(23): Show |
2 | a0001c0001t0001g0230a0007c0008t0001g0247 | 2 | HG00544.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(34): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(27): Show |
1 | a0007c0008t0001g0246 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(38): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(31): Show |
4 | a0001c0001t0001g0258a0001c0001t0001g0296a0003c0003t0001g0208others(1): Show | 4 | HG01884.hp1 HG01891.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(42): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(35): Show |
1 | a0007c0008t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(46): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(39): Show |
1 | a0007c0023t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(50): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(37): Show |
2 | a0001c0001t0001g0095a0029c0025t0001g0243 | 2 | HG03209.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6503+4113_6503+411 others(48): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346215
|
G | GAGAGAGA others(35): Show |
1 | a0028c0024t0001g0244 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6503+4113_6503+411 others(46): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346215 | ||||||
| chr12:50346216
|
A | AGAGAGAG others(5): Show |
3 | a0003c0003t0001g0034a0003c0003t0001g0205a0003c0003t0001g0232 | 3 | HG01109.hp1 HG01361.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6503+4112_6503+411 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346216 | ||||||
| chr12:50346217
|
G | GAGAGAGA others(22): Show |
1 | a0001c0001t0001g0047 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.6503+4111_6503+411 others(33): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346217 | ||||||
| chr12:50346218
|
A | AGAG | 13 | a0003c0003t0001g0022a0003c0003t0001g0049a0003c0003t0001g0050others(10): Show | 13 | HG01978.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.6503+4110_6503+411 others(7): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346218 | ||||||
| chr12:50346219
|
A | G | 50 | a0003c0003t0001g0027a0003c0003t0001g0029a0003c0003t0001g0030others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.6503+4110T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346219 | ||||||
| chr12:50346220
|
G | A | 298 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.6503+4109C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346220 | ||||||
| chr12:50346220
|
G | GA | 16 | a0003c0003t0001g0022a0003c0003t0001g0049a0003c0003t0001g0050others(13): Show | 16 | HG01978.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.6503+4108_6503+410 others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346220 | ||||||
| chr12:50346220
|
G | GAAGAAAG others(7): Show |
1 | a0003c0003t0001g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.6503+4108_6503+410 others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346220 | ||||||
| chr12:50346220
|
G | GGAAAGAA others(9): Show |
1 | a0013c0017t0001g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6503+4093_6503+410 others(20): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346220 | ||||||
| chr12:50346223
|
A | G | 51 | a0003c0003t0001g0027a0003c0003t0001g0029a0003c0003t0001g0030others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.6503+4106T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346223 | ||||||
| chr12:50346224
|
A | G | 16 | a0003c0003t0001g0022a0003c0003t0001g0049a0003c0003t0001g0050others(13): Show | 16 | HG01978.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.6503+4105T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346224 | ||||||
| chr12:50346228
|
A | G | 51 | a0003c0003t0001g0027a0003c0003t0001g0029a0003c0003t0001g0030others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.6503+4101T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346228 | ||||||
| chr12:50346229
|
G | GAAAGAAA others(10): Show |
1 | a0001c0001t0001g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6503+4099_6503+410 others(21): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346229 | ||||||
| chr12:50346237
|
A | G | 322 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.6503+4092T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346237 | ||||||
| chr12:50346241
|
G | A | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6503+4088C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346241 | ||||||
| chr12:50346262
|
A | T | 1 | a0003c0003t0001g0204 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6503+4067T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346262 | ||||||
| chr12:50346325
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.6503+4004C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346325 | ||||||
| chr12:50346356
|
C | T | 1 | a0002c0033t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6503+3973G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346356 | ||||||
| chr12:50346357
|
G | A | 1 | a0002c0002t0001g0132 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6503+3972C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346357 | ||||||
| chr12:50346569
|
C | T | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6503+3760G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346569 | ||||||
| chr12:50346663
|
C | T | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6503+3666G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346663 | ||||||
| chr12:50346739
|
C | G | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.6503+3590G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346739 | ||||||
| chr12:50346801
|
T | G | 1 | a0001c0001t0001g0291 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6503+3528A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346801 | ||||||
| chr12:50346847
|
AAAAAT | A | 10 | a0001c0001t0001g0044a0003c0003t0001g0206a0003c0003t0001g0208others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.6503+3477_6503+348 others(9): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346847 | ||||||
| chr12:50346916
|
G | GCA | 14 | a0002c0002t0001g0132a0003c0003t0001g0034a0003c0003t0001g0078others(11): Show | 14 | HG01261.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.6503+3411_6503+341 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346916 | ||||||
| chr12:50346923
|
C | A | 1 | a0019c0032t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6503+3406G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346923 | ||||||
| chr12:50346991
|
C | T | 1 | a0003c0003t0001g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6503+3338G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346991 | ||||||
| chr12:50346997
|
CA | C | 87 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0029others(84): Show | 87 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.6503+3331delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346997 | ||||||
| chr12:50346997
|
CAA | C | 15 | a0003c0003t0001g0027a0003c0003t0001g0030a0003c0003t0001g0051others(12): Show | 15 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.6503+3330_6503+333 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346997 | ||||||
| chr12:50346997
|
CAAAA | C | 8 | a0010c0019t0001g0322a0010c0019t0001g0323a0013c0017t0001g0003others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.6503+3328_6503+333 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346997 | ||||||
| chr12:50346997
|
CAAAAA | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.6503+3327_6503+333 others(9): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346997 | ||||||
| chr12:50346997
|
CAAAAAA | C | 96 | a0001c0001t0001g0015a0002c0002t0001g0073a0002c0002t0001g0113others(93): Show | 96 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.6503+3326_6503+333 others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50346997 | ||||||
| chr12:50347091
|
C | T | 5 | a0003c0003t0001g0129a0003c0003t0001g0130a0003c0003t0001g0202others(2): Show | 5 | NA18962.hp2 NA18966.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.6503+3238G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50347091 | ||||||
| chr12:50347241
|
T | C | 1 | a0003c0003t0001g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6503+3088A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50347241 | ||||||
| chr12:50347254
|
G | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6503+3075C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50347254 | ||||||
| chr12:50347674
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6503+2655T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50347674 | ||||||
| chr12:50347678
|
CA | C | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.6503+2650delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50347678 | ||||||
| chr12:50347994
|
T | G | 2 | a0003c0003t0001g0266a0021c0030t0001g0264 | 2 | HG03491.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.6503+2335A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50347994 | ||||||
| chr12:50348038
|
A | AT | 95 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0103others(92): Show | 95 | HG00408.hp2 HG00642.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.6503+2290dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50348038 | ||||||
| chr12:50348038
|
A | ATT | 108 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.6503+2289_6503+229 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50348038 | ||||||
| chr12:50348038
|
A | ATTT | 32 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0018others(29): Show | 32 | HG00140.hp1 HG00544.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.6503+2288_6503+229 others(7): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50348038 | ||||||
| chr12:50348258
|
C | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.6503+2071G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50348258 | ||||||
| chr12:50348719
|
C | T | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.6503+1610G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50348719 | ||||||
| chr12:50348834
|
A | G | 1 | a0003c0003t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6503+1495T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50348834 | ||||||
| chr12:50349112
|
A | G | 1 | a0004c0004t0001g0277 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.6503+1217T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50349112 | ||||||
| chr12:50349238
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6503+1091C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50349238 | ||||||
| chr12:50349642
|
C | G | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.6503+687G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50349642 | ||||||
| chr12:50349647
|
TTTA | T | 323 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.6503+679_6503+681d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50349647 | ||||||
| chr12:50350130
|
C | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.6503+199G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50350130 | ||||||
| chr12:50350311
|
G | A | 319 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.6503+18C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 4/7 | chr12 | 50350311 | ||||||
| chr12:50356257
|
C | A | 315 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.584-9G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356257 | ||||||
| chr12:50356510
|
C | T | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139 | 3 | HG02572.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.584-262G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356510 | ||||||
| chr12:50356523
|
C | G | 2 | a0003c0003t0001g0266a0021c0030t0001g0264 | 2 | HG03491.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.584-275G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356523 | ||||||
| chr12:50356591
|
G | A | 1 | a0007c0008t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.584-343C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356591 | ||||||
| chr12:50356688
|
G | T | 100 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.584-440C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356688 | ||||||
| chr12:50356801
|
C | G | 99 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.584-553G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356801 | ||||||
| chr12:50356903
|
G | A | 2 | a0002c0002t0001g0319a0002c0002t0001g0320 | 2 | NA18948.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.584-655C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356903 | ||||||
| chr12:50356924
|
G | A | 1 | a0003c0003t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.584-676C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356924 | ||||||
| chr12:50356999
|
AACAT | A | 7 | a0003c0003t0001g0272a0003c0003t0001g0273a0005c0005t0001g0218others(4): Show | 7 | HG01081.hp1 HG01346.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.584-755_584-752del others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356999 | ||||||
| chr12:50356999
|
AACATACA others(1): Show |
A | 14 | a0001c0001t0001g0071a0001c0001t0001g0271a0002c0002t0001g0116others(11): Show | 14 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.584-759_584-752del others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356999 | ||||||
| chr12:50356999
|
AACATACA others(5): Show |
A | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.584-763_584-752del others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356999 | ||||||
| chr12:50356999
|
AACATACA others(9): Show |
A | 94 | a0002c0002t0001g0009a0002c0002t0001g0113a0002c0002t0001g0114others(91): Show | 94 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.584-767_584-752del others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356999 | ||||||
| chr12:50356999
|
AACATACA others(13): Show |
A | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.584-771_584-752del others(20): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50356999 | ||||||
| chr12:50357018
|
A | G | 2 | a0012c0015t0001g0214a0012c0015t0001g0216 | 2 | NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.584-770T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357018 | ||||||
| chr12:50357132
|
A | G | 319 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.584-884T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357132 | ||||||
| chr12:50357234
|
C | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-986G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357234 | ||||||
| chr12:50357307
|
G | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-1059C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357307 | ||||||
| chr12:50357362
|
C | T | 1 | a0002c0002t0001g0168 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.584-1114G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357362 | ||||||
| chr12:50357363
|
G | A | 211 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.584-1115C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357363 | ||||||
| chr12:50357371
|
G | A | 8 | a0002c0002t0001g0155a0002c0002t0001g0325a0002c0002t0001g0326others(5): Show | 8 | HG01346.hp2 HG02809.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.584-1123C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357371 | ||||||
| chr12:50357434
|
G | A | 1 | a0009c0012t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.584-1186C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357434 | ||||||
| chr12:50357516
|
A | AAAG | 95 | a0001c0001t0001g0061a0002c0002t0001g0113a0002c0002t0001g0114others(92): Show | 95 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.584-1271_584-1269d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357516 | ||||||
| chr12:50357516
|
A | AAG | 116 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(113): Show | 116 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.584-1269_584-1268i others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357516 | ||||||
| chr12:50357516
|
A | AG | 4 | a0001c0001t0001g0042a0001c0001t0001g0301a0001c0001t0001g0305others(1): Show | 4 | HG00099.hp2 HG00323.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.584-1269_584-1268i others(3): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357516 | ||||||
| chr12:50357542
|
A | G | 1 | a0002c0010t0001g0197 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.584-1294T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357542 | ||||||
| chr12:50357635
|
T | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-1387A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357635 | ||||||
| chr12:50357708
|
C | T | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.584-1460G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357708 | ||||||
| chr12:50357727
|
T | G | 1 | a0001c0042t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.584-1479A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357727 | ||||||
| chr12:50357858
|
A | G | 1 | a0003c0003t0001g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.584-1610T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357858 | ||||||
| chr12:50357876
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.584-1628C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357876 | ||||||
| chr12:50357925
|
T | C | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.584-1677A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357925 | ||||||
| chr12:50357975
|
CATAA | C | 312 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.584-1731_584-1728d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357975 | ||||||
| chr12:50357975
|
CATAAATA others(5): Show |
C | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.584-1739_584-1728d others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50357975 | ||||||
| chr12:50358155
|
TA | T | 5 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG00099.hp2 HG01192.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.584-1908delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358155 | ||||||
| chr12:50358168
|
A | T | 98 | a0002c0002t0001g0073a0002c0002t0001g0113a0002c0002t0001g0114others(95): Show | 98 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.584-1920T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358168 | ||||||
| chr12:50358323
|
A | G | 1 | a0003c0003t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.584-2075T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358323 | ||||||
| chr12:50358428
|
T | TAAAAATT others(1844): Show |
1 | a0001c0001t0001g0189 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.584-2181_584-2180i others(1853): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358428 | ||||||
| chr12:50358428
|
T | TAAAAATT others(1844): Show |
1 | a0001c0001t0001g0190 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.584-2181_584-2180i others(1853): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358428 | ||||||
| chr12:50358588
|
A | T | 1 | a0014c0018t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.583+2168T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358588 | ||||||
| chr12:50358599
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.583+2157T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358599 | ||||||
| chr12:50358601
|
C | A | 224 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(221): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.583+2155G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358601 | ||||||
| chr12:50358784
|
G | A | 96 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.583+1972C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358784 | ||||||
| chr12:50358860
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.583+1896A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358860 | ||||||
| chr12:50358879
|
C | T | 1 | a0003c0003t0001g0217 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.583+1877G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358879 | ||||||
| chr12:50358912
|
G | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.583+1844C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358912 | ||||||
| chr12:50358922
|
C | CAA | 196 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(193): Show | 196 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.583+1832_583+1833d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358922 | ||||||
| chr12:50358922
|
C | CAAA | 14 | a0001c0001t0001g0019a0001c0001t0001g0048a0001c0001t0001g0095others(11): Show | 14 | HG00438.hp1 HG02055.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.583+1831_583+1833d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358922 | ||||||
| chr12:50358938
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.583+1818C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50358938 | ||||||
| chr12:50359109
|
T | TA | 22 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0057others(19): Show | 22 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.583+1646dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359109 | ||||||
| chr12:50359118
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.583+1638T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359118 | ||||||
| chr12:50359296
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.583+1460C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359296 | ||||||
| chr12:50359394
|
G | A | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+1362C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359394 | ||||||
| chr12:50359570
|
A | G | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+1186T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359570 | ||||||
| chr12:50359580
|
C | G | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+1176G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359580 | ||||||
| chr12:50359582
|
A | C | 318 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.583+1174T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359582 | ||||||
| chr12:50359603
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0103 | 2 | NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.583+1153C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50359603 | ||||||
| chr12:50360105
|
G | T | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+651C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360105 | ||||||
| chr12:50360243
|
CAA | C | 102 | a0002c0002t0001g0198a0003c0003t0001g0008a0003c0003t0001g0022others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.583+511_583+512del others(2): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360243 | ||||||
| chr12:50360243
|
CAAA | C | 60 | a0002c0002t0001g0073a0002c0002t0001g0114a0002c0002t0001g0115others(57): Show | 60 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.583+510_583+512del others(3): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360243 | ||||||
| chr12:50360243
|
CAAAA | C | 152 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.583+509_583+512del others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360243 | ||||||
| chr12:50360285
|
T | C | 9 | a0003c0003t0001g0027a0003c0003t0001g0030a0003c0003t0001g0051others(6): Show | 9 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.583+471A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360285 | ||||||
| chr12:50360351
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.583+405C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360351 | ||||||
| chr12:50360391
|
G | GT | 97 | a0002c0002t0001g0132a0003c0003t0001g0008a0003c0003t0001g0022others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.583+364dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360391 | ||||||
| chr12:50360393
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.583+363A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360393 | ||||||
| chr12:50360574
|
A | G | 97 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.583+182T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360574 | ||||||
| chr12:50360654
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.583+102G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360654 | ||||||
| chr12:50360678
|
G | GA | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.583+77dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 3/7 | chr12 | 50360678 | ||||||
| chr12:50361133
|
A | T | 6 | a0002c0002t0001g0138a0002c0002t0001g0178a0002c0002t0001g0183others(3): Show | 6 | HG02155.hp2 NA18957.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-207T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361133 | ||||||
| chr12:50361259
|
C | T | 1 | a0002c0011t0001g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413-333G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361259 | ||||||
| chr12:50361285
|
G | T | 5 | a0002c0002t0001g0137a0002c0002t0001g0154a0002c0002t0001g0168others(2): Show | 5 | NA18945.hp2 NA18967.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-359C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361285 | ||||||
| chr12:50361418
|
T | C | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.413-492A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361418 | ||||||
| chr12:50361568
|
CT | C | 9 | a0002c0002t0001g0170a0005c0005t0001g0106a0005c0005t0001g0108others(6): Show | 9 | HG02258.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.413-643delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361568 | ||||||
| chr12:50361568
|
CTT | C | 297 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(294): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.413-644_413-643del others(2): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361568 | ||||||
| chr12:50361568
|
CTTT | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0079others(14): Show | 17 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.413-645_413-643del others(3): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361568 | ||||||
| chr12:50361734
|
C | A | 1 | a0003c0003t0001g0289 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413-808G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361734 | ||||||
| chr12:50361762
|
A | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.413-836T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361762 | ||||||
| chr12:50361776
|
G | C | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-850C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50361776 | ||||||
| chr12:50362125
|
G | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+1020C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362125 | ||||||
| chr12:50362215
|
C | T | 1 | a0002c0002t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.412+930G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362215 | ||||||
| chr12:50362225
|
G | T | 1 | a0003c0003t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.412+920C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362225 | ||||||
| chr12:50362253
|
G | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.412+892C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362253 | ||||||
| chr12:50362329
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.412+816C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362329 | ||||||
| chr12:50362483
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.412+662C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362483 | ||||||
| chr12:50362492
|
C | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.412+653G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362492 | ||||||
| chr12:50362570
|
C | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.412+575G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362570 | ||||||
| chr12:50362723
|
A | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.412+422T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362723 | ||||||
| chr12:50362743
|
C | CA | 15 | a0003c0003t0001g0208a0003c0003t0001g0289a0004c0004t0001g0255others(12): Show | 15 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.412+401dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362743 | ||||||
| chr12:50362743
|
C | CAA | 66 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(63): Show | 66 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.412+400_412+401dup others(2): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362743 | ||||||
| chr12:50362743
|
C | CAAA | 14 | a0003c0003t0001g0050a0003c0003t0001g0055a0003c0003t0001g0081others(11): Show | 14 | HG01346.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.412+399_412+401dup others(3): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362743 | ||||||
| chr12:50362743
|
CAA | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0039others(11): Show | 14 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.412+400_412+401del others(2): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362743 | ||||||
| chr12:50362743
|
CAAA | C | 194 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.412+399_412+401del others(3): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362743 | ||||||
| chr12:50362743
|
CAAAA | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0189a0002c0002t0001g0245others(5): Show | 8 | HG02258.hp1 HG02717.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+398_412+401del others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362743 | ||||||
| chr12:50362774
|
G | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+371C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362774 | ||||||
| chr12:50362807
|
G | A | 5 | a0006c0007t0001g0038a0006c0007t0001g0150a0006c0007t0001g0164others(2): Show | 5 | HG01167.hp1 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+338C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 2/7 | chr12 | 50362807 | ||||||
| chr12:50363438
|
C | T | 1 | a0003c0003t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193-74G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363438 | ||||||
| chr12:50363492
|
T | C | 1 | a0005c0005t0001g0222 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.193-128A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363492 | ||||||
| chr12:50363690
|
G | A | 3 | a0001c0001t0001g0301a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG00099.hp2 HG01192.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.193-326C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363690 | ||||||
| chr12:50363760
|
T | TA | 14 | a0002c0002t0001g0179a0005c0005t0001g0106a0005c0005t0001g0108others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.193-397dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363760 | ||||||
| chr12:50363771
|
AAG | A | 7 | a0001c0001t0001g0056a0001c0001t0001g0312a0008c0009t0001g0111others(4): Show | 7 | HG01168.hp2 HG01433.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-409_193-408del others(2): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363771 | ||||||
| chr12:50363772
|
AG | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.193-409delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363772 | ||||||
| chr12:50363772
|
AGAAAG | A | 92 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.193-413_193-409del others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363772 | ||||||
| chr12:50363773
|
G | A | 105 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0009others(102): Show | 105 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.193-409C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363773 | ||||||
| chr12:50363777
|
G | A | 3 | a0003c0003t0001g0096a0003c0003t0001g0097a0004c0004t0001g0277 | 3 | HG01106.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.193-413C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363777 | ||||||
| chr12:50363845
|
G | A | 99 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.193-481C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50363845 | ||||||
| chr12:50364145
|
C | T | 2 | a0002c0002t0001g0186a0002c0002t0001g0187 | 2 | NA18963.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.193-781G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364145 | ||||||
| chr12:50364234
|
C | T | 1 | a0003c0003t0001g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.193-870G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364234 | ||||||
| chr12:50364350
|
C | T | 1 | a0003c0003t0001g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.193-986G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364350 | ||||||
| chr12:50364483
|
G | A | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-1119C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364483 | ||||||
| chr12:50364558
|
A | AAAAT | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.193-1198_193-1195d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364558 | ||||||
| chr12:50364558
|
A | AAAATAAA others(1): Show |
3 | a0001c0001t0001g0066a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG01975.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-1202_193-1195d others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364558 | ||||||
| chr12:50364598
|
A | T | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-1234T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364598 | ||||||
| chr12:50364679
|
A | G | 5 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-1315T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364679 | ||||||
| chr12:50364857
|
G | A | 2 | a0009c0012t0001g0234a0009c0012t0001g0235 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-1493C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364857 | ||||||
| chr12:50364867
|
G | A | 1 | a0030c0040t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.193-1503C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364867 | ||||||
| chr12:50364875
|
T | C | 1 | a0001c0039t0001g0064 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.193-1511A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364875 | ||||||
| chr12:50364898
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.193-1534G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364898 | ||||||
| chr12:50364995
|
A | G | 331 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.193-1631T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50364995 | ||||||
| chr12:50365038
|
C | CA | 93 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(90): Show | 93 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.193-1675dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365038 | ||||||
| chr12:50365038
|
C | CAA | 9 | a0003c0003t0001g0052a0003c0003t0001g0055a0003c0003t0001g0083others(6): Show | 9 | HG00099.hp1 HG02280.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-1676_193-1675d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365038 | ||||||
| chr12:50365038
|
C | CAAA | 24 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0056others(21): Show | 24 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-1677_193-1675d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365038 | ||||||
| chr12:50365038
|
C | CAAAA | 173 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.193-1678_193-1675d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365038 | ||||||
| chr12:50365038
|
C | CAAAAA | 18 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(15): Show | 18 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.193-1679_193-1675d others(7): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365038 | ||||||
| chr12:50365100
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.193-1736T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365100 | ||||||
| chr12:50365139
|
A | G | 1 | a0003c0003t0001g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.193-1775T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365139 | ||||||
| chr12:50365383
|
T | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-2019A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365383 | ||||||
| chr12:50365455
|
G | A | 7 | a0007c0008t0001g0088a0007c0008t0001g0246a0007c0008t0001g0247others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2091C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365455 | ||||||
| chr12:50365650
|
AAATG | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-2290_193-2287d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365650 | ||||||
| chr12:50365936
|
C | T | 6 | a0002c0002t0001g0138a0002c0002t0001g0178a0002c0002t0001g0183others(3): Show | 6 | HG02155.hp2 NA18957.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-2572G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365936 | ||||||
| chr12:50365965
|
G | T | 331 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.193-2601C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50365965 | ||||||
| chr12:50366140
|
A | G | 323 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.193-2776T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366140 | ||||||
| chr12:50366450
|
C | T | 24 | a0002c0002t0001g0116a0002c0002t0001g0126a0002c0002t0001g0135others(21): Show | 24 | HG01884.hp2 HG02155.hp2 HG02970.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-3086G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366450 | ||||||
| chr12:50366455
|
A | T | 100 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0073others(97): Show | 100 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.193-3091T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366455 | ||||||
| chr12:50366626
|
CA | C | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-3263delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366626 | ||||||
| chr12:50366626
|
CAA | C | 8 | a0003c0003t0001g0030a0003c0003t0001g0052a0003c0003t0001g0083others(5): Show | 8 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.193-3264_193-3263d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366626 | ||||||
| chr12:50366626
|
CAAA | C | 89 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(86): Show | 89 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.193-3265_193-3263d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366626 | ||||||
| chr12:50366643
|
AAAAAAC | A | 22 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0057others(19): Show | 22 | HG00642.hp1 HG00738.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.193-3285_193-3280d others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366643 | ||||||
| chr12:50366644
|
AAAAAC | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.193-3285_193-3281d others(7): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366644 | ||||||
| chr12:50366645
|
AAAAC | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0001g0105others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.193-3285_193-3282d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366645 | ||||||
| chr12:50366660
|
C | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-3296G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366660 | ||||||
| chr12:50366677
|
G | A | 2 | a0002c0011t0001g0118a0002c0011t0001g0119 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-3313C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366677 | ||||||
| chr12:50366709
|
T | TA | 97 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.193-3346dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366709 | ||||||
| chr12:50366709
|
T | TAA | 114 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0073others(111): Show | 114 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.193-3347_193-3346d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366709 | ||||||
| chr12:50366737
|
GCACAGTA others(3): Show |
G | 2 | a0002c0002t0001g0009a0002c0033t0001g0321 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.193-3383_193-3374d others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366737 | ||||||
| chr12:50366750
|
C | T | 1 | a0002c0002t0001g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.193-3386G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366750 | ||||||
| chr12:50366865
|
T | C | 1 | a0003c0003t0001g0324 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.193-3501A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366865 | ||||||
| chr12:50366936
|
C | A | 1 | a0002c0006t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.193-3572G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366936 | ||||||
| chr12:50366938
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0332 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.193-3574A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50366938 | ||||||
| chr12:50367021
|
A | G | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-3657T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367021 | ||||||
| chr12:50367033
|
T | C | 1 | a0013c0017t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.193-3669A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367033 | ||||||
| chr12:50367061
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.193-3697G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367061 | ||||||
| chr12:50367284
|
C | T | 99 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.193-3920G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367284 | ||||||
| chr12:50367335
|
T | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-3971A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367335 | ||||||
| chr12:50367516
|
CA | C | 106 | a0001c0001t0001g0020a0001c0001t0001g0063a0002c0002t0001g0178others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.193-4153delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367516 | ||||||
| chr12:50367516
|
CAA | C | 218 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.193-4154_193-4153d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367516 | ||||||
| chr12:50367582
|
A | G | 1 | a0003c0003t0001g0125 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.193-4218T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367582 | ||||||
| chr12:50367689
|
GCA | G | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-4327_193-4326d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367689 | ||||||
| chr12:50367689
|
GCACA | G | 97 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.193-4329_193-4326d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367689 | ||||||
| chr12:50367689
|
GCACACA | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-4331_193-4326d others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367689 | ||||||
| chr12:50367702
|
C | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-4338G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367702 | ||||||
| chr12:50367708
|
CACACAA | C | 3 | a0003c0003t0001g0034a0003c0003t0001g0085a0008c0009t0001g0139 | 3 | HG02717.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4350_193-4345d others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367708 | ||||||
| chr12:50367716
|
C | A | 2 | a0003c0003t0001g0034a0003c0003t0001g0085 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4352G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367716 | ||||||
| chr12:50367865
|
T | C | 2 | a0003c0003t0001g0034a0003c0003t0001g0085 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4501A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367865 | ||||||
| chr12:50367916
|
C | T | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-4552G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50367916 | ||||||
| chr12:50368178
|
G | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(10): Show | 13 | HG00544.hp2 HG01081.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-4814C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368178 | ||||||
| chr12:50368241
|
G | A | 315 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.193-4877C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368241 | ||||||
| chr12:50368337
|
C | T | 319 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.193-4973G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368337 | ||||||
| chr12:50368340
|
T | C | 319 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.193-4976A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368340 | ||||||
| chr12:50368366
|
T | C | 319 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.193-5002A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368366 | ||||||
| chr12:50368391
|
C | T | 1 | a0003c0003t0001g0289 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.193-5027G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368391 | ||||||
| chr12:50368578
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-5214C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368578 | ||||||
| chr12:50368706
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-5342C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368706 | ||||||
| chr12:50368976
|
A | AAC | 22 | a0002c0002t0001g0116a0002c0002t0001g0126a0002c0002t0001g0135others(19): Show | 22 | HG01884.hp2 HG02155.hp2 HG02970.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-5613_193-5612i others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368976 | ||||||
| chr12:50368978
|
A | AC | 74 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0073others(71): Show | 74 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.193-5615_193-5614i others(3): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368978 | ||||||
| chr12:50368978
|
A | C | 24 | a0002c0002t0001g0116a0002c0002t0001g0126a0002c0002t0001g0135others(21): Show | 24 | HG01167.hp1 HG01884.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-5614T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50368978 | ||||||
| chr12:50369221
|
T | C | 1 | a0003c0003t0001g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193-5857A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369221 | ||||||
| chr12:50369287
|
G | A | 9 | a0002c0002t0001g0113a0002c0002t0001g0132a0002c0002t0001g0133others(6): Show | 9 | HG00408.hp2 HG02083.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-5923C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369287 | ||||||
| chr12:50369357
|
G | T | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-5993C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369357 | ||||||
| chr12:50369415
|
C | T | 104 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.193-6051G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369415 | ||||||
| chr12:50369496
|
C | CA | 211 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(208): Show | 211 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.193-6133dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369496 | ||||||
| chr12:50369496
|
CA | C | 98 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.193-6133delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369496 | ||||||
| chr12:50369584
|
C | T | 1 | a0007c0008t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-6220G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369584 | ||||||
| chr12:50369632
|
G | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-6268C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369632 | ||||||
| chr12:50369642
|
C | T | 3 | a0003c0003t0001g0029a0003c0003t0001g0086a0003c0003t0001g0100 | 3 | HG01167.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.193-6278G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369642 | ||||||
| chr12:50369701
|
A | C | 95 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.193-6337T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369701 | ||||||
| chr12:50369713
|
C | T | 1 | a0009c0012t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-6349G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369713 | ||||||
| chr12:50369852
|
C | T | 2 | a0003c0003t0001g0081a0004c0004t0001g0281 | 2 | HG01071.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.193-6488G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369852 | ||||||
| chr12:50369984
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0332 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.193-6620G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50369984 | ||||||
| chr12:50370013
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.193-6649T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370013 | ||||||
| chr12:50370103
|
G | A | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-6739C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370103 | ||||||
| chr12:50370123
|
C | CA | 172 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0013others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.193-6760dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370123 | ||||||
| chr12:50370123
|
C | CAA | 36 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0023others(33): Show | 36 | HG00408.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.193-6761_193-6760d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370123 | ||||||
| chr12:50370123
|
C | CAAAAAA | 72 | a0003c0003t0001g0030a0003c0003t0001g0049a0003c0003t0001g0051others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.193-6765_193-6760d others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370123 | ||||||
| chr12:50370123
|
C | CAAAAAAA | 32 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(29): Show | 32 | HG00438.hp2 HG00673.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.193-6766_193-6760d others(9): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370123 | ||||||
| chr12:50370183
|
A | G | 4 | a0008c0009t0001g0111a0008c0009t0001g0112a0008c0009t0001g0139others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-6819T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370183 | ||||||
| chr12:50370252
|
C | T | 1 | a0003c0014t0001g0107 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.193-6888G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370252 | ||||||
| chr12:50370253
|
G | A | 1 | a0003c0003t0001g0260 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193-6889C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370253 | ||||||
| chr12:50370269
|
A | G | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-6905T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370269 | ||||||
| chr12:50370384
|
A | C | 7 | a0003c0003t0001g0008a0003c0003t0001g0125a0003c0003t0001g0210others(4): Show | 7 | HG00438.hp2 HG02071.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-7020T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370384 | ||||||
| chr12:50370790
|
T | C | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-7426A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370790 | ||||||
| chr12:50370817
|
C | T | 112 | a0002c0002t0001g0009a0002c0002t0001g0073a0002c0002t0001g0113others(109): Show | 112 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.193-7453G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370817 | ||||||
| chr12:50370928
|
G | A | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(214): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.193-7564C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50370928 | ||||||
| chr12:50371007
|
A | G | 319 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.193-7643T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371007 | ||||||
| chr12:50371053
|
T | C | 99 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.193-7689A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371053 | ||||||
| chr12:50371396
|
C | A | 1 | a0003c0003t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-8032G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371396 | ||||||
| chr12:50371413
|
G | A | 1 | a0003c0003t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.193-8049C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371413 | ||||||
| chr12:50371483
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-8119C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371483 | ||||||
| chr12:50371834
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.193-8470G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371834 | ||||||
| chr12:50371950
|
T | C | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.193-8586A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50371950 | ||||||
| chr12:50372231
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.193-8867T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372231 | ||||||
| chr12:50372379
|
G | C | 1 | a0001c0001t0001g0258 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.193-9015C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372379 | ||||||
| chr12:50372416
|
AC | A | 316 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.193-9053delG | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372416 | ||||||
| chr12:50372666
|
C | T | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-9302G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372666 | ||||||
| chr12:50372698
|
G | A | 2 | a0002c0011t0001g0118a0002c0011t0001g0119 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193-9334C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372698 | ||||||
| chr12:50372729
|
C | T | 2 | a0009c0012t0001g0234a0009c0012t0001g0235 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-9365G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372729 | ||||||
| chr12:50372806
|
G | A | 3 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0239 | 3 | HG00673.hp1 NA18747.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.193-9442C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372806 | ||||||
| chr12:50372850
|
G | A | 1 | a0029c0025t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193-9486C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372850 | ||||||
| chr12:50372855
|
G | A | 1 | a0002c0002t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.193-9491C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372855 | ||||||
| chr12:50372898
|
C | T | 1 | a0003c0003t0001g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193-9534G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372898 | ||||||
| chr12:50372901
|
C | T | 1 | a0004c0027t0001g0285 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.193-9537G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372901 | ||||||
| chr12:50372978
|
G | C | 1 | a0003c0003t0001g0212 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193-9614C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372978 | ||||||
| chr12:50372980
|
G | GAGGA | 10 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0057others(7): Show | 10 | HG00642.hp1 HG01517.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-9620_193-9617d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372980 | ||||||
| chr12:50372980
|
G | GAGGAAGG others(1): Show |
4 | a0001c0001t0001g0094a0001c0001t0001g0291a0001c0001t0001g0303others(1): Show | 4 | HG01192.hp2 HG01256.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-9624_193-9617d others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372980 | ||||||
| chr12:50372983
|
G | A | 1 | a0003c0014t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193-9619C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372983 | ||||||
| chr12:50372984
|
A | G | 1 | a0003c0003t0001g0212 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193-9620T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372984 | ||||||
| chr12:50372994
|
G | GGAAA | 13 | a0002c0002t0001g0152a0002c0002t0001g0168a0002c0002t0001g0250others(10): Show | 13 | HG00099.hp1 HG00597.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-9631_193-9630i others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
G | GGAAAGAA others(1): Show |
9 | a0002c0002t0001g0135a0002c0002t0001g0181a0002c0002t0001g0319others(6): Show | 9 | HG01496.hp2 HG01978.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-9631_193-9630i others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
G | GGAAAGAA others(5): Show |
5 | a0002c0002t0001g0117a0002c0002t0001g0184a0003c0003t0001g0087others(2): Show | 5 | HG02155.hp2 HG02165.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-9631_193-9630i others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
G | GGAAAGAA others(9): Show |
3 | a0002c0002t0001g0180a0003c0003t0001g0269a0004c0004t0001g0284 | 3 | HG01192.hp1 HG04115.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.193-9631_193-9630i others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
G | GGAAGGAA others(5): Show |
1 | a0013c0017t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.193-9631_193-9630i others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAAT | G | 55 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0036others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.193-9634_193-9631d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(1): Show |
G | 57 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0042others(54): Show | 57 | HG00544.hp1 HG00673.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.193-9638_193-9631d others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(5): Show |
G | 47 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0032others(44): Show | 47 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.193-9642_193-9631d others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(9): Show |
G | 28 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0028others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.193-9646_193-9631d others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(13): Show |
G | 10 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0080others(7): Show | 10 | HG00597.hp1 HG01081.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-9650_193-9631d others(22): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(17): Show |
G | 5 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0021others(2): Show | 5 | HG01934.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-9654_193-9631d others(26): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(21): Show |
G | 1 | a0002c0002t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-9658_193-9631d others(30): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372994
|
GGAATGAA others(45): Show |
G | 1 | a0003c0003t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.193-9682_193-9631d others(54): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372994 | ||||||
| chr12:50372995
|
GAATGAAA others(6): Show |
G | 1 | a0002c0002t0001g0141 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.193-9644_193-9632d others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372995 | ||||||
| chr12:50372998
|
T | A | 82 | a0001c0001t0001g0094a0001c0001t0001g0291a0001c0001t0001g0303others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.193-9634A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50372998
|
T | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.193-9634A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50372998
|
TGAAAGAA others(1): Show |
T | 5 | a0005c0005t0001g0108a0005c0005t0001g0218a0005c0005t0001g0223others(2): Show | 5 | HG02572.hp2 HG02622.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-9642_193-9635d others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50372998
|
TGAAAGAA others(5): Show |
T | 1 | a0005c0005t0001g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.193-9646_193-9635d others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50372998
|
TGAAAGAA others(9): Show |
T | 3 | a0005c0005t0001g0220a0008c0009t0001g0111a0008c0009t0001g0112 | 3 | HG02572.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.193-9650_193-9635d others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50372998
|
TGAAAGAA others(13): Show |
T | 1 | a0005c0005t0001g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.193-9654_193-9635d others(22): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50372998
|
TGAAAGAA others(17): Show |
T | 1 | a0005c0005t0001g0222 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.193-9658_193-9635d others(26): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50372998 | ||||||
| chr12:50373002
|
A | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.193-9638T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373002 | ||||||
| chr12:50373006
|
A | G | 41 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0025others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-9642T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373006 | ||||||
| chr12:50373010
|
A | G | 31 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(28): Show | 31 | HG01123.hp1 HG01257.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.193-9646T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373010 | ||||||
| chr12:50373014
|
A | G | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0020others(23): Show | 26 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.193-9650T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373014 | ||||||
| chr12:50373018
|
A | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0020others(14): Show | 17 | HG00438.hp1 HG00544.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.193-9654T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373018 | ||||||
| chr12:50373022
|
A | G | 13 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(10): Show | 13 | HG01081.hp2 HG01934.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-9658T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373022 | ||||||
| chr12:50373026
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0021 | 3 | HG01934.hp2 NA18953.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.193-9662T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373026 | ||||||
| chr12:50373044
|
AAAGAAAG others(4): Show |
A | 1 | a0003c0003t0001g0217 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.193-9691_193-9681d others(13): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373044 | ||||||
| chr12:50373051
|
GAAAGAAA others(15): Show |
G | 1 | a0003c0003t0001g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.193-9709_193-9688d others(24): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373051 | ||||||
| chr12:50373055
|
GAAAGAAA others(6): Show |
G | 2 | a0003c0003t0001g0206a0006c0007t0001g0150 | 2 | HG03516.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.193-9704_193-9692d others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373055 | ||||||
| chr12:50373059
|
GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.193-9708_193-9696d others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373059 | ||||||
| chr12:50373059
|
GAAAGAAA others(7): Show |
G | 1 | a0003c0003t0001g0030 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.193-9709_193-9696d others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373059 | ||||||
| chr12:50373063
|
GAAAGAAA others(3): Show |
G | 1 | a0025c0035t0001g0060 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.193-9709_193-9700d others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373063 | ||||||
| chr12:50373077
|
G | A | 2 | a0003c0003t0001g0212a0003c0003t0001g0315 | 2 | NA18954.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.193-9713C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373077 | ||||||
| chr12:50373119
|
TGG | T | 96 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.193-9757_193-9756d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373119 | ||||||
| chr12:50373254
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG01175.hp2 HG01255.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-9890C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373254 | ||||||
| chr12:50373260
|
G | A | 5 | a0005c0005t0001g0220a0005c0005t0001g0222a0005c0005t0001g0223others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-9896C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373260 | ||||||
| chr12:50373339
|
G | A | 2 | a0007c0008t0001g0088a0007c0023t0001g0054 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.193-9975C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373339 | ||||||
| chr12:50373378
|
C | T | 1 | a0002c0002t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193-10014G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373378 | ||||||
| chr12:50373447
|
C | A | 2 | a0008c0009t0001g0111a0008c0009t0001g0112 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.193-10083G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373447 | ||||||
| chr12:50373462
|
G | A | 102 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0009others(99): Show | 102 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.193-10098C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373462 | ||||||
| chr12:50373502
|
C | A | 96 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.193-10138G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373502 | ||||||
| chr12:50373589
|
C | T | 1 | a0001c0039t0001g0064 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.193-10225G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373589 | ||||||
| chr12:50373590
|
A | G | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-10226T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373590 | ||||||
| chr12:50373692
|
C | T | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-10328G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373692 | ||||||
| chr12:50373852
|
G | A | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-10488C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373852 | ||||||
| chr12:50373869
|
T | C | 103 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0009others(100): Show | 103 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.193-10505A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373869 | ||||||
| chr12:50373944
|
A | G | 3 | a0002c0011t0001g0118a0002c0011t0001g0119a0002c0011t0001g0166 | 3 | HG01891.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.193-10580T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50373944 | ||||||
| chr12:50374045
|
G | A | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-10681C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374045 | ||||||
| chr12:50374098
|
C | A | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.193-10734G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374098 | ||||||
| chr12:50374158
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0261 | 2 | NA18975.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.193-10794C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374158 | ||||||
| chr12:50374202
|
G | A | 1 | a0006c0007t0001g0164 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193-10838C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374202 | ||||||
| chr12:50374362
|
A | G | 1 | a0002c0002t0001g0326 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.193-10998T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374362 | ||||||
| chr12:50374448
|
T | C | 1 | a0002c0033t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193-11084A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374448 | ||||||
| chr12:50374452
|
G | T | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.193-11088C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374452 | ||||||
| chr12:50374528
|
C | T | 1 | a0003c0003t0001g0204 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.193-11164G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374528 | ||||||
| chr12:50374556
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.193-11192G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374556 | ||||||
| chr12:50374728
|
G | T | 1 | a0003c0003t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.193-11364C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374728 | ||||||
| chr12:50374998
|
C | T | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-11634G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50374998 | ||||||
| chr12:50375086
|
G | A | 250 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.193-11722C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375086 | ||||||
| chr12:50375247
|
C | T | 1 | a0003c0003t0001g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.193-11883G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375247 | ||||||
| chr12:50375329
|
C | T | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-11965G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375329 | ||||||
| chr12:50375537
|
G | A | 1 | a0002c0033t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193-12173C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375537 | ||||||
| chr12:50375549
|
C | CA | 10 | a0001c0001t0001g0095a0001c0001t0001g0102a0002c0002t0001g0178others(7): Show | 10 | HG02055.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-12186dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375549 | ||||||
| chr12:50375549
|
CA | C | 13 | a0001c0001t0001g0195a0001c0001t0001g0227a0002c0002t0001g0133others(10): Show | 13 | HG00099.hp1 HG01069.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.193-12186delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375549 | ||||||
| chr12:50375632
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.193-12268C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375632 | ||||||
| chr12:50375727
|
AG | A | 234 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.193-12364delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375727 | ||||||
| chr12:50375728
|
G | A | 75 | a0002c0002t0001g0009a0002c0033t0001g0321a0003c0003t0001g0008others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.193-12364C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375728 | ||||||
| chr12:50375906
|
C | T | 1 | a0022c0029t0001g0201 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.193-12542G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375906 | ||||||
| chr12:50375911
|
C | G | 1 | a0002c0002t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.193-12547G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375911 | ||||||
| chr12:50375944
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0091 | 2 | NA18747.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.193-12580A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50375944 | ||||||
| chr12:50376234
|
G | A | 1 | a0003c0003t0001g0212 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193-12870C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376234 | ||||||
| chr12:50376302
|
T | G | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-12938A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376302 | ||||||
| chr12:50376364
|
G | C | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-13000C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376364 | ||||||
| chr12:50376508
|
G | T | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-13144C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376508 | ||||||
| chr12:50376729
|
C | CCT | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-13367_193-1336 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376729 | ||||||
| chr12:50376746
|
CT | C | 305 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.193-13383delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376746 | ||||||
| chr12:50376747
|
T | TC | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-13384_193-1338 others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50376747 | ||||||
| chr12:50377044
|
C | A | 1 | a0007c0008t0001g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.193-13680G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377044 | ||||||
| chr12:50377079
|
G | A | 63 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.193-13715C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377079 | ||||||
| chr12:50377217
|
G | A | 1 | a0025c0035t0001g0060 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.193-13853C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377217 | ||||||
| chr12:50377307
|
A | G | 196 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.193-13943T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377307 | ||||||
| chr12:50377358
|
AG | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.193-13995delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377358 | ||||||
| chr12:50377478
|
A | ATACT | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-14115_193-1411 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377478 | ||||||
| chr12:50377558
|
C | T | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-14194G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377558 | ||||||
| chr12:50377591
|
G | T | 250 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.193-14227C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377591 | ||||||
| chr12:50377694
|
G | A | 1 | a0003c0003t0001g0262 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.193-14330C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377694 | ||||||
| chr12:50377757
|
C | A | 1 | a0003c0003t0001g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.193-14393G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377757 | ||||||
| chr12:50377834
|
C | CA | 305 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.193-14471dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377834 | ||||||
| chr12:50377834
|
C | CAA | 7 | a0002c0002t0001g0113a0002c0002t0001g0132a0002c0002t0001g0133others(4): Show | 7 | HG00408.hp2 HG02083.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-14472_193-1447 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377834 | ||||||
| chr12:50377844
|
A | C | 1 | a0005c0005t0001g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-14480T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377844 | ||||||
| chr12:50377925
|
T | G | 3 | a0003c0003t0001g0029a0003c0003t0001g0086a0003c0003t0001g0100 | 3 | HG01167.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.193-14561A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377925 | ||||||
| chr12:50377946
|
G | A | 1 | a0017c0043t0001g0306 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.193-14582C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50377946 | ||||||
| chr12:50378051
|
C | T | 1 | a0002c0002t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.193-14687G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378051 | ||||||
| chr12:50378155
|
C | T | 1 | a0001c0001t0001g0332 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-14791G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378155 | ||||||
| chr12:50378172
|
C | T | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-14808G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378172 | ||||||
| chr12:50378210
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0012 | 2 | NA18991.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.193-14846C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378210 | ||||||
| chr12:50378224
|
C | CA | 12 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(9): Show | 12 | HG02258.hp2 HG02572.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.193-14861dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378224 | ||||||
| chr12:50378224
|
CA | C | 312 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.193-14861delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378224 | ||||||
| chr12:50378296
|
C | T | 1 | a0004c0004t0001g0276 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.193-14932G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378296 | ||||||
| chr12:50378303
|
G | T | 63 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.193-14939C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378303 | ||||||
| chr12:50378433
|
G | A | 6 | a0002c0002t0001g0325a0002c0002t0001g0327a0002c0002t0001g0328others(3): Show | 6 | HG01346.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-15069C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378433 | ||||||
| chr12:50378503
|
C | A | 133 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.193-15139G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378503 | ||||||
| chr12:50378558
|
G | GTATA | 5 | a0005c0005t0001g0220a0005c0005t0001g0222a0005c0005t0001g0223others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-15198_193-1519 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378558 | ||||||
| chr12:50378558
|
G | GTATATA | 4 | a0002c0002t0001g0152a0002c0002t0001g0319a0002c0002t0001g0320others(1): Show | 4 | HG03486.hp1 NA18948.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-15200_193-1519 others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378558 | ||||||
| chr12:50378558
|
G | GTATATAT others(3): Show |
3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.193-15204_193-1519 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378558 | ||||||
| chr12:50378558
|
G | GTATATAT others(5): Show |
1 | a0010c0019t0001g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193-15206_193-1519 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378558 | ||||||
| chr12:50378560
|
ATATATAT others(22): Show |
A | 59 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(56): Show | 59 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.193-15225_193-1519 others(33): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378560 | ||||||
| chr12:50378562
|
ATATATAT others(20): Show |
A | 2 | a0001c0001t0001g0068a0003c0003t0001g0213 | 2 | HG02155.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.193-15225_193-1519 others(31): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378562 | ||||||
| chr12:50378564
|
ATATATAT others(18): Show |
A | 126 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.193-15225_193-1520 others(29): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378564 | ||||||
| chr12:50378566
|
ATATATAT others(16): Show |
A | 100 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 100 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.193-15225_193-1520 others(27): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378566 | ||||||
| chr12:50378568
|
ATATATAC others(14): Show |
A | 11 | a0001c0001t0001g0074a0002c0002t0001g0116a0002c0002t0001g0117others(8): Show | 11 | HG01346.hp2 HG01884.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-15225_193-1520 others(25): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378568 | ||||||
| chr12:50378570
|
ATATACAC others(12): Show |
A | 2 | a0002c0002t0001g0185a0002c0002t0001g0327 | 2 | HG02976.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.193-15225_193-1520 others(23): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378570 | ||||||
| chr12:50378589
|
G | GTA | 11 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(8): Show | 11 | HG02258.hp2 HG02572.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-15227_193-1522 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378589 | ||||||
| chr12:50378589
|
G | GTATATA | 4 | a0007c0008t0001g0246a0007c0008t0001g0247a0007c0008t0001g0248others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-15231_193-1522 others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378589 | ||||||
| chr12:50378589
|
G | GTATATAT others(30136): Show |
1 | a0002c0002t0001g0319 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.193-15226_193-1522 others(30147): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378589 | ||||||
| chr12:50378589
|
G | GTATATAT others(15044): Show |
1 | a0002c0002t0001g0320 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.193-15226_193-1522 others(15055): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378589 | ||||||
| chr12:50378594
|
T | TATATATA others(9): Show |
3 | a0003c0003t0001g0029a0003c0003t0001g0086a0003c0003t0001g0100 | 3 | HG01167.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.193-15231_193-1523 others(20): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378594 | ||||||
| chr12:50378602
|
T | C | 5 | a0001c0001t0001g0293a0003c0003t0001g0289a0013c0017t0001g0003others(2): Show | 5 | HG01168.hp1 HG02055.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-15238A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378602 | ||||||
| chr12:50378618
|
GTA | G | 66 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(63): Show | 66 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.193-15256_193-1525 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378618 | ||||||
| chr12:50378618
|
GTATA | G | 250 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.193-15258_193-1525 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378618 | ||||||
| chr12:50378671
|
A | T | 3 | a0002c0011t0001g0118a0002c0011t0001g0119a0002c0011t0001g0166 | 3 | HG01891.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.193-15307T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378671 | ||||||
| chr12:50378681
|
A | T | 1 | a0010c0019t0001g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193-15317T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378681 | ||||||
| chr12:50378784
|
G | A | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.193-15420C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378784 | ||||||
| chr12:50378963
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.193-15599C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50378963 | ||||||
| chr12:50379082
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.193-15718T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379082 | ||||||
| chr12:50379109
|
G | A | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193-15745C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379109 | ||||||
| chr12:50379169
|
G | A | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-15805C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379169 | ||||||
| chr12:50379207
|
G | C | 1 | a0003c0003t0001g0232 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.193-15843C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379207 | ||||||
| chr12:50379332
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.193-15968G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379332 | ||||||
| chr12:50379439
|
CA | C | 249 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.193-16076delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379439 | ||||||
| chr12:50379468
|
A | G | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.193-16104T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379468 | ||||||
| chr12:50379469
|
A | G | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.193-16105T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379469 | ||||||
| chr12:50379472
|
AC | A | 163 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.193-16109delG | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379472 | ||||||
| chr12:50379473
|
C | A | 149 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(146): Show | 149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.193-16109G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379473 | ||||||
| chr12:50379478
|
A | C | 1 | a0002c0002t0001g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.193-16114T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379478 | ||||||
| chr12:50379479
|
C | A | 3 | a0002c0033t0001g0321a0003c0003t0001g0289a0013c0017t0001g0003 | 3 | HG01168.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.193-16115G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379479 | ||||||
| chr12:50379481
|
A | C | 2 | a0002c0033t0001g0321a0013c0017t0001g0003 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.193-16117T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379481 | ||||||
| chr12:50379483
|
AAC | A | 306 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.193-16121_193-1612 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379483 | ||||||
| chr12:50379484
|
AC | A | 5 | a0007c0008t0001g0248a0008c0009t0001g0111a0008c0009t0001g0112others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-16121delG | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379484 | ||||||
| chr12:50379485
|
C | A | 3 | a0002c0033t0001g0321a0003c0003t0001g0289a0013c0017t0001g0003 | 3 | HG01168.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.193-16121G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379485 | ||||||
| chr12:50379509
|
G | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0305 | 2 | HG00099.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.193-16145C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379509 | ||||||
| chr12:50379686
|
TGAGGCAG others(25): Show |
T | 1 | a0009c0012t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-16354_193-1632 others(36): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379686 | ||||||
| chr12:50379701
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.193-16337C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379701 | ||||||
| chr12:50379867
|
A | C | 1 | a0019c0032t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+16426T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379867 | ||||||
| chr12:50379904
|
G | A | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.192+16389C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379904 | ||||||
| chr12:50379964
|
GGAAA | G | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.192+16325_192+1632 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50379964 | ||||||
| chr12:50380063
|
A | T | 1 | a0002c0002t0001g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.192+16230T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380063 | ||||||
| chr12:50380071
|
C | T | 1 | a0003c0003t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192+16222G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380071 | ||||||
| chr12:50380123
|
C | T | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192+16170G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380123 | ||||||
| chr12:50380197
|
G | A | 316 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.192+16096C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380197 | ||||||
| chr12:50380273
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.192+16020T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380273 | ||||||
| chr12:50380473
|
C | T | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.192+15820G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380473 | ||||||
| chr12:50380521
|
CA | C | 16 | a0002c0002t0001g0116a0002c0002t0001g0149a0002c0002t0001g0167others(13): Show | 16 | HG01934.hp1 HG01978.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.192+15771delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380521 | ||||||
| chr12:50380521
|
CAA | C | 95 | a0001c0001t0001g0033a0001c0001t0001g0196a0002c0002t0001g0009others(92): Show | 95 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.192+15770_192+1577 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380521 | ||||||
| chr12:50380521
|
CAAA | C | 150 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.192+15769_192+1577 others(7): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380521 | ||||||
| chr12:50380521
|
CAAAA | C | 60 | a0001c0001t0001g0066a0003c0003t0001g0008a0003c0003t0001g0022others(57): Show | 60 | HG00140.hp2 HG00408.hp1 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.192+15768_192+1577 others(8): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380521 | ||||||
| chr12:50380761
|
G | A | 2 | a0003c0003t0001g0029a0003c0003t0001g0100 | 2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.192+15532C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380761 | ||||||
| chr12:50380895
|
G | C | 1 | a0003c0003t0001g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192+15398C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380895 | ||||||
| chr12:50380987
|
A | AG | 331 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.192+15305dupC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50380987 | ||||||
| chr12:50381152
|
C | A | 250 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.192+15141G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50381152 | ||||||
| chr12:50381322
|
G | A | 1 | a0017c0043t0001g0306 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.192+14971C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50381322 | ||||||
| chr12:50381496
|
G | A | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.192+14797C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50381496 | ||||||
| chr12:50381630
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.192+14663C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50381630 | ||||||
| chr12:50381673
|
C | G | 313 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.192+14620G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50381673 | ||||||
| chr12:50382031
|
T | G | 63 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.192+14262A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382031 | ||||||
| chr12:50382134
|
G | A | 5 | a0007c0008t0001g0246a0007c0008t0001g0247a0007c0008t0001g0248others(2): Show | 5 | HG02109.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+14159C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382134 | ||||||
| chr12:50382220
|
T | G | 63 | a0003c0003t0001g0008a0003c0003t0001g0022a0003c0003t0001g0027others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.192+14073A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382220 | ||||||
| chr12:50382246
|
C | CA | 66 | a0001c0001t0001g0071a0002c0002t0001g0073a0003c0003t0001g0008others(63): Show | 66 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.192+14046dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382246 | ||||||
| chr12:50382246
|
CA | C | 29 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0079others(26): Show | 29 | HG00140.hp1 HG00438.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.192+14046delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382246 | ||||||
| chr12:50382297
|
C | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+13996G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382297 | ||||||
| chr12:50382407
|
T | C | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192+13886A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382407 | ||||||
| chr12:50382575
|
C | T | 5 | a0013c0017t0001g0003a0013c0017t0001g0131a0015c0016t0001g0004others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+13718G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382575 | ||||||
| chr12:50382908
|
A | G | 253 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.192+13385T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382908 | ||||||
| chr12:50382954
|
C | T | 1 | a0003c0003t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192+13339G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382954 | ||||||
| chr12:50382963
|
C | T | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+13330G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50382963 | ||||||
| chr12:50383226
|
G | C | 2 | a0002c0002t0001g0186a0002c0002t0001g0187 | 2 | NA18963.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.192+13067C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383226 | ||||||
| chr12:50383249
|
T | TAAAAAAA | 7 | a0002c0002t0001g0116a0002c0002t0001g0170a0002c0002t0001g0172others(4): Show | 7 | HG01884.hp2 HG02970.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+13037_192+1304 others(11): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383249
|
T | TAAAAAAA others(1): Show |
13 | a0002c0002t0001g0135a0002c0002t0001g0138a0002c0002t0001g0175others(10): Show | 13 | HG02155.hp2 HG03098.hp1 HG03486.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+13036_192+1304 others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383249
|
T | TAAAAAAA others(4): Show |
6 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+13033_192+1304 others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383249
|
TA | T | 7 | a0002c0002t0001g0113a0002c0002t0001g0132a0005c0005t0001g0220others(4): Show | 7 | HG02083.hp1 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+13043delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383249
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0045a0001c0001t0001g0076a0007c0008t0001g0246others(4): Show | 7 | HG02109.hp2 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+13036_192+1304 others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383249
|
TAAAAAAA others(3): Show |
T | 3 | a0001c0001t0001g0020a0001c0001t0001g0026a0006c0007t0001g0150 | 3 | HG02523.hp1 HG03516.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.192+13034_192+1304 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383249
|
TAAAAAAA others(5): Show |
T | 4 | a0006c0007t0001g0038a0006c0007t0001g0164a0006c0007t0001g0193others(1): Show | 4 | HG01167.hp1 HG02630.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+13032_192+1304 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383249 | ||||||
| chr12:50383276
|
A | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(5): Show | 8 | HG02523.hp1 HG02559.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+13017T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383276 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(9): Show |
1 | a0003c0003t0001g0273 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.192+13014_192+1301 others(20): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(8): Show |
1 | a0003c0003t0001g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.192+13014_192+1301 others(19): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(7): Show |
1 | a0002c0006t0001g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.192+13014_192+1301 others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0018 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.192+13014_192+1301 others(20): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0271 | 2 | HG03492.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.192+13014_192+1301 others(19): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(5): Show |
2 | a0002c0002t0001g0168a0002c0006t0001g0177 | 2 | HG02293.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.192+13014_192+1301 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(7): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0074others(1): Show | 4 | HG01192.hp1 HG01255.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(4): Show |
9 | a0002c0002t0001g0009a0002c0002t0001g0133a0002c0002t0001g0137others(6): Show | 9 | HG01978.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(6): Show |
26 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0014others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(17): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(3): Show |
18 | a0002c0002t0001g0115a0002c0002t0001g0120a0002c0002t0001g0121others(15): Show | 18 | HG00408.hp2 HG00738.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(5): Show |
43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0047others(40): Show | 43 | HG00099.hp1 HG00544.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.192+13014_192+1301 others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(2): Show |
13 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154others(10): Show | 13 | HG01346.hp2 HG01891.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(13): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(4): Show |
37 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0033others(34): Show | 37 | HG00673.hp2 HG01069.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0017 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.192+13014_192+1301 others(17): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(3): Show |
15 | a0001c0001t0001g0301a0001c0001t0001g0312a0002c0002t0001g0117others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAA others(5): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0063a0001c0001t0001g0065others(2): Show | 5 | HG01515.hp2 HG01517.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAAG others(4): Show |
6 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0196others(3): Show | 6 | HG00642.hp1 HG01071.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+13014_192+1301 others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAGA others(3): Show |
1 | a0001c0001t0001g0195 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.192+13014_192+1301 others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | AAAAAAGA others(5): Show |
1 | a0030c0040t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.192+13014_192+1301 others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
A | G | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(11): Show | 14 | HG02083.hp1 HG02523.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.192+13015T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383278
|
AAG | A | 48 | a0003c0003t0001g0008a0003c0003t0001g0027a0003c0003t0001g0029others(45): Show | 48 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.192+13013_192+1301 others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383278 | ||||||
| chr12:50383279
|
AG | A | 8 | a0003c0003t0001g0022a0003c0003t0001g0049a0003c0003t0001g0078others(5): Show | 8 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+13013delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383279 | ||||||
| chr12:50383280
|
G | A | 1 | a0003c0003t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.192+13013C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383280 | ||||||
| chr12:50383482
|
G | A | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192+12811C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383482 | ||||||
| chr12:50383552
|
C | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+12741G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383552 | ||||||
| chr12:50383650
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.192+12643G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383650 | ||||||
| chr12:50383790
|
C | A | 14 | a0004c0004t0001g0255a0004c0004t0001g0256a0004c0004t0001g0274others(11): Show | 14 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+12503G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383790 | ||||||
| chr12:50383846
|
G | A | 7 | a0002c0002t0001g0167a0002c0002t0001g0191a0002c0002t0001g0240others(4): Show | 7 | NA18612.hp1 NA18959.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+12447C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383846 | ||||||
| chr12:50383869
|
C | T | 1 | a0002c0002t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.192+12424G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50383869 | ||||||
| chr12:50384004
|
G | A | 1 | a0003c0003t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.192+12289C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384004 | ||||||
| chr12:50384317
|
C | T | 2 | a0002c0002t0001g0009a0002c0033t0001g0321 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.192+11976G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384317 | ||||||
| chr12:50384446
|
A | C | 1 | a0002c0002t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+11847T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384446 | ||||||
| chr12:50384521
|
C | T | 14 | a0004c0004t0001g0255a0004c0004t0001g0256a0004c0004t0001g0274others(11): Show | 14 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+11772G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384521 | ||||||
| chr12:50384547
|
A | G | 5 | a0007c0008t0001g0246a0007c0008t0001g0247a0007c0008t0001g0248others(2): Show | 5 | HG02109.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+11746T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384547 | ||||||
| chr12:50384616
|
A | G | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+11677T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384616 | ||||||
| chr12:50384668
|
AG | A | 133 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.192+11624delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384668 | ||||||
| chr12:50384670
|
C | A | 133 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.192+11623G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384670 | ||||||
| chr12:50384802
|
A | G | 5 | a0005c0005t0001g0220a0005c0005t0001g0222a0005c0005t0001g0223others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+11491T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384802 | ||||||
| chr12:50384869
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.192+11424C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384869 | ||||||
| chr12:50384969
|
C | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.192+11324G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50384969 | ||||||
| chr12:50385173
|
A | G | 1 | a0003c0003t0001g0262 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.192+11120T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385173 | ||||||
| chr12:50385186
|
G | A | 250 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.192+11107C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385186 | ||||||
| chr12:50385276
|
G | C | 4 | a0013c0017t0001g0003a0015c0016t0001g0004a0015c0016t0001g0005others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+11017C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385276 | ||||||
| chr12:50385417
|
C | CA | 11 | a0002c0002t0001g0116a0002c0002t0001g0134a0002c0002t0001g0172others(8): Show | 11 | HG00408.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+10875dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385417 | ||||||
| chr12:50385417
|
CA | C | 11 | a0001c0001t0001g0312a0002c0002t0001g0259a0002c0002t0001g0320others(8): Show | 11 | HG00408.hp1 HG01168.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+10875delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385417 | ||||||
| chr12:50385448
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.192+10845G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385448 | ||||||
| chr12:50385542
|
T | C | 1 | a0002c0002t0001g0168 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.192+10751A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385542 | ||||||
| chr12:50385550
|
T | C | 1 | a0003c0003t0001g0298 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.192+10743A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385550 | ||||||
| chr12:50385563
|
A | G | 1 | a0002c0002t0001g0117 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.192+10730T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385563 | ||||||
| chr12:50385729
|
C | T | 1 | a0026c0034t0001g0136 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.192+10564G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385729 | ||||||
| chr12:50385901
|
CA | C | 6 | a0001c0001t0001g0104a0003c0003t0001g0288a0008c0009t0001g0111others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+10391delT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50385901 | ||||||
| chr12:50386112
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.192+10181T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386112 | ||||||
| chr12:50386248
|
G | GC | 65 | a0001c0001t0001g0023a0001c0001t0001g0075a0003c0003t0001g0008others(62): Show | 65 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.192+10044dupG | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386248 | ||||||
| chr12:50386256
|
C | T | 2 | a0002c0002t0001g0009a0002c0033t0001g0321 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.192+10037G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386256 | ||||||
| chr12:50386263
|
C | T | 316 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.192+10030G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386263 | ||||||
| chr12:50386456
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.192+9837T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386456 | ||||||
| chr12:50386578
|
A | C | 106 | a0001c0001t0001g0195a0001c0001t0001g0196a0002c0002t0001g0113others(103): Show | 106 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.192+9715T>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386578 | ||||||
| chr12:50386832
|
G | A | 11 | a0001c0001t0001g0036a0001c0001t0001g0300a0001c0001t0001g0301others(8): Show | 11 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+9461C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386832 | ||||||
| chr12:50386907
|
T | G | 138 | a0001c0001t0001g0059a0001c0001t0001g0189a0001c0001t0001g0190others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.192+9386A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50386907 | ||||||
| chr12:50387223
|
C | G | 9 | a0003c0003t0001g0049a0003c0003t0001g0050a0003c0003t0001g0055others(6): Show | 9 | HG02257.hp2 HG02280.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+9070G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387223 | ||||||
| chr12:50387268
|
G | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+9025C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387268 | ||||||
| chr12:50387393
|
A | G | 107 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(104): Show | 107 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.192+8900T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387393 | ||||||
| chr12:50387562
|
C | A | 32 | a0001c0001t0001g0189a0001c0001t0001g0190a0002c0002t0001g0116others(29): Show | 32 | HG00438.hp2 HG01884.hp2 HG02155.hp2 others(29): Show |
intron_variant | MODIFIER | c.192+8731G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387562 | ||||||
| chr12:50387819
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.192+8474G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387819 | ||||||
| chr12:50387874
|
G | T | 3 | a0008c0009t0001g0111a0008c0009t0001g0112a0019c0032t0001g0231 | 3 | HG02572.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192+8419C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387874 | ||||||
| chr12:50387933
|
T | C | 331 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.192+8360A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50387933 | ||||||
| chr12:50388077
|
G | C | 1 | a0004c0027t0001g0285 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.192+8216C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388077 | ||||||
| chr12:50388114
|
C | T | 3 | a0009c0012t0001g0233a0009c0012t0001g0234a0009c0012t0001g0235 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.192+8179G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388114 | ||||||
| chr12:50388164
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG00140.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.192+8129G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388164 | ||||||
| chr12:50388330
|
T | C | 318 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.192+7963A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388330 | ||||||
| chr12:50388359
|
CTGTAATC others(7): Show |
C | 1 | a0003c0020t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.192+7920_192+7933d others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388359 | ||||||
| chr12:50388387
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.192+7906C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388387 | ||||||
| chr12:50388415
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.192+7878G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388415 | ||||||
| chr12:50388533
|
C | A | 2 | a0005c0005t0001g0226a0005c0005t0001g0251 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+7760G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388533 | ||||||
| chr12:50388615
|
G | A | 22 | a0001c0001t0001g0189a0001c0001t0001g0190a0002c0002t0001g0126others(19): Show | 22 | HG00438.hp2 HG02155.hp2 HG02293.hp2 others(19): Show |
intron_variant | MODIFIER | c.192+7678C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388615 | ||||||
| chr12:50388619
|
C | CA | 33 | a0001c0001t0001g0045a0001c0001t0001g0308a0003c0003t0001g0027others(30): Show | 33 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.192+7673dupT | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388619 | ||||||
| chr12:50388775
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.192+7518C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388775 | ||||||
| chr12:50388823
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0092 | 2 | HG00741.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.192+7470G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388823 | ||||||
| chr12:50388826
|
G | A | 105 | a0001c0001t0001g0189a0001c0001t0001g0190a0002c0002t0001g0113others(102): Show | 105 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.192+7467C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388826 | ||||||
| chr12:50388834
|
CTTGAGAT others(7): Show |
C | 1 | a0002c0002t0001g0191 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.192+7445_192+7458d others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388834 | ||||||
| chr12:50388851
|
G | C | 1 | a0027c0038t0001g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+7442C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50388851 | ||||||
| chr12:50389171
|
G | C | 1 | a0003c0003t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.192+7122C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50389171 | ||||||
| chr12:50389355
|
C | T | 1 | a0008c0009t0001g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.192+6938G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50389355 | ||||||
| chr12:50389401
|
G | A | 1 | a0003c0003t0001g0316 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.192+6892C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50389401 | ||||||
| chr12:50389525
|
G | T | 1 | a0003c0003t0001g0097 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.192+6768C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50389525 | ||||||
| chr12:50389889
|
G | T | 1 | a0022c0029t0001g0201 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.192+6404C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50389889 | ||||||
| chr12:50390048
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0076 | 2 | NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.192+6245A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390048 | ||||||
| chr12:50390081
|
A | G | 1 | a0002c0002t0001g0138 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.192+6212T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390081 | ||||||
| chr12:50390092
|
G | GGATTTTA others(33): Show |
1 | a0002c0002t0001g0138 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.192+6200_192+6201i others(42): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390092 | ||||||
| chr12:50390170
|
A | G | 1 | a0003c0003t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.192+6123T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390170 | ||||||
| chr12:50390270
|
T | G | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+6023A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390270 | ||||||
| chr12:50390529
|
T | G | 14 | a0004c0004t0001g0255a0004c0004t0001g0256a0004c0004t0001g0274others(11): Show | 14 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+5764A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390529 | ||||||
| chr12:50390573
|
A | G | 140 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.192+5720T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390573 | ||||||
| chr12:50390585
|
C | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+5708G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390585 | ||||||
| chr12:50390640
|
A | G | 1 | a0030c0040t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.192+5653T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390640 | ||||||
| chr12:50390646
|
G | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+5647C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390646 | ||||||
| chr12:50390658
|
G | A | 1 | a0001c0042t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.192+5635C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390658 | ||||||
| chr12:50390748
|
T | G | 1 | a0002c0006t0001g0192 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.192+5545A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390748 | ||||||
| chr12:50390899
|
A | T | 2 | a0005c0005t0001g0226a0005c0005t0001g0251 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+5394T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50390899 | ||||||
| chr12:50391113
|
C | G | 1 | a0003c0003t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192+5180G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391113 | ||||||
| chr12:50391161
|
G | A | 2 | a0006c0007t0001g0193a0006c0007t0001g0194 | 2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.192+5132C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391161 | ||||||
| chr12:50391304
|
T | A | 104 | a0001c0001t0001g0189a0001c0001t0001g0190a0002c0002t0001g0113others(101): Show | 104 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.192+4989A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391304 | ||||||
| chr12:50391375
|
G | A | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+4918C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391375 | ||||||
| chr12:50391397
|
C | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0046 | 3 | HG01109.hp2 HG02129.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.192+4896G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391397 | ||||||
| chr12:50391464
|
T | C | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+4829A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391464 | ||||||
| chr12:50391557
|
G | A | 1 | a0026c0034t0001g0136 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.192+4736C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391557 | ||||||
| chr12:50391581
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.192+4712A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391581 | ||||||
| chr12:50391675
|
A | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+4618T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391675 | ||||||
| chr12:50391859
|
A | G | 1 | a0003c0003t0001g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.192+4434T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391859 | ||||||
| chr12:50391995
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.192+4298T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50391995 | ||||||
| chr12:50392142
|
TG | T | 100 | a0001c0001t0001g0189a0001c0001t0001g0190a0002c0002t0001g0113others(97): Show | 100 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.192+4150delC | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392142 | ||||||
| chr12:50392143
|
G | T | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+4150C>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392143 | ||||||
| chr12:50392216
|
C | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0063others(6): Show | 9 | HG01361.hp2 HG01496.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+4077G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392216 | ||||||
| chr12:50392256
|
G | GTTGT | 10 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0039others(7): Show | 10 | HG00140.hp2 HG01361.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+4033_192+4036d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392256 | ||||||
| chr12:50392256
|
GTTGT | G | 49 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0062others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.192+4033_192+4036d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392256 | ||||||
| chr12:50392256
|
GTTGTTTG others(1): Show |
G | 14 | a0002c0002t0001g0009a0002c0033t0001g0321a0003c0003t0001g0215others(11): Show | 14 | HG01109.hp1 HG01978.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.192+4029_192+4036d others(10): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392256 | ||||||
| chr12:50392256
|
GTTGTTTG others(5): Show |
G | 1 | a0001c0001t0001g0102 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.192+4025_192+4036d others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392256 | ||||||
| chr12:50392256
|
GTTGTTTG others(9): Show |
G | 106 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(103): Show | 106 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.192+4021_192+4036d others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392256 | ||||||
| chr12:50392522
|
G | A | 1 | a0002c0010t0001g0197 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192+3771C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392522 | ||||||
| chr12:50392636
|
A | G | 1 | a0003c0003t0001g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192+3657T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392636 | ||||||
| chr12:50392650
|
G | A | 1 | a0003c0003t0001g0030 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.192+3643C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392650 | ||||||
| chr12:50392660
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.192+3633C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392660 | ||||||
| chr12:50392660
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.192+3633C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392660 | ||||||
| chr12:50392661
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.192+3632G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392661 | ||||||
| chr12:50392765
|
A | AT | 85 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.192+3527dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392765 | ||||||
| chr12:50392765
|
A | ATT | 66 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(63): Show | 66 | HG00438.hp1 HG00642.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.192+3526_192+3527d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392765 | ||||||
| chr12:50392765
|
A | ATTT | 11 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0061others(8): Show | 11 | HG01175.hp1 HG02071.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+3525_192+3527d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392765 | ||||||
| chr12:50392765
|
AT | A | 62 | a0002c0002t0001g0198a0002c0002t0001g0245a0003c0003t0001g0008others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.192+3527delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392765 | ||||||
| chr12:50392812
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.192+3481C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392812 | ||||||
| chr12:50392812
|
G | C | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+3481C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392812 | ||||||
| chr12:50392861
|
C | G | 138 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.192+3432G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392861 | ||||||
| chr12:50392929
|
CT | C | 206 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.192+3363delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392929 | ||||||
| chr12:50392995
|
T | C | 1 | a0002c0002t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.192+3298A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50392995 | ||||||
| chr12:50393033
|
T | G | 2 | a0001c0001t0001g0308a0003c0003t0001g0288 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.192+3260A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393033 | ||||||
| chr12:50393087
|
C | G | 1 | a0002c0002t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.192+3206G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393087 | ||||||
| chr12:50393147
|
C | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+3146G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393147 | ||||||
| chr12:50393203
|
T | C | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+3090A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393203 | ||||||
| chr12:50393252
|
T | C | 13 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+3041A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393252 | ||||||
| chr12:50393349
|
C | CCAACATG others(16): Show |
2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+2943_192+2944i others(25): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393349 | ||||||
| chr12:50393477
|
G | A | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+2816C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393477 | ||||||
| chr12:50393498
|
T | C | 133 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(130): Show | 133 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.192+2795A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393498 | ||||||
| chr12:50393573
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.192+2720C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393573 | ||||||
| chr12:50393601
|
C | T | 2 | a0014c0018t0001g0011a0014c0018t0001g0219 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.192+2692G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393601 | ||||||
| chr12:50393879
|
G | C | 1 | a0003c0003t0001g0289 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.192+2414C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393879 | ||||||
| chr12:50393882
|
G | A | 3 | a0007c0008t0001g0246a0007c0008t0001g0247a0007c0008t0001g0248 | 3 | HG02109.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.192+2411C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50393882 | ||||||
| chr12:50394012
|
G | A | 2 | a0002c0002t0001g0249a0002c0002t0001g0250 | 2 | NA18968.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.192+2281C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394012 | ||||||
| chr12:50394013
|
G | C | 7 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+2280C>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394013 | ||||||
| chr12:50394106
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192+2187C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394106 | ||||||
| chr12:50394131
|
T | C | 130 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.192+2162A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394131 | ||||||
| chr12:50394269
|
A | G | 1 | a0005c0005t0001g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.192+2024T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394269 | ||||||
| chr12:50394380
|
G | A | 130 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.192+1913C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394380 | ||||||
| chr12:50394509
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.192+1784C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394509 | ||||||
| chr12:50394570
|
T | C | 4 | a0005c0005t0001g0106a0005c0005t0001g0108a0005c0005t0001g0109others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1723A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394570 | ||||||
| chr12:50394664
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.192+1629G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394664 | ||||||
| chr12:50394732
|
C | CT | 95 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.192+1560dupA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTT | 21 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0115others(18): Show | 21 | HG00438.hp2 HG00597.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+1559_192+1560d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.192+1551_192+1560d others(12): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(4): Show |
3 | a0003c0014t0001g0107a0005c0005t0001g0108a0005c0005t0001g0109 | 3 | HG02897.hp2 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+1550_192+1560d others(13): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0105a0005c0005t0001g0106 | 3 | HG02258.hp2 NA18988.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.192+1549_192+1560d others(14): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(6): Show |
10 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0101others(7): Show | 10 | HG01069.hp1 HG01167.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+1548_192+1560d others(15): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(7): Show |
34 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(31): Show | 34 | HG01257.hp2 HG01261.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.192+1547_192+1560d others(16): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(8): Show |
24 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(21): Show | 24 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.192+1546_192+1560d others(17): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(4): Show | 7 | HG00673.hp2 HG00741.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1545_192+1560d others(18): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0028a0003c0003t0001g0029a0003c0003t0001g0030 | 3 | HG00140.hp2 HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.192+1544_192+1560d others(19): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(11): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01081.hp2 HG01975.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1543_192+1560d others(20): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(12): Show |
7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1542_192+1560d others(21): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG01255.hp1 HG01934.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.192+1541_192+1560d others(22): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0012a0014c0018t0001g0011a0033c0021t0001g0002 | 3 | HG02257.hp1 HG02257.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.192+1537_192+1560d others(26): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.192+1536_192+1560d others(27): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
CT | C | 9 | a0001c0001t0001g0257a0001c0001t0001g0258a0002c0002t0001g0259others(6): Show | 9 | HG00738.hp2 HG01433.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1560delA | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
CTT | C | 32 | a0001c0001t0001g0261a0001c0001t0001g0271a0003c0003t0001g0260others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.192+1559_192+1560d others(4): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
CTTT | C | 20 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.192+1558_192+1560d others(5): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394732
|
CTTTT | C | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0003c0003t0001g0311others(6): Show | 9 | HG01168.hp2 HG02132.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1557_192+1560d others(6): Show |
FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394732 | ||||||
| chr12:50394761
|
A | T | 1 | a0002c0002t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.192+1532T>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394761 | ||||||
| chr12:50394827
|
A | G | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+1466T>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50394827 | ||||||
| chr12:50395151
|
T | A | 2 | a0002c0002t0001g0319a0002c0002t0001g0320 | 2 | NA18948.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.192+1142A>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395151 | ||||||
| chr12:50395189
|
G | A | 1 | a0002c0033t0001g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.192+1104C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395189 | ||||||
| chr12:50395388
|
C | G | 1 | a0003c0003t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.192+905G>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395388 | ||||||
| chr12:50395465
|
T | G | 2 | a0010c0019t0001g0322a0010c0019t0001g0323 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+828A>C | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395465 | ||||||
| chr12:50395599
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.192+694G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395599 | ||||||
| chr12:50395617
|
T | C | 1 | a0003c0003t0001g0324 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.192+676A>G | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395617 | ||||||
| chr12:50395642
|
G | A | 7 | a0002c0002t0001g0325a0002c0002t0001g0326a0002c0002t0001g0327others(4): Show | 7 | HG01346.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+651C>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395642 | ||||||
| chr12:50395869
|
C | A | 1 | a0001c0001t0001g0332 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+424G>T | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50395869 | ||||||
| chr12:50396058
|
C | T | 4 | a0013c0017t0001g0003a0015c0016t0001g0004a0015c0016t0001g0005others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+235G>A | FAM186A | ENSG00000185958.10 | transcript | ENST00000327337.6 | protein_coding | 1/7 | chr12 | 50396058 |