Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MSGVV others(376): Show |
chr7 | 2723105 | 2849308 |
| a0002 | 0/0 | 381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | MSGVV others(376): Show |
chr7 | 2723105 | 2849308 |
| a0003 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | MSGVV others(376): Show |
chr7 | 2723105 | 2849308 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1143 | 298 | 71 | 54 | 118 | 13 | 40 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 | ||
| a0001c0002 | 0/0 | 1143 | 11 | 11 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 | ||
| a0001c0003 | 0/0 | 1143 | 5 | 0 | 0 | 5 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 | ||
| a0001c0004 | 0/0 | 1143 | 5 | 3 | 1 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 | ||
| a0001c0007 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 | ||
| a0002c0006 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 | ||
| a0003c0005 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | ATGTC others(1138): Show |
chr7 | 2723105 | 2849308 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4365 | 83 | 27 | 21 | 22 | 2 | 11 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0002 | 0/0 | 4369 | 67 | 11 | 14 | 27 | 7 | 8 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0003 | 1/1 | 4369 | 56 | 0 | 5 | 35 | 2 | 12 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0004 | 0/0 | 4369 | 18 | 1 | 11 | 1 | 2 | 3 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0005 | 0/0 | 4369 | 10 | 0 | 0 | 10 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0006 | 0/0 | 4369 | 10 | 5 | 1 | 3 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0007 | 0/0 | 4365 | 9 | 0 | 0 | 8 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0008 | 0/0 | 4369 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0009 | 0/0 | 4369 | 4 | 0 | 0 | 4 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0010 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0011 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0012 | 0/0 | 4369 | 3 | 0 | 0 | 3 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0014 | 0/0 | 4369 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0015 | 0/0 | 4369 | 2 | 0 | 0 | 0 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0016 | 0/0 | 4369 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0018 | 0/0 | 4369 | 2 | 1 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0019 | 0/0 | 4365 | 2 | 0 | 0 | 0 | 0 | 2 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0020 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0021 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0022 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0023 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0024 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0025 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0027 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0028 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0029 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0030 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0031 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0032 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0033 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0034 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0001t0035 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0002t0001 | 0/0 | 4365 | 11 | 11 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4360): Show |
chr7 | 2723105 | 2849308 |
| a0001c0003t0002 | 0/0 | 4369 | 5 | 0 | 0 | 5 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0004t0013 | 0/0 | 4369 | 3 | 3 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0004t0017 | 0/0 | 4369 | 2 | 0 | 1 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0001c0007t0003 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0002c0006t0026 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| a0003c0005t0002 | 0/0 | 4369 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | CTCGG others(4364): Show |
chr7 | 2723105 | 2849308 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0020 | 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 |
| a0001c0001t0003g0037 | 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 |
| a0001c0001t0003g0041 | 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 |
| a0001c0001t0003g0047 | 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 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0003g0167 | 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 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0011g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0012g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0014g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0015g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0016g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0018g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0018g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0019g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0019g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0021g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0022g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0023g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0024g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0025g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0027g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0028g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0029g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0030g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0031g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0032g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0033g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0034g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0001t0035g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0013g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0017g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0001c0004t0017g0266 | 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 |
| a0002c0006t0026g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| a0003c0005t0002g0257 | 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 | g0152 | EUR | GBR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | GBR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | FIN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0092 | EUR | FIN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0309 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0307 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00741 | hp1 | a0001 | c0004 | t0017 | g0265 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0308 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0315 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | 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 | t0004 | g0301 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01109 | hp1 | a0001 | c0001 | t0024 | g0073 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0313 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01192 | hp2 | a0001 | c0001 | t0018 | g0275 | AMR | PUR | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | 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 | t0004 | g0304 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0303 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0261 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0302 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0305 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01884 | hp1 | a0001 | c0001 | t0020 | g0048 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0159 | 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 | t0001 | g0028 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02056 | hp1 | a0001 | c0001 | t0007 | g0069 | 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 | t0002 | g0258 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02129 | hp2 | a0001 | c0001 | t0023 | g0039 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CDX | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02258 | hp1 | a0001 | c0001 | t0025 | g0288 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0311 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0160 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0319 | AMR | PEL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0162 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02523 | hp1 | a0001 | c0001 | t0021 | g0109 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02602 | hp2 | a0001 | c0001 | t0019 | g0024 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0161 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0300 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02717 | hp2 | a0001 | c0001 | t0028 | g0182 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0049 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02735 | hp1 | a0001 | c0001 | t0019 | g0023 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02818 | hp2 | a0001 | c0004 | t0013 | g0285 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0298 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02896 | hp2 | a0001 | c0004 | t0013 | g0286 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02922 | hp1 | a0001 | c0004 | t0013 | g0287 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02965 | hp2 | a0001 | c0001 | t0016 | g0272 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02970 | hp2 | a0001 | c0001 | t0034 | g0297 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0184 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0268 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0271 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03139 | hp1 | a0001 | c0001 | t0027 | g0284 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0317 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0273 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03453 | hp2 | a0002 | c0006 | t0026 | g0170 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0169 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0318 | AFR | ESN | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03540 | hp2 | a0001 | c0001 | t0018 | g0276 | AFR | GWD | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0299 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0306 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0137 | 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 | t0002 | g0229 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04115 | hp2 | a0001 | c0001 | t0015 | g0150 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0133 | SAS | BEB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | 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 | g0097 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0070 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | YRI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18906 | hp2 | a0001 | c0001 | t0033 | g0125 | AFR | YRI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0063 | 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 | t0002 | g0232 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18956 | hp1 | a0001 | c0001 | t0012 | g0277 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18956 | hp2 | a0001 | c0001 | t0009 | g0096 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18960 | hp1 | a0001 | c0001 | t0009 | g0089 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18960 | hp2 | a0001 | c0001 | t0032 | g0129 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18974 | hp1 | a0001 | c0001 | t0030 | g0181 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18979 | hp2 | a0001 | c0001 | t0012 | g0278 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0037 | 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 | t0002 | g0257 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0016 | 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 | t0001 | g0128 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18992 | hp1 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19004 | hp2 | a0001 | c0001 | t0009 | g0091 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19005 | hp1 | a0001 | c0001 | t0012 | g0279 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0237 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19012 | hp1 | a0001 | c0001 | t0009 | g0082 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19030 | hp1 | a0001 | c0001 | t0035 | g0296 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19043 | hp1 | a0001 | c0001 | t0031 | g0254 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19056 | hp1 | a0001 | c0001 | t0007 | g0283 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | 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 | t0002 | g0227 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0235 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19076 | hp1 | a0001 | c0001 | t0022 | g0019 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19076 | hp2 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0238 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ASW | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ASW | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20752 | hp1 | a0001 | c0004 | t0017 | g0266 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0262 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0214 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0264 | EUR | TSI | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20905 | hp2 | a0001 | c0001 | t0015 | g0149 | SAS | GIH | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0274 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0316 | AFR | MSL | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0269 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0310 | AFR | USA | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA21309 | hp1 | a0001 | c0001 | t0029 | g0213 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | LWK | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0165 | REF | REF | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0100 | REF | REF | GNA12_chr7_2723105_2849308 | GNA12 | chr7 | 2723105 | 2849308 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0029 | 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 | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(17): 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 | a0001c0001t0027 | 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 | a0001c0001t0016 | 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 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0015 others(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 | a0001c0001t0012 | 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 | a0001c0001t0030 | 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 | a0001c0004t0013 | 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 | 11 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(8): 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 | a0001c0001t0015 | 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 | 11 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(8): 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 | a0001c0001t0032 | 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 | a0001c0001t0027 | 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 | a0001c0001t0014 a0001c0001t0031 a0001c0001t0034 |
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 | a0002c0006t0026 | 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 | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(19): 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 | 12 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(9): 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 | a0001c0001t0023 | 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 | 20 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(17): 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 | a0001c0001t0019 | 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 | a0001c0001t0010 a0001c0001t0011 |
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 | a0001c0004t0017 | 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 | a0001c0001t0009 | 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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0033 |
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 | a0001c0001t0018 | 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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(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 | a0001c0001t0020 | 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 | a0001c0001t0024 | 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 | a0001c0001t0007 | 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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(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 | a0001c0001t0031 | 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 | a0001c0004t0013 | 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 | a0001c0001t0005 | 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 | 10 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(7): 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 | a0001c0001t0008 | 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 | a0001c0001t0014 a0001c0001t0034 |
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 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0034 others(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 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0034 others(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 |
| view | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0018 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0002g0224 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0289 a0001c0001t0004g0313 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0316 a0001c0001t0011g0317 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0035g0296 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(254): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): 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 | a0001c0001t0003g0041 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0002t0001g0099 | 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 | a0001c0001t0001g0029 | 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 | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(254): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): 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 | a0001c0001t0003g0016 | 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 | a0001c0001t0001g0282 a0001c0001t0002g0222 |
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 | a0001c0001t0010g0273 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0003g0016 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
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 | a0001c0001t0004g0313 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0008g0274 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0003g0071 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 237 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(234): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0024g0073 | 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 | a0001c0001t0005g0088 | 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0012g0278 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0011g0316 | 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 | a0001c0001t0016g0272 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0179 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0179 a0001c0001t0004g0299 others(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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0033g0125 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0057 | 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 | a0001c0001t0011g0318 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0273 a0001c0001t0033g0125 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0002t0001g0099 | 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 | a0001c0001t0002g0007 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0078 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(129): Show |
133 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(130): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0005g0114 | 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 | a0001c0001t0019g0023 a0001c0001t0019g0024 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0157 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0009 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0252 | 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 | a0001c0001t0007g0068 | 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 | a0001c0001t0002g0262 a0001c0001t0007g0064 |
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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0206 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0001t0003g0062 a0001c0001t0003g0084 a0001c0001t0003g0152 others(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 | 3 | a0001c0001t0003g0092 a0001c0001t0003g0123 a0001c0001t0003g0147 |
3 | HG00280.hp2 HG03927.hp1 NA19068.hp2 |
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 | a0001c0001t0003g0095 a0001c0001t0003g0167 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0004t0013g0285 | 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 | a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0016g0271 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0016g0272 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0106 a0001c0001t0032g0129 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0003g0079 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0077 a0001c0001t0003g0122 others(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 | 12 | a0001c0001t0003g0041 a0001c0001t0003g0062 a0001c0001t0003g0084 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01934.hp1 others(9): 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 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0280 others(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 | a0001c0001t0006g0005 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0153 a0001c0001t0001g0255 others(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 | 201 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0006g0192 others(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 | a0001c0001t0025g0288 a0001c0004t0013g0285 a0001c0004t0013g0286 others(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 | a0001c0001t0003g0016 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0027g0284 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0002g0218 a0001c0001t0005g0246 |
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 | a0001c0001t0008g0160 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0002g0191 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0008g0268 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0011g0316 a0001c0001t0011g0317 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0005g0114 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0033 a0001c0001t0003g0040 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0264 a0001c0002t0001g0098 a0001c0002t0001g0099 others(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 | a0001c0003t0002g0227 a0001c0003t0002g0236 a0001c0003t0002g0237 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0005g0042 a0001c0001t0005g0045 |
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 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0007g0070 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0027g0284 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0108 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0216 a0001c0001t0002g0219 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0211 a0001c0001t0002g0215 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0107 | 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 | a0001c0002t0001g0121 a0001c0002t0001g0141 a0001c0002t0001g0142 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0011 a0001c0001t0002g0264 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0216 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0090 | 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 | a0001c0001t0004g0312 | 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 | a0001c0001t0010g0183 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0002g0256 a0001c0001t0002g0259 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0016g0272 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0003g0075 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0153 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | 72 | a0001c0001t0003g0012 a0001c0001t0003g0016 a0001c0001t0003g0020 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(69): 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0107 a0001c0001t0003g0199 |
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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0023g0039 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0002g0206 a0001c0001t0002g0224 a0001c0001t0002g0225 others(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 | a0001c0001t0012g0277 a0001c0001t0012g0279 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0203 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0148 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0024g0073 | 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 | a0001c0001t0006g0192 a0001c0001t0006g0193 a0001c0001t0006g0194 |
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 | a0001c0001t0003g0047 a0001c0002t0001g0098 a0001c0002t0001g0118 others(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 | a0001c0001t0003g0047 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0003g0047 | 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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0003g0079 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0085 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0001c0001t0002g0290 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0010g0003 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0027g0284 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0007g0151 a0001c0001t0007g0283 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0051 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | 90 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(87): 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 | a0001c0001t0002g0239 a0001c0001t0002g0260 a0001c0001t0002g0261 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0018 a0001c0001t0011g0298 |
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 | a0001c0001t0002g0007 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0024g0073 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0010g0003 | 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 | a0001c0001t0002g0242 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0006g0194 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0004g0314 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0003g0122 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0004g0300 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0002g0007 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0023g0039 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0184 others(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 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0184 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0018g0275 | 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 | a0001c0001t0018g0275 | 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 | a0001c0001t0018g0275 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0007g0067 a0001c0001t0007g0151 a0001c0001t0007g0283 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0002g0250 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0003g0154 | 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 | a0001c0002t0001g0099 | 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 | a0001c0002t0001g0099 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0002t0001g0099 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0312 others(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 | a0001c0002t0001g0098 a0001c0002t0001g0118 a0001c0002t0001g0119 |
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 | a0001c0001t0002g0251 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0289 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0005g0025 a0001c0001t0005g0189 |
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 | a0001c0001t0018g0275 | 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 | a0001c0001t0035g0296 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0217 | 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 | a0001c0001t0011g0316 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0041 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0159 a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0024g0073 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0004t0013g0287 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0018g0275 a0001c0001t0018g0276 a0001c0001t0025g0288 others(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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0116 | 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 | a0001c0004t0017g0265 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0153 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0173 a0001c0001t0002g0248 a0001c0001t0002g0249 others(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 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0003g0035 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0001g0159 a0001c0001t0002g0009 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0002g0247 | 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 | a0001c0001t0003g0016 a0001c0001t0003g0038 a0001c0001t0003g0071 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0024g0073 | 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 | a0001c0001t0003g0032 a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0024g0073 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0159 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0036 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0148 |
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 | a0001c0001t0003g0032 | 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 | a0001c0001t0003g0038 | 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 | a0001c0001t0007g0068 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0003g0133 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0159 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0007g0065 a0001c0001t0007g0069 a0001c0001t0007g0070 |
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 | a0001c0001t0001g0294 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0215 others(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 | a0001c0001t0004g0312 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0029g0213 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0024g0073 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0084 | 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 | a0001c0001t0002g0240 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0159 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0143 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0001c0001t0002g0290 others(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 | a0001c0001t0004g0302 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0224 a0001c0001t0010g0003 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0226 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0004g0313 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0094 others(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 | a0001c0001t0007g0069 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0002g0008 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0008g0160 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0038 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0025g0288 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
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 | a0001c0001t0010g0183 a0001c0001t0010g0273 a0001c0001t0011g0316 others(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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0188 | 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 | a0001c0001t0003g0136 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0159 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0250 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0007g0070 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0014g0161 | 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 | a0001c0001t0002g0233 | 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 | a0001c0001t0001g0159 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0202 others(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 | a0001c0001t0012g0277 a0001c0001t0012g0278 a0001c0003t0002g0237 others(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 | a0001c0001t0002g0220 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0051 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0159 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0038 a0001c0001t0003g0071 others(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 | |||||||
| chr7:2757574 | G | A | 1 | a0001c0001t0002g0215 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0159 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): 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 | a0001c0001t0002g0243 | 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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0226 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0028g0182 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0024g0073 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0002g0206 others(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 | a0001c0001t0002g0212 a0001c0001t0003g0034 a0001c0003t0002g0236 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0003g0084 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0103 a0001c0001t0001g0128 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0006g0006 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0030g0181 | 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 | a0001c0001t0025g0288 | 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 | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(165): Show |
170 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(167): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0051 | 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 | a0001c0001t0003g0084 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0008g0274 | 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 | a0001c0001t0008g0274 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | 72 | a0001c0001t0001g0163 a0001c0001t0003g0012 a0001c0001t0003g0016 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(69): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0006g0184 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0172 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0003c0005t0002g0257 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0204 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0002g0248 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0003g0122 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0002g0211 | 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 | a0001c0001t0019g0024 | 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 | a0001c0001t0031g0254 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0010g0273 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0035g0296 | 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 | a0001c0001t0002g0009 a0001c0001t0002g0173 a0001c0001t0002g0202 others(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 | a0001c0001t0003g0095 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0031g0254 | 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 | a0001c0001t0001g0051 a0001c0001t0006g0185 |
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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0002g0263 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0006g0184 others(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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0033g0125 | 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 | a0001c0001t0033g0125 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0113 | 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 | a0001c0001t0006g0005 | 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 | 21 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(18): 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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0052 others(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 | a0001c0004t0013g0287 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0289 a0001c0001t0008g0274 a0001c0001t0025g0288 |
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 | a0001c0001t0018g0275 | 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 | a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0018g0276 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0014g0161 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0016g0271 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0016g0272 | 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 | a0001c0001t0001g0171 a0001c0001t0003g0124 a0001c0001t0008g0267 others(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 | a0001c0001t0001g0178 a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0002g0206 a0001c0001t0002g0224 a0001c0001t0002g0225 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0004g0313 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0024g0073 | 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 | 8 | a0001c0001t0001g0163 a0001c0001t0003g0041 a0001c0001t0003g0075 others(5): Show |
8 | NA18975.hp1 NA18977.hp1 NA18984.hp1 others(5): 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 | a0001c0001t0020g0049 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0002g0247 a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0031g0254 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0004t0013g0286 | 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 | a0001c0001t0002g0242 | 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 | a0001c0001t0003g0077 a0001c0001t0003g0078 a0001c0001t0005g0025 others(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 | a0001c0001t0001g0282 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0010 a0001c0001t0002g0204 a0001c0001t0003g0081 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0003c0005t0002g0257 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0224 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0002g0222 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0095 others(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 | a0001c0001t0001g0057 a0001c0001t0007g0067 a0001c0001t0007g0151 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0031g0254 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0011g0317 | 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 | a0001c0001t0003g0016 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0004t0017g0265 | 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 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0006g0006 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0005g0083 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0220 | 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 | a0001c0001t0008g0274 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0108 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0030g0181 | 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 | a0001c0001t0004g0313 | 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 | a0001c0001t0024g0073 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0010g0003 | 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 | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(311): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0001c0001t0002g0290 others(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 | a0001c0001t0031g0254 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0033g0125 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0037 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0005g0042 | 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 | a0001c0001t0002g0247 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0020g0049 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0027g0284 | 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 | a0001c0001t0006g0006 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0014g0162 | 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 | a0001c0004t0017g0266 | 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 | a0001c0004t0017g0265 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0002t0001g0118 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0273 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0003g0154 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0030g0181 | 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 | a0001c0001t0030g0181 | 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 | a0001c0001t0003g0092 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0002g0248 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0209 | 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 | a0001c0001t0002g0211 a0001c0001t0002g0215 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0002t0001g0119 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0247 a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): 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 | a0001c0001t0023g0039 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0034g0297 a0002c0006t0026g0170 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0018g0276 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0006g0005 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0038 a0001c0001t0003g0071 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0002g0206 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0003g0020 a0001c0001t0022g0019 |
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 | a0001c0001t0023g0039 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0006g0005 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0003g0084 | 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 | a0001c0001t0006g0006 | 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 | a0001c0001t0007g0065 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0027g0284 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(301): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): 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 | a0001c0001t0003g0077 a0001c0001t0003g0078 a0001c0001t0003g0122 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0146 |
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 | a0001c0001t0004g0312 | 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 | a0001c0001t0001g0002 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0031g0254 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0247 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0003g0033 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0033 a0001c0001t0003g0040 |
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 | a0001c0001t0002g0247 a0001c0001t0008g0160 a0001c0001t0008g0267 others(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 | a0001c0001t0003g0033 a0001c0001t0003g0040 |
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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0022g0019 | 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 | a0001c0001t0010g0003 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0051 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0002c0006t0026g0170 | 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 | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(313): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): 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 | a0001c0001t0003g0092 | 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 | a0001c0001t0002g0250 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0027g0284 | 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 | 8 | a0001c0001t0001g0163 a0001c0001t0003g0041 a0001c0001t0003g0075 others(5): Show |
8 | NA18975.hp1 NA18977.hp1 NA18984.hp1 others(5): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0007g0069 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0218 | 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 | a0001c0001t0015g0149 a0001c0001t0015g0150 |
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 | a0001c0001t0003g0093 a0001c0001t0003g0147 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0140 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0005g0083 a0001c0001t0005g0088 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0146 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0006g0005 | 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 | a0001c0001t0022g0019 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0022g0019 | 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 | a0001c0001t0022g0019 | 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 | a0001c0001t0022g0019 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0002g0206 a0001c0001t0002g0224 a0001c0001t0002g0225 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0010g0183 a0001c0001t0010g0273 a0001c0001t0011g0298 others(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 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0004g0314 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0030 |
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 | a0001c0001t0003g0076 | 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 | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(313): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): 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 | a0001c0001t0004g0300 a0001c0001t0004g0312 a0001c0001t0004g0313 others(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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 others(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 | a0001c0001t0001g0090 a0001c0001t0010g0003 a0001c0001t0010g0183 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0006g0269 | 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 | a0001c0001t0006g0270 | 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 | a0001c0001t0004g0303 a0001c0001t0004g0306 |
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 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0311 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0313 others(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 | a0001c0001t0004g0307 a0001c0001t0004g0309 a0001c0001t0004g0310 others(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 | a0001c0001t0004g0308 | 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 | a0001c0001t0004g0304 | 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 | a0001c0001t0010g0273 a0001c0001t0011g0317 |
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 | a0001c0001t0010g0183 | 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 | a0001c0004t0017g0266 | 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 | a0001c0001t0010g0003 a0001c0001t0011g0298 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0028g0182 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0216 a0001c0001t0002g0231 a0001c0001t0002g0232 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0003t0002g0227 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0190 a0001c0001t0002g0203 others(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 | a0001c0001t0002g0173 a0001c0001t0002g0191 a0001c0001t0002g0202 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0033g0125 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(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 | 7 | a0001c0001t0001g0117 a0001c0001t0003g0041 a0001c0001t0003g0075 others(4): Show |
7 | HG01433.hp1 HG01884.hp1 HG03834.hp1 others(4): 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 | a0001c0001t0001g0107 a0001c0001t0001g0177 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0172 a0001c0001t0003g0033 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0102 a0001c0001t0003g0034 a0001c0001t0007g0069 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0060 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0094 a0001c0001t0003g0076 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0038 a0001c0001t0003g0071 others(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 | a0001c0001t0023g0039 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0003g0137 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0006g0184 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0007 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0015g0149 a0001c0001t0015g0150 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0209 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0002g0258 | 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 | a0001c0001t0007g0064 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0027g0284 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0002g0112 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0105 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0148 a0001c0001t0002g0216 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0050 others(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 |
31 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0030 others(28): Show |
32 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(29): 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 | a0001c0001t0001g0010 a0001c0001t0001g0140 a0001c0001t0002g0202 others(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 | a0001c0001t0002g0210 a0001c0001t0002g0214 a0001c0001t0002g0240 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0239 a0001c0001t0002g0260 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0209 a0001c0001t0002g0212 others(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 | a0001c0001t0029g0213 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0004g0299 a0001c0001t0016g0271 a0001c0001t0027g0284 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0033g0125 | 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 | a0001c0001t0003g0077 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0002g0263 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0019g0023 a0001c0001t0019g0024 |
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 | a0001c0001t0003g0138 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0003g0136 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0035g0296 | 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0012g0278 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0316 a0001c0001t0011g0317 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0016g0271 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0006g0269 a0001c0001t0006g0270 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0002g0191 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0228 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0001g0094 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0029 others(69): Show |
74 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(71): 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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0172 a0001c0001t0003g0016 others(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 | a0001c0002t0001g0026 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0117 a0001c0001t0002g0112 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0006g0005 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0006g0269 a0001c0001t0006g0270 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0176 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0006g0169 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0003g0062 | 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 | a0001c0001t0006g0192 a0001c0001t0006g0193 a0001c0001t0006g0194 others(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 | a0001c0002t0001g0141 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0050 | 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 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
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 | a0001c0001t0019g0023 a0001c0001t0019g0024 |
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 | a0001c0001t0001g0140 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0216 a0001c0001t0002g0219 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0002g0239 | 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 | a0001c0001t0015g0149 a0001c0001t0015g0150 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0062 | 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 | a0001c0001t0001g0085 | 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 | a0002c0006t0026g0170 | 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 | a0001c0003t0002g0227 | 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 | a0001c0001t0007g0069 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0063 a0001c0001t0003g0062 |
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 | a0001c0001t0001g0144 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | 10 | a0001c0001t0001g0163 a0001c0001t0003g0041 a0001c0001t0003g0075 others(7): Show |
10 | HG02965.hp2 HG03098.hp2 NA18975.hp1 others(7): 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0006g0006 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0148 |
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 | a0001c0001t0003g0166 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0015g0149 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0015g0149 a0001c0001t0015g0150 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0022g0019 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0015g0150 | 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 | a0001c0001t0001g0074 a0001c0001t0024g0073 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0018g0276 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0276 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0002c0006t0026g0170 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0008g0274 | 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 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0001c0001t0002g0290 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0103 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(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 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0206 a0001c0001t0002g0263 a0001c0001t0010g0273 others(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 | a0001c0001t0011g0318 a0001c0001t0014g0161 |
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 | a0001c0001t0010g0003 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0008g0274 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0077 a0001c0001t0003g0078 a0001c0001t0003g0122 |
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 | a0001c0001t0003g0081 | 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 | a0001c0001t0003g0081 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0010g0273 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0027g0284 | 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 | a0001c0003t0002g0236 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0018g0275 | 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 | a0001c0001t0006g0269 a0001c0001t0006g0270 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0025g0288 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0002g0217 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0033g0125 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0002g0242 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0016g0272 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0312 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0060 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | |||||||
| chr7:2793013 | G | A | 5 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0168 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0010 a0001c0001t0010g0003 a0001c0001t0010g0183 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0018g0275 | 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 | a0001c0001t0018g0275 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): 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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0158 a0001c0001t0014g0161 a0001c0001t0014g0162 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0117 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0117 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0003g0081 | 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 | a0001c0001t0001g0116 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0002c0006t0026g0170 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0005g0189 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0004t0017g0266 | 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 | a0001c0001t0005g0042 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0273 a0001c0004t0013g0285 others(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 | a0001c0001t0008g0274 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0004g0303 a0001c0001t0004g0304 a0001c0001t0004g0307 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0061 others(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 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
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 | a0001c0001t0004g0314 | 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 | a0001c0001t0001g0022 a0001c0001t0014g0161 a0001c0001t0014g0162 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0103 others(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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0153 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0002g0293 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0016g0271 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0002g0216 a0001c0001t0002g0231 a0001c0001t0002g0232 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0143 others(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 | a0001c0001t0008g0268 | 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 | a0001c0001t0002g0264 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0008g0160 | 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 | a0001c0001t0001g0171 a0001c0001t0003g0043 a0001c0001t0003g0047 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0107 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0031 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0228 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0004g0303 a0001c0001t0004g0304 a0001c0001t0004g0307 others(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 | a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0003g0097 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0003g0033 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0316 a0001c0001t0011g0317 |
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 | a0001c0001t0003g0152 | 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 | a0001c0001t0004g0307 a0001c0001t0004g0308 |
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 | a0001c0001t0001g0010 | 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 | a0001c0001t0004g0314 | 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 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0007g0069 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0016g0271 others(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 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0006g0192 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0060 others(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 | a0001c0001t0002g0264 | 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 | a0001c0001t0001g0111 a0001c0001t0021g0109 |
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 | a0001c0001t0002g0242 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0002g0229 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0024g0073 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0113 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0003g0081 | 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 | a0001c0001t0018g0275 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0002g0210 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0002c0006t0026g0170 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0002g0216 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0003g0147 | 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 | a0001c0001t0009g0082 a0001c0001t0009g0089 a0001c0001t0009g0091 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0095 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0016g0271 a0001c0001t0016g0272 a0001c0001t0018g0275 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0103 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0003g0012 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0031g0254 | 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 | a0001c0001t0002g0218 | 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 | a0001c0001t0007g0067 a0001c0001t0007g0151 a0001c0001t0007g0283 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0002g0256 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0168 a0001c0001t0004g0299 others(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 | a0001c0001t0004g0309 a0001c0001t0004g0310 a0001c0001t0010g0183 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0143 a0001c0001t0002g0007 others(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 | a0001c0001t0020g0048 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0005g0080 a0001c0001t0005g0114 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0003g0034 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0018g0276 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0175 | 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 | a0001c0002t0001g0120 | 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 | a0001c0001t0010g0003 a0001c0001t0010g0273 a0001c0004t0017g0265 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0159 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0273 a0001c0001t0014g0161 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0016g0272 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0061 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0008g0267 a0001c0001t0008g0268 a0001c0001t0008g0274 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0273 a0001c0004t0017g0265 others(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 | a0001c0001t0008g0274 | 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 | a0001c0001t0005g0088 | 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 | a0001c0001t0007g0064 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0007g0068 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0003g0081 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0016g0272 | 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 | a0001c0001t0004g0310 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0183 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0014 | 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 | a0001c0004t0017g0266 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0024g0073 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0273 a0001c0004t0017g0265 others(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 | a0001c0001t0002g0242 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0317 others(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 | a0001c0001t0011g0316 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0090 a0001c0001t0033g0125 |
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 | a0001c0001t0003g0075 | 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 | a0001c0001t0004g0301 a0001c0001t0004g0302 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0003g0020 a0001c0001t0022g0019 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0028g0182 | 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 | a0001c0001t0003g0062 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0204 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0004g0299 | 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 | a0001c0001t0002g0173 a0001c0001t0002g0248 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0051 a0001c0001t0006g0185 |
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 | 2 | a0001c0001t0003g0164 a0001c0001t0003g0166 |
2 | NA18977.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.310-17354G>A | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2812497 | |||||||
| chr7:2812589 | A | G | 1 | a0001c0001t0002g0250 | 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 | 43 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0052 others(40): Show |
43 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(40): 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 | a0001c0001t0001g0011 a0001c0001t0001g0146 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0117 a0001c0001t0006g0005 a0001c0001t0007g0068 others(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 | a0001c0001t0001g0002 a0001c0001t0007g0067 a0001c0001t0011g0298 |
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 | a0001c0001t0001g0110 a0001c0001t0004g0313 a0001c0001t0007g0066 |
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 | a0001c0001t0007g0065 | 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 | a0001c0001t0004g0311 | 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 | a0001c0001t0006g0006 a0001c0001t0006g0270 |
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 | a0001c0001t0004g0310 a0001c0001t0006g0269 |
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 | a0001c0001t0004g0302 | 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 | a0001c0001t0004g0309 | 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 | a0001c0001t0004g0299 a0001c0001t0004g0308 a0001c0001t0004g0319 |
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 | a0001c0001t0004g0301 | 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 | a0001c0001t0004g0303 a0001c0001t0004g0306 a0001c0001t0004g0307 |
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 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
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 | a0001c0001t0004g0300 a0001c0001t0006g0184 |
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 | a0001c0001t0004g0305 a0001c0001t0006g0169 |
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 | a0001c0001t0004g0312 | 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 | a0001c0001t0004g0304 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0050 a0001c0001t0003g0201 a0001c0001t0010g0003 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0208 a0001c0001t0030g0181 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0133 a0001c0001t0003g0134 a0001c0001t0003g0135 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0005g0042 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 a0002c0006t0026g0170 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0024g0073 | 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 | a0001c0001t0024g0073 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0030g0181 | 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 | a0001c0001t0002g0216 a0001c0001t0002g0231 a0001c0001t0002g0232 others(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 | a0001c0001t0001g0002 | 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 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0003g0012 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0030g0181 | 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 | a0001c0001t0003g0016 a0001c0001t0003g0071 a0001c0001t0003g0076 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0034 a0001c0001t0003g0133 a0001c0001t0008g0160 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0018g0275 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0016g0272 a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0002g0250 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0016g0272 | 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 | a0001c0004t0017g0266 | 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 | a0001c0001t0028g0182 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0095 others(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 | a0001c0001t0001g0094 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0002c0006t0026g0170 | 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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0016g0272 a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0051 a0001c0001t0006g0185 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0207 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0314 | 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 | a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0008g0268 | 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 | a0001c0001t0004g0302 | 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 | a0001c0001t0001g0168 | 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 | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(311): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): 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 | a0001c0001t0001g0111 a0001c0001t0021g0109 |
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 | a0001c0001t0002g0216 a0001c0001t0002g0251 a0001c0003t0002g0235 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0012 a0001c0001t0016g0272 |
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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0010g0003 | 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 | a0001c0001t0003g0097 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0074 a0001c0001t0024g0073 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0153 a0001c0001t0001g0255 |
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 | a0001c0001t0003g0043 | 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 | a0001c0001t0002g0243 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0247 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0009 a0001c0001t0002g0202 a0001c0001t0002g0239 others(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 | a0001c0001t0003g0033 a0001c0001t0003g0040 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0016g0272 a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0008g0274 | 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 | a0001c0001t0010g0003 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0075 | 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 | a0001c0001t0002g0009 | 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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0027g0284 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0003g0133 a0001c0001t0003g0134 a0001c0001t0003g0135 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0002 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0011g0298 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0202 | 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 | a0001c0001t0003g0095 | 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 | a0001c0001t0007g0070 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0031g0254 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0027g0284 a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | |||||||
| chr7:2819891 | A | G | 1 | a0001c0001t0027g0284 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0005g0046 | 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 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0004g0303 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0011g0298 a0001c0001t0011g0316 a0001c0001t0011g0317 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0111 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0002g0209 | 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 | a0001c0001t0002g0209 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0005g0042 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0003g0097 a0001c0001t0003g0174 a0001c0001t0003g0186 |
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 | a0001c0001t0005g0246 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0190 | 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 | a0001c0001t0028g0182 | 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 | a0001c0001t0003g0062 | 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 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0060 others(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 | a0001c0001t0033g0125 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0071 a0001c0001t0003g0123 a0001c0001t0003g0124 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0051 a0001c0001t0006g0185 |
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 | 100 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
100 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(97): 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 | a0001c0001t0002g0009 a0001c0001t0002g0173 a0001c0001t0002g0190 others(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 | a0001c0001t0030g0181 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0146 others(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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0032 | 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 | a0001c0001t0002g0009 a0001c0001t0002g0173 a0001c0001t0002g0190 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0005g0246 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0008g0274 a0001c0001t0010g0273 |
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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0020g0048 a0001c0001t0020g0049 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0006g0005 a0001c0001t0006g0006 a0001c0001t0028g0182 |
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 | a0001c0001t0001g0180 a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0008g0274 | 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 | a0001c0001t0004g0301 a0001c0001t0004g0302 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0008g0274 | 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 | a0001c0001t0007g0151 a0001c0001t0007g0283 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0003g0152 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0003g0113 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 |
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 | a0001c0001t0002g0264 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0018g0276 | 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 | a0001c0001t0027g0284 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0004g0315 | 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 | a0001c0001t0003g0166 | 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 | a0001c0001t0002g0247 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0031g0254 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0025g0288 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0003g0047 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0005g0042 a0001c0001t0005g0045 a0001c0001t0005g0046 |
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 | a0001c0001t0001g0294 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0173 a0001c0001t0002g0248 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0173 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0001g0158 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0006g0185 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0187 a0001c0001t0001g0280 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0033 a0001c0001t0003g0040 |
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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0032 a0001c0001t0003g0033 others(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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0004g0299 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0008g0160 | 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 | a0001c0001t0002g0256 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0030 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0122 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0025g0288 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
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 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0167 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0002g0190 | 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 | a0001c0001t0003g0154 | 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 | a0001c0004t0017g0265 a0001c0004t0017g0266 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0002g0009 a0001c0001t0002g0155 a0001c0001t0002g0156 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
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 | a0001c0001t0008g0274 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0206 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0005g0025 | 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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0033g0125 | 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0018g0275 a0001c0001t0018g0276 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0027g0284 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0003g0020 a0001c0001t0022g0019 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
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 | a0001c0001t0006g0269 a0001c0001t0006g0270 a0001c0001t0008g0160 others(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 | a0001c0001t0003g0133 a0001c0001t0003g0134 a0001c0001t0003g0135 others(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 | a0001c0001t0006g0184 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0140 a0001c0001t0006g0184 a0001c0001t0006g0269 others(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 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0031g0254 | 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 | a0001c0002t0001g0142 | 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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0017 a0001c0001t0005g0189 a0001c0001t0006g0184 others(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 | a0001c0001t0003g0147 a0001c0001t0004g0299 a0001c0001t0004g0300 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0016 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0010g0183 a0001c0001t0011g0298 a0001c0001t0011g0316 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0011g0298 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0005g0189 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0025g0288 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0185 a0001c0001t0006g0269 others(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 | a0001c0001t0001g0011 | 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 | a0002c0006t0026g0170 | 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 | a0001c0001t0027g0284 a0001c0004t0013g0285 a0001c0004t0013g0286 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0015g0149 a0001c0001t0015g0150 |
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 | a0001c0001t0008g0160 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0002c0006t0026g0170 | 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 | a0001c0001t0007g0151 a0001c0001t0007g0283 |
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 | a0001c0001t0001g0010 | 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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0002g0256 a0001c0001t0002g0258 a0001c0001t0002g0259 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0301 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0185 a0001c0001t0006g0269 others(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 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
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 | a0001c0001t0003g0152 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0016g0271 a0001c0001t0016g0272 |
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 | a0001c0001t0002g0293 | 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 | a0001c0001t0011g0298 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0014g0161 a0001c0001t0014g0162 a0001c0001t0034g0297 |
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 | a0001c0001t0006g0185 | 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 | a0001c0001t0002g0262 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0003g0154 | 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 | 4 | a0001c0001t0001g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(1): Show |
4 | NA18977.hp1 NA18984.hp1 NA19001.hp2 others(1): 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 | a0001c0001t0001g0255 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0158 | 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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0159 | 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 | a0001c0001t0002g0263 | 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 | a0001c0001t0006g0184 a0001c0001t0006g0185 a0001c0001t0006g0269 others(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 | a0001c0001t0006g0184 a0001c0001t0006g0185 a0001c0001t0006g0269 others(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 | 4 | a0001c0001t0001g0163 a0001c0001t0003g0164 a0001c0001t0003g0166 others(1): Show |
4 | NA18977.hp1 NA18984.hp1 NA19001.hp2 others(1): 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 | a0001c0001t0011g0318 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0303 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0008g0274 a0001c0001t0010g0003 a0001c0001t0010g0273 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0171 a0001c0001t0001g0255 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0029 others(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 | a0001c0001t0010g0003 a0001c0001t0010g0273 |
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 | a0001c0001t0034g0297 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0255 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0255 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0010g0003 a0001c0001t0028g0182 |
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 | a0001c0001t0008g0274 a0001c0001t0025g0288 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0255 a0001c0001t0002g0007 others(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 | a0001c0004t0013g0285 a0001c0004t0013g0286 a0001c0004t0013g0287 |
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 | a0001c0001t0002g0264 a0001c0001t0008g0267 a0001c0001t0008g0268 others(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 | a0001c0001t0010g0273 | 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 | a0001c0001t0010g0273 | 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 | a0001c0001t0010g0273 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0255 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0255 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0255 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0255 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0255 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0006g0269 a0001c0001t0006g0270 a0001c0001t0016g0271 others(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 | a0001c0001t0011g0316 a0001c0001t0011g0317 a0001c0001t0011g0318 |
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 | a0001c0001t0006g0184 a0001c0001t0006g0185 |
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 | a0001c0001t0006g0269 a0001c0001t0006g0270 a0001c0001t0016g0271 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0255 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0280 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0003g0186 |
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 | a0001c0001t0001g0255 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0012g0277 a0001c0001t0012g0278 a0001c0001t0012g0279 |
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 | a0001c0001t0001g0255 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0255 a0001c0001t0002g0190 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0007g0283 a0001c0001t0027g0284 a0001c0004t0013g0285 others(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 | a0001c0001t0025g0288 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0294 | 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 | a0001c0001t0004g0319 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.309+79C>T | GNA12 | ENSG00000146535.14 | transcript | ENST00000275364.8 | protein_coding | 1/3 | chr7 | 2843774 |