Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2768 |
|---|---|
| ensemblid | ENSG00000146535.14 |
| hgncid | 4380 |
| symbol | GNA12 |
| name | G protein subunit alpha 12 |
| refseq_nuc | NM_007353.3 |
| refseq_prot | NP_031379.2 |
| ensembl_nuc | ENST00000275364.8 |
| ensembl_prot | ENSP00000275364.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 2728105 |
| end | 2844308 |
| strand | - |
| ver | v1.2 |
| region | chr7:2728105-2844308 |
| region5000 | chr7:2723105-2849308 |
| regionname0 | GNA12_chr7_2728105_2844308 |
| regionname5000 | GNA12_chr7_2723105_2849308 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 381 | 320 | 85 | 56 | 123 | 14 | 40 | 95 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0002 | 0/0 | 381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0003 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1146 | 298 | 71 | 54 | 118 | 13 | 40 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| c0002 | 0/0 | 1146 | 11 | 11 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| c0003 | 0/0 | 1146 | 5 | 0 | 0 | 5 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| c0004 | 0/0 | 1146 | 5 | 3 | 1 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| c0005 | 0/0 | 1146 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| c0006 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| c0007 | 0/0 | 1146 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3224 | 73 | 11 | 14 | 33 | 7 | 8 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0002 | 0/0 | 3220 | 58 | 28 | 16 | 12 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0003 | 1/1 | 3224 | 57 | 0 | 6 | 35 | 2 | 12 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0004 | 0/0 | 3222 | 36 | 10 | 5 | 10 | 2 | 9 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0005 | 0/0 | 3224 | 18 | 1 | 11 | 1 | 2 | 3 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0006 | 0/0 | 3224 | 10 | 0 | 0 | 10 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0007 | 0/0 | 3224 | 10 | 5 | 1 | 3 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0008 | 0/0 | 3222 | 9 | 0 | 0 | 8 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0009 | 0/0 | 3224 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0010 | 0/0 | 3224 | 4 | 0 | 0 | 4 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0011 | 0/0 | 3220 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0012 | 0/0 | 3220 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0013 | 0/0 | 3224 | 3 | 0 | 0 | 3 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0014 | 0/0 | 3224 | 3 | 3 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0015 | 0/0 | 3224 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0016 | 0/0 | 3226 | 2 | 0 | 0 | 0 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0017 | 0/0 | 3224 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0018 | 0/0 | 3224 | 2 | 0 | 1 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0019 | 0/0 | 3224 | 2 | 1 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0020 | 0/0 | 3220 | 2 | 0 | 0 | 0 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0021 | 0/0 | 3220 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0022 | 0/0 | 3224 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0023 | 0/0 | 3224 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0024 | 0/0 | 3224 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0025 | 0/0 | 3224 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0026 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0027 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0028 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0029 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0030 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0031 | 0/0 | 3224 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0032 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0033 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0034 | 0/0 | 3220 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0035 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| t0036 | 0/0 | 3220 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1146 | 298 | 71 | 54 | 118 | 13 | 40 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0002 | 0/0 | 1146 | 11 | 11 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0003 | 0/0 | 1146 | 5 | 0 | 0 | 5 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0004 | 0/0 | 1146 | 5 | 3 | 1 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0007 | 0/0 | 1146 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0002c0006 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0003c0005 | 0/0 | 1146 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4369 | 67 | 11 | 14 | 27 | 7 | 8 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0002 | 0/0 | 4365 | 47 | 17 | 16 | 12 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0003 | 1/1 | 4369 | 56 | 0 | 5 | 35 | 2 | 12 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0004 | 0/0 | 4367 | 36 | 10 | 5 | 10 | 2 | 9 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0005 | 0/0 | 4369 | 18 | 1 | 11 | 1 | 2 | 3 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0006 | 0/0 | 4369 | 10 | 0 | 0 | 10 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0007 | 0/0 | 4369 | 10 | 5 | 1 | 3 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0008 | 0/0 | 4367 | 9 | 0 | 0 | 8 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0009 | 0/0 | 4369 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0010 | 0/0 | 4369 | 4 | 0 | 0 | 4 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0011 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0012 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0013 | 0/0 | 4369 | 3 | 0 | 0 | 3 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0015 | 0/0 | 4369 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0016 | 0/0 | 4371 | 2 | 0 | 0 | 0 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0017 | 0/0 | 4369 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0019 | 0/0 | 4369 | 2 | 1 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0020 | 0/0 | 4365 | 2 | 0 | 0 | 0 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0021 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0022 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0023 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0024 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0025 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0026 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0028 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0029 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0030 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0031 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0032 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0033 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0034 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0035 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0001t0036 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0002t0002 | 0/0 | 4365 | 11 | 11 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0003t0001 | 0/0 | 4369 | 5 | 0 | 0 | 5 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0004t0014 | 0/0 | 4369 | 3 | 3 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0004t0018 | 0/0 | 4369 | 2 | 0 | 1 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0001c0007t0003 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0002c0006t0027 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| a0003c0005t0001 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | copy fasta | chr7 | 2723105 | 2849308 |
| 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 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0013g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0013g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0013g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0015g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0016g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0017g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0017g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0019g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0020g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0021g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0021g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0022g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0023g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0024g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0025g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0026g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0028g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0029g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0030g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0031g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0032g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0033g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0034g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0035g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0036g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0014g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0018g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0018g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0007t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0002c0006t0027g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0003c0005t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0133 | EUR | GBR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0075 | EUR | FIN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0246 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0309 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0307 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00741 | hp1 | a0001 | c0004 | t0018 | g0265 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0314 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0315 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01106 | hp1 | a0001 | c0007 | t0003 | g0295 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0301 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01109 | hp1 | a0001 | c0001 | t0025 | g0057 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0313 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01192 | hp2 | a0001 | c0001 | t0019 | g0275 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0304 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0100 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0303 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0302 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0305 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01884 | hp1 | a0001 | c0001 | t0021 | g0044 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0049 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02129 | hp2 | a0001 | c0001 | t0024 | g0037 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02258 | hp1 | a0001 | c0001 | t0026 | g0288 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0311 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0319 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0141 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02523 | hp1 | a0001 | c0001 | t0022 | g0092 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02602 | hp2 | a0001 | c0001 | t0020 | g0025 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0140 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0300 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02717 | hp2 | a0001 | c0001 | t0029 | g0182 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02723 | hp2 | a0001 | c0001 | t0021 | g0045 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02735 | hp1 | a0001 | c0001 | t0020 | g0024 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02818 | hp2 | a0001 | c0004 | t0014 | g0285 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0298 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02896 | hp2 | a0001 | c0004 | t0014 | g0286 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02922 | hp1 | a0001 | c0004 | t0014 | g0287 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02965 | hp2 | a0001 | c0001 | t0017 | g0272 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0082 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02970 | hp2 | a0001 | c0001 | t0035 | g0297 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0268 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03098 | hp2 | a0001 | c0001 | t0017 | g0271 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03139 | hp1 | a0001 | c0001 | t0028 | g0284 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0317 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0273 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03453 | hp2 | a0002 | c0006 | t0027 | g0149 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0148 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0318 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0276 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0299 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0306 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0086 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04115 | hp2 | a0001 | c0001 | t0016 | g0131 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0054 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | YRI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18906 | hp2 | a0001 | c0001 | t0034 | g0107 | AFR | YRI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18956 | hp1 | a0001 | c0001 | t0013 | g0277 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18956 | hp2 | a0001 | c0001 | t0010 | g0079 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0072 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18960 | hp2 | a0001 | c0001 | t0033 | g0110 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0194 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18974 | hp1 | a0001 | c0001 | t0031 | g0181 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18979 | hp2 | a0001 | c0001 | t0013 | g0279 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18983 | hp2 | a0003 | c0005 | t0001 | g0257 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18992 | hp2 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0074 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19005 | hp1 | a0001 | c0001 | t0013 | g0278 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19012 | hp1 | a0001 | c0001 | t0010 | g0066 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19030 | hp1 | a0001 | c0001 | t0036 | g0296 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19043 | hp1 | a0001 | c0001 | t0032 | g0254 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19056 | hp1 | a0001 | c0001 | t0008 | g0283 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19062 | hp2 | a0001 | c0001 | t0008 | g0050 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19067 | hp2 | a0001 | c0001 | t0008 | g0052 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19076 | hp1 | a0001 | c0001 | t0023 | g0020 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19076 | hp2 | a0001 | c0001 | t0008 | g0048 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19083 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | ASW | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ASW | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20752 | hp1 | a0001 | c0004 | t0018 | g0266 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | GIH | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20905 | hp2 | a0001 | c0001 | t0016 | g0130 | SAS | GIH | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0089 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0185 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0316 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0269 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0310 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA21309 | hp1 | a0001 | c0001 | t0030 | g0213 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0270 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0144 | REF | REF | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0084 | REF | REF | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2731369
|
C | T | 1 | a0002 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.958G>A | p.Asp320Asn | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1105/4369 | 958/1146 | 320/381 | chr7 | 2731369 | ||
| chr7:2795050
|
C | T | 1 | a0003 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.403G>A | p.Glu135Lys | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/4 | 550/4369 | 403/1146 | 135/381 | chr7 | 2795050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2731265
|
G | A | 1 | a0001c0003 | 5 | NA19011.hp1 NA19056.hp2 NA19057.hp2 others(2): Show |
synonymous_variant | LOW | c.1062C>T | p.Ile354Ile | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1209/4369 | 1062/1146 | 354/381 | chr7 | 2731265 | ||
| chr7:2731349
|
G | A | 1 | a0001c0002 | 11 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
synonymous_variant | LOW | c.978C>T | p.Asp326Asp | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1125/4369 | 978/1146 | 326/381 | chr7 | 2731349 | ||
| chr7:2794943
|
T | C | 1 | a0001c0004 | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.510A>G | p.Arg170Arg | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/4 | 657/4369 | 510/1146 | 170/381 | chr7 | 2794943 | ||
| chr7:2795120
|
T | C | 1 | a0001c0004 | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.333A>G | p.Ala111Ala | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/4 | 480/4369 | 333/1146 | 111/381 | chr7 | 2795120 | ||
| chr7:2844042
|
G | A | 1 | a0001c0007 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.120C>T | p.Ser40Ser | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/4 | 267/4369 | 120/1146 | 40/381 | chr7 | 2844042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2728235
|
C | T | 1 | a0001c0001t0030 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2946G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2946 | chr7 | 2728235 | |||||
| chr7:2728305
|
T | C | 21 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(18): Show | 201 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*2876A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2876 | chr7 | 2728305 | |||||
| chr7:2728314
|
T | C | 1 | a0001c0001t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2867A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2867 | chr7 | 2728314 | |||||
| chr7:2728410
|
A | G | 1 | a0001c0001t0017 | 2 | HG02965.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2771T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2771 | chr7 | 2728410 | |||||
| chr7:2728721
|
A | ATG | 4 | a0001c0001t0004a0001c0001t0008a0001c0001t0016others(1): Show | 48 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2458_*2459dupCA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2459 | chr7 | 2728721 | |||||
| chr7:2728741
|
T | C | 1 | a0001c0001t0013 | 3 | NA18956.hp1 NA18979.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2440A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2440 | chr7 | 2728741 | |||||
| chr7:2728756
|
G | A | 1 | a0001c0001t0031 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2425C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2425 | chr7 | 2728756 | |||||
| chr7:2728836
|
G | A | 1 | a0001c0004t0014 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2345C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2345 | chr7 | 2728836 | |||||
| chr7:2728927
|
C | T | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(9): Show | 120 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2254G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2254 | chr7 | 2728927 | |||||
| chr7:2728937
|
G | A | 1 | a0001c0001t0016 | 2 | HG04115.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2244C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2244 | chr7 | 2728937 | |||||
| chr7:2728992
|
C | T | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(9): Show | 120 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2189G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2189 | chr7 | 2728992 | |||||
| chr7:2729016
|
C | T | 1 | a0001c0001t0033 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2165G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2165 | chr7 | 2729016 | |||||
| chr7:2729057
|
A | G | 1 | a0001c0001t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2124T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2124 | chr7 | 2729057 | |||||
| chr7:2729138
|
C | T | 3 | a0001c0001t0015a0001c0001t0032a0001c0001t0035 | 4 | HG02451.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2043G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 2043 | chr7 | 2729138 | |||||
| chr7:2729191
|
G | T | 1 | a0002c0006t0027 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1990 | chr7 | 2729191 | |||||
| chr7:2729230
|
T | C | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(20): Show | 204 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1951A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1951 | chr7 | 2729230 | |||||
| chr7:2729263
|
C | T | 13 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(10): Show | 121 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1918G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1918 | chr7 | 2729263 | |||||
| chr7:2729276
|
G | A | 1 | a0001c0001t0024 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1905C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1905 | chr7 | 2729276 | |||||
| chr7:2729301
|
G | T | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(18): Show | 138 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1880C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1880 | chr7 | 2729301 | |||||
| chr7:2729388
|
T | A | 1 | a0001c0001t0020 | 2 | HG02602.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1793A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1793 | chr7 | 2729388 | |||||
| chr7:2729496
|
C | T | 2 | a0001c0001t0011a0001c0001t0012 | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1685G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1685 | chr7 | 2729496 | |||||
| chr7:2729555
|
G | A | 1 | a0001c0004t0018 | 2 | HG00741.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1626C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1626 | chr7 | 2729555 | |||||
| chr7:2729677
|
C | T | 1 | a0001c0001t0010 | 4 | NA18956.hp2 NA18960.hp1 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1504G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1504 | chr7 | 2729677 | |||||
| chr7:2729879
|
G | A | 3 | a0001c0001t0011a0001c0001t0012a0001c0001t0034 | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1302C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1302 | chr7 | 2729879 | |||||
| chr7:2729886
|
T | A | 1 | a0001c0001t0019 | 2 | HG01192.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1295A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 1295 | chr7 | 2729886 | |||||
| chr7:2730287
|
G | A | 21 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(18): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*894C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 894 | chr7 | 2730287 | |||||
| chr7:2730310
|
G | C | 1 | a0001c0001t0021 | 2 | HG01884.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*871C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 871 | chr7 | 2730310 | |||||
| chr7:2730349
|
G | T | 1 | a0001c0001t0025 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 832 | chr7 | 2730349 | |||||
| chr7:2730393
|
G | A | 1 | a0001c0001t0008 | 9 | HG02056.hp1 HG02071.hp2 HG04204.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*788C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 788 | chr7 | 2730393 | |||||
| chr7:2730433
|
G | C | 21 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(18): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*748C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 748 | chr7 | 2730433 | |||||
| chr7:2730587
|
G | A | 1 | a0001c0001t0032 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 594 | chr7 | 2730587 | |||||
| chr7:2730759
|
T | G | 1 | a0001c0004t0014 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*422A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 422 | chr7 | 2730759 | |||||
| chr7:2730840
|
C | G | 1 | a0001c0001t0006 | 10 | HG00423.hp1 HG00597.hp2 NA18942.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 341 | chr7 | 2730840 | |||||
| chr7:2730858
|
CAATT | C | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(8): Show | 118 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*322delAATT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 319 | chr7 | 2730858 | |||||
| chr7:2730972
|
C | T | 1 | a0001c0001t0009 | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*209G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 209 | chr7 | 2730972 | |||||
| chr7:2730998
|
A | T | 2 | a0001c0001t0015a0001c0001t0035 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 4/4 | 183 | chr7 | 2730998 | |||||
| chr7:2844293
|
C | A | 4 | a0001c0001t0005a0001c0001t0012a0001c0001t0035others(1): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-132G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/4 | 132 | chr7 | 2844293 | |||||
| chr7:2844294
|
T | G | 4 | a0001c0001t0005a0001c0001t0012a0001c0001t0035others(1): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-133A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/4 | 133 | chr7 | 2844294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2731761
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.577-11G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2731761 | ||||||
| chr7:2731870
|
C | A | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.577-120G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2731870 | ||||||
| chr7:2732008
|
G | A | 27 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(24): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.577-258C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732008 | ||||||
| chr7:2732037
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.577-287C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732037 | ||||||
| chr7:2732082
|
A | AT | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.577-333dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732082 | ||||||
| chr7:2732211
|
G | A | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.577-461C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732211 | ||||||
| chr7:2732474
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.577-724T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732474 | ||||||
| chr7:2732496
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.577-746G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732496 | ||||||
| chr7:2732525
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.577-775C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732525 | ||||||
| chr7:2732627
|
T | C | 175 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(172): Show | 176 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.576+824A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732627 | ||||||
| chr7:2732632
|
A | C | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+819T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732632 | ||||||
| chr7:2732656
|
T | C | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 179 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.576+795A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732656 | ||||||
| chr7:2732657
|
G | A | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.576+794C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732657 | ||||||
| chr7:2732688
|
G | A | 2 | a0001c0001t0004g0289a0001c0001t0005g0313 | 2 | HG01169.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.576+763C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732688 | ||||||
| chr7:2732797
|
A | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.576+654T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732797 | ||||||
| chr7:2732879
|
T | C | 4 | a0001c0001t0011g0183a0001c0001t0012g0316a0001c0001t0012g0317others(1): Show | 4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+572A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2732879 | ||||||
| chr7:2733138
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.576+313C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2733138 | ||||||
| chr7:2733156
|
T | C | 174 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 175 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.576+295A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2733156 | ||||||
| chr7:2733161
|
G | T | 1 | a0001c0001t0036g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.576+290C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2733161 | ||||||
| chr7:2733321
|
C | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.576+130G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2733321 | ||||||
| chr7:2733401
|
C | CAT | 258 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.576+49_576+50insAT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2733401 | ||||||
| chr7:2733423
|
G | T | 1 | a0001c0001t0003g0038 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.576+28C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 3/3 | chr7 | 2733423 | ||||||
| chr7:2733537
|
G | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-36C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2733537 | ||||||
| chr7:2733589
|
T | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-88A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2733589 | ||||||
| chr7:2733770
|
C | T | 1 | a0001c0002t0002g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526-269G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2733770 | ||||||
| chr7:2733836
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.526-335G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2733836 | ||||||
| chr7:2733971
|
A | G | 258 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.526-470T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2733971 | ||||||
| chr7:2734027
|
G | C | 1 | a0001c0001t0003g0017 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.526-526C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734027 | ||||||
| chr7:2734134
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0002g0282 | 2 | HG01109.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.526-633G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734134 | ||||||
| chr7:2734199
|
G | A | 1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.526-698C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734199 | ||||||
| chr7:2734225
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.526-724G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734225 | ||||||
| chr7:2734228
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.526-727C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734228 | ||||||
| chr7:2734296
|
C | G | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-795G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734296 | ||||||
| chr7:2734337
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.526-836T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734337 | ||||||
| chr7:2734352
|
G | A | 1 | a0001c0001t0005g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.526-851C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734352 | ||||||
| chr7:2734491
|
G | A | 19 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(16): Show | 19 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.526-990C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734491 | ||||||
| chr7:2734497
|
G | A | 2 | a0001c0001t0009g0267a0001c0001t0009g0268 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-996C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734497 | ||||||
| chr7:2734546
|
C | T | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526-1045G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734546 | ||||||
| chr7:2734560
|
G | A | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 12 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-1059C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734560 | ||||||
| chr7:2734749
|
G | A | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-1248C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734749 | ||||||
| chr7:2734771
|
T | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-1270A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734771 | ||||||
| chr7:2734822
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-1321G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734822 | ||||||
| chr7:2734840
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-1339G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734840 | ||||||
| chr7:2734847
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-1346G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734847 | ||||||
| chr7:2734904
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-1403C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734904 | ||||||
| chr7:2734924
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-1423G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734924 | ||||||
| chr7:2734926
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.526-1425C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734926 | ||||||
| chr7:2734951
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-1450G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734951 | ||||||
| chr7:2734970
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-1469G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734970 | ||||||
| chr7:2734974
|
C | T | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-1473G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734974 | ||||||
| chr7:2734977
|
G | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-1476C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2734977 | ||||||
| chr7:2735041
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-1540G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735041 | ||||||
| chr7:2735115
|
T | TC | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 182 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.526-1615dupG | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735115 | ||||||
| chr7:2735155
|
T | G | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.526-1654A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735155 | ||||||
| chr7:2735159
|
G | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-1658C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735159 | ||||||
| chr7:2735169
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-1668C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735169 | ||||||
| chr7:2735180
|
C | T | 1 | a0001c0001t0006g0071 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.526-1679G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735180 | ||||||
| chr7:2735194
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.526-1693C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735194 | ||||||
| chr7:2735195
|
G | C | 1 | a0001c0001t0013g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.526-1694C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735195 | ||||||
| chr7:2735357
|
G | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-1856C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735357 | ||||||
| chr7:2735363
|
C | T | 1 | a0001c0001t0012g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.526-1862G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735363 | ||||||
| chr7:2735384
|
A | T | 1 | a0001c0001t0017g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.526-1883T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735384 | ||||||
| chr7:2735454
|
GAC | G | 50 | a0001c0001t0002g0179a0001c0001t0002g0280a0001c0001t0002g0281others(47): Show | 51 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.526-1955_526-1954d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735454 | ||||||
| chr7:2735468
|
G | A | 28 | a0001c0001t0002g0179a0001c0001t0004g0012a0001c0001t0005g0299others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.526-1967C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735468 | ||||||
| chr7:2735481
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-1980C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735481 | ||||||
| chr7:2735533
|
G | A | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.526-2032C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735533 | ||||||
| chr7:2735544
|
C | T | 22 | a0001c0001t0002g0001a0001c0001t0002g0046a0001c0001t0002g0047others(19): Show | 23 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.526-2043G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735544 | ||||||
| chr7:2735650
|
C | G | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-2149G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735650 | ||||||
| chr7:2735650
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.526-2149G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735650 | ||||||
| chr7:2735701
|
T | C | 1 | a0001c0001t0012g0318 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.526-2200A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735701 | ||||||
| chr7:2735827
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-2326C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735827 | ||||||
| chr7:2735841
|
G | C | 3 | a0001c0001t0011g0003a0001c0001t0011g0273a0001c0001t0034g0107 | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2340C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735841 | ||||||
| chr7:2735908
|
G | C | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.526-2407C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735908 | ||||||
| chr7:2735923
|
T | G | 1 | a0001c0002t0002g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526-2422A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735923 | ||||||
| chr7:2735973
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0005g0299a0001c0001t0005g0300others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.526-2472C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735973 | ||||||
| chr7:2735985
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-2484A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735985 | ||||||
| chr7:2735987
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.526-2486G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735987 | ||||||
| chr7:2735997
|
A | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(176): Show | 181 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.526-2496T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2735997 | ||||||
| chr7:2736028
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.526-2527C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736028 | ||||||
| chr7:2736045
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.526-2544G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736045 | ||||||
| chr7:2736050
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-2549C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736050 | ||||||
| chr7:2736055
|
C | T | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 10 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.526-2554G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736055 | ||||||
| chr7:2736076
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.526-2575G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736076 | ||||||
| chr7:2736084
|
G | A | 71 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(68): Show | 72 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.526-2583C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736084 | ||||||
| chr7:2736131
|
A | G | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 182 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.526-2630T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736131 | ||||||
| chr7:2736160
|
T | C | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 179 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.526-2659A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736160 | ||||||
| chr7:2736191
|
A | T | 133 | a0001c0001t0001g0264a0001c0001t0002g0001a0001c0001t0002g0004others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.526-2690T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736191 | ||||||
| chr7:2736222
|
C | T | 1 | a0001c0001t0004g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.526-2721G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736222 | ||||||
| chr7:2736245
|
C | T | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-2744G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736245 | ||||||
| chr7:2736269
|
G | C | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-2768C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736269 | ||||||
| chr7:2736410
|
C | A | 163 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 164 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.526-2909G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736410 | ||||||
| chr7:2736414
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-2913G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736414 | ||||||
| chr7:2736432
|
CAG | C | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-2933_526-2932d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736432 | ||||||
| chr7:2736495
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526-2994C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736495 | ||||||
| chr7:2736498
|
A | G | 160 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 161 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.526-2997T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736498 | ||||||
| chr7:2736572
|
G | T | 1 | a0001c0001t0006g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.526-3071C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736572 | ||||||
| chr7:2736762
|
G | A | 2 | a0001c0001t0020g0024a0001c0001t0020g0025 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.526-3261C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736762 | ||||||
| chr7:2736764
|
A | G | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 182 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.526-3263T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736764 | ||||||
| chr7:2736768
|
C | T | 1 | a0001c0001t0002g0150 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.526-3267G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736768 | ||||||
| chr7:2736803
|
G | A | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-3302C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736803 | ||||||
| chr7:2736908
|
G | T | 8 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-3407C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736908 | ||||||
| chr7:2736940
|
G | A | 8 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-3439C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736940 | ||||||
| chr7:2736993
|
T | C | 160 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 161 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.526-3492A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2736993 | ||||||
| chr7:2737064
|
T | G | 173 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.526-3563A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737064 | ||||||
| chr7:2737110
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-3609C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737110 | ||||||
| chr7:2737116
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.526-3615C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737116 | ||||||
| chr7:2737150
|
G | T | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-3649C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737150 | ||||||
| chr7:2737263
|
AGTTTTGT others(3): Show |
A | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0137others(28): Show | 31 | HG00609.hp1 HG00735.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.526-3772_526-3763d others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737263 | ||||||
| chr7:2737263
|
AGTTTTGT others(18): Show |
A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-3787_526-3763d others(27): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737263 | ||||||
| chr7:2737264
|
GTTTTGTT others(4): Show |
G | 40 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0191others(37): Show | 40 | HG00140.hp2 HG00423.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.526-3774_526-3764d others(13): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737264 | ||||||
| chr7:2737264
|
GTTTTGTT others(5): Show |
G | 1 | a0001c0001t0001g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.526-3775_526-3764d others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737264 | ||||||
| chr7:2737264
|
GTTTTGTT others(8): Show |
G | 1 | a0001c0001t0008g0052 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.526-3778_526-3764d others(17): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737264 | ||||||
| chr7:2737264
|
GTTTTGTT others(9): Show |
G | 2 | a0001c0001t0001g0262a0001c0001t0008g0048 | 2 | NA19076.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.526-3779_526-3764d others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737264 | ||||||
| chr7:2737265
|
TTTTGTTT others(2): Show |
T | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0206others(4): Show | 7 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-3773_526-3765d others(11): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737265 | ||||||
| chr7:2737267
|
TTGTTTTG others(15): Show |
T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.526-3788_526-3767d others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737267 | ||||||
| chr7:2737269
|
G | GT | 5 | a0001c0001t0003g0133a0001c0001t0003g0143a0001c0001t0003g0145others(2): Show | 5 | HG00140.hp1 NA18977.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-3769dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
G | GTT | 4 | a0001c0001t0003g0075a0001c0001t0003g0128a0001c0001t0003g0144others(1): Show | 4 | HG00280.hp2 HG03927.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-3770_526-3769d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
G | T | 2 | a0001c0001t0003g0078a0001c0001t0003g0146 | 2 | HG01934.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.526-3768C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
GTTTTGTT others(3): Show |
G | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-3778_526-3769d others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
GTTTTGTT others(4): Show |
G | 1 | a0001c0004t0014g0285 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.526-3779_526-3769d others(13): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
GTTTTGTT others(5): Show |
G | 2 | a0001c0004t0014g0286a0001c0004t0014g0287 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-3780_526-3769d others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
GTTTTGTT others(6): Show |
G | 1 | a0001c0001t0017g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.526-3781_526-3769d others(15): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
GTTTTGTT others(7): Show |
G | 4 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0017g0272others(1): Show | 4 | HG02451.hp2 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-3782_526-3769d others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737269
|
GTTTTGTT others(8): Show |
G | 4 | a0001c0001t0004g0086a0001c0001t0004g0087a0001c0001t0004g0125others(1): Show | 4 | HG02148.hp1 HG03927.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-3783_526-3769d others(17): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737269 | ||||||
| chr7:2737272
|
TTGTTTTT others(10): Show |
T | 2 | a0001c0001t0004g0089a0001c0001t0033g0110 | 2 | HG01123.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.526-3788_526-3772d others(19): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737272 | ||||||
| chr7:2737273
|
TGTTTTTT others(9): Show |
T | 37 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(34): Show | 38 | HG01074.hp1 HG01192.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.526-3788_526-3773d others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737273 | ||||||
| chr7:2737274
|
G | GT | 24 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0073others(21): Show | 24 | HG01106.hp1 HG01258.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.526-3774dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737274 | ||||||
| chr7:2737274
|
G | GTT | 9 | a0001c0001t0002g0014a0001c0001t0003g0061a0001c0001t0003g0096others(6): Show | 9 | HG00597.hp2 HG01175.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-3775_526-3774d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737274 | ||||||
| chr7:2737274
|
G | GTTT | 8 | a0001c0001t0003g0017a0001c0001t0003g0062a0001c0001t0003g0105others(5): Show | 8 | HG02615.hp2 HG02895.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-3776_526-3774d others(5): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737274 | ||||||
| chr7:2737274
|
G | T | 13 | a0001c0001t0003g0038a0001c0001t0003g0075a0001c0001t0003g0076others(10): Show | 13 | HG00140.hp1 HG00280.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-3773C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737274 | ||||||
| chr7:2737279
|
T | G | 5 | a0001c0001t0002g0068a0001c0001t0002g0280a0001c0001t0002g0281others(2): Show | 5 | HG00639.hp2 HG03195.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-3778A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737279 | ||||||
| chr7:2737279
|
TTTTTTTT others(3): Show |
T | 5 | a0001c0001t0007g0005a0001c0001t0007g0184a0001c0001t0007g0269others(2): Show | 5 | HG01167.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-3788_526-3779d others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737279 | ||||||
| chr7:2737281
|
TTTTTTTT others(1): Show |
T | 16 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0302others(13): Show | 16 | HG00639.hp1 HG01069.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.526-3788_526-3781d others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737281 | ||||||
| chr7:2737284
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-3783A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737284 | ||||||
| chr7:2737287
|
T | G | 1 | a0001c0001t0003g0195 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.526-3786A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737287 | ||||||
| chr7:2737289
|
G | GT | 24 | a0001c0001t0002g0001a0001c0001t0002g0046a0001c0001t0002g0047others(21): Show | 25 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.526-3789dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737289 | ||||||
| chr7:2737289
|
G | GTT | 6 | a0001c0001t0002g0085a0001c0001t0002g0171a0001c0001t0002g0255others(3): Show | 6 | HG01123.hp2 HG01934.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-3790_526-3789d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737289 | ||||||
| chr7:2737289
|
G | T | 202 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.526-3788C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737289 | ||||||
| chr7:2737294
|
T | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-3793A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737294 | ||||||
| chr7:2737309
|
G | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-3808C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737309 | ||||||
| chr7:2737314
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0007g0192others(2): Show | 5 | HG00423.hp2 NA18970.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-3813T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737314 | ||||||
| chr7:2737319
|
C | T | 6 | a0001c0001t0026g0288a0001c0004t0014g0285a0001c0004t0014g0286others(3): Show | 6 | HG00741.hp1 HG02258.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3818G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737319 | ||||||
| chr7:2737320
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.526-3819C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737320 | ||||||
| chr7:2737328
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-3827C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737328 | ||||||
| chr7:2737333
|
G | A | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.526-3832C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737333 | ||||||
| chr7:2737414
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-3913C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737414 | ||||||
| chr7:2737434
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-3933C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737434 | ||||||
| chr7:2737449
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-3948G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737449 | ||||||
| chr7:2737478
|
G | A | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-3977C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737478 | ||||||
| chr7:2737508
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-4007G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737508 | ||||||
| chr7:2737580
|
C | T | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-4079G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737580 | ||||||
| chr7:2737581
|
G | A | 5 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-4080C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737581 | ||||||
| chr7:2737584
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-4083G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737584 | ||||||
| chr7:2737669
|
G | C | 2 | a0001c0001t0001g0218a0001c0001t0006g0246 | 2 | HG00423.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.526-4168C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737669 | ||||||
| chr7:2737681
|
T | C | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.526-4180A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737681 | ||||||
| chr7:2737721
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-4220C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737721 | ||||||
| chr7:2737735
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.526-4234T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737735 | ||||||
| chr7:2737760
|
T | A | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526-4259A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737760 | ||||||
| chr7:2737764
|
A | G | 1 | a0001c0001t0009g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.526-4263T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737764 | ||||||
| chr7:2737830
|
G | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-4329C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737830 | ||||||
| chr7:2737971
|
C | G | 2 | a0001c0001t0012g0316a0001c0001t0012g0317 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.526-4470G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2737971 | ||||||
| chr7:2738050
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-4549A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738050 | ||||||
| chr7:2738134
|
G | T | 1 | a0001c0001t0006g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.526-4633C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738134 | ||||||
| chr7:2738191
|
A | G | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(91): Show | 94 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.526-4690T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738191 | ||||||
| chr7:2738271
|
T | G | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.526-4770A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738271 | ||||||
| chr7:2738283
|
TA | T | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.526-4783delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738283 | ||||||
| chr7:2738321
|
G | A | 9 | a0001c0001t0001g0264a0001c0002t0002g0081a0001c0002t0002g0082others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-4820C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738321 | ||||||
| chr7:2738322
|
A | C | 4 | a0001c0003t0001g0227a0001c0003t0001g0236a0001c0003t0001g0237others(1): Show | 4 | NA19011.hp1 NA19056.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-4821T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738322 | ||||||
| chr7:2738363
|
C | T | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 180 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.526-4862G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738363 | ||||||
| chr7:2738423
|
C | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-4922G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738423 | ||||||
| chr7:2738428
|
G | A | 2 | a0001c0001t0006g0039a0001c0001t0006g0041 | 2 | HG00597.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.526-4927C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738428 | ||||||
| chr7:2738443
|
C | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0008g0054 | 3 | HG01515.hp1 HG01517.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.526-4942G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738443 | ||||||
| chr7:2738450
|
G | A | 1 | a0001c0001t0004g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.526-4949C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738450 | ||||||
| chr7:2738468
|
C | T | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-4967G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738468 | ||||||
| chr7:2738479
|
A | G | 1 | a0001c0001t0004g0087 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.526-4978T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738479 | ||||||
| chr7:2738486
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-4985C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738486 | ||||||
| chr7:2738494
|
C | G | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-4993G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738494 | ||||||
| chr7:2738539
|
G | C | 1 | a0001c0001t0004g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526-5038C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738539 | ||||||
| chr7:2738706
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-5205A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738706 | ||||||
| chr7:2738800
|
A | G | 7 | a0001c0001t0001g0203a0001c0001t0001g0216a0001c0001t0001g0222others(4): Show | 7 | NA18612.hp2 NA18943.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-5299T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738800 | ||||||
| chr7:2738810
|
C | T | 34 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(31): Show | 34 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.526-5309G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738810 | ||||||
| chr7:2738847
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0215 | 2 | HG01346.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.526-5346C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738847 | ||||||
| chr7:2738856
|
C | G | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-5355G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738856 | ||||||
| chr7:2738862
|
G | A | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-5361C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738862 | ||||||
| chr7:2738953
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526-5452G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2738953 | ||||||
| chr7:2739065
|
C | T | 3 | a0001c0002t0002g0104a0001c0002t0002g0122a0001c0002t0002g0123 | 3 | HG03516.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.526-5564G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739065 | ||||||
| chr7:2739068
|
A | G | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-5567T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739068 | ||||||
| chr7:2739094
|
T | G | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 173 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.526-5593A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739094 | ||||||
| chr7:2739115
|
G | A | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-5614C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739115 | ||||||
| chr7:2739121
|
C | T | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-5620G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739121 | ||||||
| chr7:2739238
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.526-5737G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739238 | ||||||
| chr7:2739252
|
G | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-5751C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739252 | ||||||
| chr7:2739271
|
A | G | 51 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(48): Show | 53 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(50): Show |
intron_variant | MODIFIER | c.526-5770T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739271 | ||||||
| chr7:2739321
|
GCTTT | G | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-5824_526-5821d others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739321 | ||||||
| chr7:2739491
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-5990C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739491 | ||||||
| chr7:2739493
|
A | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-5992T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739493 | ||||||
| chr7:2739495
|
AT | A | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 180 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.526-5995delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739495 | ||||||
| chr7:2739642
|
T | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-6141A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739642 | ||||||
| chr7:2739644
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-6143G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739644 | ||||||
| chr7:2739750
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-6249G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739750 | ||||||
| chr7:2739800
|
G | A | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-6299C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739800 | ||||||
| chr7:2739871
|
C | T | 2 | a0001c0001t0004g0187a0001c0001t0004g0188 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.526-6370G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2739871 | ||||||
| chr7:2740021
|
C | A | 1 | a0001c0001t0004g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.526-6520G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740021 | ||||||
| chr7:2740026
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0004g0012 | 2 | HG02055.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.526-6525G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740026 | ||||||
| chr7:2740027
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-6526C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740027 | ||||||
| chr7:2740153
|
ACTCCAGT others(16): Show |
A | 1 | a0001c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.526-6675_526-6653d others(25): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740153 | ||||||
| chr7:2740158
|
A | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 171 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.526-6657T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740158 | ||||||
| chr7:2740203
|
C | G | 1 | a0001c0001t0003g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.526-6702G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740203 | ||||||
| chr7:2740278
|
C | A | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.526-6777G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740278 | ||||||
| chr7:2740370
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-6869G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740370 | ||||||
| chr7:2740371
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.526-6870C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740371 | ||||||
| chr7:2740441
|
C | A | 1 | a0001c0001t0005g0312 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.526-6940G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740441 | ||||||
| chr7:2740487
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.526-6986G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740487 | ||||||
| chr7:2740588
|
T | C | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-7087A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740588 | ||||||
| chr7:2740644
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.526-7143T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740644 | ||||||
| chr7:2740711
|
A | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-7210T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740711 | ||||||
| chr7:2740758
|
T | C | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-7257A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740758 | ||||||
| chr7:2740767
|
C | T | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-7266G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740767 | ||||||
| chr7:2740820
|
G | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0259 | 2 | HG02165.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.526-7319C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740820 | ||||||
| chr7:2740888
|
C | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.526-7387G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740888 | ||||||
| chr7:2740901
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-7400G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740901 | ||||||
| chr7:2740906
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.526-7405C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740906 | ||||||
| chr7:2740996
|
G | C | 1 | a0001c0001t0017g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.526-7495C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2740996 | ||||||
| chr7:2741024
|
G | A | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-7523C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741024 | ||||||
| chr7:2741032
|
G | A | 34 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(31): Show | 34 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.526-7531C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741032 | ||||||
| chr7:2741038
|
C | A | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-7537G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741038 | ||||||
| chr7:2741040
|
G | A | 1 | a0001c0001t0003g0059 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.526-7539C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741040 | ||||||
| chr7:2741045
|
A | AAAAC | 4 | a0001c0001t0002g0165a0001c0001t0002g0171a0001c0001t0002g0255others(1): Show | 4 | HG01069.hp2 HG01123.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-7548_526-7545d others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741045 | ||||||
| chr7:2741045
|
AAAAC | A | 90 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(87): Show | 91 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.526-7548_526-7545d others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741045 | ||||||
| chr7:2741097
|
A | T | 8 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-7596T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741097 | ||||||
| chr7:2741132
|
T | C | 44 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(41): Show | 45 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.526-7631A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741132 | ||||||
| chr7:2741174
|
G | A | 12 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(9): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-7673C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741174 | ||||||
| chr7:2741191
|
G | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-7690C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741191 | ||||||
| chr7:2741229
|
C | A | 73 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0021others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.526-7728G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741229 | ||||||
| chr7:2741290
|
G | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-7789C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741290 | ||||||
| chr7:2741308
|
T | C | 2 | a0001c0001t0003g0199a0001c0001t0004g0090 | 2 | HG01993.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.526-7807A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741308 | ||||||
| chr7:2741354
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.526-7853G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741354 | ||||||
| chr7:2741389
|
A | G | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 173 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.526-7888T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741389 | ||||||
| chr7:2741401
|
A | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-7900T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741401 | ||||||
| chr7:2741421
|
G | T | 1 | a0001c0001t0024g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.526-7920C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741421 | ||||||
| chr7:2741426
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-7925G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741426 | ||||||
| chr7:2741430
|
A | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-7929T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741430 | ||||||
| chr7:2741456
|
C | A | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 173 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.526-7955G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741456 | ||||||
| chr7:2741615
|
G | C | 78 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(75): Show | 79 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.526-8114C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741615 | ||||||
| chr7:2741670
|
T | TA | 44 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(41): Show | 45 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.526-8170dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741670 | ||||||
| chr7:2741694
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-8193A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741694 | ||||||
| chr7:2741818
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.526-8317A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741818 | ||||||
| chr7:2741877
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0221a0001c0001t0001g0225others(1): Show | 4 | HG01358.hp1 HG02257.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-8376G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741877 | ||||||
| chr7:2741922
|
A | G | 2 | a0001c0001t0013g0277a0001c0001t0013g0278 | 2 | NA18956.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.526-8421T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2741922 | ||||||
| chr7:2742048
|
G | A | 42 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0012others(39): Show | 43 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(40): Show |
intron_variant | MODIFIER | c.526-8547C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742048 | ||||||
| chr7:2742147
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.526-8646C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742147 | ||||||
| chr7:2742178
|
T | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0129 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526-8677A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742178 | ||||||
| chr7:2742180
|
C | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-8679G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742180 | ||||||
| chr7:2742258
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.526-8757A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742258 | ||||||
| chr7:2742324
|
G | C | 44 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(41): Show | 45 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.526-8823C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742324 | ||||||
| chr7:2742336
|
A | G | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-8835T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742336 | ||||||
| chr7:2742449
|
G | T | 3 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194 | 3 | NA18970.hp2 NA18992.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.526-8948C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742449 | ||||||
| chr7:2742479
|
C | A | 5 | a0001c0001t0003g0043a0001c0002t0002g0081a0001c0002t0002g0101others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-8978G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742479 | ||||||
| chr7:2742482
|
T | C | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526-8981A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742482 | ||||||
| chr7:2742484
|
T | G | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526-8983A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742484 | ||||||
| chr7:2742485
|
A | T | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526-8984T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742485 | ||||||
| chr7:2742486
|
T | C | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526-8985A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742486 | ||||||
| chr7:2742488
|
T | A | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.526-8987A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742488 | ||||||
| chr7:2742518
|
T | C | 313 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.526-9017A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742518 | ||||||
| chr7:2742556
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-9055G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742556 | ||||||
| chr7:2742614
|
A | G | 1 | a0001c0001t0003g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.526-9113T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742614 | ||||||
| chr7:2742768
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-9267G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742768 | ||||||
| chr7:2742859
|
C | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.526-9358G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742859 | ||||||
| chr7:2742927
|
T | C | 3 | a0001c0001t0002g0018a0001c0001t0002g0027a0001c0001t0002g0068 | 3 | HG00639.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.526-9426A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742927 | ||||||
| chr7:2742958
|
C | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.526-9457G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2742958 | ||||||
| chr7:2743016
|
G | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-9515C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743016 | ||||||
| chr7:2743192
|
G | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-9691C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743192 | ||||||
| chr7:2743206
|
G | A | 7 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0290others(4): Show | 7 | HG02165.hp2 NA18953.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-9705C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743206 | ||||||
| chr7:2743342
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-9841G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743342 | ||||||
| chr7:2743402
|
CA | C | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-9902delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743402 | ||||||
| chr7:2743459
|
T | A | 1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.526-9958A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743459 | ||||||
| chr7:2743542
|
A | G | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-10041T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743542 | ||||||
| chr7:2743550
|
T | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-10049A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743550 | ||||||
| chr7:2743573
|
A | T | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-10072T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743573 | ||||||
| chr7:2743587
|
C | T | 2 | a0001c0001t0008g0132a0001c0001t0008g0283 | 2 | NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.526-10086G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743587 | ||||||
| chr7:2743604
|
C | A | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-10103G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743604 | ||||||
| chr7:2743605
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.526-10104C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743605 | ||||||
| chr7:2743609
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-10108C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743609 | ||||||
| chr7:2743644
|
C | G | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-10143G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743644 | ||||||
| chr7:2743672
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.526-10171A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743672 | ||||||
| chr7:2743704
|
C | T | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.526-10203G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743704 | ||||||
| chr7:2743705
|
G | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-10204C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743705 | ||||||
| chr7:2743710
|
G | A | 91 | a0001c0001t0002g0004a0001c0001t0002g0014a0001c0001t0002g0015others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.526-10209C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743710 | ||||||
| chr7:2743720
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG01070.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.526-10219C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743720 | ||||||
| chr7:2743726
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-10225G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743726 | ||||||
| chr7:2743794
|
A | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 171 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.526-10293T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743794 | ||||||
| chr7:2743857
|
G | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-10356C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743857 | ||||||
| chr7:2743888
|
G | A | 1 | a0001c0001t0004g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526-10387C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743888 | ||||||
| chr7:2743892
|
G | A | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 10 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.526-10391C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743892 | ||||||
| chr7:2743964
|
G | T | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-10463C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743964 | ||||||
| chr7:2743983
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-10482G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743983 | ||||||
| chr7:2743994
|
A | T | 2 | a0001c0001t0004g0022a0001c0001t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.526-10493T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2743994 | ||||||
| chr7:2744112
|
A | G | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-10611T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744112 | ||||||
| chr7:2744148
|
C | T | 2 | a0001c0001t0002g0019a0001c0001t0012g0298 | 2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.526-10647G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744148 | ||||||
| chr7:2744170
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.526-10669A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744170 | ||||||
| chr7:2744173
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.526-10672A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744173 | ||||||
| chr7:2744181
|
C | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.526-10680G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744181 | ||||||
| chr7:2744208
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-10707C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744208 | ||||||
| chr7:2744210
|
G | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-10709C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744210 | ||||||
| chr7:2744229
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.526-10728C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744229 | ||||||
| chr7:2744248
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | NA18953.hp1 NA19012.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-10747C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744248 | ||||||
| chr7:2744258
|
G | C | 1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.526-10757C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744258 | ||||||
| chr7:2744295
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.526-10794G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744295 | ||||||
| chr7:2744329
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-10828C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744329 | ||||||
| chr7:2744331
|
A | G | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-10830T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744331 | ||||||
| chr7:2744349
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-10848A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744349 | ||||||
| chr7:2744362
|
A | G | 1 | a0001c0001t0007g0194 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.526-10861T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744362 | ||||||
| chr7:2744367
|
C | A | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-10866G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744367 | ||||||
| chr7:2744369
|
G | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-10868C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744369 | ||||||
| chr7:2744376
|
T | C | 1 | a0001c0001t0005g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.526-10875A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744376 | ||||||
| chr7:2744549
|
A | T | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-11048T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744549 | ||||||
| chr7:2744626
|
A | G | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.526-11125T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744626 | ||||||
| chr7:2744650
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-11149G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744650 | ||||||
| chr7:2744889
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.526-11388G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744889 | ||||||
| chr7:2744898
|
G | C | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.526-11397C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744898 | ||||||
| chr7:2744969
|
A | C | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.526-11468T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744969 | ||||||
| chr7:2744975
|
A | G | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-11474T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744975 | ||||||
| chr7:2744987
|
C | T | 1 | a0001c0001t0003g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.526-11486G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2744987 | ||||||
| chr7:2745111
|
G | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-11610C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745111 | ||||||
| chr7:2745156
|
G | T | 37 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0012others(34): Show | 38 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.526-11655C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745156 | ||||||
| chr7:2745210
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-11709T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745210 | ||||||
| chr7:2745214
|
T | C | 1 | a0001c0001t0005g0300 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.526-11713A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745214 | ||||||
| chr7:2745233
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-11732A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745233 | ||||||
| chr7:2745277
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.526-11776T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745277 | ||||||
| chr7:2745301
|
T | G | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-11800A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745301 | ||||||
| chr7:2745336
|
C | T | 1 | a0001c0001t0024g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.526-11835G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745336 | ||||||
| chr7:2745340
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-11839G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745340 | ||||||
| chr7:2745383
|
T | G | 1 | a0001c0001t0004g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.526-11882A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745383 | ||||||
| chr7:2745386
|
T | C | 1 | a0001c0001t0004g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526-11885A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745386 | ||||||
| chr7:2745491
|
G | C | 7 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0184others(4): Show | 7 | HG01167.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.526-11990C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745491 | ||||||
| chr7:2745494
|
T | A | 7 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0184others(4): Show | 7 | HG01167.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.526-11993A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745494 | ||||||
| chr7:2745506
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-12005T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745506 | ||||||
| chr7:2745529
|
T | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-12028A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745529 | ||||||
| chr7:2745561
|
T | A | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.526-12060A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745561 | ||||||
| chr7:2745563
|
A | T | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.526-12062T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745563 | ||||||
| chr7:2745567
|
A | G | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.526-12066T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745567 | ||||||
| chr7:2745678
|
T | C | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-12177A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745678 | ||||||
| chr7:2745692
|
G | A | 1 | a0001c0001t0004g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.526-12191C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745692 | ||||||
| chr7:2745759
|
T | G | 2 | a0001c0001t0009g0267a0001c0001t0009g0268 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-12258A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745759 | ||||||
| chr7:2745764
|
T | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-12263A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745764 | ||||||
| chr7:2745854
|
C | T | 3 | a0001c0001t0008g0051a0001c0001t0008g0132a0001c0001t0008g0283 | 3 | NA18992.hp1 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.526-12353G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745854 | ||||||
| chr7:2745864
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.526-12363C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745864 | ||||||
| chr7:2745873
|
GTC | G | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-12374_526-1237 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745873 | ||||||
| chr7:2745908
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.526-12407G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745908 | ||||||
| chr7:2745957
|
CAAG | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-12459_526-1245 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745957 | ||||||
| chr7:2745963
|
G | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-12462C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2745963 | ||||||
| chr7:2746113
|
A | G | 1 | a0001c0001t0003g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.526-12612T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746113 | ||||||
| chr7:2746124
|
T | C | 1 | a0001c0002t0002g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526-12623A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746124 | ||||||
| chr7:2746148
|
T | C | 1 | a0001c0002t0002g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526-12647A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746148 | ||||||
| chr7:2746153
|
C | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-12652G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746153 | ||||||
| chr7:2746166
|
A | G | 1 | a0001c0002t0002g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526-12665T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746166 | ||||||
| chr7:2746185
|
G | A | 4 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(1): Show | 4 | HG03834.hp1 NA19067.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-12684C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746185 | ||||||
| chr7:2746264
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.526-12763A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746264 | ||||||
| chr7:2746376
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-12875C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746376 | ||||||
| chr7:2746410
|
A | G | 6 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0312others(3): Show | 6 | HG01074.hp2 HG01081.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-12909T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746410 | ||||||
| chr7:2746444
|
G | T | 3 | a0001c0002t0002g0081a0001c0002t0002g0101a0001c0002t0002g0102 | 3 | HG02559.hp2 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.526-12943C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746444 | ||||||
| chr7:2746460
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.526-12959A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746460 | ||||||
| chr7:2746482
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-12981G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746482 | ||||||
| chr7:2746533
|
A | T | 43 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(40): Show | 44 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.526-13032T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746533 | ||||||
| chr7:2746533
|
AT | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-13033delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746533 | ||||||
| chr7:2746640
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-13139G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746640 | ||||||
| chr7:2746641
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-13140G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746641 | ||||||
| chr7:2746735
|
T | G | 2 | a0001c0001t0004g0093a0001c0001t0004g0289 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.526-13234A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746735 | ||||||
| chr7:2746757
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-13256G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746757 | ||||||
| chr7:2746766
|
C | T | 2 | a0001c0001t0006g0026a0001c0001t0006g0189 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.526-13265G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746766 | ||||||
| chr7:2746788
|
G | A | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.526-13287C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746788 | ||||||
| chr7:2746800
|
G | C | 1 | a0001c0001t0036g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.526-13299C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2746800 | ||||||
| chr7:2747185
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-13684G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747185 | ||||||
| chr7:2747200
|
T | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-13699A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747200 | ||||||
| chr7:2747216
|
A | G | 1 | a0001c0001t0003g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.526-13715T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747216 | ||||||
| chr7:2747251
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-13750G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747251 | ||||||
| chr7:2747253
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-13752A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747253 | ||||||
| chr7:2747302
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.526-13801G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747302 | ||||||
| chr7:2747402
|
C | T | 1 | a0001c0001t0012g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.526-13901G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747402 | ||||||
| chr7:2747428
|
C | T | 12 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(9): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-13927G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747428 | ||||||
| chr7:2747486
|
A | G | 1 | a0001c0001t0003g0038 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.526-13985T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747486 | ||||||
| chr7:2747512
|
G | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-14011C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747512 | ||||||
| chr7:2747657
|
G | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-14156C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747657 | ||||||
| chr7:2747662
|
C | T | 12 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(9): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-14161G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747662 | ||||||
| chr7:2747673
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0225a0001c0001t0002g0172 | 3 | HG01358.hp1 HG01993.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.526-14172G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747673 | ||||||
| chr7:2747700
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-14199C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747700 | ||||||
| chr7:2747746
|
C | T | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-14245G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747746 | ||||||
| chr7:2747833
|
A | T | 1 | a0001c0004t0014g0287 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.526-14332T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747833 | ||||||
| chr7:2747900
|
C | G | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-14399G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747900 | ||||||
| chr7:2747910
|
T | C | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.526-14409A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747910 | ||||||
| chr7:2747983
|
C | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-14482G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2747983 | ||||||
| chr7:2748059
|
G | A | 8 | a0001c0001t0019g0275a0001c0001t0019g0276a0001c0001t0026g0288others(5): Show | 8 | HG01192.hp2 HG02258.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.526-14558C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748059 | ||||||
| chr7:2748065
|
A | G | 313 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.526-14564T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748065 | ||||||
| chr7:2748097
|
T | C | 1 | a0001c0001t0004g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.526-14596A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748097 | ||||||
| chr7:2748241
|
G | A | 1 | a0001c0001t0004g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.526-14740C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748241 | ||||||
| chr7:2748496
|
C | A | 1 | a0001c0004t0018g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.526-14995G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748496 | ||||||
| chr7:2748570
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-15069A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748570 | ||||||
| chr7:2748605
|
G | A | 3 | a0001c0001t0002g0171a0001c0001t0004g0022a0001c0001t0004g0023 | 3 | HG01934.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.526-15104C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748605 | ||||||
| chr7:2748738
|
A | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-15237T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748738 | ||||||
| chr7:2748742
|
A | C | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-15241T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748742 | ||||||
| chr7:2748822
|
C | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-15321G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748822 | ||||||
| chr7:2748837
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-15336T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748837 | ||||||
| chr7:2748847
|
A | G | 5 | a0001c0001t0001g0173a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG00609.hp1 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-15346T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748847 | ||||||
| chr7:2748853
|
C | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01358.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.526-15352G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748853 | ||||||
| chr7:2748984
|
T | C | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.526-15483A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748984 | ||||||
| chr7:2748987
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-15486A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748987 | ||||||
| chr7:2748988
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-15487C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2748988 | ||||||
| chr7:2749103
|
C | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-15602G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749103 | ||||||
| chr7:2749163
|
A | G | 49 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(46): Show | 50 | HG01074.hp1 HG01123.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.526-15662T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749163 | ||||||
| chr7:2749180
|
T | TA | 26 | a0001c0001t0004g0010a0001c0001t0004g0022a0001c0001t0004g0023others(23): Show | 26 | HG01123.hp1 HG01361.hp2 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.526-15680dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749180 | ||||||
| chr7:2749191
|
G | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-15690C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749191 | ||||||
| chr7:2749205
|
T | C | 1 | a0001c0001t0003g0034 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.526-15704A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749205 | ||||||
| chr7:2749221
|
T | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-15720A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749221 | ||||||
| chr7:2749224
|
C | T | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-15723G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749224 | ||||||
| chr7:2749278
|
T | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0173a0001c0001t0001g0190others(83): Show | 86 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.526-15777A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749278 | ||||||
| chr7:2749386
|
T | C | 174 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 175 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.526-15885A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749386 | ||||||
| chr7:2749387
|
C | T | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-15886G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749387 | ||||||
| chr7:2749494
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.526-15993G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749494 | ||||||
| chr7:2749568
|
G | A | 9 | a0001c0001t0003g0017a0001c0001t0003g0036a0001c0001t0003g0055others(6): Show | 9 | HG00609.hp2 HG02135.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-16067C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749568 | ||||||
| chr7:2749627
|
G | A | 10 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(7): Show | 11 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-16126C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749627 | ||||||
| chr7:2749629
|
T | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-16128A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749629 | ||||||
| chr7:2749639
|
T | G | 173 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.526-16138A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749639 | ||||||
| chr7:2749646
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-16145C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749646 | ||||||
| chr7:2749735
|
G | C | 3 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0035 | 3 | HG00544.hp2 HG02080.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.526-16234C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749735 | ||||||
| chr7:2749884
|
A | T | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-16383T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2749884 | ||||||
| chr7:2750070
|
G | A | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 148 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.526-16569C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750070 | ||||||
| chr7:2750089
|
A | G | 15 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(12): Show | 15 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.526-16588T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750089 | ||||||
| chr7:2750139
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-16638C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750139 | ||||||
| chr7:2750175
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.526-16674C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750175 | ||||||
| chr7:2750246
|
A | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.526-16745T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750246 | ||||||
| chr7:2750458
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-16957T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750458 | ||||||
| chr7:2750470
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.526-16969G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750470 | ||||||
| chr7:2750647
|
C | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-17146G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750647 | ||||||
| chr7:2750674
|
G | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0129 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.526-17173C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750674 | ||||||
| chr7:2750688
|
C | A | 1 | a0001c0001t0003g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.526-17187G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750688 | ||||||
| chr7:2750694
|
C | CGGGGGAC others(46): Show |
1 | a0001c0001t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.526-17246_526-1719 others(57): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750694 | ||||||
| chr7:2750721
|
C | A | 1 | a0001c0001t0008g0052 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.526-17220G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750721 | ||||||
| chr7:2750752
|
G | A | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-17251C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750752 | ||||||
| chr7:2750758
|
C | T | 171 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 173 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.526-17257G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750758 | ||||||
| chr7:2750778
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | NA18982.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.526-17277A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750778 | ||||||
| chr7:2750811
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.526-17310C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750811 | ||||||
| chr7:2750814
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-17313G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750814 | ||||||
| chr7:2750925
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.526-17424G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2750925 | ||||||
| chr7:2751051
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.526-17550A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751051 | ||||||
| chr7:2751117
|
G | A | 3 | a0001c0001t0008g0049a0001c0001t0008g0053a0001c0001t0008g0054 | 3 | HG02056.hp1 HG02071.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.526-17616C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751117 | ||||||
| chr7:2751244
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.526-17743T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751244 | ||||||
| chr7:2751315
|
C | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-17814G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751315 | ||||||
| chr7:2751323
|
C | T | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-17822G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751323 | ||||||
| chr7:2751399
|
G | GA | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 99 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.526-17899dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751399 | ||||||
| chr7:2751399
|
G | GAA | 13 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0215others(10): Show | 13 | HG00741.hp2 HG01346.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.526-17900_526-1789 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751399 | ||||||
| chr7:2751410
|
A | C | 1 | a0001c0001t0005g0312 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.526-17909T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751410 | ||||||
| chr7:2751509
|
G | A | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-18008C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751509 | ||||||
| chr7:2751520
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.526-18019A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751520 | ||||||
| chr7:2751754
|
C | T | 1 | a0001c0001t0030g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.526-18253G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751754 | ||||||
| chr7:2751782
|
TA | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-18282delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751782 | ||||||
| chr7:2751878
|
C | T | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-18377G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751878 | ||||||
| chr7:2751944
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-18443G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751944 | ||||||
| chr7:2751964
|
A | T | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526-18463T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751964 | ||||||
| chr7:2751988
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-18487G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2751988 | ||||||
| chr7:2752030
|
C | T | 1 | a0001c0001t0003g0169 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.526-18529G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752030 | ||||||
| chr7:2752103
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.526-18602A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752103 | ||||||
| chr7:2752196
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-18695A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752196 | ||||||
| chr7:2752234
|
T | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-18733A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752234 | ||||||
| chr7:2752379
|
G | A | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.526-18878C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752379 | ||||||
| chr7:2752414
|
C | T | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-18913G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752414 | ||||||
| chr7:2752446
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.526-18945C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752446 | ||||||
| chr7:2752503
|
A | C | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-19002T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752503 | ||||||
| chr7:2752629
|
A | C | 5 | a0001c0001t0002g0159a0001c0001t0002g0161a0001c0001t0004g0124others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-19128T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752629 | ||||||
| chr7:2752657
|
A | G | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-19156T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752657 | ||||||
| chr7:2752764
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-19263C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752764 | ||||||
| chr7:2752773
|
G | A | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.526-19272C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752773 | ||||||
| chr7:2752874
|
G | A | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-19373C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752874 | ||||||
| chr7:2752890
|
G | A | 31 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(28): Show | 31 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.526-19389C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752890 | ||||||
| chr7:2752956
|
C | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-19455G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2752956 | ||||||
| chr7:2753139
|
C | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0290others(4): Show | 7 | HG02165.hp2 NA18953.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-19638G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753139 | ||||||
| chr7:2753144
|
C | G | 1 | a0001c0001t0005g0302 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.526-19643G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753144 | ||||||
| chr7:2753151
|
C | T | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG00741.hp1 NA19067.hp1 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-19650G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753151 | ||||||
| chr7:2753154
|
C | CT | 12 | a0001c0001t0001g0007a0001c0001t0001g0221a0001c0001t0011g0003others(9): Show | 13 | HG00741.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.526-19654dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753154 | ||||||
| chr7:2753154
|
CT | C | 31 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(28): Show | 31 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.526-19654delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753154 | ||||||
| chr7:2753165
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.526-19664A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753165 | ||||||
| chr7:2753166
|
A | T | 9 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(6): Show | 10 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-19665T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753166 | ||||||
| chr7:2753167
|
A | T | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.526-19666T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753167 | ||||||
| chr7:2753281
|
G | C | 1 | a0001c0001t0003g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.526-19780C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753281 | ||||||
| chr7:2753391
|
T | TCCTCCTG others(6): Show |
178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 180 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.526-19891_526-1989 others(17): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753391 | ||||||
| chr7:2753408
|
G | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-19907C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753408 | ||||||
| chr7:2753457
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.526-19956A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753457 | ||||||
| chr7:2753501
|
T | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-20000A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753501 | ||||||
| chr7:2753589
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-20088A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753589 | ||||||
| chr7:2753672
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-20171C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753672 | ||||||
| chr7:2753804
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-20303A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753804 | ||||||
| chr7:2753958
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.526-20457G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753958 | ||||||
| chr7:2753973
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-20472A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2753973 | ||||||
| chr7:2754003
|
G | T | 1 | a0001c0001t0005g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.526-20502C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754003 | ||||||
| chr7:2754075
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-20574A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754075 | ||||||
| chr7:2754446
|
T | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-20945A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754446 | ||||||
| chr7:2754476
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.526-20975G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754476 | ||||||
| chr7:2754495
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.526-20994G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754495 | ||||||
| chr7:2754508
|
C | G | 6 | a0001c0001t0002g0077a0001c0001t0004g0056a0001c0001t0004g0058others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-21007G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754508 | ||||||
| chr7:2754513
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.526-21012G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754513 | ||||||
| chr7:2754577
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.526-21076A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754577 | ||||||
| chr7:2754582
|
TA | T | 80 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0012others(77): Show | 81 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.526-21082delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754582 | ||||||
| chr7:2754582
|
TAA | T | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 6 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-21083_526-2108 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754582 | ||||||
| chr7:2754643
|
G | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-21142C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754643 | ||||||
| chr7:2754754
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.526-21253C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754754 | ||||||
| chr7:2754827
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-21326G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754827 | ||||||
| chr7:2754840
|
C | T | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.526-21339G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754840 | ||||||
| chr7:2754861
|
A | T | 1 | a0001c0001t0003g0201 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.526-21360T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754861 | ||||||
| chr7:2754955
|
T | A | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.526-21454A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754955 | ||||||
| chr7:2754964
|
A | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-21463T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754964 | ||||||
| chr7:2754984
|
T | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-21483A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2754984 | ||||||
| chr7:2755254
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.526-21753G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755254 | ||||||
| chr7:2755275
|
A | G | 9 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0026g0288others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-21774T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755275 | ||||||
| chr7:2755283
|
G | A | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG02922.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.526-21782C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755283 | ||||||
| chr7:2755430
|
C | T | 6 | a0001c0001t0011g0183a0001c0001t0011g0273a0001c0001t0012g0316others(3): Show | 6 | HG03195.hp2 HG03209.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-21929G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755430 | ||||||
| chr7:2755636
|
C | G | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-22135G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755636 | ||||||
| chr7:2755829
|
C | T | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526-22328G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755829 | ||||||
| chr7:2755843
|
A | C | 1 | a0001c0001t0004g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.526-22342T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755843 | ||||||
| chr7:2755896
|
A | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-22395T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755896 | ||||||
| chr7:2755910
|
T | G | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.526-22409A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755910 | ||||||
| chr7:2755932
|
T | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-22431A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755932 | ||||||
| chr7:2755936
|
A | T | 1 | a0001c0001t0004g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.526-22435T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2755936 | ||||||
| chr7:2756221
|
G | T | 1 | a0001c0001t0003g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.526-22720C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756221 | ||||||
| chr7:2756248
|
T | G | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.526-22747A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756248 | ||||||
| chr7:2756280
|
G | A | 55 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(52): Show | 56 | HG00741.hp1 HG01074.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.526-22779C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756280 | ||||||
| chr7:2756309
|
T | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-22808A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756309 | ||||||
| chr7:2756319
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.526-22818T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756319 | ||||||
| chr7:2756323
|
A | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.526-22822T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756323 | ||||||
| chr7:2756329
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-22828A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756329 | ||||||
| chr7:2756379
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.526-22878T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756379 | ||||||
| chr7:2756428
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-22927A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756428 | ||||||
| chr7:2756474
|
G | T | 5 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0197others(2): Show | 5 | HG02056.hp2 NA18952.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-22973C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756474 | ||||||
| chr7:2756605
|
T | TCAAA | 35 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(32): Show | 35 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.526-23108_526-2310 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756605 | ||||||
| chr7:2756605
|
T | TCAAACAA others(1): Show |
42 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0011others(39): Show | 43 | HG01074.hp1 HG01123.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.526-23112_526-2310 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756605 | ||||||
| chr7:2756634
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-23133A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756634 | ||||||
| chr7:2756664
|
G | A | 1 | a0001c0001t0008g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.526-23163C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756664 | ||||||
| chr7:2756697
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-23196C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756697 | ||||||
| chr7:2756836
|
G | C | 1 | a0001c0001t0015g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-23335C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2756836 | ||||||
| chr7:2757061
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.526-23560G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757061 | ||||||
| chr7:2757128
|
C | CT | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 55 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.526-23628_526-2362 others(5): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757128 | ||||||
| chr7:2757128
|
C | CTT | 22 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.526-23628_526-2362 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757128 | ||||||
| chr7:2757128
|
C | CTTT | 4 | a0001c0001t0013g0277a0001c0001t0013g0279a0001c0003t0001g0237others(1): Show | 4 | NA18956.hp1 NA18979.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-23628_526-2362 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757128 | ||||||
| chr7:2757128
|
CCTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.526-23637_526-2362 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757128 | ||||||
| chr7:2757129
|
C | CT | 36 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0046others(33): Show | 36 | HG00544.hp2 HG01175.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.526-23629dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757129 | ||||||
| chr7:2757129
|
C | CTTTTTTT others(33): Show |
1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-23629_526-2362 others(44): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757129 | ||||||
| chr7:2757129
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.526-23628G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757129 | ||||||
| chr7:2757129
|
CTTTTT | C | 46 | a0001c0001t0004g0002a0001c0001t0004g0010a0001c0001t0004g0012others(43): Show | 47 | HG01074.hp1 HG01123.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.526-23633_526-2362 others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757129 | ||||||
| chr7:2757129
|
CTTTTTT | C | 22 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(19): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-23634_526-2362 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757129 | ||||||
| chr7:2757129
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0003g0017a0001c0001t0003g0036a0001c0001t0003g0055others(1): Show | 4 | HG00609.hp2 HG02135.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-23641_526-2362 others(17): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757129 | ||||||
| chr7:2757277
|
A | AG | 318 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(315): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.526-23777dupC | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757277 | ||||||
| chr7:2757574
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.526-24073C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757574 | ||||||
| chr7:2757620
|
T | G | 12 | a0001c0001t0004g0002a0001c0001t0004g0100a0001c0001t0004g0127others(9): Show | 13 | HG01074.hp1 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-24119A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757620 | ||||||
| chr7:2757633
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.526-24132A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757633 | ||||||
| chr7:2757832
|
CAT | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-24333_526-2433 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2757832 | ||||||
| chr7:2758116
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-24615C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758116 | ||||||
| chr7:2758240
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-24739A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758240 | ||||||
| chr7:2758311
|
C | G | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-24810G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758311 | ||||||
| chr7:2758370
|
A | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-24869T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758370 | ||||||
| chr7:2758410
|
G | C | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(311): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.526-24909C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758410 | ||||||
| chr7:2758528
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.526-25027C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758528 | ||||||
| chr7:2758621
|
G | C | 313 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.526-25120C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758621 | ||||||
| chr7:2758621
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.526-25120C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758621 | ||||||
| chr7:2758627
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.526-25126G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758627 | ||||||
| chr7:2758660
|
C | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.526-25159G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758660 | ||||||
| chr7:2758705
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.526-25204G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758705 | ||||||
| chr7:2758895
|
A | G | 5 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-25394T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2758895 | ||||||
| chr7:2759071
|
C | T | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.526-25570G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759071 | ||||||
| chr7:2759075
|
G | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-25574C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759075 | ||||||
| chr7:2759096
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.526-25595G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759096 | ||||||
| chr7:2759097
|
A | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.526-25596T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759097 | ||||||
| chr7:2759113
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-25612G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759113 | ||||||
| chr7:2759139
|
CAAAATAA others(5): Show |
C | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-25650_526-2563 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759139 | ||||||
| chr7:2759140
|
A | AAAAT | 9 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0259others(6): Show | 9 | HG01358.hp2 HG01934.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-25643_526-2564 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
A | AAAATAAA others(1): Show |
3 | a0001c0001t0001g0212a0001c0001t0003g0032a0001c0003t0001g0236 | 3 | HG00140.hp2 NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.526-25647_526-2564 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
AAAAT | A | 23 | a0001c0001t0001g0173a0001c0001t0001g0247a0001c0001t0001g0262others(20): Show | 23 | HG00544.hp2 HG01169.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.526-25643_526-2564 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
AAAATAAA others(1): Show |
A | 27 | a0001c0001t0002g0004a0001c0001t0003g0169a0001c0001t0004g0100others(24): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.526-25647_526-2564 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
AAAATAAA others(5): Show |
A | 11 | a0001c0001t0002g0163a0001c0001t0004g0010a0001c0001t0004g0086others(8): Show | 11 | HG00741.hp1 HG01361.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-25651_526-2564 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
AAAATAAA others(9): Show |
A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-25655_526-2564 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
AAAATAAA others(13): Show |
A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-25659_526-2564 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759140
|
AAAATAAA others(17): Show |
A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-25663_526-2564 others(28): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759140 | ||||||
| chr7:2759175
|
A | G | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.526-25674T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759175 | ||||||
| chr7:2759188
|
T | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.526-25687A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759188 | ||||||
| chr7:2759284
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-25783T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759284 | ||||||
| chr7:2759361
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(4): Show | 7 | HG00280.hp1 HG01261.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-25860A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759361 | ||||||
| chr7:2759369
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-25868G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759369 | ||||||
| chr7:2759372
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-25871G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759372 | ||||||
| chr7:2759378
|
T | C | 8 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-25877A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759378 | ||||||
| chr7:2759424
|
G | C | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.526-25923C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759424 | ||||||
| chr7:2759531
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.526-26030C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759531 | ||||||
| chr7:2759550
|
T | C | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.526-26049A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759550 | ||||||
| chr7:2759751
|
G | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00280.hp1 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.526-26250C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759751 | ||||||
| chr7:2759829
|
G | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-26328C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759829 | ||||||
| chr7:2759858
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0184a0001c0001t0007g0269others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-26357G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759858 | ||||||
| chr7:2759859
|
GCCC | G | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-26361_526-2635 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759859 | ||||||
| chr7:2759908
|
G | A | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-26407C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759908 | ||||||
| chr7:2759933
|
C | A | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.526-26432G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759933 | ||||||
| chr7:2759948
|
T | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-26447A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2759948 | ||||||
| chr7:2760052
|
G | T | 169 | a0001c0001t0001g0264a0001c0001t0002g0001a0001c0001t0002g0004others(166): Show | 171 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.526-26551C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760052 | ||||||
| chr7:2760098
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-26597A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760098 | ||||||
| chr7:2760215
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.526-26714C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760215 | ||||||
| chr7:2760249
|
C | T | 1 | a0001c0001t0003g0169 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.526-26748G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760249 | ||||||
| chr7:2760277
|
C | T | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.526-26776G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760277 | ||||||
| chr7:2760318
|
G | A | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526-26817C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760318 | ||||||
| chr7:2760319
|
C | T | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526-26818G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760319 | ||||||
| chr7:2760435
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-26934G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760435 | ||||||
| chr7:2760492
|
A | G | 73 | a0001c0001t0002g0142a0001c0001t0003g0013a0001c0001t0003g0017others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.526-26991T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760492 | ||||||
| chr7:2760568
|
A | G | 2 | a0001c0001t0004g0022a0001c0001t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.526-27067T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760568 | ||||||
| chr7:2760575
|
C | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.526-27074G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760575 | ||||||
| chr7:2760584
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-27083G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760584 | ||||||
| chr7:2760585
|
G | A | 1 | a0001c0001t0007g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.526-27084C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760585 | ||||||
| chr7:2760649
|
C | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-27148G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760649 | ||||||
| chr7:2760824
|
A | C | 3 | a0001c0001t0004g0088a0001c0001t0004g0098a0001c0001t0004g0151 | 3 | HG02129.hp1 NA18943.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.526-27323T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760824 | ||||||
| chr7:2760887
|
A | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.526-27386T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760887 | ||||||
| chr7:2760914
|
G | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-27413C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760914 | ||||||
| chr7:2760927
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0259a0003c0005t0001g0257 | 3 | HG02165.hp2 NA18983.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.526-27426T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2760927 | ||||||
| chr7:2761007
|
A | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-27506T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761007 | ||||||
| chr7:2761068
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.526-27567C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761068 | ||||||
| chr7:2761158
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526-27657C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761158 | ||||||
| chr7:2761191
|
C | T | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-27690G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761191 | ||||||
| chr7:2761239
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.526-27738G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761239 | ||||||
| chr7:2761241
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(4): Show | 7 | HG00280.hp1 HG01261.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-27740A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761241 | ||||||
| chr7:2761342
|
C | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-27841G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761342 | ||||||
| chr7:2761353
|
C | T | 1 | a0001c0001t0003g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.526-27852G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761353 | ||||||
| chr7:2761391
|
T | G | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-27890A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761391 | ||||||
| chr7:2761532
|
G | A | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-28031C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761532 | ||||||
| chr7:2761533
|
G | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526-28032C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761533 | ||||||
| chr7:2761599
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.526-28098T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761599 | ||||||
| chr7:2761738
|
A | G | 1 | a0001c0001t0020g0025 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.526-28237T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761738 | ||||||
| chr7:2761739
|
G | C | 1 | a0001c0001t0003g0200 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.526-28238C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761739 | ||||||
| chr7:2761837
|
T | A | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-28336A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761837 | ||||||
| chr7:2761908
|
G | A | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.526-28407C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761908 | ||||||
| chr7:2761955
|
C | T | 1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.526-28454G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2761955 | ||||||
| chr7:2762047
|
G | A | 1 | a0001c0001t0004g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.526-28546C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762047 | ||||||
| chr7:2762101
|
A | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-28600T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762101 | ||||||
| chr7:2762135
|
C | T | 1 | a0001c0001t0036g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.526-28634G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762135 | ||||||
| chr7:2762169
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0173a0001c0001t0001g0202others(43): Show | 46 | HG00140.hp2 HG00609.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.526-28668G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762169 | ||||||
| chr7:2762273
|
G | T | 1 | a0001c0001t0003g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526-28772C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762273 | ||||||
| chr7:2762356
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-28855G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762356 | ||||||
| chr7:2762363
|
A | AG | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.526-28863dupC | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762363 | ||||||
| chr7:2762391
|
T | G | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-28890A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762391 | ||||||
| chr7:2762464
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0007g0185 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.526-28963A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762464 | ||||||
| chr7:2762513
|
G | A | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-29012C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762513 | ||||||
| chr7:2762536
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.526-29035C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762536 | ||||||
| chr7:2762539
|
T | C | 30 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(27): Show | 31 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.526-29038A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762539 | ||||||
| chr7:2762657
|
T | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-29156A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762657 | ||||||
| chr7:2762850
|
C | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-29349G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762850 | ||||||
| chr7:2762862
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.526-29361T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762862 | ||||||
| chr7:2762888
|
T | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.526-29387A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762888 | ||||||
| chr7:2762899
|
G | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-29398C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762899 | ||||||
| chr7:2762926
|
C | T | 5 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0184others(2): Show | 5 | HG01167.hp1 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-29425G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762926 | ||||||
| chr7:2762944
|
G | A | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526-29443C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762944 | ||||||
| chr7:2762983
|
C | G | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.526-29482G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2762983 | ||||||
| chr7:2763012
|
C | T | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.526-29511G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763012 | ||||||
| chr7:2763024
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-29523C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763024 | ||||||
| chr7:2763043
|
C | A | 1 | a0001c0001t0003g0096 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.526-29542G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763043 | ||||||
| chr7:2763190
|
CAACACAC others(5): Show |
C | 1 | a0001c0001t0007g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.526-29701_526-2969 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763190 | ||||||
| chr7:2763191
|
A | AAC | 22 | a0001c0001t0001g0095a0001c0001t0002g0068a0001c0001t0002g0083others(19): Show | 22 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-29692_526-2969 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACAC | 37 | a0001c0001t0002g0004a0001c0001t0002g0073a0001c0001t0002g0162others(34): Show | 38 | HG00280.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.526-29694_526-2969 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACAC | 34 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0027others(31): Show | 34 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.526-29696_526-2969 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(1): Show |
36 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(33): Show | 36 | HG01074.hp1 HG01081.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.526-29698_526-2969 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(3): Show |
14 | a0001c0001t0002g0177a0001c0001t0003g0115a0001c0001t0004g0022others(11): Show | 14 | HG01361.hp2 HG02148.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.526-29700_526-2969 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(5): Show |
11 | a0001c0001t0002g0158a0001c0001t0003g0118a0001c0001t0004g0010others(8): Show | 11 | HG01192.hp1 HG01433.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-29702_526-2969 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(7): Show |
1 | a0001c0004t0014g0287 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.526-29704_526-2969 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(9): Show |
2 | a0001c0001t0004g0011a0001c0001t0004g0093 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526-29706_526-2969 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(11): Show |
3 | a0001c0001t0004g0289a0001c0001t0009g0274a0001c0001t0026g0288 | 3 | HG02258.hp1 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.526-29708_526-2969 others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(17): Show |
1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.526-29714_526-2969 others(28): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(25): Show |
2 | a0001c0001t0015g0141a0001c0001t0035g0297 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.526-29722_526-2969 others(36): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(27): Show |
1 | a0001c0001t0019g0276 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526-29724_526-2969 others(38): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(29): Show |
2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.526-29726_526-2969 others(40): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(31): Show |
1 | a0001c0001t0015g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-29728_526-2969 others(42): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(35): Show |
2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.526-29691_526-2969 others(46): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(37): Show |
1 | a0001c0001t0017g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.526-29691_526-2969 others(48): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(41): Show |
1 | a0001c0001t0002g0282 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.526-29691_526-2969 others(52): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
A | AACACACA others(67): Show |
1 | a0001c0001t0017g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.526-29691_526-2969 others(78): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
AAC | A | 5 | a0001c0001t0002g0150a0001c0001t0003g0106a0001c0001t0009g0267others(2): Show | 5 | HG03098.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-29692_526-2969 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
AACACAC | A | 3 | a0001c0001t0002g0178a0001c0001t0011g0003a0001c0001t0011g0273 | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-29696_526-2969 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0206a0001c0001t0001g0221a0001c0001t0001g0225others(6): Show | 9 | HG00609.hp1 HG01358.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-29700_526-2969 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
AACACACA others(5): Show |
A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.526-29702_526-2969 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763191
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0005g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.526-29704_526-2969 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763191 | ||||||
| chr7:2763309
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.526-29808C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763309 | ||||||
| chr7:2763349
|
G | C | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.526-29848C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763349 | ||||||
| chr7:2763365
|
G | C | 9 | a0001c0001t0002g0142a0001c0001t0003g0038a0001c0001t0003g0059others(6): Show | 9 | NA18975.hp1 NA18977.hp1 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-29864C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763365 | ||||||
| chr7:2763379
|
G | A | 1 | a0001c0001t0021g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.526-29878C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763379 | ||||||
| chr7:2763403
|
A | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.526-29902T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763403 | ||||||
| chr7:2763450
|
G | T | 2 | a0001c0001t0004g0093a0001c0001t0004g0289 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.526-29949C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763450 | ||||||
| chr7:2763468
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.526-29967T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763468 | ||||||
| chr7:2763694
|
T | C | 3 | a0001c0001t0001g0247a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.526-30193A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763694 | ||||||
| chr7:2763714
|
A | G | 1 | a0001c0001t0004g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526-30213T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763714 | ||||||
| chr7:2763834
|
C | A | 3 | a0001c0001t0004g0010a0001c0001t0004g0108a0001c0001t0004g0109 | 3 | NA18942.hp2 NA18990.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.526-30333G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763834 | ||||||
| chr7:2763876
|
C | T | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.526-30375G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763876 | ||||||
| chr7:2763995
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.526-30494T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2763995 | ||||||
| chr7:2764034
|
G | C | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-30533C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764034 | ||||||
| chr7:2764088
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | NA18939.hp1 NA18955.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.526-30587A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764088 | ||||||
| chr7:2764170
|
T | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-30669A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764170 | ||||||
| chr7:2764191
|
G | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-30690C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764191 | ||||||
| chr7:2764214
|
G | A | 1 | a0001c0004t0014g0286 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.526-30713C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764214 | ||||||
| chr7:2764219
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.525+30709G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764219 | ||||||
| chr7:2764244
|
C | CT | 6 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0006g0026others(3): Show | 6 | HG00423.hp1 NA18962.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+30683dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764244 | ||||||
| chr7:2764244
|
CT | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.525+30683delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764244 | ||||||
| chr7:2764248
|
T | C | 33 | a0001c0001t0001g0204a0001c0001t0003g0065a0001c0001t0004g0011others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.525+30680A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764248 | ||||||
| chr7:2764249
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.525+30679A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764249 | ||||||
| chr7:2764317
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.525+30611C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764317 | ||||||
| chr7:2764325
|
C | A | 1 | a0001c0001t0004g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.525+30603G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764325 | ||||||
| chr7:2764391
|
T | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0259a0003c0005t0001g0257 | 3 | HG02165.hp2 NA18983.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.525+30537A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764391 | ||||||
| chr7:2764394
|
T | A | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.525+30534A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764394 | ||||||
| chr7:2764523
|
C | A | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+30405G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764523 | ||||||
| chr7:2764524
|
G | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+30404C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764524 | ||||||
| chr7:2764679
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.525+30249G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764679 | ||||||
| chr7:2764694
|
T | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+30234A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764694 | ||||||
| chr7:2764857
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.525+30071A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764857 | ||||||
| chr7:2764891
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.525+30037C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764891 | ||||||
| chr7:2764999
|
A | G | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+29929T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2764999 | ||||||
| chr7:2765001
|
T | C | 4 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0078others(1): Show | 4 | HG00280.hp2 HG01934.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+29927A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765001 | ||||||
| chr7:2765150
|
C | CT | 6 | a0001c0001t0002g0163a0001c0001t0008g0051a0001c0001t0008g0132others(3): Show | 6 | HG01361.hp1 HG02717.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+29777dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765150 | ||||||
| chr7:2765150
|
CT | C | 12 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(9): Show | 13 | HG00741.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+29777delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765150 | ||||||
| chr7:2765151
|
T | G | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525+29777A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765151 | ||||||
| chr7:2765170
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+29758G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765170 | ||||||
| chr7:2765186
|
C | T | 1 | a0001c0001t0012g0317 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.525+29742G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765186 | ||||||
| chr7:2765217
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.525+29711C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765217 | ||||||
| chr7:2765241
|
G | A | 8 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(5): Show | 8 | HG02451.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+29687C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765241 | ||||||
| chr7:2765253
|
T | C | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+29675A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765253 | ||||||
| chr7:2765282
|
G | A | 1 | a0001c0004t0018g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.525+29646C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765282 | ||||||
| chr7:2765309
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | NA18953.hp1 NA19012.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+29619C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765309 | ||||||
| chr7:2765380
|
A | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+29548T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765380 | ||||||
| chr7:2765380
|
A | T | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.525+29548T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765380 | ||||||
| chr7:2765549
|
T | G | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.525+29379A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765549 | ||||||
| chr7:2765587
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.525+29341C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765587 | ||||||
| chr7:2765615
|
GTT | G | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+29311_525+2931 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765615 | ||||||
| chr7:2765657
|
G | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+29271C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765657 | ||||||
| chr7:2765686
|
G | A | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.525+29242C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765686 | ||||||
| chr7:2765708
|
A | C | 2 | a0001c0001t0004g0187a0001c0001t0004g0188 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.525+29220T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765708 | ||||||
| chr7:2765789
|
C | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+29139G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765789 | ||||||
| chr7:2765834
|
T | G | 1 | a0001c0001t0004g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.525+29094A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765834 | ||||||
| chr7:2765853
|
A | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0184a0001c0001t0007g0269others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+29075T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765853 | ||||||
| chr7:2765875
|
G | GC | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.525+29052dupG | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765875 | ||||||
| chr7:2765887
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+29041A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765887 | ||||||
| chr7:2765891
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.525+29037G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765891 | ||||||
| chr7:2765906
|
TGCTGGGA others(8): Show |
T | 1 | a0001c0001t0006g0067 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.525+29007_525+2902 others(19): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765906 | ||||||
| chr7:2765963
|
G | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+28965C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765963 | ||||||
| chr7:2765963
|
G | T | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.525+28965C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2765963 | ||||||
| chr7:2766259
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.525+28669G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766259 | ||||||
| chr7:2766360
|
A | G | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.525+28568T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766360 | ||||||
| chr7:2766365
|
T | C | 5 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+28563A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766365 | ||||||
| chr7:2766387
|
C | CT | 11 | a0001c0001t0002g0160a0001c0001t0002g0164a0001c0001t0002g0172others(8): Show | 11 | HG01358.hp2 HG01993.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+28540dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766387 | ||||||
| chr7:2766387
|
CT | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.525+28540delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766387 | ||||||
| chr7:2766388
|
T | G | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.525+28540A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766388 | ||||||
| chr7:2766397
|
T | G | 1 | a0001c0001t0005g0313 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.525+28531A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766397 | ||||||
| chr7:2766474
|
T | C | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.525+28454A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766474 | ||||||
| chr7:2766644
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+28284G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766644 | ||||||
| chr7:2766666
|
G | A | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+28262C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766666 | ||||||
| chr7:2766770
|
T | C | 1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.525+28158A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766770 | ||||||
| chr7:2766796
|
T | C | 315 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(312): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.525+28132A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766796 | ||||||
| chr7:2766920
|
A | C | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.525+28008T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766920 | ||||||
| chr7:2766969
|
T | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+27959A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766969 | ||||||
| chr7:2766997
|
A | C | 7 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0290others(4): Show | 7 | HG02165.hp2 NA18953.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+27931T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2766997 | ||||||
| chr7:2767040
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.525+27888C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767040 | ||||||
| chr7:2767404
|
T | C | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525+27524A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767404 | ||||||
| chr7:2767415
|
C | T | 10 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(7): Show | 11 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+27513G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767415 | ||||||
| chr7:2767475
|
T | C | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.525+27453A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767475 | ||||||
| chr7:2767499
|
G | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+27429C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767499 | ||||||
| chr7:2767614
|
T | TA | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.525+27313dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767614 | ||||||
| chr7:2767813
|
T | C | 1 | a0001c0001t0003g0035 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.525+27115A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767813 | ||||||
| chr7:2767869
|
G | T | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+27059C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767869 | ||||||
| chr7:2767990
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+26938C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767990 | ||||||
| chr7:2767995
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+26933G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2767995 | ||||||
| chr7:2768038
|
A | T | 1 | a0001c0001t0006g0039 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.525+26890T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768038 | ||||||
| chr7:2768121
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.525+26807A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768121 | ||||||
| chr7:2768172
|
T | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+26756A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768172 | ||||||
| chr7:2768209
|
C | G | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.525+26719G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768209 | ||||||
| chr7:2768304
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+26624T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768304 | ||||||
| chr7:2768366
|
A | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+26562T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768366 | ||||||
| chr7:2768367
|
G | T | 1 | a0001c0001t0021g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.525+26561C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768367 | ||||||
| chr7:2768464
|
C | T | 22 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0121others(19): Show | 23 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.525+26464G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768464 | ||||||
| chr7:2768525
|
A | ATAT | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+26402_525+2640 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768525 | ||||||
| chr7:2768527
|
G | GTTT | 13 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(10): Show | 13 | HG00741.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+26400_525+2640 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768527 | ||||||
| chr7:2768527
|
G | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+26401C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768527 | ||||||
| chr7:2768550
|
T | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+26378A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768550 | ||||||
| chr7:2768617
|
AAATT | A | 5 | a0001c0001t0007g0006a0001c0001t0007g0184a0001c0001t0007g0269others(2): Show | 5 | HG02572.hp1 HG02976.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+26307_525+2631 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768617 | ||||||
| chr7:2768666
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0015g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.525+26252_525+2626 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768666 | ||||||
| chr7:2768666
|
T | TAAAAAAA others(6): Show |
1 | a0001c0004t0018g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.525+26261_525+2626 others(17): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768666 | ||||||
| chr7:2768666
|
T | TAAAAAAA others(9): Show |
1 | a0001c0004t0018g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.525+26261_525+2626 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768666 | ||||||
| chr7:2768672
|
A | C | 42 | a0001c0001t0002g0073a0001c0001t0002g0160a0001c0001t0002g0163others(39): Show | 43 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.525+26256T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768672 | ||||||
| chr7:2768677
|
C | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.525+26251G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768677 | ||||||
| chr7:2768678
|
A | AAC | 79 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.525+26249_525+2625 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768678 | ||||||
| chr7:2768679
|
A | C | 2 | a0001c0001t0009g0267a0001c0001t0009g0268 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+26249T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768679 | ||||||
| chr7:2768682
|
C | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.525+26246G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768682 | ||||||
| chr7:2768686
|
A | C | 29 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+26242T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768686 | ||||||
| chr7:2768687
|
C | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 124 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.525+26241G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768687 | ||||||
| chr7:2768687
|
CA | C | 41 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(38): Show | 42 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(39): Show |
intron_variant | MODIFIER | c.525+26240delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768687 | ||||||
| chr7:2768690
|
A | C | 29 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+26238T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768690 | ||||||
| chr7:2768691
|
A | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.525+26237T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768691 | ||||||
| chr7:2768692
|
A | C | 1 | a0001c0002t0002g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.525+26236T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768692 | ||||||
| chr7:2768697
|
A | AC | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+26230_525+2623 others(5): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768697 | ||||||
| chr7:2768723
|
G | C | 1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.525+26205C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768723 | ||||||
| chr7:2768835
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.525+26093T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768835 | ||||||
| chr7:2768883
|
T | C | 21 | a0001c0001t0003g0134a0001c0001t0005g0299a0001c0001t0005g0300others(18): Show | 21 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.525+26045A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768883 | ||||||
| chr7:2768961
|
C | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.525+25967G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768961 | ||||||
| chr7:2768980
|
G | A | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.525+25948C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768980 | ||||||
| chr7:2768998
|
G | C | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.525+25930C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2768998 | ||||||
| chr7:2769017
|
C | A | 1 | a0001c0001t0003g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.525+25911G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769017 | ||||||
| chr7:2769083
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.525+25845A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769083 | ||||||
| chr7:2769098
|
T | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.525+25830A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769098 | ||||||
| chr7:2769188
|
G | C | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+25740C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769188 | ||||||
| chr7:2769208
|
T | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+25720A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769208 | ||||||
| chr7:2769443
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.525+25485G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769443 | ||||||
| chr7:2769453
|
G | A | 37 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(34): Show | 38 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.525+25475C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769453 | ||||||
| chr7:2769459
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.525+25469C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769459 | ||||||
| chr7:2769482
|
G | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0215 | 2 | HG01346.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.525+25446C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769482 | ||||||
| chr7:2769572
|
A | G | 16 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(13): Show | 16 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.525+25356T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769572 | ||||||
| chr7:2769613
|
G | C | 1 | a0001c0002t0002g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.525+25315C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769613 | ||||||
| chr7:2769651
|
C | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+25277G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769651 | ||||||
| chr7:2769663
|
G | T | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.525+25265C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769663 | ||||||
| chr7:2769681
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.525+25247G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769681 | ||||||
| chr7:2769696
|
G | A | 13 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(10): Show | 13 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+25232C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769696 | ||||||
| chr7:2769712
|
G | C | 1 | a0001c0001t0003g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.525+25216C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769712 | ||||||
| chr7:2769840
|
C | T | 16 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(13): Show | 16 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.525+25088G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769840 | ||||||
| chr7:2769962
|
G | A | 3 | a0001c0001t0001g0247a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.525+24966C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769962 | ||||||
| chr7:2769965
|
C | A | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+24963G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2769965 | ||||||
| chr7:2770141
|
A | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+24787T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770141 | ||||||
| chr7:2770302
|
G | A | 314 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(311): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.525+24626C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770302 | ||||||
| chr7:2770307
|
G | C | 1 | a0001c0001t0024g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.525+24621C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770307 | ||||||
| chr7:2770643
|
ATAACAAC | A | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.525+24278_525+2428 others(11): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770643 | ||||||
| chr7:2770650
|
C | CAACAA | 158 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 160 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.525+24273_525+2427 others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770650 | ||||||
| chr7:2770811
|
C | T | 2 | a0001c0001t0035g0297a0002c0006t0027g0149 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.525+24117G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770811 | ||||||
| chr7:2770844
|
T | C | 13 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(10): Show | 13 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+24084A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2770844 | ||||||
| chr7:2771016
|
C | T | 1 | a0001c0001t0019g0276 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.525+23912G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771016 | ||||||
| chr7:2771047
|
T | C | 4 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(1): Show | 4 | HG02258.hp1 NA19067.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+23881A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771047 | ||||||
| chr7:2771062
|
G | A | 1 | a0001c0001t0007g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.525+23866C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771062 | ||||||
| chr7:2771112
|
G | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.525+23816C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771112 | ||||||
| chr7:2771205
|
C | T | 4 | a0001c0001t0003g0017a0001c0001t0003g0036a0001c0001t0003g0055others(1): Show | 4 | HG00609.hp2 HG02135.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+23723G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771205 | ||||||
| chr7:2771232
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.525+23696G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771232 | ||||||
| chr7:2771302
|
A | C | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.525+23626T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771302 | ||||||
| chr7:2771312
|
C | CA | 6 | a0001c0001t0001g0206a0001c0001t0002g0047a0001c0001t0003g0114others(3): Show | 6 | HG02055.hp1 HG03492.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+23615dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771312 | ||||||
| chr7:2771437
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.525+23491G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771437 | ||||||
| chr7:2771439
|
T | C | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+23489A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771439 | ||||||
| chr7:2771518
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0023g0020 | 2 | NA18939.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.525+23410G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771518 | ||||||
| chr7:2771607
|
C | T | 1 | a0001c0001t0024g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.525+23321G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771607 | ||||||
| chr7:2771615
|
T | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+23313A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771615 | ||||||
| chr7:2771666
|
A | C | 1 | a0001c0001t0007g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.525+23262T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771666 | ||||||
| chr7:2771713
|
T | C | 7 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+23215A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771713 | ||||||
| chr7:2771738
|
A | G | 1 | a0001c0001t0002g0150 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.525+23190T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771738 | ||||||
| chr7:2771814
|
CAT | C | 13 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(10): Show | 13 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+23112_525+2311 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771814 | ||||||
| chr7:2771909
|
T | C | 183 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.525+23019A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2771909 | ||||||
| chr7:2772035
|
T | G | 1 | a0001c0001t0003g0169 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.525+22893A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772035 | ||||||
| chr7:2772066
|
G | A | 1 | a0001c0001t0007g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.525+22862C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772066 | ||||||
| chr7:2772204
|
G | C | 1 | a0001c0001t0008g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.525+22724C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772204 | ||||||
| chr7:2772310
|
C | G | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.525+22618G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772310 | ||||||
| chr7:2772337
|
G | A | 32 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(29): Show | 32 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.525+22591C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772337 | ||||||
| chr7:2772375
|
A | C | 12 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(9): Show | 12 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+22553T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772375 | ||||||
| chr7:2772440
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.525+22488C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772440 | ||||||
| chr7:2772476
|
C | T | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.525+22452G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772476 | ||||||
| chr7:2772559
|
C | CAA | 12 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(9): Show | 12 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+22367_525+2236 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772559 | ||||||
| chr7:2772578
|
A | C | 12 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(9): Show | 12 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+22350T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772578 | ||||||
| chr7:2772621
|
G | C | 32 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(29): Show | 32 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.525+22307C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772621 | ||||||
| chr7:2772727
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+22201A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772727 | ||||||
| chr7:2772773
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+22155T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772773 | ||||||
| chr7:2772830
|
C | A | 12 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(9): Show | 12 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+22098G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772830 | ||||||
| chr7:2772906
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+22022C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772906 | ||||||
| chr7:2772948
|
A | C | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+21980T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772948 | ||||||
| chr7:2772948
|
A | T | 305 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(302): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.525+21980T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772948 | ||||||
| chr7:2772990
|
G | GA | 3 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0105 | 3 | NA18970.hp1 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.525+21937dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772990 | ||||||
| chr7:2772998
|
C | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.525+21930G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2772998 | ||||||
| chr7:2773022
|
TA | T | 3 | a0001c0001t0004g0088a0001c0001t0004g0098a0001c0001t0004g0151 | 3 | HG02129.hp1 NA18943.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.525+21905delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773022 | ||||||
| chr7:2773025
|
A | C | 3 | a0001c0001t0004g0088a0001c0001t0004g0098a0001c0001t0004g0151 | 3 | HG02129.hp1 NA18943.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.525+21903T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773025 | ||||||
| chr7:2773026
|
C | T | 3 | a0001c0001t0004g0002a0001c0001t0004g0100a0001c0001t0004g0127 | 4 | HG01074.hp1 HG01433.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+21902G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773026 | ||||||
| chr7:2773041
|
A | G | 1 | a0001c0001t0005g0312 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.525+21887T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773041 | ||||||
| chr7:2773080
|
G | A | 1 | a0001c0001t0004g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.525+21848C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773080 | ||||||
| chr7:2773083
|
G | A | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+21845C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773083 | ||||||
| chr7:2773302
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.525+21626C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773302 | ||||||
| chr7:2773329
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.525+21599G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773329 | ||||||
| chr7:2773444
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+21484G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773444 | ||||||
| chr7:2773510
|
C | G | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525+21418G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773510 | ||||||
| chr7:2773528
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.525+21400G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773528 | ||||||
| chr7:2773641
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+21287G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773641 | ||||||
| chr7:2773738
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.525+21190G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773738 | ||||||
| chr7:2773857
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+21071C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773857 | ||||||
| chr7:2773901
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.525+21027G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2773901 | ||||||
| chr7:2774127
|
G | C | 1 | a0001c0001t0002g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.525+20801C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774127 | ||||||
| chr7:2774134
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.525+20794C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774134 | ||||||
| chr7:2774172
|
G | A | 31 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(28): Show | 31 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.525+20756C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774172 | ||||||
| chr7:2774187
|
C | G | 15 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(12): Show | 15 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.525+20741G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774187 | ||||||
| chr7:2774434
|
G | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+20494C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774434 | ||||||
| chr7:2774527
|
G | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+20401C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774527 | ||||||
| chr7:2774609
|
G | T | 1 | a0001c0001t0003g0029 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.525+20319C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774609 | ||||||
| chr7:2774637
|
A | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.525+20291T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774637 | ||||||
| chr7:2774710
|
T | G | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.525+20218A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774710 | ||||||
| chr7:2774771
|
A | C | 13 | a0001c0001t0001g0247a0001c0001t0009g0139a0001c0001t0009g0267others(10): Show | 13 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+20157T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774771 | ||||||
| chr7:2774848
|
T | C | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.525+20080A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774848 | ||||||
| chr7:2774974
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.525+19954G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2774974 | ||||||
| chr7:2775001
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.525+19927G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775001 | ||||||
| chr7:2775100
|
A | G | 45 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(42): Show | 46 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(43): Show |
intron_variant | MODIFIER | c.525+19828T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775100 | ||||||
| chr7:2775104
|
A | C | 1 | a0001c0001t0023g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.525+19824T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775104 | ||||||
| chr7:2775221
|
G | C | 1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.525+19707C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775221 | ||||||
| chr7:2775299
|
G | C | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+19629C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775299 | ||||||
| chr7:2775309
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0184a0001c0001t0007g0269others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+19619C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775309 | ||||||
| chr7:2775385
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+19543A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775385 | ||||||
| chr7:2775506
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.525+19422C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775506 | ||||||
| chr7:2775604
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.525+19324G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775604 | ||||||
| chr7:2775606
|
A | C | 12 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(9): Show | 12 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+19322T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775606 | ||||||
| chr7:2775697
|
C | T | 2 | a0001c0001t0005g0314a0001c0001t0005g0315 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.525+19231G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775697 | ||||||
| chr7:2775819
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+19109C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775819 | ||||||
| chr7:2775824
|
C | G | 6 | a0001c0001t0002g0121a0001c0001t0002g0159a0001c0001t0002g0161others(3): Show | 6 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+19104G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775824 | ||||||
| chr7:2775897
|
C | A | 24 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0121others(21): Show | 25 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.525+19031G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775897 | ||||||
| chr7:2775917
|
G | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+19011C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775917 | ||||||
| chr7:2775926
|
A | G | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(314): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.525+19002T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775926 | ||||||
| chr7:2775969
|
G | T | 1 | a0001c0001t0003g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.525+18959C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2775969 | ||||||
| chr7:2776000
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.525+18928C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776000 | ||||||
| chr7:2776040
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+18888G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776040 | ||||||
| chr7:2776113
|
C | T | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+18815G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776113 | ||||||
| chr7:2776135
|
A | G | 9 | a0001c0001t0002g0142a0001c0001t0003g0038a0001c0001t0003g0059others(6): Show | 9 | NA18975.hp1 NA18977.hp1 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+18793T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776135 | ||||||
| chr7:2776225
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+18703G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776225 | ||||||
| chr7:2776486
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.525+18442A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776486 | ||||||
| chr7:2776519
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.525+18409G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776519 | ||||||
| chr7:2776640
|
G | C | 12 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(9): Show | 12 | HG00741.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.525+18288C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776640 | ||||||
| chr7:2776750
|
A | G | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.525+18178T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776750 | ||||||
| chr7:2776778
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+18150C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776778 | ||||||
| chr7:2776903
|
C | T | 49 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(46): Show | 50 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.525+18025G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776903 | ||||||
| chr7:2776956
|
TAAG | T | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.525+17969_525+1797 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2776956 | ||||||
| chr7:2777003
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.525+17925A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777003 | ||||||
| chr7:2777093
|
T | G | 2 | a0001c0001t0016g0130a0001c0001t0016g0131 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.525+17835A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777093 | ||||||
| chr7:2777123
|
G | A | 2 | a0001c0001t0003g0076a0001c0001t0003g0128 | 2 | HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.525+17805C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777123 | ||||||
| chr7:2777149
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.525+17779A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777149 | ||||||
| chr7:2777156
|
G | A | 9 | a0001c0001t0002g0121a0001c0001t0002g0159a0001c0001t0002g0161others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+17772C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777156 | ||||||
| chr7:2777240
|
C | A | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+17688G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777240 | ||||||
| chr7:2777262
|
T | C | 2 | a0001c0001t0006g0067a0001c0001t0006g0071 | 2 | NA18969.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.525+17666A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777262 | ||||||
| chr7:2777295
|
G | A | 12 | a0001c0001t0004g0002a0001c0001t0004g0100a0001c0001t0004g0127others(9): Show | 13 | HG01074.hp1 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.525+17633C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777295 | ||||||
| chr7:2777383
|
A | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+17545T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777383 | ||||||
| chr7:2777390
|
T | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+17538A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777390 | ||||||
| chr7:2777435
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+17493G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777435 | ||||||
| chr7:2777443
|
T | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+17485A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777443 | ||||||
| chr7:2777665
|
G | C | 1 | a0001c0001t0007g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.525+17263C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777665 | ||||||
| chr7:2777690
|
C | G | 1 | a0001c0001t0023g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.525+17238G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777690 | ||||||
| chr7:2777741
|
C | A | 2 | a0001c0001t0004g0022a0001c0001t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.525+17187G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777741 | ||||||
| chr7:2777766
|
G | A | 1 | a0001c0001t0023g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.525+17162C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777766 | ||||||
| chr7:2777767
|
A | G | 1 | a0001c0001t0023g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.525+17161T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777767 | ||||||
| chr7:2777789
|
A | T | 1 | a0001c0001t0023g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.525+17139T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777789 | ||||||
| chr7:2777821
|
G | T | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.525+17107C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777821 | ||||||
| chr7:2777871
|
G | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+17057C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777871 | ||||||
| chr7:2777877
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.525+17051T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777877 | ||||||
| chr7:2777929
|
G | C | 4 | a0001c0001t0001g0206a0001c0001t0001g0221a0001c0001t0001g0225others(1): Show | 4 | HG01358.hp1 HG02257.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+16999C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777929 | ||||||
| chr7:2777995
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+16933G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2777995 | ||||||
| chr7:2778087
|
C | T | 6 | a0001c0001t0011g0183a0001c0001t0011g0273a0001c0001t0012g0298others(3): Show | 6 | HG02886.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+16841G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778087 | ||||||
| chr7:2778108
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG01109.hp2 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.525+16820G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778108 | ||||||
| chr7:2778122
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+16806A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778122 | ||||||
| chr7:2778234
|
C | G | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+16694G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778234 | ||||||
| chr7:2778266
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(2): Show | 5 | HG02258.hp1 NA18953.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+16662G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778266 | ||||||
| chr7:2778795
|
C | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+16133G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778795 | ||||||
| chr7:2778809
|
G | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+16119C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778809 | ||||||
| chr7:2778997
|
T | G | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.525+15931A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2778997 | ||||||
| chr7:2779029
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+15899C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779029 | ||||||
| chr7:2779048
|
T | C | 1 | a0001c0001t0005g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.525+15880A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779048 | ||||||
| chr7:2779304
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0027 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.525+15624G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779304 | ||||||
| chr7:2779386
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.525+15542C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779386 | ||||||
| chr7:2779436
|
C | G | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(314): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.525+15492G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779436 | ||||||
| chr7:2779495
|
G | C | 6 | a0001c0001t0005g0300a0001c0001t0005g0312a0001c0001t0005g0313others(3): Show | 6 | HG01074.hp2 HG01081.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+15433C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779495 | ||||||
| chr7:2779710
|
T | C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.525+15218A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779710 | ||||||
| chr7:2779713
|
T | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+15215A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779713 | ||||||
| chr7:2779714
|
G | A | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+15214C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779714 | ||||||
| chr7:2779753
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.525+15175T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779753 | ||||||
| chr7:2779889
|
G | T | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+15039C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779889 | ||||||
| chr7:2779896
|
C | T | 8 | a0001c0001t0002g0073a0001c0001t0011g0003a0001c0001t0011g0183others(5): Show | 9 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+15032G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2779896 | ||||||
| chr7:2780022
|
C | G | 39 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(36): Show | 40 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.525+14906G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780022 | ||||||
| chr7:2780046
|
G | GTATATGT others(9): Show |
1 | a0001c0001t0007g0269 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.525+14881_525+1488 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(13): Show |
1 | a0001c0001t0007g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.525+14881_525+1488 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(3): Show |
2 | a0001c0001t0005g0303a0001c0001t0005g0306 | 2 | HG01433.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.525+14881_525+1488 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(9): Show |
6 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0311others(3): Show | 6 | HG01074.hp2 HG01106.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+14881_525+1488 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(11): Show |
4 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0313others(1): Show | 4 | HG01081.hp1 HG01169.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+14881_525+1488 others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(13): Show |
5 | a0001c0001t0005g0307a0001c0001t0005g0309a0001c0001t0005g0310others(2): Show | 5 | HG00639.hp1 HG00735.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+14881_525+1488 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(15): Show |
1 | a0001c0001t0005g0308 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.525+14881_525+1488 others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
G | GTATATGT others(25): Show |
1 | a0001c0001t0005g0304 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.525+14881_525+1488 others(36): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(3): Show |
G | 2 | a0001c0001t0011g0273a0001c0001t0012g0317 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.525+14872_525+1488 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(5): Show |
G | 1 | a0001c0001t0011g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.525+14870_525+1488 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(7): Show |
G | 1 | a0001c0004t0018g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.525+14868_525+1488 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(9): Show |
G | 2 | a0001c0001t0011g0003a0001c0001t0012g0298 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.525+14866_525+1488 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(17): Show |
G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+14858_525+1488 others(28): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(23): Show |
G | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.525+14852_525+1488 others(34): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780046
|
GTGTACAT others(25): Show |
G | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.525+14850_525+1488 others(36): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780046 | ||||||
| chr7:2780048
|
G | A | 27 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(24): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.525+14880C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780048
|
GTACATAT others(1): Show |
G | 4 | a0001c0001t0001g0216a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | NA18943.hp2 NA18952.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+14872_525+1487 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780048
|
GTACATAT others(3): Show |
G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0003t0001g0227 | 3 | HG03491.hp2 HG03492.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.525+14870_525+1487 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780048
|
GTACATAT others(5): Show |
G | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+14868_525+1487 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780048
|
GTACATAT others(7): Show |
G | 11 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0203others(8): Show | 11 | HG00738.hp2 HG01070.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+14866_525+1487 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780048
|
GTACATAT others(9): Show |
G | 54 | a0001c0001t0001g0173a0001c0001t0001g0191a0001c0001t0001g0202others(51): Show | 54 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.525+14864_525+1487 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780048
|
GTACATAT others(13): Show |
G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+14860_525+1487 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780048 | ||||||
| chr7:2780051
|
C | CAT | 35 | a0001c0001t0001g0095a0001c0001t0002g0018a0001c0001t0002g0027others(32): Show | 36 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.525+14875_525+1487 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATACATA others(3): Show |
1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.525+14876_525+1487 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATAT | 27 | a0001c0001t0001g0264a0001c0001t0002g0014a0001c0001t0002g0015others(24): Show | 27 | HG00544.hp2 HG01175.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.525+14873_525+1487 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATATAT | 8 | a0001c0001t0003g0038a0001c0001t0003g0059a0001c0001t0003g0096others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+14871_525+1487 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATATATA others(1): Show |
11 | a0001c0001t0002g0177a0001c0001t0003g0031a0001c0001t0003g0040others(8): Show | 11 | HG00280.hp2 HG02080.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+14869_525+1487 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATATATA others(3): Show |
7 | a0001c0001t0003g0029a0001c0001t0003g0043a0001c0001t0003g0145others(4): Show | 7 | HG02080.hp2 HG03704.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+14867_525+1487 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATATATA others(5): Show |
1 | a0001c0001t0004g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.525+14865_525+1487 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | CATATATA others(7): Show |
3 | a0001c0001t0002g0085a0001c0001t0003g0032a0001c0001t0008g0053 | 3 | HG02056.hp1 HG02622.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.525+14863_525+1487 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
C | T | 34 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(31): Show | 34 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.525+14877G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CAT | C | 11 | a0001c0001t0002g0160a0001c0001t0002g0162a0001c0001t0002g0255others(8): Show | 11 | HG01070.hp1 HG01123.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+14875_525+1487 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATAT | C | 10 | a0001c0001t0002g0150a0001c0001t0002g0158a0001c0001t0002g0163others(7): Show | 10 | HG01192.hp1 HG01358.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+14873_525+1487 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATAT | C | 17 | a0001c0001t0002g0047a0001c0001t0002g0157a0001c0001t0002g0166others(14): Show | 17 | HG00597.hp1 HG02165.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+14871_525+1487 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0002g0001a0001c0001t0002g0121a0001c0001t0002g0155others(4): Show | 8 | HG00544.hp1 HG02572.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+14869_525+1487 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(3): Show |
C | 2 | a0001c0001t0002g0077a0001c0001t0003g0060 | 2 | HG02155.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.525+14867_525+1487 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(5): Show |
C | 8 | a0001c0001t0003g0017a0001c0001t0003g0036a0001c0001t0003g0055others(5): Show | 8 | HG00609.hp2 HG02135.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.525+14865_525+1487 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0024g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.525+14863_525+1487 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(11): Show |
C | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.525+14859_525+1487 others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0003g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.525+14855_525+1487 others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780051
|
CATATATA others(19): Show |
C | 1 | a0001c0001t0004g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.525+14851_525+1487 others(30): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780051 | ||||||
| chr7:2780056
|
A | G | 1 | a0001c0001t0007g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.525+14872T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780056 | ||||||
| chr7:2780093
|
T | A | 104 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.525+14835A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780093 | ||||||
| chr7:2780093
|
T | TATATATA others(3): Show |
1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+14834_525+1483 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780093 | ||||||
| chr7:2780222
|
G | C | 2 | a0001c0001t0016g0130a0001c0001t0016g0131 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.525+14706C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780222 | ||||||
| chr7:2780422
|
T | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+14506A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780422 | ||||||
| chr7:2780432
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.525+14496C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780432 | ||||||
| chr7:2780530
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+14398A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780530 | ||||||
| chr7:2780558
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.525+14370C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780558 | ||||||
| chr7:2780569
|
T | C | 53 | a0001c0001t0001g0095a0001c0001t0003g0096a0001c0001t0004g0002others(50): Show | 55 | HG01074.hp1 HG01123.hp1 HG01346.hp2 others(52): Show |
intron_variant | MODIFIER | c.525+14359A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780569 | ||||||
| chr7:2780629
|
T | C | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.525+14299A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780629 | ||||||
| chr7:2780688
|
C | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+14240G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780688 | ||||||
| chr7:2780695
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+14233T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780695 | ||||||
| chr7:2780741
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.525+14187A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780741 | ||||||
| chr7:2780805
|
A | G | 1 | a0001c0001t0008g0048 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.525+14123T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780805 | ||||||
| chr7:2780808
|
T | C | 17 | a0001c0001t0001g0264a0001c0001t0002g0014a0001c0001t0002g0015others(14): Show | 17 | HG01081.hp2 HG02257.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+14120A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780808 | ||||||
| chr7:2780849
|
A | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+14079T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780849 | ||||||
| chr7:2780976
|
T | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+13952A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780976 | ||||||
| chr7:2780990
|
T | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+13938A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780990 | ||||||
| chr7:2780996
|
C | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+13932G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2780996 | ||||||
| chr7:2781023
|
G | A | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.525+13905C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781023 | ||||||
| chr7:2781055
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.525+13873A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781055 | ||||||
| chr7:2781063
|
T | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+13865A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781063 | ||||||
| chr7:2781155
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.525+13773A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781155 | ||||||
| chr7:2781222
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.525+13706C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781222 | ||||||
| chr7:2781412
|
C | CTG | 9 | a0001c0001t0001g0206a0001c0001t0001g0226a0001c0001t0003g0036others(6): Show | 9 | HG00609.hp2 HG02129.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+13514_525+1351 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTG | 13 | a0001c0001t0001g0216a0001c0001t0001g0231a0001c0001t0001g0232others(10): Show | 13 | HG02559.hp1 HG02630.hp2 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.525+13512_525+1351 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTG | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.525+13510_525+1351 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTGT others(1): Show |
32 | a0001c0001t0001g0224a0001c0001t0001g0233a0001c0001t0001g0247others(29): Show | 33 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.525+13508_525+1351 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTGT others(3): Show |
15 | a0001c0001t0001g0202a0001c0001t0001g0220a0001c0001t0001g0223others(12): Show | 15 | HG01109.hp2 HG01934.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.525+13506_525+1351 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTGT others(5): Show |
9 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0240others(6): Show | 9 | HG00735.hp2 HG00741.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+13504_525+1351 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTGT others(7): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0239a0001c0001t0001g0260others(2): Show | 5 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+13502_525+1351 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTGT others(9): Show |
7 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0001g0242others(4): Show | 7 | HG00140.hp2 HG01496.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+13500_525+1351 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0030g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.525+13498_525+1351 others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
C | G | 1 | a0001c0001t0004g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.525+13516G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
CTG | C | 44 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(41): Show | 45 | HG01074.hp1 HG01361.hp2 HG01433.hp1 others(42): Show |
intron_variant | MODIFIER | c.525+13514_525+1351 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
CTGTG | C | 7 | a0001c0001t0005g0299a0001c0001t0017g0271a0001c0001t0028g0284others(4): Show | 7 | HG02717.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+13512_525+1351 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
CTGTGTG | C | 32 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(29): Show | 32 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.525+13510_525+1351 others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.525+13504_525+1351 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781412
|
CTGTGTGT others(17): Show |
C | 1 | a0001c0001t0003g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.525+13492_525+1351 others(28): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781412 | ||||||
| chr7:2781500
|
A | C | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.525+13428T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781500 | ||||||
| chr7:2781502
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.525+13426A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781502 | ||||||
| chr7:2781637
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.525+13291G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781637 | ||||||
| chr7:2781656
|
T | C | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.525+13272A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781656 | ||||||
| chr7:2781677
|
T | C | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.525+13251A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781677 | ||||||
| chr7:2781801
|
C | T | 2 | a0001c0001t0020g0024a0001c0001t0020g0025 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.525+13127G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781801 | ||||||
| chr7:2781842
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.525+13086G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781842 | ||||||
| chr7:2781966
|
T | C | 31 | a0001c0001t0002g0001a0001c0001t0002g0046a0001c0001t0002g0047others(28): Show | 32 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.525+12962A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2781966 | ||||||
| chr7:2782043
|
A | C | 31 | a0001c0001t0002g0001a0001c0001t0002g0046a0001c0001t0002g0047others(28): Show | 32 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.525+12885T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782043 | ||||||
| chr7:2782057
|
G | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+12871C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782057 | ||||||
| chr7:2782128
|
C | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+12800G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782128 | ||||||
| chr7:2782176
|
T | C | 1 | a0001c0001t0003g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.525+12752A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782176 | ||||||
| chr7:2782373
|
T | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+12555A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782373 | ||||||
| chr7:2782477
|
T | C | 1 | a0001c0001t0004g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.525+12451A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782477 | ||||||
| chr7:2782517
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.525+12411G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782517 | ||||||
| chr7:2782548
|
C | G | 1 | a0001c0001t0004g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.525+12380G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782548 | ||||||
| chr7:2782629
|
G | A | 1 | a0001c0001t0036g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.525+12299C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782629 | ||||||
| chr7:2782657
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.525+12271C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782657 | ||||||
| chr7:2782696
|
C | T | 1 | a0001c0001t0013g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.525+12232G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782696 | ||||||
| chr7:2782782
|
G | A | 44 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(41): Show | 45 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.525+12146C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782782 | ||||||
| chr7:2782786
|
A | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+12142T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782786 | ||||||
| chr7:2782840
|
T | G | 4 | a0001c0001t0011g0183a0001c0001t0012g0316a0001c0001t0012g0317others(1): Show | 4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+12088A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2782840 | ||||||
| chr7:2783105
|
G | A | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+11823C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783105 | ||||||
| chr7:2783139
|
G | A | 7 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0017g0271others(4): Show | 7 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+11789C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783139 | ||||||
| chr7:2783236
|
G | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+11692C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783236 | ||||||
| chr7:2783299
|
C | T | 45 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(42): Show | 46 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(43): Show |
intron_variant | MODIFIER | c.525+11629G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783299 | ||||||
| chr7:2783352
|
T | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.525+11576A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783352 | ||||||
| chr7:2783361
|
G | T | 2 | a0001c0001t0007g0269a0001c0001t0007g0270 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+11567C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783361 | ||||||
| chr7:2783368
|
C | T | 1 | a0001c0001t0004g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.525+11560G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783368 | ||||||
| chr7:2783403
|
C | T | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+11525G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783403 | ||||||
| chr7:2783457
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.525+11471G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783457 | ||||||
| chr7:2783463
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.525+11465G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783463 | ||||||
| chr7:2783503
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.525+11425G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783503 | ||||||
| chr7:2783531
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.525+11397C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783531 | ||||||
| chr7:2783570
|
T | C | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.525+11358A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783570 | ||||||
| chr7:2783624
|
C | A | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.525+11304G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783624 | ||||||
| chr7:2783634
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+11294A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783634 | ||||||
| chr7:2783649
|
C | CATTT | 73 | a0001c0001t0001g0264a0001c0001t0002g0001a0001c0001t0002g0046others(70): Show | 75 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.525+11275_525+1127 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
C | CATTTATT others(1): Show |
32 | a0001c0001t0002g0019a0001c0001t0002g0085a0001c0001t0002g0156others(29): Show | 33 | HG01069.hp2 HG01070.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.525+11271_525+1127 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
C | CATTTATT others(5): Show |
29 | a0001c0001t0002g0121a0001c0001t0002g0129a0001c0001t0003g0013others(26): Show | 29 | HG00280.hp2 HG00609.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+11267_525+1127 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
C | CATTTATT others(9): Show |
13 | a0001c0001t0002g0147a0001c0001t0004g0022a0001c0001t0004g0023others(10): Show | 13 | HG01978.hp1 HG02055.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.525+11263_525+1127 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
C | CATTTATT others(13): Show |
6 | a0001c0001t0003g0017a0001c0001t0003g0062a0001c0001t0003g0197others(3): Show | 6 | HG02056.hp2 HG04228.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+11259_525+1127 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
C | CATTTATT others(21): Show |
1 | a0001c0002t0002g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.525+11251_525+1127 others(32): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
CATTT | C | 15 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0175others(12): Show | 15 | HG00140.hp1 HG01081.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.525+11275_525+1127 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
CATTTATT others(1): Show |
C | 7 | a0001c0001t0001g0095a0001c0001t0001g0250a0001c0001t0003g0128others(4): Show | 7 | HG01346.hp2 HG01433.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+11271_525+1127 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
CATTTATT others(5): Show |
C | 12 | a0001c0001t0001g0173a0001c0001t0001g0219a0001c0001t0001g0248others(9): Show | 12 | HG00609.hp1 HG02155.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.525+11267_525+1127 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
CATTTATT others(9): Show |
C | 68 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0191others(65): Show | 68 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.525+11263_525+1127 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783649
|
CATTTATT others(13): Show |
C | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(41): Show | 44 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.525+11259_525+1127 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783649 | ||||||
| chr7:2783702
|
T | A | 1 | a0001c0001t0002g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.525+11226A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783702 | ||||||
| chr7:2783725
|
C | T | 1 | a0001c0001t0007g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.525+11203G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783725 | ||||||
| chr7:2783809
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+11119G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783809 | ||||||
| chr7:2783842
|
G | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.525+11086C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2783842 | ||||||
| chr7:2784334
|
G | A | 2 | a0001c0001t0007g0269a0001c0001t0007g0270 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+10594C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784334 | ||||||
| chr7:2784495
|
T | A | 4 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+10433A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784495 | ||||||
| chr7:2784632
|
A | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+10296T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784632 | ||||||
| chr7:2784684
|
C | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+10244G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784684 | ||||||
| chr7:2784746
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.525+10182G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784746 | ||||||
| chr7:2784787
|
T | C | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+10141A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784787 | ||||||
| chr7:2784831
|
T | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+10097A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784831 | ||||||
| chr7:2784944
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.525+9984A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2784944 | ||||||
| chr7:2785008
|
A | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+9920T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785008 | ||||||
| chr7:2785073
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.525+9855C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785073 | ||||||
| chr7:2785089
|
A | G | 1 | a0001c0001t0007g0148 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.525+9839T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785089 | ||||||
| chr7:2785180
|
G | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+9748C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785180 | ||||||
| chr7:2785276
|
T | G | 1 | a0001c0001t0003g0168 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.525+9652A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785276 | ||||||
| chr7:2785461
|
G | A | 5 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(2): Show | 5 | HG00741.hp1 NA18970.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+9467C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785461 | ||||||
| chr7:2785477
|
G | A | 1 | a0001c0002t0002g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.525+9451C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785477 | ||||||
| chr7:2785651
|
TATACACA others(38): Show |
T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+9232_525+9276d others(47): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785651 | ||||||
| chr7:2785682
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.525+9246C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785682 | ||||||
| chr7:2785732
|
G | T | 2 | a0001c0001t0005g0314a0001c0001t0005g0315 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.525+9196C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785732 | ||||||
| chr7:2785740
|
A | G | 2 | a0001c0001t0020g0024a0001c0001t0020g0025 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.525+9188T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785740 | ||||||
| chr7:2785751
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.525+9177A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785751 | ||||||
| chr7:2785821
|
T | C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.525+9107A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785821 | ||||||
| chr7:2785931
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.525+8997C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785931 | ||||||
| chr7:2785957
|
C | G | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.525+8971G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2785957 | ||||||
| chr7:2786061
|
C | T | 7 | a0001c0001t0001g0203a0001c0001t0001g0216a0001c0001t0001g0222others(4): Show | 7 | NA18612.hp2 NA18943.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+8867G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786061 | ||||||
| chr7:2786068
|
A | G | 8 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+8860T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786068 | ||||||
| chr7:2786093
|
G | A | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+8835C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786093 | ||||||
| chr7:2786176
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.525+8752G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786176 | ||||||
| chr7:2786177
|
A | G | 2 | a0001c0001t0016g0130a0001c0001t0016g0131 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.525+8751T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786177 | ||||||
| chr7:2786217
|
C | G | 1 | a0001c0001t0004g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.525+8711G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786217 | ||||||
| chr7:2786288
|
C | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.525+8640G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786288 | ||||||
| chr7:2786314
|
G | T | 1 | a0001c0001t0003g0168 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.525+8614C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786314 | ||||||
| chr7:2786320
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.525+8608A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786320 | ||||||
| chr7:2786354
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+8574G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786354 | ||||||
| chr7:2786451
|
T | C | 1 | a0001c0003t0001g0227 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.525+8477A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786451 | ||||||
| chr7:2786506
|
A | C | 1 | a0001c0001t0008g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.525+8422T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786506 | ||||||
| chr7:2786542
|
A | G | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+8386T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786542 | ||||||
| chr7:2786571
|
A | G | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.525+8357T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786571 | ||||||
| chr7:2786639
|
G | A | 2 | a0001c0001t0002g0047a0001c0001t0003g0168 | 2 | NA18949.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.525+8289C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786639 | ||||||
| chr7:2786676
|
T | C | 1 | a0001c0001t0004g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.525+8252A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786676 | ||||||
| chr7:2786725
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+8203A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786725 | ||||||
| chr7:2786810
|
C | T | 11 | a0001c0001t0002g0142a0001c0001t0003g0038a0001c0001t0003g0059others(8): Show | 11 | HG02965.hp2 HG03098.hp2 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+8118G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786810 | ||||||
| chr7:2786841
|
A | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+8087T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786841 | ||||||
| chr7:2786860
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0184a0001c0001t0007g0269others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+8068G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786860 | ||||||
| chr7:2786873
|
C | G | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+8055G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2786873 | ||||||
| chr7:2787054
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0002g0129 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.525+7874G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787054 | ||||||
| chr7:2787113
|
C | A | 1 | a0001c0001t0003g0145 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.525+7815G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787113 | ||||||
| chr7:2787188
|
G | A | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.525+7740C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787188 | ||||||
| chr7:2787313
|
C | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0070 | 2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.525+7615G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787313 | ||||||
| chr7:2787332
|
C | A | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+7596G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787332 | ||||||
| chr7:2787559
|
A | G | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+7369T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787559 | ||||||
| chr7:2787574
|
C | T | 1 | a0001c0001t0016g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.525+7354G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787574 | ||||||
| chr7:2787642
|
T | C | 183 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.525+7286A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787642 | ||||||
| chr7:2787767
|
C | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | NA18939.hp1 NA18955.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.525+7161G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787767 | ||||||
| chr7:2787778
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.525+7150C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787778 | ||||||
| chr7:2787884
|
A | G | 1 | a0001c0001t0004g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.525+7044T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787884 | ||||||
| chr7:2787920
|
A | G | 189 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 191 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.525+7008T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787920 | ||||||
| chr7:2787943
|
CA | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+6984delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2787943 | ||||||
| chr7:2788047
|
C | T | 2 | a0001c0001t0016g0130a0001c0001t0016g0131 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.525+6881G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788047 | ||||||
| chr7:2788152
|
C | CA | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.525+6775dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788152 | ||||||
| chr7:2788267
|
C | G | 25 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.525+6661G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788267 | ||||||
| chr7:2788330
|
CTG | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+6596_525+6597d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788330 | ||||||
| chr7:2788339
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+6589G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788339 | ||||||
| chr7:2788375
|
G | T | 1 | a0001c0001t0023g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.525+6553C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788375 | ||||||
| chr7:2788401
|
G | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+6527C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788401 | ||||||
| chr7:2788456
|
G | A | 1 | a0001c0001t0016g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.525+6472C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788456 | ||||||
| chr7:2788488
|
C | G | 2 | a0001c0001t0004g0058a0001c0001t0025g0057 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.525+6440G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788488 | ||||||
| chr7:2788521
|
G | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+6407C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788521 | ||||||
| chr7:2788558
|
A | G | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.525+6370T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788558 | ||||||
| chr7:2788574
|
A | T | 1 | a0001c0001t0019g0276 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.525+6354T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788574 | ||||||
| chr7:2788702
|
G | A | 3 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0276 | 3 | HG02965.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.525+6226C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788702 | ||||||
| chr7:2788902
|
C | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.525+6026G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788902 | ||||||
| chr7:2788960
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+5968G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788960 | ||||||
| chr7:2788967
|
C | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+5961G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2788967 | ||||||
| chr7:2789052
|
A | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+5876T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789052 | ||||||
| chr7:2789062
|
C | A | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.525+5866G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789062 | ||||||
| chr7:2789082
|
T | C | 7 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0290others(4): Show | 7 | HG02165.hp2 NA18953.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+5846A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789082 | ||||||
| chr7:2789091
|
A | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+5837T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789091 | ||||||
| chr7:2789109
|
C | T | 144 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 144 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.525+5819G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789109 | ||||||
| chr7:2789118
|
ACCCCTTC others(307): Show |
A | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+5496_525+5809d others(2): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789118 | ||||||
| chr7:2789132
|
C | CT | 10 | a0001c0001t0002g0015a0001c0001t0002g0068a0001c0001t0002g0147others(7): Show | 10 | HG00544.hp2 HG00639.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+5795dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT | 7 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0113others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+5789_525+5795d others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(1): Show |
48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0256others(45): Show | 48 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.525+5788_525+5795d others(10): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(2): Show |
59 | a0001c0001t0001g0009a0001c0001t0001g0173a0001c0001t0001g0202others(56): Show | 59 | HG00140.hp2 HG00609.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.525+5787_525+5795d others(11): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(3): Show |
23 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0205others(20): Show | 23 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.525+5786_525+5795d others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0206a0001c0001t0001g0263a0001c0001t0011g0273others(4): Show | 7 | HG01175.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+5785_525+5795d others(13): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0012g0318a0001c0001t0015g0140 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.525+5784_525+5795d others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.525+5782_525+5795d others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0282 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.525+5776_525+5795d others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.525+5795_525+5796i others(30): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789132
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0281 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.525+5795_525+5796i others(36): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789132 | ||||||
| chr7:2789205
|
G | A | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.525+5723C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789205 | ||||||
| chr7:2789222
|
G | A | 4 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(1): Show | 4 | HG02258.hp1 NA19067.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+5706C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789222 | ||||||
| chr7:2789237
|
G | A | 3 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0105 | 3 | NA18970.hp1 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.525+5691C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789237 | ||||||
| chr7:2789284
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.525+5644G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789284 | ||||||
| chr7:2789290
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.525+5638A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789290 | ||||||
| chr7:2789532
|
C | T | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.525+5396G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789532 | ||||||
| chr7:2789543
|
T | C | 1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.525+5385A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789543 | ||||||
| chr7:2789663
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+5265G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789663 | ||||||
| chr7:2789747
|
T | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+5181A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2789747 | ||||||
| chr7:2790001
|
T | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+4927A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790001 | ||||||
| chr7:2790150
|
T | C | 1 | a0001c0003t0001g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.525+4778A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790150 | ||||||
| chr7:2790220
|
C | T | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.525+4708G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790220 | ||||||
| chr7:2790223
|
T | C | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.525+4705A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790223 | ||||||
| chr7:2790311
|
G | C | 2 | a0001c0001t0007g0269a0001c0001t0007g0270 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+4617C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790311 | ||||||
| chr7:2790397
|
C | T | 18 | a0001c0001t0004g0002a0001c0001t0004g0012a0001c0001t0004g0093others(15): Show | 19 | HG01074.hp1 HG01433.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.525+4531G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790397 | ||||||
| chr7:2790476
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.525+4452G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790476 | ||||||
| chr7:2790609
|
T | G | 182 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(179): Show | 184 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.525+4319A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790609 | ||||||
| chr7:2790630
|
T | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+4298A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790630 | ||||||
| chr7:2790702
|
T | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+4226A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790702 | ||||||
| chr7:2790809
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.525+4119T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790809 | ||||||
| chr7:2790821
|
A | C | 1 | a0001c0001t0003g0201 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.525+4107T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790821 | ||||||
| chr7:2790864
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.525+4064G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790864 | ||||||
| chr7:2790962
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.525+3966T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790962 | ||||||
| chr7:2790974
|
T | TA | 44 | a0001c0001t0001g0137a0001c0001t0001g0241a0001c0001t0003g0118others(41): Show | 45 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.525+3953dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2790974 | ||||||
| chr7:2791054
|
A | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+3874T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791054 | ||||||
| chr7:2791157
|
A | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+3771T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791157 | ||||||
| chr7:2791208
|
CTCTG | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+3716_525+3719d others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791208 | ||||||
| chr7:2791449
|
T | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.525+3479A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791449 | ||||||
| chr7:2791495
|
T | C | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.525+3433A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791495 | ||||||
| chr7:2791773
|
G | T | 13 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(10): Show | 14 | HG00741.hp1 HG02818.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+3155C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791773 | ||||||
| chr7:2791917
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.525+3011A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791917 | ||||||
| chr7:2791968
|
A | G | 164 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 165 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.525+2960T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791968 | ||||||
| chr7:2791982
|
T | C | 1 | a0001c0001t0004g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.525+2946A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791982 | ||||||
| chr7:2791982
|
T | TACAAATG others(13): Show |
1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+2926_525+2945d others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2791982 | ||||||
| chr7:2792160
|
T | A | 1 | a0001c0001t0002g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.525+2768A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792160 | ||||||
| chr7:2792187
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.525+2741C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792187 | ||||||
| chr7:2792260
|
G | A | 1 | a0001c0001t0017g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.525+2668C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792260 | ||||||
| chr7:2792333
|
A | G | 17 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0312others(14): Show | 17 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+2595T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792333 | ||||||
| chr7:2792476
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.525+2452G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792476 | ||||||
| chr7:2792520
|
A | G | 6 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0156others(3): Show | 7 | HG00544.hp1 HG00597.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+2408T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792520 | ||||||
| chr7:2792645
|
C | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+2283G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792645 | ||||||
| chr7:2792649
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.525+2279G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792649 | ||||||
| chr7:2792731
|
T | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.525+2197A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2792731 | ||||||
| chr7:2793012
|
C | T | 1 | a0001c0001t0003g0144 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.525+1916G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793012 | ||||||
| chr7:2793013
|
G | A | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1915C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793013 | ||||||
| chr7:2793070
|
C | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18939.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.525+1858G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793070 | ||||||
| chr7:2793074
|
A | C | 12 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(9): Show | 12 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.525+1854T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793074 | ||||||
| chr7:2793211
|
C | T | 26 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(23): Show | 26 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.525+1717G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793211 | ||||||
| chr7:2793280
|
G | C | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.525+1648C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793280 | ||||||
| chr7:2793282
|
G | GCGCGAGA others(17): Show |
5 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(2): Show | 5 | HG01192.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1622_525+1645d others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793282 | ||||||
| chr7:2793282
|
GCGCGAGA others(17): Show |
G | 1 | a0001c0007t0003g0295 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.525+1622_525+1645d others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793282 | ||||||
| chr7:2793282
|
GCGCGAGA others(41): Show |
G | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1598_525+1645d others(50): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793282 | ||||||
| chr7:2793322
|
C | T | 8 | a0001c0001t0004g0011a0001c0001t0011g0003a0001c0001t0011g0183others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+1606G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793322 | ||||||
| chr7:2793339
|
G | A | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.525+1589C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793339 | ||||||
| chr7:2793339
|
G | GAAGCAGC others(17): Show |
2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.525+1588_525+1589i others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793339 | ||||||
| chr7:2793359
|
A | G | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1569T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793359 | ||||||
| chr7:2793614
|
G | A | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1314C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793614 | ||||||
| chr7:2793621
|
A | G | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1307T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793621 | ||||||
| chr7:2793717
|
C | T | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1211G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793717 | ||||||
| chr7:2793745
|
T | G | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.525+1183A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793745 | ||||||
| chr7:2793746
|
G | T | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.525+1182C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793746 | ||||||
| chr7:2793751
|
T | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1177A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793751 | ||||||
| chr7:2793808
|
A | G | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1120T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793808 | ||||||
| chr7:2793854
|
G | C | 313 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.525+1074C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793854 | ||||||
| chr7:2793866
|
C | T | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.525+1062G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793866 | ||||||
| chr7:2793867
|
G | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1061C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793867 | ||||||
| chr7:2793881
|
CA | C | 11 | a0001c0001t0004g0138a0001c0001t0015g0140a0001c0001t0015g0141others(8): Show | 11 | HG01192.hp2 HG01361.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+1046delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793881 | ||||||
| chr7:2793881
|
CAA | C | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.525+1045_525+1046d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793881 | ||||||
| chr7:2793898
|
A | AAG | 16 | a0001c0001t0004g0002a0001c0001t0004g0012a0001c0001t0004g0100others(13): Show | 17 | HG01074.hp1 HG01433.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+1029_525+1030i others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793898 | ||||||
| chr7:2793898
|
A | AGAAG | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+1029_525+1030i others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793898 | ||||||
| chr7:2793900
|
G | A | 21 | a0001c0001t0004g0002a0001c0001t0004g0012a0001c0001t0004g0100others(18): Show | 22 | HG00741.hp1 HG01074.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.525+1028C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793900 | ||||||
| chr7:2793938
|
C | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+990G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793938 | ||||||
| chr7:2793942
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+986A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2793942 | ||||||
| chr7:2794006
|
G | T | 1 | a0001c0001t0003g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.525+922C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794006 | ||||||
| chr7:2794131
|
G | A | 1 | a0001c0001t0004g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.525+797C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794131 | ||||||
| chr7:2794218
|
T | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.525+710A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794218 | ||||||
| chr7:2794243
|
G | A | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+685C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794243 | ||||||
| chr7:2794262
|
G | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+666C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794262 | ||||||
| chr7:2794311
|
AT | A | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+616delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794311 | ||||||
| chr7:2794354
|
A | G | 1 | a0001c0001t0006g0189 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.525+574T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794354 | ||||||
| chr7:2794356
|
G | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.525+572C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794356 | ||||||
| chr7:2794463
|
G | A | 1 | a0001c0004t0018g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.525+465C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794463 | ||||||
| chr7:2794473
|
G | A | 1 | a0001c0001t0006g0039 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.525+455C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794473 | ||||||
| chr7:2794568
|
A | G | 7 | a0001c0001t0011g0003a0001c0001t0011g0273a0001c0004t0014g0285others(4): Show | 8 | HG00741.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+360T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794568 | ||||||
| chr7:2794664
|
A | G | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.525+264T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794664 | ||||||
| chr7:2794667
|
G | C | 5 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287others(2): Show | 5 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+261C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794667 | ||||||
| chr7:2794779
|
G | A | 147 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.525+149C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794779 | ||||||
| chr7:2794808
|
C | A | 8 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0307others(5): Show | 8 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+120G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 2/3 | chr7 | 2794808 | ||||||
| chr7:2795183
|
C | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.310-40G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795183 | ||||||
| chr7:2795203
|
G | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-60C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795203 | ||||||
| chr7:2795235
|
C | T | 146 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.310-92G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795235 | ||||||
| chr7:2795400
|
G | C | 5 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0156others(2): Show | 6 | HG00544.hp1 NA18612.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-257C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795400 | ||||||
| chr7:2795420
|
C | G | 2 | a0001c0001t0005g0314a0001c0001t0005g0315 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.310-277G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795420 | ||||||
| chr7:2795434
|
C | T | 1 | a0001c0001t0005g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.310-291G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795434 | ||||||
| chr7:2795627
|
C | CA | 9 | a0001c0001t0004g0023a0001c0001t0015g0140a0001c0001t0015g0141others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-485dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795627 | ||||||
| chr7:2795627
|
C | CAA | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.310-486_310-485dup others(2): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795627 | ||||||
| chr7:2795682
|
A | C | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.310-539T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795682 | ||||||
| chr7:2795816
|
CT | C | 15 | a0001c0001t0001g0210a0001c0001t0002g0165a0001c0001t0002g0171others(12): Show | 15 | HG00609.hp2 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.310-674delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795816 | ||||||
| chr7:2795816
|
CTT | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.310-675_310-674del others(2): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795816 | ||||||
| chr7:2795816
|
CTTT | C | 24 | a0001c0001t0001g0293a0001c0001t0005g0299a0001c0001t0005g0300others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.310-676_310-674del others(3): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795816 | ||||||
| chr7:2795930
|
C | G | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-787G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2795930 | ||||||
| chr7:2796021
|
C | T | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.310-878G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796021 | ||||||
| chr7:2796088
|
A | G | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-945T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796088 | ||||||
| chr7:2796095
|
ACCTCAGC others(11): Show |
A | 7 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0017g0271others(4): Show | 7 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-970_310-953del others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796095 | ||||||
| chr7:2796109
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.310-966C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796109 | ||||||
| chr7:2796126
|
C | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-983G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796126 | ||||||
| chr7:2796178
|
C | T | 3 | a0001c0001t0001g0216a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | NA18952.hp2 NA18959.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.310-1035G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796178 | ||||||
| chr7:2796184
|
A | G | 5 | a0001c0001t0002g0159a0001c0001t0002g0161a0001c0001t0004g0124others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-1041T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796184 | ||||||
| chr7:2796216
|
C | T | 1 | a0001c0001t0009g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.310-1073G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796216 | ||||||
| chr7:2796276
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.310-1133C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796276 | ||||||
| chr7:2796383
|
A | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-1240T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796383 | ||||||
| chr7:2796385
|
C | T | 159 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(156): Show | 160 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.310-1242G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796385 | ||||||
| chr7:2796427
|
G | C | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.310-1284C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796427 | ||||||
| chr7:2796666
|
T | C | 9 | a0001c0001t0002g0150a0001c0001t0003g0040a0001c0001t0003g0043others(6): Show | 9 | HG02132.hp1 NA18956.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-1523A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796666 | ||||||
| chr7:2796704
|
G | A | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-1561C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796704 | ||||||
| chr7:2796721
|
G | A | 152 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 152 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.310-1578C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796721 | ||||||
| chr7:2796736
|
G | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-1593C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796736 | ||||||
| chr7:2796799
|
A | G | 27 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(24): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.310-1656T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796799 | ||||||
| chr7:2796880
|
C | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-1737G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2796880 | ||||||
| chr7:2797214
|
T | G | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.310-2071A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797214 | ||||||
| chr7:2797325
|
G | A | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-2182C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797325 | ||||||
| chr7:2797385
|
C | T | 1 | a0001c0001t0004g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.310-2242G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797385 | ||||||
| chr7:2797439
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-2296G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797439 | ||||||
| chr7:2797517
|
G | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-2374C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797517 | ||||||
| chr7:2797544
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.310-2401A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797544 | ||||||
| chr7:2797571
|
C | A | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-2428G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797571 | ||||||
| chr7:2797618
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.310-2475G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797618 | ||||||
| chr7:2797740
|
C | G | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-2597G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797740 | ||||||
| chr7:2797761
|
T | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-2618A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797761 | ||||||
| chr7:2797965
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.310-2822A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797965 | ||||||
| chr7:2797996
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-2853G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2797996 | ||||||
| chr7:2798059
|
T | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.310-2916A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798059 | ||||||
| chr7:2798126
|
TG | T | 8 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0307others(5): Show | 8 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-2984delC | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798126 | ||||||
| chr7:2798289
|
T | G | 2 | a0001c0001t0009g0267a0001c0001t0009g0268 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.310-3146A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798289 | ||||||
| chr7:2798290
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.310-3147T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798290 | ||||||
| chr7:2798308
|
CTAGAA | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.310-3170_310-3166d others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798308 | ||||||
| chr7:2798438
|
C | G | 1 | a0001c0001t0003g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.310-3295G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798438 | ||||||
| chr7:2798492
|
T | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.310-3349A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798492 | ||||||
| chr7:2798546
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.310-3403G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798546 | ||||||
| chr7:2798602
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.310-3459A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798602 | ||||||
| chr7:2798819
|
T | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-3676A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798819 | ||||||
| chr7:2798851
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.310-3708C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798851 | ||||||
| chr7:2798873
|
GC | G | 7 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0086others(4): Show | 7 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-3731delG | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798873 | ||||||
| chr7:2798926
|
G | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-3783C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798926 | ||||||
| chr7:2798944
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-3801A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798944 | ||||||
| chr7:2798964
|
G | A | 3 | a0001c0001t0011g0183a0001c0001t0012g0316a0001c0001t0012g0317 | 3 | HG03195.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.310-3821C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798964 | ||||||
| chr7:2798964
|
G | C | 1 | a0001c0001t0003g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.310-3821C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798964 | ||||||
| chr7:2798971
|
G | A | 2 | a0001c0001t0005g0307a0001c0001t0005g0308 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.310-3828C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2798971 | ||||||
| chr7:2799224
|
G | C | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.310-4081C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799224 | ||||||
| chr7:2799409
|
G | A | 1 | a0001c0001t0005g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.310-4266C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799409 | ||||||
| chr7:2799454
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.310-4311G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799454 | ||||||
| chr7:2799502
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.310-4359T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799502 | ||||||
| chr7:2799548
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.310-4405G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799548 | ||||||
| chr7:2799620
|
T | C | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-4477A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799620 | ||||||
| chr7:2799620
|
T | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-4477A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799620 | ||||||
| chr7:2799680
|
A | T | 14 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0229others(11): Show | 14 | HG00140.hp2 HG01346.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.310-4537T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799680 | ||||||
| chr7:2799681
|
T | A | 6 | a0001c0001t0002g0046a0001c0001t0002g0157a0001c0001t0002g0280others(3): Show | 6 | HG02165.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-4538A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799681 | ||||||
| chr7:2799682
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.310-4539A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799682 | ||||||
| chr7:2799766
|
T | C | 7 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0017g0271others(4): Show | 7 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-4623A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799766 | ||||||
| chr7:2799864
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0007g0192others(2): Show | 5 | HG00423.hp2 NA18970.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-4721T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799864 | ||||||
| chr7:2799899
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-4756G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2799899 | ||||||
| chr7:2800095
|
T | C | 7 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0150others(4): Show | 8 | HG00544.hp1 HG00597.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-4952A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800095 | ||||||
| chr7:2800211
|
A | C | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.310-5068T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800211 | ||||||
| chr7:2800311
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0022g0092 | 2 | HG02523.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.310-5168C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800311 | ||||||
| chr7:2800609
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310-5466C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800609 | ||||||
| chr7:2800650
|
A | G | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.310-5507T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800650 | ||||||
| chr7:2800677
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.310-5534T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800677 | ||||||
| chr7:2800855
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-5712G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800855 | ||||||
| chr7:2800856
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-5713C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800856 | ||||||
| chr7:2800881
|
G | C | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.310-5738C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2800881 | ||||||
| chr7:2801039
|
G | A | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.310-5896C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801039 | ||||||
| chr7:2801078
|
C | T | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-5935G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801078 | ||||||
| chr7:2801199
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-6056C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801199 | ||||||
| chr7:2801287
|
A | C | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-6144T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801287 | ||||||
| chr7:2801381
|
G | A | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG00280.hp1 HG01261.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-6238C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801381 | ||||||
| chr7:2801474
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-6331G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801474 | ||||||
| chr7:2801475
|
G | A | 1 | a0001c0001t0003g0096 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.310-6332C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801475 | ||||||
| chr7:2801482
|
T | C | 187 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 189 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.310-6339A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801482 | ||||||
| chr7:2801530
|
G | A | 88 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.310-6387C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801530 | ||||||
| chr7:2801782
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.310-6639C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801782 | ||||||
| chr7:2801873
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-6730C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801873 | ||||||
| chr7:2801950
|
T | C | 9 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(6): Show | 9 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-6807A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801950 | ||||||
| chr7:2801963
|
T | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-6820A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2801963 | ||||||
| chr7:2802072
|
G | C | 1 | a0001c0001t0003g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.310-6929C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802072 | ||||||
| chr7:2802133
|
T | C | 1 | a0001c0001t0019g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.310-6990A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802133 | ||||||
| chr7:2802392
|
T | TG | 30 | a0001c0001t0001g0263a0001c0001t0004g0099a0001c0001t0004g0111others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.310-7250_310-7249i others(3): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802392 | ||||||
| chr7:2802393
|
T | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 171 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.310-7250A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802393 | ||||||
| chr7:2802401
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.310-7258A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802401 | ||||||
| chr7:2802402
|
G | A | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-7259C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802402 | ||||||
| chr7:2802441
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.310-7298G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802441 | ||||||
| chr7:2802643
|
G | T | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-7500C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802643 | ||||||
| chr7:2802792
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-7649G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802792 | ||||||
| chr7:2802932
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-7789G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802932 | ||||||
| chr7:2802993
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-7850G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2802993 | ||||||
| chr7:2803052
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-7909G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803052 | ||||||
| chr7:2803098
|
G | GA | 183 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.310-7956dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803098 | ||||||
| chr7:2803120
|
T | G | 4 | a0001c0001t0001g0204a0001c0001t0002g0280a0001c0001t0002g0281others(1): Show | 4 | HG03490.hp2 NA19067.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-7977A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803120 | ||||||
| chr7:2803132
|
A | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 6 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-7989T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803132 | ||||||
| chr7:2803261
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.310-8118G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803261 | ||||||
| chr7:2803264
|
C | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-8121G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803264 | ||||||
| chr7:2803304
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-8161C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803304 | ||||||
| chr7:2803327
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.310-8184C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803327 | ||||||
| chr7:2803332
|
G | T | 4 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0074others(1): Show | 4 | NA18956.hp2 NA18960.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-8189C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803332 | ||||||
| chr7:2803527
|
C | G | 183 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.310-8384G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803527 | ||||||
| chr7:2803640
|
A | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-8497T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803640 | ||||||
| chr7:2803793
|
C | CA | 4 | a0001c0001t0001g0210a0001c0001t0002g0280a0001c0001t0002g0281others(1): Show | 4 | HG02738.hp2 NA19067.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-8651dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803793 | ||||||
| chr7:2803798
|
C | A | 183 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.310-8655G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803798 | ||||||
| chr7:2803803
|
C | A | 183 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.310-8660G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803803 | ||||||
| chr7:2803821
|
C | T | 4 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0078others(1): Show | 4 | HG00280.hp2 HG01934.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-8678G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803821 | ||||||
| chr7:2803823
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-8680T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803823 | ||||||
| chr7:2803911
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-8768G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803911 | ||||||
| chr7:2803955
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.310-8812C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2803955 | ||||||
| chr7:2804085
|
G | A | 4 | a0001c0001t0017g0271a0001c0001t0017g0272a0001c0001t0019g0275others(1): Show | 4 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-8942C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804085 | ||||||
| chr7:2804122
|
A | AAC | 10 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(7): Show | 11 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.310-8981_310-8980d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804122 | ||||||
| chr7:2804128
|
A | C | 184 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 186 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.310-8985T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804128 | ||||||
| chr7:2804243
|
C | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-9100G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804243 | ||||||
| chr7:2804290
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(4): Show | 7 | HG00280.hp1 HG01261.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-9147A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804290 | ||||||
| chr7:2804376
|
C | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-9233G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804376 | ||||||
| chr7:2804811
|
C | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-9668G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804811 | ||||||
| chr7:2804811
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310-9668G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804811 | ||||||
| chr7:2804854
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.310-9711A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804854 | ||||||
| chr7:2804906
|
T | TA | 155 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(152): Show | 157 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.310-9764dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804906 | ||||||
| chr7:2804907
|
A | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-9764T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2804907 | ||||||
| chr7:2805014
|
C | T | 46 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(43): Show | 47 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.310-9871G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805014 | ||||||
| chr7:2805022
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-9879C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805022 | ||||||
| chr7:2805106
|
A | G | 1 | a0001c0001t0004g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.310-9963T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805106 | ||||||
| chr7:2805220
|
G | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-10077C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805220 | ||||||
| chr7:2805326
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0003g0013 | 3 | HG01261.hp2 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.310-10183A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805326 | ||||||
| chr7:2805379
|
C | G | 46 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(43): Show | 47 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.310-10236G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805379 | ||||||
| chr7:2805419
|
G | C | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.310-10276C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805419 | ||||||
| chr7:2805495
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.310-10352C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805495 | ||||||
| chr7:2805568
|
G | C | 3 | a0001c0001t0008g0051a0001c0001t0008g0132a0001c0001t0008g0283 | 3 | NA18992.hp1 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.310-10425C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805568 | ||||||
| chr7:2805737
|
A | G | 182 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(179): Show | 184 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.310-10594T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2805737 | ||||||
| chr7:2806086
|
T | C | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.310-10943A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806086 | ||||||
| chr7:2806141
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-10998G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806141 | ||||||
| chr7:2806200
|
C | T | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-11057G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806200 | ||||||
| chr7:2806216
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-11073G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806216 | ||||||
| chr7:2806291
|
C | A | 46 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(43): Show | 47 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.310-11148G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806291 | ||||||
| chr7:2806299
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.310-11156A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806299 | ||||||
| chr7:2806308
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-11165T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806308 | ||||||
| chr7:2806338
|
G | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-11195C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806338 | ||||||
| chr7:2806398
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.310-11255A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806398 | ||||||
| chr7:2806457
|
C | CA | 27 | a0001c0001t0002g0156a0001c0001t0002g0160a0001c0001t0002g0165others(24): Show | 27 | HG00544.hp1 HG01069.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.310-11315dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806457 | ||||||
| chr7:2806457
|
C | CAA | 23 | a0001c0001t0002g0147a0001c0001t0002g0172a0001c0001t0005g0299others(20): Show | 23 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.310-11316_310-1131 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806457 | ||||||
| chr7:2806457
|
C | CAAA | 9 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0011g0183others(6): Show | 9 | HG00639.hp1 HG02886.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-11317_310-1131 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806457 | ||||||
| chr7:2806457
|
CA | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.310-11315delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806457 | ||||||
| chr7:2806457
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0021g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.310-11327_310-1131 others(17): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806457 | ||||||
| chr7:2806466
|
A | AG | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-11324_310-1132 others(5): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806466 | ||||||
| chr7:2806539
|
C | A | 2 | a0001c0001t0006g0064a0001c0001t0006g0097 | 2 | NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.310-11396G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806539 | ||||||
| chr7:2806623
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-11480A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806623 | ||||||
| chr7:2806684
|
A | G | 1 | a0001c0001t0003g0032 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.310-11541T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806684 | ||||||
| chr7:2806784
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-11641A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2806784 | ||||||
| chr7:2807117
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-11974C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807117 | ||||||
| chr7:2807250
|
CTTTTATA others(5): Show |
C | 4 | a0001c0001t0007g0006a0001c0001t0007g0184a0001c0001t0007g0269others(1): Show | 4 | HG02572.hp1 HG02976.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-12119_310-1210 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807250 | ||||||
| chr7:2807260
|
G | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.310-12117C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807260 | ||||||
| chr7:2807343
|
A | C | 46 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(43): Show | 47 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.310-12200T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807343 | ||||||
| chr7:2807372
|
C | T | 29 | a0001c0001t0003g0096a0001c0001t0004g0010a0001c0001t0004g0012others(26): Show | 29 | HG01106.hp1 HG01123.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.310-12229G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807372 | ||||||
| chr7:2807577
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-12434T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807577 | ||||||
| chr7:2807583
|
G | C | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-12440C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807583 | ||||||
| chr7:2807585
|
G | GA | 14 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(11): Show | 15 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.310-12443dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807585 | ||||||
| chr7:2807744
|
A | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.310-12601T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807744 | ||||||
| chr7:2807783
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(4): Show | 7 | HG00280.hp1 HG01261.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-12640A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807783 | ||||||
| chr7:2807862
|
A | G | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.310-12719T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807862 | ||||||
| chr7:2807863
|
A | G | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.310-12720T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807863 | ||||||
| chr7:2807880
|
G | A | 1 | a0001c0001t0019g0276 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.310-12737C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807880 | ||||||
| chr7:2807920
|
C | T | 1 | a0001c0001t0004g0028 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.310-12777G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807920 | ||||||
| chr7:2807928
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.310-12785G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2807928 | ||||||
| chr7:2808056
|
C | T | 1 | a0001c0002t0002g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.310-12913G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808056 | ||||||
| chr7:2808159
|
G | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0273a0001c0004t0018g0265others(1): Show | 5 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-13016C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808159 | ||||||
| chr7:2808189
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-13046G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808189 | ||||||
| chr7:2808190
|
A | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0164a0001c0001t0002g0172 | 3 | HG01358.hp2 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.310-13047T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808190 | ||||||
| chr7:2808241
|
T | C | 10 | a0001c0001t0011g0003a0001c0001t0011g0273a0001c0001t0015g0140others(7): Show | 11 | HG00741.hp1 HG01192.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.310-13098A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808241 | ||||||
| chr7:2808255
|
C | G | 6 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0017g0272others(3): Show | 6 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-13112G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808255 | ||||||
| chr7:2808516
|
G | C | 51 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(48): Show | 52 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.310-13373C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808516 | ||||||
| chr7:2808529
|
G | A | 6 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0150others(3): Show | 7 | HG00544.hp1 NA18612.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-13386C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808529 | ||||||
| chr7:2808550
|
C | G | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-13407G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808550 | ||||||
| chr7:2808556
|
A | C | 3 | a0001c0001t0009g0267a0001c0001t0009g0268a0001c0001t0009g0274 | 3 | HG02486.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.310-13413T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808556 | ||||||
| chr7:2808558
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0273a0001c0004t0018g0265others(1): Show | 5 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-13415T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808558 | ||||||
| chr7:2808568
|
G | A | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-13425C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808568 | ||||||
| chr7:2808610
|
G | A | 1 | a0001c0001t0006g0071 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.310-13467C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808610 | ||||||
| chr7:2808641
|
C | T | 1 | a0001c0001t0008g0048 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.310-13498G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808641 | ||||||
| chr7:2808944
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-13801G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808944 | ||||||
| chr7:2808964
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.310-13821C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808964 | ||||||
| chr7:2808975
|
C | T | 1 | a0001c0001t0008g0052 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.310-13832G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2808975 | ||||||
| chr7:2809015
|
A | G | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.310-13872T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809015 | ||||||
| chr7:2809117
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.310-13974C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809117 | ||||||
| chr7:2809174
|
C | G | 1 | a0001c0001t0003g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.310-14031G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809174 | ||||||
| chr7:2809193
|
G | T | 163 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 164 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.310-14050C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809193 | ||||||
| chr7:2809275
|
G | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-14132C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809275 | ||||||
| chr7:2809378
|
T | C | 1 | a0001c0001t0017g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.310-14235A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809378 | ||||||
| chr7:2809401
|
A | T | 1 | a0001c0001t0005g0310 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.310-14258T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809401 | ||||||
| chr7:2809450
|
G | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-14307C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809450 | ||||||
| chr7:2809459
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-14316G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809459 | ||||||
| chr7:2809534
|
C | A | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.310-14391G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809534 | ||||||
| chr7:2809574
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.310-14431C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809574 | ||||||
| chr7:2809591
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.310-14448A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809591 | ||||||
| chr7:2809818
|
A | T | 2 | a0001c0001t0003g0115a0001c0001t0003g0116 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.310-14675T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2809818 | ||||||
| chr7:2810129
|
T | C | 8 | a0001c0001t0011g0003a0001c0001t0011g0183a0001c0001t0011g0273others(5): Show | 9 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.310-14986A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810129 | ||||||
| chr7:2810180
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.310-15037T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810180 | ||||||
| chr7:2810248
|
C | T | 1 | a0001c0004t0018g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.310-15105G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810248 | ||||||
| chr7:2810420
|
G | A | 43 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(40): Show | 44 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.310-15277C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810420 | ||||||
| chr7:2810433
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.310-15290C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810433 | ||||||
| chr7:2810535
|
TG | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.310-15393delC | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810535 | ||||||
| chr7:2810547
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0273a0001c0004t0018g0265others(1): Show | 5 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-15404T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810547 | ||||||
| chr7:2810590
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310-15447C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810590 | ||||||
| chr7:2810854
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.310-15711G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810854 | ||||||
| chr7:2810901
|
A | AAAAG | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 124 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.310-15762_310-1575 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810901 | ||||||
| chr7:2810901
|
A | AAAAGAAA others(5): Show |
4 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0317others(1): Show | 4 | HG02886.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-15770_310-1575 others(16): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810901 | ||||||
| chr7:2810901
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0012g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.310-15774_310-1575 others(20): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810901 | ||||||
| chr7:2810901
|
AAAAG | A | 49 | a0001c0001t0003g0096a0001c0001t0004g0002a0001c0001t0004g0010others(46): Show | 51 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.310-15762_310-1575 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810901 | ||||||
| chr7:2810948
|
C | G | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.310-15805G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810948 | ||||||
| chr7:2810970
|
C | T | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.310-15827G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810970 | ||||||
| chr7:2810999
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-15856G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2810999 | ||||||
| chr7:2811009
|
C | T | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.310-15866G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811009 | ||||||
| chr7:2811167
|
C | G | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 6 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-16024G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811167 | ||||||
| chr7:2811244
|
A | G | 35 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(32): Show | 36 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.310-16101T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811244 | ||||||
| chr7:2811310
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0034g0107 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.310-16167C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811310 | ||||||
| chr7:2811390
|
C | G | 1 | a0001c0001t0003g0059 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.310-16247G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811390 | ||||||
| chr7:2811394
|
A | C | 2 | a0001c0001t0005g0301a0001c0001t0005g0302 | 2 | HG01106.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.310-16251T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811394 | ||||||
| chr7:2811499
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-16356A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811499 | ||||||
| chr7:2811519
|
CTT | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.310-16378_310-1637 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811519 | ||||||
| chr7:2811560
|
A | G | 2 | a0001c0001t0003g0021a0001c0001t0023g0020 | 2 | NA18939.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.310-16417T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811560 | ||||||
| chr7:2811622
|
G | A | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 6 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-16479C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811622 | ||||||
| chr7:2811641
|
T | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-16498A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811641 | ||||||
| chr7:2811823
|
A | C | 48 | a0001c0001t0002g0085a0001c0001t0002g0129a0001c0001t0003g0096others(45): Show | 49 | HG01074.hp1 HG01106.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.310-16680T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811823 | ||||||
| chr7:2811834
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.310-16691G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811834 | ||||||
| chr7:2811969
|
A | G | 1 | a0001c0001t0003g0168 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.310-16826T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2811969 | ||||||
| chr7:2812055
|
G | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-16912C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812055 | ||||||
| chr7:2812135
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.310-16992C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812135 | ||||||
| chr7:2812140
|
A | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.310-16997T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812140 | ||||||
| chr7:2812298
|
C | T | 1 | a0001c0001t0005g0299 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.310-17155G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812298 | ||||||
| chr7:2812404
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG00609.hp1 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-17261G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812404 | ||||||
| chr7:2812432
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0007g0185 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.310-17289G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812432 | ||||||
| chr7:2812497
|
C | T | 3 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0145 | 3 | NA18977.hp1 NA19084.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.310-17354G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812497 | ||||||
| chr7:2812589
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.310-17446T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812589 | ||||||
| chr7:2812636
|
A | AACATC | 44 | a0001c0001t0002g0004a0001c0001t0002g0014a0001c0001t0002g0158others(41): Show | 44 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.310-17498_310-1749 others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(3): Show |
8 | a0001c0001t0002g0129a0001c0001t0004g0012a0001c0001t0004g0127others(5): Show | 8 | HG01074.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.310-17503_310-1749 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(8): Show |
6 | a0001c0001t0004g0100a0001c0001t0007g0005a0001c0001t0008g0052others(3): Show | 6 | HG01167.hp1 HG01433.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-17508_310-1749 others(19): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(13): Show |
3 | a0001c0001t0004g0002a0001c0001t0008g0051a0001c0001t0012g0298 | 4 | HG01516.hp1 HG01517.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-17513_310-1749 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(18): Show |
3 | a0001c0001t0004g0093a0001c0001t0005g0313a0001c0001t0008g0050 | 3 | HG01169.hp1 HG03579.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.310-17518_310-1749 others(29): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(23): Show |
1 | a0001c0001t0008g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.310-17523_310-1749 others(34): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(28): Show |
1 | a0001c0001t0005g0311 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.310-17528_310-1749 others(39): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(43): Show |
2 | a0001c0001t0007g0006a0001c0001t0007g0270 | 2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.310-17543_310-1749 others(54): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(53): Show |
2 | a0001c0001t0005g0310a0001c0001t0007g0269 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.310-17553_310-1749 others(64): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(58): Show |
1 | a0001c0001t0005g0302 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.310-17494_310-1749 others(69): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(68): Show |
1 | a0001c0001t0005g0309 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.310-17494_310-1749 others(79): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(73): Show |
3 | a0001c0001t0005g0299a0001c0001t0005g0308a0001c0001t0005g0319 | 3 | HG01069.hp1 HG02300.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.310-17494_310-1749 others(84): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(78): Show |
1 | a0001c0001t0005g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.310-17494_310-1749 others(89): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(83): Show |
3 | a0001c0001t0005g0303a0001c0001t0005g0306a0001c0001t0005g0307 | 3 | HG00735.hp1 HG01433.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.310-17494_310-1749 others(94): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(88): Show |
2 | a0001c0001t0005g0314a0001c0001t0005g0315 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.310-17494_310-1749 others(99): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(103): Show |
2 | a0001c0001t0005g0300a0001c0001t0007g0184 | 2 | HG02698.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.310-17494_310-1749 others(114): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(108): Show |
2 | a0001c0001t0005g0305a0001c0001t0007g0148 | 2 | HG01516.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.310-17494_310-1749 others(119): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(113): Show |
1 | a0001c0001t0005g0312 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.310-17494_310-1749 others(124): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
A | AACATCAC others(118): Show |
1 | a0001c0001t0005g0304 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.310-17494_310-1749 others(129): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
AACATC | A | 30 | a0001c0001t0001g0095a0001c0001t0001g0264a0001c0001t0002g0046others(27): Show | 30 | HG00609.hp2 HG01123.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.310-17498_310-1749 others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
AACATCAC others(3): Show |
A | 6 | a0001c0001t0002g0157a0001c0001t0003g0201a0001c0001t0011g0003others(3): Show | 7 | HG02165.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-17503_310-1749 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
AACATCAC others(8): Show |
A | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0217others(9): Show | 12 | HG00423.hp1 HG00423.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.310-17508_310-1749 others(19): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
AACATCAC others(13): Show |
A | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.310-17513_310-1749 others(24): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812636
|
AACATCAC others(18): Show |
A | 2 | a0001c0001t0001g0208a0001c0001t0031g0181 | 2 | NA18955.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.310-17518_310-1749 others(29): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812636 | ||||||
| chr7:2812729
|
C | T | 9 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(6): Show | 10 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.310-17586G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812729 | ||||||
| chr7:2812783
|
A | C | 12 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(9): Show | 13 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.310-17640T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812783 | ||||||
| chr7:2812847
|
G | A | 6 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 6 | HG03239.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-17704C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812847 | ||||||
| chr7:2812942
|
T | A | 1 | a0001c0001t0003g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.310-17799A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812942 | ||||||
| chr7:2812976
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-17833G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812976 | ||||||
| chr7:2813028
|
C | G | 1 | a0001c0001t0006g0039 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.310-17885G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813028 | ||||||
| chr7:2813032
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-17889G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813032 | ||||||
| chr7:2813148
|
T | C | 6 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-18005A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813148 | ||||||
| chr7:2813172
|
G | C | 6 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-18029C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813172 | ||||||
| chr7:2813201
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.310-18058A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813201 | ||||||
| chr7:2813434
|
C | G | 3 | a0001c0004t0018g0265a0001c0004t0018g0266a0002c0006t0027g0149 | 3 | HG00741.hp1 HG03453.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.310-18291G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813434 | ||||||
| chr7:2813457
|
T | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-18314A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813457 | ||||||
| chr7:2813502
|
G | A | 6 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-18359C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813502 | ||||||
| chr7:2813579
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-18436T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813579 | ||||||
| chr7:2813647
|
G | A | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.310-18504C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813647 | ||||||
| chr7:2813649
|
G | T | 1 | a0001c0001t0025g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.310-18506C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813649 | ||||||
| chr7:2813672
|
C | CA | 6 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-18530dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813672 | ||||||
| chr7:2813786
|
C | T | 1 | a0001c0001t0004g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.310-18643G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813786 | ||||||
| chr7:2813955
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-18812G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2813955 | ||||||
| chr7:2814284
|
C | A | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.310-19141G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814284 | ||||||
| chr7:2814335
|
G | C | 5 | a0001c0001t0001g0216a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | NA18943.hp2 NA18952.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-19192C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814335 | ||||||
| chr7:2814361
|
C | T | 1 | a0001c0001t0004g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.310-19218G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814361 | ||||||
| chr7:2814375
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0003g0013 | 3 | HG01261.hp2 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.310-19232A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814375 | ||||||
| chr7:2814376
|
G | A | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.310-19233C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814376 | ||||||
| chr7:2814595
|
C | T | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.310-19452G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814595 | ||||||
| chr7:2814612
|
A | G | 7 | a0001c0001t0003g0017a0001c0001t0003g0055a0001c0001t0003g0060others(4): Show | 7 | HG02135.hp2 HG02155.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-19469T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814612 | ||||||
| chr7:2814616
|
C | T | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.310-19473G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814616 | ||||||
| chr7:2814635
|
C | CT | 8 | a0001c0001t0003g0032a0001c0001t0003g0114a0001c0001t0009g0139others(5): Show | 9 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.310-19493dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814635 | ||||||
| chr7:2814635
|
CT | C | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 170 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.310-19493delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814635 | ||||||
| chr7:2814635
|
CTT | C | 8 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0019g0275others(5): Show | 8 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-19494_310-1949 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814635 | ||||||
| chr7:2814637
|
T | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-19494A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814637 | ||||||
| chr7:2814746
|
A | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.310-19603T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814746 | ||||||
| chr7:2814832
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.310-19689C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814832 | ||||||
| chr7:2814913
|
A | G | 3 | a0001c0001t0017g0272a0001c0001t0019g0275a0001c0001t0019g0276 | 3 | HG01192.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-19770T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814913 | ||||||
| chr7:2814951
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.310-19808A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814951 | ||||||
| chr7:2814955
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-19812G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814955 | ||||||
| chr7:2814967
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.310-19824C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814967 | ||||||
| chr7:2814982
|
G | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-19839C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2814982 | ||||||
| chr7:2815031
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.310-19888G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815031 | ||||||
| chr7:2815131
|
C | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-19988G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815131 | ||||||
| chr7:2815157
|
A | G | 1 | a0001c0001t0017g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.310-20014T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815157 | ||||||
| chr7:2815163
|
C | A | 1 | a0001c0004t0018g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.310-20020G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815163 | ||||||
| chr7:2815186
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.310-20043G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815186 | ||||||
| chr7:2815235
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-20092G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815235 | ||||||
| chr7:2815380
|
T | C | 4 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0078others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-20237A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815380 | ||||||
| chr7:2815474
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.310-20331A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815474 | ||||||
| chr7:2815535
|
A | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-20392T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815535 | ||||||
| chr7:2815535
|
A | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-20392T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815535 | ||||||
| chr7:2815669
|
A | C | 313 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.310-20526T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815669 | ||||||
| chr7:2815692
|
G | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.310-20549C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815692 | ||||||
| chr7:2815692
|
G | C | 3 | a0001c0001t0017g0272a0001c0001t0019g0275a0001c0001t0019g0276 | 3 | HG01192.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-20549C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815692 | ||||||
| chr7:2815703
|
T | C | 139 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 140 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.310-20560A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815703 | ||||||
| chr7:2815720
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-20577G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815720 | ||||||
| chr7:2815738
|
G | A | 2 | a0001c0001t0002g0046a0001c0001t0007g0185 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.310-20595C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815738 | ||||||
| chr7:2815793
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-20650C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815793 | ||||||
| chr7:2815801
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.310-20658G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815801 | ||||||
| chr7:2815802
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.310-20659A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815802 | ||||||
| chr7:2815849
|
C | T | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.310-20706G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815849 | ||||||
| chr7:2815895
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.310-20752C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815895 | ||||||
| chr7:2815960
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.310-20817A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815960 | ||||||
| chr7:2815991
|
C | T | 1 | a0001c0001t0005g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.310-20848G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815991 | ||||||
| chr7:2815998
|
C | G | 2 | a0001c0001t0009g0267a0001c0001t0009g0268 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.310-20855G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2815998 | ||||||
| chr7:2816016
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-20873C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816016 | ||||||
| chr7:2816033
|
G | A | 1 | a0001c0001t0009g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.310-20890C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816033 | ||||||
| chr7:2816045
|
G | A | 1 | a0001c0001t0005g0302 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.310-20902C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816045 | ||||||
| chr7:2816162
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.310-21019T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816162 | ||||||
| chr7:2816169
|
C | T | 315 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(312): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.310-21026G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816169 | ||||||
| chr7:2816208
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0022g0092 | 2 | HG02523.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.310-21065C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816208 | ||||||
| chr7:2816240
|
C | CTTTTTTT | 6 | a0001c0001t0001g0216a0001c0001t0001g0251a0001c0003t0001g0235others(3): Show | 6 | NA18959.hp1 NA18969.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-21104_310-2109 others(11): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816240 | ||||||
| chr7:2816240
|
C | CTTTTTTT others(1): Show |
79 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.310-21105_310-2109 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816240 | ||||||
| chr7:2816240
|
C | CTTTTTTT others(2): Show |
39 | a0001c0001t0001g0207a0001c0001t0002g0280a0001c0001t0002g0281others(36): Show | 39 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.310-21106_310-2109 others(13): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816240 | ||||||
| chr7:2816240
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0003g0013a0001c0001t0017g0272 | 2 | HG02273.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.310-21098_310-2109 others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816240 | ||||||
| chr7:2816240
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-21098_310-2109 others(15): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816240 | ||||||
| chr7:2816333
|
C | T | 1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.310-21190G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816333 | ||||||
| chr7:2816406
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.310-21263A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816406 | ||||||
| chr7:2816534
|
C | A | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.310-21391G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816534 | ||||||
| chr7:2816543
|
T | G | 48 | a0001c0001t0002g0085a0001c0001t0002g0129a0001c0001t0003g0096others(45): Show | 49 | HG01074.hp1 HG01123.hp1 HG01361.hp2 others(46): Show |
intron_variant | MODIFIER | c.310-21400A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816543 | ||||||
| chr7:2816568
|
T | C | 5 | a0001c0001t0004g0093a0001c0001t0004g0124a0001c0001t0004g0125others(2): Show | 5 | HG02922.hp2 HG03041.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-21425A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816568 | ||||||
| chr7:2816585
|
C | A | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-21442G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816585 | ||||||
| chr7:2816620
|
T | C | 2 | a0001c0001t0004g0058a0001c0001t0025g0057 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.310-21477A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816620 | ||||||
| chr7:2816643
|
T | C | 3 | a0001c0001t0002g0165a0001c0001t0002g0171a0001c0001t0002g0255 | 3 | HG01069.hp2 HG01123.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.310-21500A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816643 | ||||||
| chr7:2816672
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.310-21529A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816672 | ||||||
| chr7:2816773
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.310-21630A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816773 | ||||||
| chr7:2816809
|
T | G | 184 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 186 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.310-21666A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816809 | ||||||
| chr7:2816849
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-21706C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816849 | ||||||
| chr7:2816894
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.310-21751A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816894 | ||||||
| chr7:2816899
|
G | A | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.310-21756C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816899 | ||||||
| chr7:2816919
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.310-21776C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2816919 | ||||||
| chr7:2817105
|
T | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0202a0001c0001t0001g0239others(9): Show | 12 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.310-21962A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817105 | ||||||
| chr7:2817158
|
C | T | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.310-22015G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817158 | ||||||
| chr7:2817233
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-22090A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817233 | ||||||
| chr7:2817253
|
C | T | 3 | a0001c0001t0017g0272a0001c0001t0019g0275a0001c0001t0019g0276 | 3 | HG01192.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-22110G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817253 | ||||||
| chr7:2817453
|
G | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.310-22310C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817453 | ||||||
| chr7:2817503
|
G | A | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-22360C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817503 | ||||||
| chr7:2817558
|
A | G | 1 | a0001c0001t0011g0003 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.310-22415T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817558 | ||||||
| chr7:2817742
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-22599G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817742 | ||||||
| chr7:2817767
|
G | A | 6 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-22624C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817767 | ||||||
| chr7:2817777
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.310-22634G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2817777 | ||||||
| chr7:2818242
|
T | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.310-23099A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818242 | ||||||
| chr7:2818328
|
C | T | 1 | a0001c0001t0003g0059 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.310-23185G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818328 | ||||||
| chr7:2818405
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.310-23262G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818405 | ||||||
| chr7:2818407
|
G | C | 7 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(4): Show | 7 | HG02717.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-23264C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818407 | ||||||
| chr7:2818420
|
T | A | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-23277A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818420 | ||||||
| chr7:2818444
|
G | GTAATAAA others(14): Show |
1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.310-23322_310-2330 others(25): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818444 | ||||||
| chr7:2818521
|
G | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-23378C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818521 | ||||||
| chr7:2818523
|
G | A | 6 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 6 | HG03239.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-23380C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818523 | ||||||
| chr7:2818606
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.310-23463A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818606 | ||||||
| chr7:2818624
|
A | G | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-23481T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818624 | ||||||
| chr7:2818633
|
T | G | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.310-23490A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818633 | ||||||
| chr7:2818681
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.310-23538A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818681 | ||||||
| chr7:2818759
|
G | GA | 36 | a0001c0001t0001g0216a0001c0001t0002g0129a0001c0001t0002g0280others(33): Show | 36 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.310-23617dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818759 | ||||||
| chr7:2818759
|
G | GAA | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.310-23618_310-2361 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818759 | ||||||
| chr7:2818814
|
G | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.310-23671C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818814 | ||||||
| chr7:2818835
|
G | A | 6 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(3): Show | 6 | HG01192.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-23692C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818835 | ||||||
| chr7:2818836
|
CT | C | 22 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(19): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.310-23694delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818836 | ||||||
| chr7:2818877
|
C | T | 1 | a0001c0001t0004g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.310-23734G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818877 | ||||||
| chr7:2818932
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.310-23789G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2818932 | ||||||
| chr7:2819009
|
G | C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-23866C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819009 | ||||||
| chr7:2819046
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.310-23903A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819046 | ||||||
| chr7:2819060
|
C | A | 1 | a0001c0001t0012g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.310-23917G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819060 | ||||||
| chr7:2819100
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-23957T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819100 | ||||||
| chr7:2819123
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.310-23980G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819123 | ||||||
| chr7:2819128
|
T | G | 1 | a0001c0001t0003g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.310-23985A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819128 | ||||||
| chr7:2819136
|
T | A | 1 | a0001c0001t0008g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.310-23993A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819136 | ||||||
| chr7:2819175
|
T | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.310-24032A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819175 | ||||||
| chr7:2819218
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-24075G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819218 | ||||||
| chr7:2819272
|
A | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.310-24129T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819272 | ||||||
| chr7:2819273
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.310-24130G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819273 | ||||||
| chr7:2819319
|
C | T | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.310-24176G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819319 | ||||||
| chr7:2819427
|
A | T | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 129 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.310-24284T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819427 | ||||||
| chr7:2819575
|
A | G | 3 | a0001c0001t0028g0284a0001c0004t0018g0265a0001c0004t0018g0266 | 3 | HG00741.hp1 HG03139.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+24278T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819575 | ||||||
| chr7:2819781
|
G | C | 1 | a0001c0001t0003g0144 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.309+24072C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819781 | ||||||
| chr7:2819891
|
A | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.309+23962T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819891 | ||||||
| chr7:2819994
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+23859G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2819994 | ||||||
| chr7:2820185
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+23668G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820185 | ||||||
| chr7:2820213
|
G | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.309+23640C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820213 | ||||||
| chr7:2820216
|
C | G | 6 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+23637G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820216 | ||||||
| chr7:2820253
|
G | C | 1 | a0001c0001t0006g0042 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.309+23600C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820253 | ||||||
| chr7:2820295
|
T | C | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG01258.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.309+23558A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820295 | ||||||
| chr7:2820316
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+23537G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820316 | ||||||
| chr7:2820401
|
C | CT | 20 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(17): Show | 20 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.309+23451dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820401
|
C | CTTT | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.309+23449_309+2345 others(7): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820401
|
C | CTTTT | 6 | a0001c0001t0005g0303a0001c0001t0007g0184a0001c0001t0007g0269others(3): Show | 6 | HG01433.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+23448_309+2345 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820401
|
C | CTTTTTTT | 6 | a0001c0001t0012g0298a0001c0001t0012g0316a0001c0001t0012g0317others(3): Show | 6 | HG02886.hp1 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+23445_309+2345 others(11): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820401
|
C | CTTTTTTT others(7): Show |
2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+23438_309+2345 others(18): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820401
|
CT | C | 9 | a0001c0001t0002g0157a0001c0001t0003g0017a0001c0001t0004g0023others(6): Show | 9 | HG02129.hp2 HG02165.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.309+23451delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820401
|
CTTTT | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+23448_309+2345 others(8): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820401 | ||||||
| chr7:2820562
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.309+23291T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820562 | ||||||
| chr7:2820575
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.309+23278T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820575 | ||||||
| chr7:2820583
|
A | C | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.309+23270T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820583 | ||||||
| chr7:2820649
|
C | A | 1 | a0001c0001t0006g0039 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.309+23204G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820649 | ||||||
| chr7:2820719
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.309+23134C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820719 | ||||||
| chr7:2820895
|
T | C | 3 | a0001c0001t0003g0080a0001c0001t0003g0174a0001c0001t0003g0186 | 3 | HG03834.hp1 HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.309+22958A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820895 | ||||||
| chr7:2820949
|
C | G | 1 | a0001c0001t0006g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.309+22904G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820949 | ||||||
| chr7:2820969
|
G | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+22884C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2820969 | ||||||
| chr7:2821090
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.309+22763T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2821090 | ||||||
| chr7:2821753
|
G | C | 1 | a0001c0001t0029g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.309+22100C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2821753 | ||||||
| chr7:2821950
|
T | C | 1 | a0001c0001t0003g0168 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.309+21903A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2821950 | ||||||
| chr7:2821961
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(5): Show | 8 | HG00140.hp2 HG01346.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+21892G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2821961 | ||||||
| chr7:2822104
|
CTAGCTAA others(4): Show |
C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.309+21738_309+2174 others(15): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822104 | ||||||
| chr7:2822121
|
G | C | 7 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0150others(4): Show | 8 | HG00544.hp1 HG00597.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+21732C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822121 | ||||||
| chr7:2822450
|
T | C | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.309+21403A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822450 | ||||||
| chr7:2822540
|
G | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+21313C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822540 | ||||||
| chr7:2822614
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.309+21239A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822614 | ||||||
| chr7:2822750
|
T | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+21103A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822750 | ||||||
| chr7:2822791
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.309+21062C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822791 | ||||||
| chr7:2822841
|
A | G | 4 | a0001c0001t0003g0055a0001c0001t0003g0106a0001c0001t0003g0146others(1): Show | 4 | HG02135.hp2 NA18975.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+21012T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822841 | ||||||
| chr7:2822908
|
C | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.309+20945G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822908 | ||||||
| chr7:2822912
|
C | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+20941G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2822912 | ||||||
| chr7:2823040
|
T | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+20813A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823040 | ||||||
| chr7:2823041
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0007g0185 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.309+20812T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823041 | ||||||
| chr7:2823257
|
C | T | 101 | a0001c0001t0002g0004a0001c0001t0002g0018a0001c0001t0002g0019others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.309+20596G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823257 | ||||||
| chr7:2823272
|
C | T | 75 | a0001c0001t0001g0009a0001c0001t0001g0173a0001c0001t0001g0190others(72): Show | 75 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.309+20581G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823272 | ||||||
| chr7:2823341
|
G | A | 1 | a0001c0001t0031g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.309+20512C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823341 | ||||||
| chr7:2823398
|
C | T | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 12 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+20455G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823398 | ||||||
| chr7:2823505
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+20348G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823505 | ||||||
| chr7:2823655
|
A | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.309+20198T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823655 | ||||||
| chr7:2823660
|
A | G | 10 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(7): Show | 10 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+20193T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823660 | ||||||
| chr7:2823698
|
TA | T | 17 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(14): Show | 17 | HG00140.hp2 HG01081.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.309+20154delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823698 | ||||||
| chr7:2823809
|
T | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.309+20044A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823809 | ||||||
| chr7:2823871
|
A | T | 1 | a0001c0001t0003g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.309+19982T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823871 | ||||||
| chr7:2823940
|
G | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0173a0001c0001t0001g0190others(72): Show | 75 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.309+19913C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823940 | ||||||
| chr7:2823947
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.309+19906T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823947 | ||||||
| chr7:2823989
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+19864G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2823989 | ||||||
| chr7:2824069
|
A | T | 7 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(4): Show | 7 | HG01192.hp2 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+19784T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824069 | ||||||
| chr7:2824076
|
G | C | 1 | a0001c0001t0006g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.309+19777C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824076 | ||||||
| chr7:2824172
|
A | G | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+19681T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824172 | ||||||
| chr7:2824215
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.309+19638C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824215 | ||||||
| chr7:2824233
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.309+19620C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824233 | ||||||
| chr7:2824396
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+19457A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824396 | ||||||
| chr7:2824449
|
C | A | 2 | a0001c0001t0009g0274a0001c0001t0011g0273 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.309+19404G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824449 | ||||||
| chr7:2824459
|
C | A | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.309+19394G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824459 | ||||||
| chr7:2824477
|
C | A | 2 | a0001c0001t0021g0044a0001c0001t0021g0045 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.309+19376G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824477 | ||||||
| chr7:2824559
|
G | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+19294C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824559 | ||||||
| chr7:2824563
|
G | A | 3 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0029g0182 | 3 | HG01167.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.309+19290C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824563 | ||||||
| chr7:2824728
|
A | G | 3 | a0001c0001t0002g0180a0001c0004t0018g0265a0001c0004t0018g0266 | 3 | HG00741.hp1 HG03041.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.309+19125T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824728 | ||||||
| chr7:2824806
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+19047G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824806 | ||||||
| chr7:2824807
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+19046C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824807 | ||||||
| chr7:2824851
|
C | G | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+19002G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824851 | ||||||
| chr7:2824934
|
TTTCCGAC others(41): Show |
T | 1 | a0001c0001t0002g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.309+18871_309+1891 others(52): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824934 | ||||||
| chr7:2824952
|
G | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.309+18901C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824952 | ||||||
| chr7:2824978
|
C | A | 1 | a0001c0001t0004g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.309+18875G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2824978 | ||||||
| chr7:2825040
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.309+18813C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825040 | ||||||
| chr7:2825072
|
C | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+18781G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825072 | ||||||
| chr7:2825107
|
C | T | 2 | a0001c0001t0004g0187a0001c0001t0004g0188 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.309+18746G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825107 | ||||||
| chr7:2825153
|
G | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+18700C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825153 | ||||||
| chr7:2825196
|
C | T | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.309+18657G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825196 | ||||||
| chr7:2825329
|
C | T | 2 | a0001c0001t0005g0301a0001c0001t0005g0302 | 2 | HG01106.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.309+18524G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825329 | ||||||
| chr7:2825428
|
GC | G | 24 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.309+18424delG | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825428 | ||||||
| chr7:2825449
|
C | T | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.309+18404G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825449 | ||||||
| chr7:2825639
|
G | A | 2 | a0001c0001t0008g0132a0001c0001t0008g0283 | 2 | NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.309+18214C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825639 | ||||||
| chr7:2825678
|
C | G | 7 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(4): Show | 7 | HG01192.hp2 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+18175G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825678 | ||||||
| chr7:2825735
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.309+18118T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825735 | ||||||
| chr7:2825768
|
G | C | 1 | a0001c0007t0003g0295 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.309+18085C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825768 | ||||||
| chr7:2825782
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.309+18071G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825782 | ||||||
| chr7:2825802
|
G | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+18051C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825802 | ||||||
| chr7:2825859
|
TCCCACCA | T | 7 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(4): Show | 7 | HG01192.hp2 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+17987_309+1799 others(11): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825859 | ||||||
| chr7:2825887
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.309+17966A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825887 | ||||||
| chr7:2825945
|
C | T | 3 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270 | 3 | HG02976.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.309+17908G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2825945 | ||||||
| chr7:2826037
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.309+17816A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826037 | ||||||
| chr7:2826105
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+17748C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826105 | ||||||
| chr7:2826143
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+17710G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826143 | ||||||
| chr7:2826230
|
T | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 12 | HG00741.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+17623A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826230 | ||||||
| chr7:2826376
|
C | CA | 10 | a0001c0001t0002g0018a0001c0001t0003g0030a0001c0001t0003g0038others(7): Show | 10 | HG01169.hp2 HG01175.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+17476dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826376 | ||||||
| chr7:2826376
|
CA | C | 35 | a0001c0001t0002g0001a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 36 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.309+17476delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826376 | ||||||
| chr7:2826376
|
CAA | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.309+17475_309+1747 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826376 | ||||||
| chr7:2826389
|
A | C | 11 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(8): Show | 11 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.309+17464T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826389 | ||||||
| chr7:2826512
|
T | A | 1 | a0001c0001t0019g0276 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.309+17341A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826512 | ||||||
| chr7:2826524
|
C | G | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.309+17329G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826524 | ||||||
| chr7:2826527
|
A | G | 10 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(7): Show | 10 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+17326T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826527 | ||||||
| chr7:2826716
|
C | T | 22 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(19): Show | 23 | HG00741.hp1 HG01192.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.309+17137G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826716 | ||||||
| chr7:2826734
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.309+17119C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826734 | ||||||
| chr7:2826778
|
G | A | 1 | a0001c0001t0004g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.309+17075C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826778 | ||||||
| chr7:2826834
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.309+17019C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826834 | ||||||
| chr7:2826844
|
T | G | 118 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.309+17009A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826844 | ||||||
| chr7:2826895
|
G | A | 27 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(24): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.309+16958C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826895 | ||||||
| chr7:2826988
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.309+16865A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2826988 | ||||||
| chr7:2827043
|
G | A | 1 | a0001c0001t0005g0315 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.309+16810C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827043 | ||||||
| chr7:2827121
|
G | A | 1 | a0001c0001t0003g0145 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.309+16732C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827121 | ||||||
| chr7:2827199
|
G | C | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.309+16654C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827199 | ||||||
| chr7:2827381
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.309+16472C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827381 | ||||||
| chr7:2827505
|
G | A | 10 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(7): Show | 10 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+16348C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827505 | ||||||
| chr7:2827662
|
A | G | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.309+16191T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827662 | ||||||
| chr7:2827790
|
G | C | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.309+16063C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827790 | ||||||
| chr7:2827796
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+16057C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827796 | ||||||
| chr7:2827923
|
A | AT | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.309+15929dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2827923 | ||||||
| chr7:2828015
|
A | C | 1 | a0001c0001t0003g0174 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.309+15838T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828015 | ||||||
| chr7:2828396
|
C | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.309+15457G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828396 | ||||||
| chr7:2828471
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+15382C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828471 | ||||||
| chr7:2828499
|
A | T | 7 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(4): Show | 7 | HG01192.hp2 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+15354T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828499 | ||||||
| chr7:2828599
|
C | G | 1 | a0001c0001t0003g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.309+15254G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828599 | ||||||
| chr7:2828606
|
C | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+15247G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828606 | ||||||
| chr7:2828634
|
C | T | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+15219G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828634 | ||||||
| chr7:2828756
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.309+15097A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828756 | ||||||
| chr7:2828904
|
C | T | 3 | a0001c0001t0006g0039a0001c0001t0006g0041a0001c0001t0006g0042 | 3 | HG00597.hp2 NA18942.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.309+14949G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828904 | ||||||
| chr7:2828940
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.309+14913C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2828940 | ||||||
| chr7:2829073
|
AG | A | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.309+14779delC | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829073 | ||||||
| chr7:2829075
|
G | A | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG01192.hp2 HG03540.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+14778C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829075 | ||||||
| chr7:2829096
|
A | G | 110 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.309+14757T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829096 | ||||||
| chr7:2829112
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG00609.hp1 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+14741C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829112 | ||||||
| chr7:2829190
|
C | G | 132 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.309+14663G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829190 | ||||||
| chr7:2829211
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.309+14642G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829211 | ||||||
| chr7:2829314
|
G | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+14539C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829314 | ||||||
| chr7:2829363
|
T | C | 39 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(36): Show | 39 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.309+14490A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829363 | ||||||
| chr7:2829463
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+14390A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829463 | ||||||
| chr7:2829606
|
A | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.309+14247T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829606 | ||||||
| chr7:2829640
|
G | A | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.309+14213C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829640 | ||||||
| chr7:2829695
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+14158A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829695 | ||||||
| chr7:2829703
|
T | C | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+14150A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829703 | ||||||
| chr7:2829730
|
A | T | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.309+14123T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829730 | ||||||
| chr7:2829757
|
T | C | 132 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.309+14096A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829757 | ||||||
| chr7:2829772
|
T | A | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+14081A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829772 | ||||||
| chr7:2829849
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.309+14004A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829849 | ||||||
| chr7:2829852
|
T | C | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+14001A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829852 | ||||||
| chr7:2829888
|
G | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.309+13965C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2829888 | ||||||
| chr7:2830207
|
G | C | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+13646C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830207 | ||||||
| chr7:2830226
|
C | CA | 16 | a0001c0001t0001g0264a0001c0001t0002g0014a0001c0001t0002g0015others(13): Show | 16 | HG01081.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.309+13626dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830226 | ||||||
| chr7:2830351
|
T | C | 88 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 89 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.309+13502A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830351 | ||||||
| chr7:2830363
|
T | C | 1 | a0001c0001t0003g0021 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.309+13490A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830363 | ||||||
| chr7:2830571
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.309+13282T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830571 | ||||||
| chr7:2830584
|
G | T | 2 | a0001c0001t0009g0267a0001c0001t0009g0268 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.309+13269C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830584 | ||||||
| chr7:2830820
|
T | G | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+13033A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830820 | ||||||
| chr7:2830910
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+12943G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830910 | ||||||
| chr7:2830953
|
GA | G | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.309+12899delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830953 | ||||||
| chr7:2830981
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | NA18939.hp1 NA18955.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.309+12872T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2830981 | ||||||
| chr7:2831126
|
T | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+12727A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831126 | ||||||
| chr7:2831141
|
G | A | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+12712C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831141 | ||||||
| chr7:2831151
|
T | C | 1 | a0001c0001t0007g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.309+12702A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831151 | ||||||
| chr7:2831254
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.309+12599G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831254 | ||||||
| chr7:2831340
|
C | G | 1 | a0001c0001t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.309+12513G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831340 | ||||||
| chr7:2831404
|
C | CT | 100 | a0001c0001t0001g0009a0001c0001t0001g0173a0001c0001t0001g0202others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.309+12448dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831404 | ||||||
| chr7:2831404
|
C | CTT | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0135others(11): Show | 14 | HG00280.hp1 HG00741.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.309+12447_309+1244 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831404 | ||||||
| chr7:2831453
|
GAGTGC | G | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.309+12395_309+1239 others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831453 | ||||||
| chr7:2831459
|
AGTGGCGC others(1): Show |
A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+12386_309+1239 others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831459 | ||||||
| chr7:2831464
|
C | G | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.309+12389G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831464 | ||||||
| chr7:2831466
|
C | A | 41 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.309+12387G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831466 | ||||||
| chr7:2831558
|
C | T | 12 | a0001c0001t0003g0021a0001c0001t0003g0029a0001c0001t0003g0030others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.309+12295G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831558 | ||||||
| chr7:2831564
|
C | T | 41 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.309+12289G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831564 | ||||||
| chr7:2831604
|
C | T | 1 | a0001c0001t0005g0299 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.309+12249G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831604 | ||||||
| chr7:2831641
|
G | A | 8 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(5): Show | 8 | HG01192.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+12212C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831641 | ||||||
| chr7:2831683
|
A | G | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.309+12170T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831683 | ||||||
| chr7:2831687
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.309+12166T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831687 | ||||||
| chr7:2831700
|
G | T | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.309+12153C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831700 | ||||||
| chr7:2831731
|
A | C | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+12122T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831731 | ||||||
| chr7:2831891
|
C | T | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.309+11962G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2831891 | ||||||
| chr7:2832206
|
A | C | 1 | a0001c0001t0001g0256 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.309+11647T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832206 | ||||||
| chr7:2832237
|
C | G | 8 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(5): Show | 8 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+11616G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832237 | ||||||
| chr7:2832279
|
T | C | 1 | a0001c0001t0004g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.309+11574A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832279 | ||||||
| chr7:2832299
|
C | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0027 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.309+11554G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832299 | ||||||
| chr7:2832599
|
A | G | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.309+11254T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832599 | ||||||
| chr7:2832723
|
G | C | 1 | a0001c0001t0003g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.309+11130C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832723 | ||||||
| chr7:2832812
|
G | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.309+11041C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832812 | ||||||
| chr7:2832952
|
C | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+10901G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2832952 | ||||||
| chr7:2833056
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+10797G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833056 | ||||||
| chr7:2833106
|
G | A | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+10747C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833106 | ||||||
| chr7:2833178
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.309+10675A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833178 | ||||||
| chr7:2833189
|
T | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+10664A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833189 | ||||||
| chr7:2833490
|
C | T | 16 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(13): Show | 17 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.309+10363G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833490 | ||||||
| chr7:2833502
|
C | T | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+10351G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833502 | ||||||
| chr7:2833535
|
A | G | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.309+10318T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833535 | ||||||
| chr7:2833600
|
C | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(98): Show | 102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.309+10253G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833600 | ||||||
| chr7:2833613
|
C | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.309+10240G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833613 | ||||||
| chr7:2833645
|
G | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.309+10208C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833645 | ||||||
| chr7:2833660
|
C | T | 22 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(19): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+10193G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833660 | ||||||
| chr7:2833739
|
CTG | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+10112_309+1011 others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833739 | ||||||
| chr7:2833775
|
T | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+10078A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833775 | ||||||
| chr7:2833783
|
C | T | 8 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(5): Show | 8 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+10070G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833783 | ||||||
| chr7:2833860
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.309+9993G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2833860 | ||||||
| chr7:2834014
|
A | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+9839T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834014 | ||||||
| chr7:2834129
|
G | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.309+9724C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834129 | ||||||
| chr7:2834171
|
G | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+9682C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834171 | ||||||
| chr7:2834290
|
A | T | 3 | a0001c0002t0002g0152a0001c0002t0002g0153a0001c0002t0002g0154 | 3 | HG02055.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.309+9563T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834290 | ||||||
| chr7:2834370
|
T | G | 3 | a0001c0001t0003g0106a0001c0001t0003g0146a0001c0001t0003g0170 | 3 | NA18975.hp2 NA18984.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.309+9483A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834370 | ||||||
| chr7:2834593
|
A | C | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+9260T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834593 | ||||||
| chr7:2834694
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.309+9159T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834694 | ||||||
| chr7:2834733
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.309+9120A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834733 | ||||||
| chr7:2834755
|
C | T | 2 | a0001c0004t0018g0265a0001c0004t0018g0266 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.309+9098G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834755 | ||||||
| chr7:2834758
|
T | C | 16 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(13): Show | 17 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.309+9095A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834758 | ||||||
| chr7:2834772
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+9081G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834772 | ||||||
| chr7:2834906
|
C | T | 76 | a0001c0001t0001g0009a0001c0001t0001g0135a0001c0001t0001g0136others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.309+8947G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834906 | ||||||
| chr7:2834935
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.309+8918C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834935 | ||||||
| chr7:2834947
|
G | A | 1 | a0001c0001t0009g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.309+8906C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834947 | ||||||
| chr7:2834959
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+8894G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834959 | ||||||
| chr7:2834959
|
CGCGATGC others(13): Show |
C | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.309+8874_309+8893d others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834959 | ||||||
| chr7:2834960
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+8893C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834960 | ||||||
| chr7:2834967
|
A | G | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.309+8886T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2834967 | ||||||
| chr7:2835151
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.309+8702G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835151 | ||||||
| chr7:2835201
|
T | C | 17 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(14): Show | 18 | HG01192.hp2 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.309+8652A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835201 | ||||||
| chr7:2835258
|
C | G | 1 | a0001c0001t0006g0026 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.309+8595G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835258 | ||||||
| chr7:2835348
|
T | C | 28 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+8505A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835348 | ||||||
| chr7:2835378
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | NA18982.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.309+8475A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835378 | ||||||
| chr7:2835392
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.309+8461T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835392 | ||||||
| chr7:2835445
|
C | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+8408G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835445 | ||||||
| chr7:2835562
|
G | C | 1 | a0001c0001t0034g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.309+8291C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835562 | ||||||
| chr7:2835573
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.309+8280G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835573 | ||||||
| chr7:2835786
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+8067C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835786 | ||||||
| chr7:2835936
|
G | A | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.309+7917C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835936 | ||||||
| chr7:2835940
|
C | T | 22 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(19): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+7913G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835940 | ||||||
| chr7:2835956
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.309+7897T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835956 | ||||||
| chr7:2835969
|
G | T | 2 | a0001c0001t0004g0022a0001c0001t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.309+7884C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2835969 | ||||||
| chr7:2836119
|
C | CA | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.309+7733dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836119 | ||||||
| chr7:2836139
|
G | A | 3 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.309+7714C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836139 | ||||||
| chr7:2836456
|
T | C | 7 | a0001c0001t0004g0010a0001c0001t0004g0108a0001c0001t0004g0109others(4): Show | 7 | NA18942.hp2 NA18949.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.309+7397A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836456 | ||||||
| chr7:2836523
|
G | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.309+7330C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836523 | ||||||
| chr7:2836540
|
C | G | 2 | a0001c0001t0019g0275a0001c0001t0019g0276 | 2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.309+7313G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836540 | ||||||
| chr7:2836543
|
C | T | 16 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(13): Show | 17 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.309+7310G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836543 | ||||||
| chr7:2836667
|
T | C | 1 | a0001c0001t0028g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.309+7186A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836667 | ||||||
| chr7:2836721
|
CG | C | 16 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(13): Show | 17 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.309+7131delC | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836721 | ||||||
| chr7:2836898
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0023g0020 | 2 | NA18939.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.309+6955G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2836898 | ||||||
| chr7:2837611
|
G | T | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+6242C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837611 | ||||||
| chr7:2837618
|
G | A | 15 | a0001c0001t0007g0269a0001c0001t0007g0270a0001c0001t0009g0139others(12): Show | 16 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.309+6235C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837618 | ||||||
| chr7:2837674
|
G | A | 6 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 6 | HG03239.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+6179C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837674 | ||||||
| chr7:2837778
|
G | C | 10 | a0001c0001t0007g0184a0001c0001t0007g0269a0001c0001t0007g0270others(7): Show | 10 | HG01192.hp2 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+6075C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837778 | ||||||
| chr7:2837802
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.309+6051C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837802 | ||||||
| chr7:2837840
|
T | TA | 17 | a0001c0001t0002g0121a0001c0001t0007g0184a0001c0001t0007g0269others(14): Show | 18 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.309+6012dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837840 | ||||||
| chr7:2837859
|
T | C | 2 | a0001c0001t0005g0314a0001c0001t0005g0315 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.309+5994A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837859 | ||||||
| chr7:2837888
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.309+5965T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2837888 | ||||||
| chr7:2838035
|
T | C | 1 | a0001c0001t0032g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.309+5818A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838035 | ||||||
| chr7:2838074
|
G | C | 1 | a0001c0002t0002g0123 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.309+5779C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838074 | ||||||
| chr7:2838141
|
T | TA | 8 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(5): Show | 9 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.309+5711dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838141 | ||||||
| chr7:2838177
|
A | G | 22 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(19): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+5676T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838177 | ||||||
| chr7:2838244
|
G | A | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG02922.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.309+5609C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838244 | ||||||
| chr7:2838280
|
T | TA | 27 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0263others(24): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.309+5572dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838280 | ||||||
| chr7:2838280
|
T | TAA | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.309+5571_309+5572d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838280 | ||||||
| chr7:2838280
|
TA | T | 14 | a0001c0001t0002g0018a0001c0001t0006g0189a0001c0001t0007g0184others(11): Show | 15 | HG01169.hp2 HG01192.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+5572delT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838280 | ||||||
| chr7:2838307
|
G | A | 22 | a0001c0001t0003g0128a0001c0001t0005g0299a0001c0001t0005g0300others(19): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+5546C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838307 | ||||||
| chr7:2838382
|
C | G | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.309+5471G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838382 | ||||||
| chr7:2838469
|
G | A | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.309+5384C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838469 | ||||||
| chr7:2838539
|
G | T | 1 | a0001c0001t0003g0017 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.309+5314C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838539 | ||||||
| chr7:2838570
|
A | G | 10 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(7): Show | 10 | HG00741.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+5283T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838570 | ||||||
| chr7:2838608
|
G | T | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+5245C>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838608 | ||||||
| chr7:2838739
|
A | T | 8 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(5): Show | 8 | HG01081.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+5114T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838739 | ||||||
| chr7:2838762
|
T | C | 5 | a0001c0001t0011g0183a0001c0001t0012g0298a0001c0001t0012g0316others(2): Show | 5 | HG02886.hp1 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+5091A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838762 | ||||||
| chr7:2838845
|
T | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+5008A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838845 | ||||||
| chr7:2838873
|
C | G | 1 | a0001c0001t0012g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.309+4980G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838873 | ||||||
| chr7:2838876
|
A | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.309+4977T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838876 | ||||||
| chr7:2838971
|
G | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+4882C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2838971 | ||||||
| chr7:2839073
|
G | A | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.309+4780C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839073 | ||||||
| chr7:2839145
|
T | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.309+4708A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839145 | ||||||
| chr7:2839223
|
G | C | 19 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(16): Show | 19 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.309+4630C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839223 | ||||||
| chr7:2839242
|
C | CT | 83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.309+4610dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839242 | ||||||
| chr7:2839349
|
C | T | 1 | a0001c0001t0006g0189 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.309+4504G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839349 | ||||||
| chr7:2839362
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.309+4491G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839362 | ||||||
| chr7:2839363
|
A | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+4490T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839363 | ||||||
| chr7:2839388
|
A | G | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+4465T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839388 | ||||||
| chr7:2839401
|
T | C | 21 | a0001c0001t0007g0184a0001c0001t0007g0185a0001c0001t0007g0269others(18): Show | 22 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.309+4452A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839401 | ||||||
| chr7:2839422
|
C | T | 1 | a0001c0001t0004g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.309+4431G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839422 | ||||||
| chr7:2839441
|
T | C | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+4412A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839441 | ||||||
| chr7:2839528
|
C | T | 4 | a0001c0001t0028g0284a0001c0004t0014g0285a0001c0004t0014g0286others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+4325G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839528 | ||||||
| chr7:2839604
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.309+4249C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839604 | ||||||
| chr7:2839690
|
T | C | 2 | a0001c0001t0016g0130a0001c0001t0016g0131 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.309+4163A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839690 | ||||||
| chr7:2839729
|
C | T | 10 | a0001c0001t0009g0139a0001c0001t0009g0267a0001c0001t0009g0268others(7): Show | 11 | HG02280.hp1 HG02486.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.309+4124G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839729 | ||||||
| chr7:2839771
|
C | T | 1 | a0002c0006t0027g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+4082G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839771 | ||||||
| chr7:2839791
|
G | A | 2 | a0001c0001t0008g0132a0001c0001t0008g0283 | 2 | NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.309+4062C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839791 | ||||||
| chr7:2839827
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.309+4026G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839827 | ||||||
| chr7:2839854
|
C | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+3999G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839854 | ||||||
| chr7:2839928
|
G | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+3925C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839928 | ||||||
| chr7:2839976
|
C | A | 9 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0259others(6): Show | 9 | HG02071.hp1 HG02165.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.309+3877G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2839976 | ||||||
| chr7:2840062
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+3791T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840062 | ||||||
| chr7:2840121
|
C | T | 21 | a0001c0001t0005g0299a0001c0001t0005g0300a0001c0001t0005g0301others(18): Show | 21 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.309+3732G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840121 | ||||||
| chr7:2840131
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.309+3722G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840131 | ||||||
| chr7:2840171
|
T | C | 21 | a0001c0001t0007g0184a0001c0001t0007g0185a0001c0001t0007g0269others(18): Show | 22 | HG01192.hp2 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.309+3682A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840171 | ||||||
| chr7:2840200
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.309+3653A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840200 | ||||||
| chr7:2840355
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.309+3498A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840355 | ||||||
| chr7:2840367
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+3486A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840367 | ||||||
| chr7:2840552
|
G | A | 2 | a0001c0001t0017g0271a0001c0001t0017g0272 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.309+3301C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840552 | ||||||
| chr7:2840676
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.309+3177A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840676 | ||||||
| chr7:2840781
|
C | T | 1 | a0001c0001t0012g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.309+3072G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840781 | ||||||
| chr7:2840805
|
A | C | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.309+3048T>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840805 | ||||||
| chr7:2840844
|
ACT | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+3007_309+3008d others(4): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840844 | ||||||
| chr7:2840916
|
C | A | 3 | a0001c0001t0015g0140a0001c0001t0015g0141a0001c0001t0035g0297 | 3 | HG02451.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.309+2937G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840916 | ||||||
| chr7:2840921
|
G | A | 1 | a0001c0001t0007g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.309+2932C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840921 | ||||||
| chr7:2840939
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.309+2914C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840939 | ||||||
| chr7:2840960
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.309+2893A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2840960 | ||||||
| chr7:2841014
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.309+2839A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841014 | ||||||
| chr7:2841175
|
G | A | 5 | a0001c0001t0002g0142a0001c0001t0003g0143a0001c0001t0003g0144others(2): Show | 5 | NA18977.hp1 NA18984.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+2678C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841175 | ||||||
| chr7:2841301
|
G | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.309+2552C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841301 | ||||||
| chr7:2841389
|
T | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+2464A>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841389 | ||||||
| chr7:2841407
|
G | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+2446C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841407 | ||||||
| chr7:2841420
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.309+2433C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841420 | ||||||
| chr7:2841497
|
AGAC | A | 3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+2353_309+2355d others(5): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841497 | ||||||
| chr7:2841501
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.309+2352C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841501 | ||||||
| chr7:2841540
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.309+2313A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841540 | ||||||
| chr7:2841579
|
C | CT | 20 | a0001c0001t0007g0184a0001c0001t0007g0185a0001c0001t0007g0269others(17): Show | 21 | HG01192.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.309+2273dupA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841579 | ||||||
| chr7:2841583
|
G | C | 20 | a0001c0001t0007g0184a0001c0001t0007g0185a0001c0001t0007g0269others(17): Show | 21 | HG01192.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.309+2270C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841583 | ||||||
| chr7:2841716
|
G | A | 5 | a0001c0001t0002g0142a0001c0001t0003g0143a0001c0001t0003g0144others(2): Show | 5 | NA18977.hp1 NA18984.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+2137C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841716 | ||||||
| chr7:2841733
|
G | C | 1 | a0001c0001t0012g0318 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.309+2120C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841733 | ||||||
| chr7:2841905
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.309+1948C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841905 | ||||||
| chr7:2841916
|
G | C | 33 | a0001c0001t0001g0264a0001c0001t0002g0280a0001c0001t0002g0281others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.309+1937C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841916 | ||||||
| chr7:2841990
|
G | C | 16 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0303others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.309+1863C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2841990 | ||||||
| chr7:2842001
|
T | TAGGGAGG others(17): Show |
37 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(34): Show | 37 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.309+1851_309+1852i others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842001 | ||||||
| chr7:2842001
|
T | TAGGGAGG others(21): Show |
4 | a0001c0001t0009g0274a0001c0001t0011g0003a0001c0001t0011g0273others(1): Show | 5 | HG02486.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+1851_309+1852i others(30): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842001 | ||||||
| chr7:2842005
|
G | GAGGGAGG others(13): Show |
97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 97 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.309+1847_309+1848i others(22): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842005 | ||||||
| chr7:2842005
|
G | GAGGGAGG others(17): Show |
3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+1847_309+1848i others(26): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842005 | ||||||
| chr7:2842014
|
AGAAAGGA others(3): Show |
A | 1 | a0001c0001t0004g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.309+1829_309+1838d others(12): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842014 | ||||||
| chr7:2842016
|
A | G | 1 | a0001c0001t0004g0010 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.309+1837T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842016 | ||||||
| chr7:2842016
|
AAAGGAAG others(5): Show |
A | 24 | a0001c0001t0002g0001a0001c0001t0002g0155a0001c0001t0002g0156others(21): Show | 26 | HG00544.hp1 HG00597.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.309+1825_309+1836d others(14): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842016 | ||||||
| chr7:2842031
|
G | A | 2 | a0001c0001t0011g0003a0001c0001t0011g0273 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.309+1822C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842031 | ||||||
| chr7:2842090
|
AAAGGAAG others(6): Show |
A | 1 | a0001c0001t0035g0297 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.309+1750_309+1762d others(15): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842090 | ||||||
| chr7:2842099
|
A | AAGAGAAG | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.309+1753_309+1754i others(9): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842099 | ||||||
| chr7:2842104
|
A | G | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.309+1749T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842104 | ||||||
| chr7:2842106
|
G | GAAAA | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+1746_309+1747i others(6): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842106 | ||||||
| chr7:2842108
|
A | AAAGGAAG others(73): Show |
2 | a0001c0001t0011g0003a0001c0001t0029g0182 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.309+1744_309+1745i others(82): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842108 | ||||||
| chr7:2842108
|
A | AAAGGAAG others(64): Show |
2 | a0001c0001t0009g0274a0001c0001t0026g0288 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.309+1744_309+1745i others(73): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842108 | ||||||
| chr7:2842108
|
A | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+1745T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842108 | ||||||
| chr7:2842110
|
G | A | 8 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(5): Show | 9 | HG02258.hp1 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.309+1743C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842110 | ||||||
| chr7:2842110
|
G | GAATGGAA others(21): Show |
91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.309+1742_309+1743i others(30): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842110 | ||||||
| chr7:2842110
|
G | GAGAAGAA others(37): Show |
3 | a0001c0004t0014g0285a0001c0004t0014g0286a0001c0004t0014g0287 | 3 | HG02818.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+1742_309+1743i others(46): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842110 | ||||||
| chr7:2842110
|
G | GGGAAGAA others(37): Show |
5 | a0001c0001t0001g0264a0001c0001t0009g0267a0001c0001t0009g0268others(2): Show | 5 | HG00741.hp1 HG03098.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+1742_309+1743i others(46): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842110 | ||||||
| chr7:2842116
|
G | GAAAGGAA others(52): Show |
1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.309+1736_309+1737i others(61): Show |
GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842116 | ||||||
| chr7:2842117
|
G | A | 1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.309+1736C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842117 | ||||||
| chr7:2842129
|
A | G | 1 | a0001c0001t0011g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.309+1724T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842129 | ||||||
| chr7:2842275
|
G | C | 39 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(36): Show | 40 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.309+1578C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842275 | ||||||
| chr7:2842283
|
A | G | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.309+1570T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842283 | ||||||
| chr7:2842322
|
AT | A | 45 | a0001c0001t0002g0004a0001c0001t0002g0280a0001c0001t0002g0281others(42): Show | 46 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.309+1530delA | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842322 | ||||||
| chr7:2842396
|
T | C | 137 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(134): Show | 138 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.309+1457A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842396 | ||||||
| chr7:2842521
|
C | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+1332G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842521 | ||||||
| chr7:2842563
|
G | C | 6 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(3): Show | 6 | HG01081.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1290C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842563 | ||||||
| chr7:2842569
|
A | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+1284T>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842569 | ||||||
| chr7:2842628
|
G | A | 133 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(130): Show | 134 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.309+1225C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842628 | ||||||
| chr7:2842787
|
G | A | 88 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.309+1066C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842787 | ||||||
| chr7:2842987
|
A | G | 88 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.309+866T>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2842987 | ||||||
| chr7:2843062
|
G | A | 6 | a0001c0001t0007g0269a0001c0001t0007g0270a0001c0001t0017g0271others(3): Show | 6 | HG01192.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+791C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843062 | ||||||
| chr7:2843147
|
G | A | 3 | a0001c0001t0012g0316a0001c0001t0012g0317a0001c0001t0012g0318 | 3 | HG03195.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.309+706C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843147 | ||||||
| chr7:2843153
|
T | C | 2 | a0001c0001t0007g0184a0001c0001t0007g0185 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.309+700A>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843153 | ||||||
| chr7:2843181
|
C | T | 4 | a0001c0001t0007g0269a0001c0001t0007g0270a0001c0001t0017g0271others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+672G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843181 | ||||||
| chr7:2843193
|
C | T | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+660G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843193 | ||||||
| chr7:2843195
|
G | A | 132 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(129): Show | 133 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.309+658C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843195 | ||||||
| chr7:2843221
|
C | G | 30 | a0001c0001t0002g0004a0001c0001t0002g0280a0001c0001t0002g0281others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.309+632G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843221 | ||||||
| chr7:2843292
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+561G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843292 | ||||||
| chr7:2843359
|
G | A | 3 | a0001c0001t0003g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | HG03688.hp1 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.309+494C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843359 | ||||||
| chr7:2843370
|
G | C | 87 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.309+483C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843370 | ||||||
| chr7:2843372
|
C | A | 3 | a0001c0001t0013g0277a0001c0001t0013g0278a0001c0001t0013g0279 | 3 | NA18956.hp1 NA18979.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.309+481G>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843372 | ||||||
| chr7:2843372
|
C | G | 84 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.309+481G>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843372 | ||||||
| chr7:2843437
|
G | A | 96 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.309+416C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843437 | ||||||
| chr7:2843455
|
G | A | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | NA19067.hp1 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.309+398C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843455 | ||||||
| chr7:2843481
|
C | CA | 5 | a0001c0001t0008g0283a0001c0001t0028g0284a0001c0004t0014g0285others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+371dupT | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843481 | ||||||
| chr7:2843507
|
G | C | 1 | a0001c0001t0026g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309+346C>G | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843507 | ||||||
| chr7:2843525
|
T | G | 1 | a0001c0001t0004g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.309+328A>C | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843525 | ||||||
| chr7:2843568
|
G | A | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | NA18953.hp1 NA19012.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+285C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843568 | ||||||
| chr7:2843687
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.309+166C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843687 | ||||||
| chr7:2843774
|
G | A | 1 | a0001c0001t0005g0319 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.309+79C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843774 |